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Lori Jacobs
Date: Dec 2024
Diagnosis: Autoimmune Disease (Scleroderma)
Jacob’s Testimonial
Back in 2009 or 2010, I began facing serious health challenges. I was diagnosed with cancer in several areas of my body, and eventually with scleroderma—an autoimmune disease related to lupus and arthritis, both of which run in my family. It felt like my body was shutting down, and the conventional treatments just weren’t helping. I tried to stay hopeful, but deep down, I knew I needed a different approach.
At first, I followed the doctors’ recommendations. I went through chemotherapy and medications like Cytoxan, and took other prescriptions from UCLA. But the side effects were overwhelming, and I didn’t feel like I was making progress. That’s when I met a nurse who understood integrated health. Her knowledge and encouragement opened the door for me to explore alternative therapies—and that changed everything.
I first heard about Poly-MVA in 2009, of all places, at my veterinarian’s office. I was there with my rescue dog Samantha, who had cancer. An integrative vet introduced me to Poly-MVA, and I remember another pet owner there telling me how it helped his labrador, who had been given only two weeks to live—but went on to thrive for much longer.
That was all the inspiration I needed. I started giving Poly-MVA to Samantha, and soon after, began taking it myself. I started with two teaspoons a day, and now I take one teaspoon daily. It’s helped me in so many ways—my energy came back, my appetite improved, and I truly believe it played a major role in my remission.
It’s also become part of my wider wellness circle. My ex-husband, who lives with diabetes, high blood pressure, and struggles with weight, now takes Poly-MVA too. And most recently, I started giving it to our dog, Kida, who was diagnosed with hemangiosarcoma. Her prognosis wasn’t good, but since taking Poly-MVA, she’s become more energetic and playful again. It’s been incredible to see.
Poly-MVA has been nothing short of a miracle for me. It’s easy to take, has a mild taste, and has given me hope during my hardest moments. I just wish it were more affordable so more people and pets could experience its benefits.
I’m 66 now, and I thank God every day that I found Poly-MVA, I give full permission for you to share my story. This is my journey—everything I’ve been through, and everything I’ve learned along the way.
Gene Johnson
Date: August 8, 2009
Diagnosis: Bladder Cancer
Personal story
On 8/8/09 after cutting grass on a riding lawn motor for 2 hours I went to urinate and was passing blood. I went to my regular Doctor and he immediately made an appointment to Dr. Lange of urology group of Fort Smith. After they scooped my bladder they found a massive cancerous tumor in my bladder.
The next day I was in surgery to remove it. They could not get it all for fear of getting in to the bladder wall. A month later they went back in to surgery with success; two months later one more time to clear it up again. They suggested a chemo treatment for the bladder.
In the meantime I became acquainted with Dr. Jerry Vin who lived across the street from US. I started on Poly-MVA as recommended. I did not take the chemo treatment! I have had periodic exams every 3 months, then six months. It has not reoccurred!
For the last 6 months I am now using poly mva in a maintenance dose every day. I am so pleased to have the peace of mind that I am doing something positive for my system that through the continue maintenance program!
Thank you Amarc Enterprises and your cancer research program,! I am 75 years and still alive.
Gene
Angelo Stefanelli
Date: August 2004
Diagnosis: Bladder Cancer
2 Updates 7-13-2011 – 5-5-2015
Personal story
After my bladder cancer operation in 08/04, I began taking Poly-MVA. Since that time I have being going back to the V.A. Hospital every 3 months for observation. I underwent ten B.C.G treatments, but I also took Poly-MVA and vitamins and minerals.
I have always been active and I still am. Several months ago during my exam the doctor stated that there was not even a scar where my tumor was removed. I am currently on a maintenance dose of poly-MVA. My wife also takes Poly-MVA.
Thanks,
Angelo
7-13-2011
Spoke to Angelo and his cancer is doing well…. tumor in bladder was not very deep. He will be doing more check ups. Still shares the PMVA with his wife and continues to use.
5-5-2015
Had a great talk with Angelo. He is doing very well and is cancer free. I also told him I would like to keep in touch and call him and update his testimonial. He said he was more than willing.
Dr. Carl F. Gugino
Date: February, 2011
Diagnosis: Bladder Cancer
3 Updates 5-13-15 – 6-10-16 – 1-14-17
Personal story
I was diagnosed with bladder cancer in February 2011. I had a tumor removed from my bladder in March 2011. I started all alternative medical treatments in April 2011. I have been and continued to take poly-MVA.
I recently had some cancer cells in my urine, so I had a biopsy and it came back negative for malignancy or dysplasia, with no deep muscle invasion. I underwent 6 weeks of BCG treatment which I just completed.
I will continue to take poly-MVA because I feel it has helped me. I was originally told I would need to have my bladder removed. As of today, 2 years later, I still have my bladder!
Thank you,
Dr. Carl F. Gugino
5-13-2015
Dr Gugino had surgery and refused any further targeted therapies. He went to Hope For Cancer where Poly was part of his treatment protocol. He has been on Poly ever since and is now over 3 years cancer free and continues to take 1 tsp daily. He is 86 years old and continues to do some international teaching and is flying to Japan for 3 weeks as of next week. He and his wife come out to Rancho La Puerta everything Thanksgiving.
6-10-16
Dr. Gugino is traveling a lot. He is on his way to Japan. Doing well.
1-14-2017
Doctor is still taking daily maintenance dose.
Marjorie Delin
Date: January 2004
Diagnosis: Bladder
Personal story
To Whom It May Concern: September 20, 2005
I would like to share with you my remarkable journey of healing from bladder cancer using PolyMVA. In January of 2004 I noticed blood in my urine. After a Urologist determined the cause was a large tumor, he told me it needed to be removed and biopsied. I was operated on Jan. 14th, 2004 and the biopsy showed it was stage 4 level 4 Bladder cancer. The surgeon suggested removing my bladder, uterus and vagina in a 12 hour operation which would leave me with a bag and would be a dangerous operation for me at 86 years old, especially since I would still need chemo afterwards.
My daughter, a certified acupressurist, had heard about PolyMVA through a publication in the mail and after researching it, I decided to try it instead, along with other natural supplements given to me by my holistic chiropractor. I began using it on 2/24/04, taking 2tsp 2 times a day, then increased it to 2 tsp 4 times a day on 3/7/04.
After 3 months of this regime an exam revealed the tumor was back, and again the Dr. suggested the operation plus chemo to save my life. I decided to seek a second opinion and the other Urologist said he wouldn’t want to do such extensive surgery on an 86 yr old woman, He recommended a low dose of chemo, which I began on 6/9/04 with 2 drugs, Cisplatim and Gemzar having them every two weeks, finishing the last treatment on 10/5/04 (9 treatments in all). I never lost my hair and had few side effects except a couple days of nausea and fatigue following each treatment.
When the Urologist looked in my bladder, all that was left of the large tumor was a small piece of tissue which he removed where the tumor had been. He and the Oncologist were very pleased with how well the chemo did the job. (I believe it was the combination of it and the Poly). He recommended I do more chemo until all cells in the wall of the bladder were gone. At that time, I decided to just do the Poly and supplements, since I was experiencing some shortness of breath/weakness from the accumulation of chemo at that time.
After doing only Poly for 3 months I received a report that the CT scan showed no tumors or growths, so I cut back on the Poly (1 tsp 3x/a day). The next CT scan 3 months later showed some lymph nodes that were enlarged in my groin and a couple other areas, so I increased the Poly back to 2 tsp 4 times a day and started taking CoQ10 with each dose.
My last CT scan in August 05 showed those lymph nodes were “no longer active/growing” and had shrunk, therefore I did not need further chemo. The Urologist did find a small finger nail sized growth which he removed to prevent it from spreading, however no further activity in any other areas. They will continue to monitor me with regular CT scans and bladder scopes every 3 months.
I feel Poly is a powerful antioxidant and has been a valuable resource which has helped me heal to this point. I will continue to take it and my other supplements (CoQ10, Coral Calcium, Liver Support etc.) and I thank God for his guidance in this direction and leading me to this wonderful supplement!
Sincerely,
Marge Delin
Nancy Farley
Date: August 19, 1999
Diagnosis: Bladder Cancer
E-Mail: nfhaven@comcast.net
8 Updates 6-27-01 - 1-20-03 - 2-20-04 - 1-26-07 - 1-3-09 6-03-10 – 5-06-15 – 11-15-17
Personal story
August 19, 1999
Dear Dr. Sanchez,
Thank you for giving me the opportunity to share my journey in fighting this most dreaded disease. I am a 65 year old Psychologist who in 1996 was diagnosed with bladder cancer. A transurethral resection was followed by periodic cystoscopy examinations at Emory Hospital, Atlanta, Georgia. By patient preference, I chose not to undergo suggested chemotherapy. I remained asymptomatic until December 1998 when laboratory studies revealed active cancer again. I had the Arthur Malignancy Index or AMID test performed which showed a large tumor mass; The Smith Kline Laboratory panels revealed an NK Cell count of 2, clearly indicative of immune system degeneration. This test was performed several times to rule out erroneous results.
William Crawford, a naturopath, was my physician. Dr. Crawford was on staff at the Oasis Hospital in Baja, California. I followed the nutritional protocol developed for me by Dr. Crawford, which included using Poly-MVA twice daily. At this time I am doing well as evidenced by the laboratory reports I have received, and, more importantly, by the way I feel.
The Poly-MVA has done remarkable things to my immune system with repeated AMID tests showing an excellent rating of "GOOD;" Recent NK numbers are now at an amazing level of 59. Tests also show a diminished tumor mass in me. I am faithfully continuing complimentary and/or alternative healthcare.
I have been very pleased with the results obtained by taking Poly-MVA used in conjunction with Clodronate. My energy level has soared and has sustained at the point I was 4 years ago. My total program includes proper nutrition, exercise and a positive spiritual understanding that life is a gift from God, to be used wisely. It is my desire and prayer to encourage and inform others, with special emphasis on Poly-MVA. Nancy C. Farley, Ph.D
2nd UPDATE - June 27, 2001
Dear Tim,
It was good of you to pursue and persist and push for this update. Part of the delay was my desire to have the most recent chemical Lab tests in hand to further substantiate the good work of Poly. So here goes: For several months now I have been talking on the phone with a number of you who are vitally interested in PolyMVA, either for yourselves or someone you love and care for. I trust this update will serve as encouragement and incentive to give PolyMVA continued opportunity to do it's unique work.
In 1996 I put aside plans to open a counseling center in the Atlanta area. It took several months after cancer was diagnosed to recuperate from a transurethral resection of the bladder. The immune system was severely compromised, and pneumonia persisted. By patient preference, I did not have the suggested chemotheraphy or radiation, but chose to embark on an intense search to find well documented, well tested alternative treatments for cancer. It did not take long to find Al Sanchez who was fully prepared to explain and substantiate why PolyMVA was excellent in building up and supporting the entire immune system. For extended periods, PolyMVA was a defined part of my prevention protocol. However, during my husband's illness, my system became weakened. An elevated count of cancer cells was found again last December. With Al Sanchez's encouragement, I went back on a heavy program of PolyMVA, and thank God, I am now considered to be in remission. All the lab work is within normal range, and balance has been regained. It takes work, determination and persistance to maintain the battle against cancer.
PolyMVA has been the the foundation for my ongoing treatment of cancer. "It is THE super, free-radical scavanger and extremely powerful antioxident" which I believe has helped to bring me to this chapter of remission. I continue to take a maintenance dosage of PolyMVA daily, and am pleased with my energy level. In fact I have had no further lung infections or pneumonia which plagued me for several months after my dear husband died last year. It is a noteworthy that good nutrition is essential for continued good health, so I am careful to choose the right diet. As you all know, it takes special care to get enough rest and exercise.
Above all, I am thankful to God for an extended time period in which to fulfill the dream my husband and I began to put together in early 2000. It was our prayer and desire to open a retreat center in the mountains north of Atlanta, with the main purpose of providing a place for patients to come who had been given diagnoses of cancer. Tender care can be provided at this Christian Retreat called The Haven, to help individuals deal with levels of fear, anger and denial. Family members who need support and guidance from understanding counselors can be taught to cope more effectively With renewed courage and strength, The Haven is becoming a reality.
As you continue your own courageous journey, remember we are doing much more than just surviving, We are learning to be thriving in body, soul and spirit with God's help! I pray you will be blessed, and I have been, by all that is experienced in living fully while He lends us breath.
Nancy Farley
3rd UPDATE- January 20, 2003
It is especially meaningful for me to share that the sixth year post diagnosis of bladder cancer report is excellent. The latest medical examination found "the bladder to be normal with smooth walls with no abnormalities, no lesions seen and no areas or erythema appreciated." In layman’s terms, this means I am still free of tumors with no sign of cancer. The specialist repeated verbatim his statement from last year that he was both pleased and surprised. "It is very unusual for your type of cancer not to reappear.You are my only patient that has experienced this." When I reminded him of Poly MVA, he remarked, "Whatever you're doing, just keep it up." I smiled saying " My times are in God's hands, and I've got a good plan going."
My maintenance dose of PolyMVA, is still in order, taking 1/2 teaspoon morning and 1/2 teaspoon evening. Much of my continued energy level I owe to Poly, ever grateful there has been no recurrence of pneumonia or flu for the past two years. In the absence of my beloved Carl who died July of 2002 of liver cancer, I must choose to keep positive, choose to keep disciplined, choose to keep planning proper nutrition and exercise. I must to create fun times, including a coveted art class and strengthen bonds with friends. All of this combines to give a good measure of "inner and outer strength" for hours of counseling and teaching which I love, and development of The Haven, a Christian Retreat Center in the beautiful Georgia mountains. This is some retirement program!
No doubt other survivors have found, as have I, that there is an exquisite balance we must seek. Continued care of ourselves must not lead to selfish preoccupation, or morbid introspection. But, with God's help, we who have responded well to PolyMVA can offer solid information to others who may still be confused and doubting. Accurate, timely sharing allows for God to reveal creative ways for each of us to live life more fully and love more clearly. It's our choice. Let's rejoice!
4th UPDATE: February 20, 2004
I am going to have tests repeated in March, and will happily send you a current update. At this time I am strong, well and wonderfully busy in the ministry of counseling. I still go one week to Birmingham, 3 l/1 hrs away where I counsel about 21 people in the 3 days there. Then I go to North Carolina to see cancer patients, an autistic child and several other dear folk the next week. I do telephone counseling and office counseling here in Atlanta; the cup...AND saucer are full. It's an unusual package God has put together, but I love it.
There is a "keeping power of God" which encircles those of us who trust Him. May you be very aware of His Presence this day May His love guide you as you reach many, many travelers on this journey. Love in Him, Nancy Farley nfhaven@comcast.net
5th UPDATE: May 12, 2004
Tim, Greetings!! I'm delighted to let you know the latest Lab Reports show excellent levels and a strong Immune System. These just came in yesterday, so I'm thanking the Lord I have good news to pass on. A Black Field Microscopy test in January showed slight cancer activity, but that also is now reduced. I waited until now to give the latest and most accurate report.
I am continuing the protocol of Poly maintenance of 1/2 teaspoon AM and PM along with the supplements that keep me in good health. I came thru a flu attack in January which lasted only days instead of the usual debilitating 4 weeks. I attribute this to Poly which provides an excellent defense against such infections.
In a few weeks I will be celebrating my 70th! I asked the Lord to give me more life in my years, and not just years to my life, and He has. I am full of energy and working strong and steady in the counseling ministry.
Hope all is well with you and Al. Please give him a "fuerte abrazo" from me.
Cordially, Nancy Farley
6th UPDATE: July 17, 2004
Hello Tim, I'm excited about the upcoming Convention since this year I really have a testimonial that continues to amaze me. The newest Lab Reports and even the Osteoporosis report are well within normal range, signifying good maintenance and positive progress.
My medical friends, which are many, are still shaking their heads. One MD who is the main Breast Cancer Surgeon on staff at the YUB Hospital in Birmingham can't reckon with the fact I did not submit to his knife, but am coming up with excellent Lab reports and no cancer cells evident!
I thank the Lord daily for His healing thru the Poly protocol and just keep taking on God's assignments in counseling ministry wherever he opens the doors.
Special greetings to Al,
Nancy Farley
7th UPDATE: January 26, 2007
This is an update on January 26, 2007 for Nancy Farley PhD Bladder Cancer Survivor in remission for 6 years. Thank you for your call asking for an update. I have been waiting to contact you until I received the latest Cancer Report. I just finished the yearly Cystoscopy Exam last week and the Dr has declared again I am cancer free. Hallelujah!! Several other tests he took also came in showing no Cancer cells at all! So I am passing along good news, and thanking God for His watchful healing.
I still get 1 to 2 calls weekly, asking for support or info and I gladly pass on what Poly has done for my cancer levels. I remain a loyal supporter!
In Him, Nancy Farley
8th UPDATE: July 3, 2009
Nancy Farley PhD---Nancy called today to report that she had a scan of her bladder this past March 2009 and her bladder continues to be totally cancer free. Her Oncologist told her that she is his only bladder cancer patient in 25 years that has not had a recurrence. She is beating all of the odds. Nancy was diagnosed in 1996. She started on Poly-MVA in 1998 and has been in complete remission from bladder cancer since 1999. Nancy feels that Poly-MVA is the primary reason she is alive and well. She continues taking 1 teaspoon daily for maintenance. She still receives many calls regarding her story and refers them on to Poly-MVA. She also continues to thank God for Poly-MVA, Dr. Sanchez, Tim, Gary and all of those involved in this wonderful protocol.
6-03-2010
Nancy had delayed to respond because today was her 6 month check up. The Doctor told her all is clear and she continues to be cancer free after 14 years. She had surgery but refused chemo and radiation. She has continued her healthy diet and takes Poly every day.
5-06-2015
Nancy sold her home in Woodstock in august of 2014. I called Dr. Crawford and he told me she was just dx with Parkinson's. He will let her know I would love to talk to her.
11-15-2017
I reached Nancy on her cell phone. Had a great talk. She wanted to know about Dr. Al and how Poly was doing. She has Parkinsons and wondered if Poly could help.
George Holliday MD
Personal story
“I have been fighting bladder cancer since July 4, 1972, with many recurrences. Regular doses of chemotherapy went on for several years, with multiple hospitalizations for various procedures. Finally, I began to tire of the chemo and decided to investigate other possibilities on the internet. In 2003 after speaking with Cardiologist Dr. Steven Sinatra who was prescribing and using PolyMVA for his cardiovascular patients is when I discovered Poly-MVA. After discussion with Gary Matson and Dr. Garnett, the decision was made. I began taking Poly-MVA in March 2003, and in October my urine lab test came back NEGATIVE…meaning I was in remission. PolyMVA was the only thing I added to a basic supplement routine. I started low at 1 teaspoon per day and got to 10 teaspoons. Stayed on that higher dose for 6 months and I was feeling great! I have continued to take small doses 2 to 4 teaspoons of Poly-MVA since then, and my annual urine tests have remained negative, thus continual remission. I will take Poly-MVA for the remainder of my life. I am now 76 and plan to live to the 90s with God’s blessing!”
– George E. Holladay, MD Passed away peacefully April 5, 2013 at the age of 87
C. Piazza
Date: April 2016
Diagnosis: Gliomatosis Cerebri Tumors * Extensively infiltrative diffuse glioma cells
1 Update 6-29-2020
Personal story
In April of 2016 during a usual Saturday AM, I began to have double vision. I sat on the floor as I was also afraid I was going to fall. I then could feel my heart start to race. My husband then took my blood pressure and although I don’t remember the number it was alarming enough for us to immediately go to the ER as I never had high blood pressure.
Upon arrival at the ER I told the admitting staff that I thought I was having a stroke. The Dr. immediately ruled out a stroke but decided to do a CT scan as there clearly was a reason for my symptoms. The CT scan came back and it was clear that I had a very large mass on my occipital lobe. However, it was difficult to see what it was so a MRI was ordered. When we got the MRI results we could see a large mass on my occipital lobe that had grown tentacles that literally infiltrated themselves throughout most of my brain.
I told the neurologist that I obviously don’t know anything about reading MRI’s but that didn’t look good. She confirmed and told me it wasn’t good. The hospital discharged me but made an appointment so I could meet with a neurosurgeon in Philadelphia. This surgeon was at a conference so I couldn’t get in for a little over a week.
When we got home my husband went to US News and World Reports to research the best neuro dr’s/hospitals in the country and made appointments and travel plans. I appreciated this as I wanted to meet with as many Dr’s as I could and learn everything about this disease. So far, all I knew was it was a astrocytoma.
I had many meetings but the overall consensus was this disease by definition was gliomatosisis cerebri as it was an extensively infiltrative diffuse glioma involving at least three lobes. I never had a biopsy so the grade was unknown.
At first it appeared to be low grade because I was not having any symptoms, there was not any enhancement and at first it looked to be slow growing. I learned that when a glioma has this type of migratory behavior patients have a much worse prognosis than patients with diffuse gliomas of corresponding grades. Basically the grade was not relevant when it got to this point.
I asked every surgeon and oncologist I met if there was a chance of a cure/remission or even the possibility to extend my life? The answer was always no on all accounts.
I did learn that the benefit of treatment is prolonged progression free survival but not overall survival. I decided this wasn’t going to be the route for me as I didn’t want my immune system busy recovering from treatments but rather support my immune system to focus on this large mass that invaded my brain. Perhaps if there was any chance in improving overall survival I might have thought differently. I did a cost benefit analysis and decided to do nothing else but routine scans after my initial consults.
At first things were smooth sailing. I went back to work and life as usual and was just starting to believe I just might be able to live with this disease but in December of 2016 things started to change drastically. I had violent episodes of vomiting multiple times per day, I was passing out and I started having visual, smell and taste hallucinations.
All of these symptoms caused fatigue that I never could have imagined. I was sleeping most of the day. I was asleep for many more hours than I was awake. I literally lost all concept of time. It was not a surprise to be that the tumor was now starting to enhance. Although the rest of the tumor didn’t grow the enhanced part was growing. I was also starting to become convinced the contrast was contributing to my problems and the potential malignant transformation of my tumor.
I had one more scan in February of 2017 and became violently ill and haven’t been back to see a Dr or have a scan. I saw enough patients in the waiting rooms and met many patients and caregivers online and knew I would never receive any treatments.
I decided to focus on this disease and treat it as a mitochondrial metabolic disease based on professor Seyfried’s book Cancer as a Metabolic Disease. This is how I found Poly MVA.
The first thing I noticed was how much more energy I had. I was no longer sleeping all day and didn’t worry about where I was going to be when the fatigue hit as there was no way of staying awake when this happened. The increased energy and ability to focus was profound and a life changer. I was feeling so guilty as I was literally not the mother or wife I wanted to be.
We went to Boston this summer for a week and I forgot my Poly. All of my previous symptoms reoccurred. It got so bad that at one point my husband was begging me to go to the ER. I declined but on the way home we decided I’m never going to ever stop taking POLY for the rest of my life.
Don’t ever underestimate the Power of Poly! I’m so convinced of it’s safety and efficacy I’ve started my family on a maintenance dose.
Thank you!
Carrollann
Lynn Rivers
Date: October 8, 2009
Diagnosis: Meningioma (Benign)
E-Mail: not available
My Poly-MVA Story
I have a recurrent Benign Meningioma. My first surgery was in 1993. I had a second surgery for recurrence in 1998. Between those two surgeries I had regular follow-up scans. After the second surgery I declined to have any further scans. My reasoning was that if I was feeling fine; I preferred to just go about my life.
In April of 2008 I decided to have another scan as I had been having some "twinging" in my head on occasion. That scan revealed yet another recurrence adjacent to the previous site. The concern this time was that the recurrence was on the motor strip in my brain. A good friend of mine was participating in the Poly-MVA study. After reading the booklet on Poly-MVA and how it works in the cell I decided that I wanted to be in the study. My thought was that any tumor benign or cancerous constitutes abnormal cells and therefore the poly should work the same for me as it would for someone with cancer. I started the protocol on November 1st 2008. I am soon to finish my one year participation in the study. My last MRI scan was this past April.
What was encouraging to me was that this scan showed absolutely no change from the scan the year before. Meningioma is a slow growing tumor. Between the first two surgeries when I was scanned every 3 months during the year prior to surgery number two they were able to detect continued growth of the tumor. So, the fact that there was no change for a whole year said to me that the tumor is not growing. I have not experienced anything that I would call a symptom since I've been on the poly. No change in extremity strength, balance or function of any kind. My surgeon knows that I tend to be conservative as to how I manage my situation and therefore recommended that I have another scan in 18 months. That means that 1 year from this month (Oct. 09) I'll have another MRI. I intend to stay on poly-mva daily as a maintenance program and even though I'm done with the study I fully intend to contact AMARC as to the results of my next scan. I expect those results to be no change seen. Thank you! Lynn
Larry Puckett
Date: January 2007
Diagnosis: Glioblastoma Stage IV
3 Update 5-13-13 – 4-08-14 – 3-01-18
Personal story
I was diagnosed with stage 4 glioblastoma in Jan 2007. I recently had an MRI. It showed that nothing has changed as of 10/29/09. I have had good results since I have been taking poly-mva. I have been on it almost three years.
I feel much better when I take polymva. My doctor told not to change anything I am doing because my MRI showed nothing was growing. Thanks for Polymva.
Larry Puckett
5-13-2013
I am working every day like I did before cancer. I work at a food store during the day, farm and ranch after that. My Doctors are calling it a miracle to just be alive.
Poly-MVA deserves a lot credit. If it was not for Poly-MVA, I don’t think I would be doing this well. In fact, I just got married.
Larry
4-08-2014
I talked to Larry’s wife, Peggy. She said Larry is doing well but working late. They just celebrated their one year anniversary last Sunday. She will let him know that I called.
3-01-2018
Spoke to Larry. He is doing well and continues to take Poly MVA.
Jim Storc
Date: February 13, 2007
Diagnosed: Thanksgiving night, 2003
Diagnosis: GBM4 Brain Tumor
Email: jcstorc@ameritech.net
2 Updates 2-08-2010 - 1-29-20019
Date Started Poly-MVA: January '04
Dosage Amount: started at 8 tsp a day. Now at 1 tsp a day
Personal story
My Poly-MVA Story...as written by my wife, Cindy It was Thanksgiving night, 2003, after a wonderful time with family, that Jim had a Grand Mal Seizure. I was sound asleep when I heard the crash as he fell to the floor. We have led a very charmed life and I had never seen anyone in that condition before. I didn't know what was happening as I called 911, held onto Jim and begged God to spare his life. He came to as the rescue squad arrived and he was so confused. I remember being thankful it wasn't a heart attack...little did I know at that time but our life was going to be turned upside down.
While sitting in the car waiting for the rescue squad to leave I made some phone calls to ask friends to start praying. I was blessed when I pulled up to the hospital and Jim's brother was waiting for me. My sister in law had gone in with the ETM's. She is in the medical profession and held our hands through out the whole thing. When I got to Jim he looked fine...a little tired but I thought wow, they are going to check him out and we'll be able to go home. He went home a week in a half later minus a piece of his brain.
The diagnosis was GBM...glioblastoma multiforme which is a grade 4 brain tumor. His surgery was on December 3rd, 2003. We were told to enjoy our Christmas together because it would probably be our last. Jim never believed them but I felt my whole world was falling apart. Twenty people came over right after his surgery to pray over him and anoint him with oil. That was the beginning of my prayer chain and my link to sanity. I asked people to pray as I searched on line for survivors and alternative treatments.
He took one chemo pill as I read the warnings to him. We both were in shock as we read them. I called our family doctor and he called the oncologist who said they didn't really have any good statistics on the Temodar. I asked if he would give it to his wife and he said no.
Well, that was that. I needed to find something fast. Jim was 2 weeks out of surgery and on his way to 6 weeks of radiation followed by the rotating gamma. I spent day and night researching what other survivors were doing and put together a protocol that I could only pray would work. I spent a month on the computer and realized my anxiety issues stemmed from all the reading I was doing...so many were dying...I couldn't take it anymore. I decided I needed to move on but what if I missed that magic pill?
I gave it one more shot praying that if I missed something it would show up and low and behold PolyMVA showed up. I can't remember how it happened but there it was. I had never seen it before but it was here now. I did some research on the poly and I emailed people. They wrote back with wonderful testimonies and Jim decided he would give it a try.
He continued to have seizures, his left side getting weaker and weaker. As summer progressed they got worse. Jim went to a neurologist for an adjustment on the seizures meds and the doctor was horrible. He basically said it was back and if it wasn't it would be. He sent us on our way with a handful of anti depressants saying he would need them. We got into the car and cried.
On the way home, we decided we didn't have to believe him. He spent all of 5 minutes with us and decided Jim's life was over....no way! This was in August '04.
Jim was still having seizures and his neuro-surgeon said he thought they were caused by edema from radio-necrosis. We had planned a 3 week camping trip in September and had a wonderful time but I could see Jim was going down hill. September 21, '04 MRI came back slight thickening therefore a PET scan was ordered for 10/7. In the mean time he started dropping things and his speech was slurred. He was dragging his leg and his eyes looked blank. They kept increasing his Decadron and he would appear to get better only for a short time.
On 10/11 he had a really bad seizure in the morning...the worst since his grand mal 10 months earlier. That afternoon he had a double whammy grand mal in our pickup. He almost didn't make it. Here we are again in ER waiting...always waiting! The surgeon said it was back. The PET had come back showing no cancer activity but the surgeon didn't agree. Oct. 18th, 2004 another surgery but it was 98% necrosis(DEAD TISSUE) and they couldn't identify the remaining 2 %.
It has been a rough road and after the 2nd surgery things didn't look good but here he is 3+ years later. Still tumor free! He never quit running his business, rides his bike (weather permitting) 20-30 miles 4-5 days a week. He skis, goes white water rafting....in general is living a very healthy life.
Jim with his Family during their Ski Trip to Breckenridge, Colorado in February 2007 We believe prayer, PolyMVA along with diet change and other nutritional support were key to Jim's survival. As of 2/13/07 Jim's MRI's continue to come back cancer free. The only problems he has ever had were caused by radiation damage.
Cindy Storc
UPDATE: February 8, 2010
Friends, Most of you don't realize but we have come back to IL for Jim's MRI. He had his tests today and saw the Dr. and again his tests all came back clear. We are feeling very blessed and very happy. He is now over 6 years tumor free.
Six years ago we couldn't see any further then the end of the day and now we talk about our future. I know I have said it before but again, thank you for your support and prayers over the years.
We are loving Colorado and spending time with our beautiful little grand daughter. It has been great to come "home" and see friends and family but are looking forward to getting back to our new home. We should be back some time next summer for Jim's next MRI. Again, thank you for caring and love to all,
Jim and Cindy
1-29-2019
Wow, I can't believe it has been so long since I last updated Jim's journey! This is January 29th 2019. I never thought I would have my dear husband still with me. The Dr's. were not encouraging us...very little hope given. It has now been 15 years...NO recurrence.
GBM is not a death sentence! In 2013 we had a Neurologist say she didn't believe the dx because he shouldn't be alive. She thinks they made a mistake in the dx even though we had so much proof of the dx!
In 2014 we moved to Ecuador for 3 years. Had the time of our lives making wonderful friends and having amazing adventures. Moving back to the states in 2017 we decided to become full time RVer's. Now we are living a whole new adventure. The first year back we put on over 30,000 miles driving around the country and Canada.
At 63 years of age Jim has a very positive attitude about his life. He is riding his bike 15-20 miles a day,. loves spending time with family and friends and finding new adventures around every corner.
Over the years he has lived his life to the fullest. Skiing, whitewater rafting, biking, hiking, camping.... We are so thankful for God's many blessings on us, for answered prayers and for all the support we have had through out the last 15 years. Thank you! Cindy, wife of Jim
Daniel Morrison
Date: September 21, 2003
Diagnosis: Astrocytoma/Glioma
E-Mail: dennysbutton@gmail.com
Phone: 775-781-9191
Daniel's Testimonial
Dear Survivors:
On January 29, 2002 our son, Daniel Morrison, was walking through the house holding onto his right arm like he had had a stroke. It was limp and he told me, "Mommy, my arm doesn't work anymore." I was beside myself. My fiancee', EZ, had noticed that Daniel's arm wasn't right a couple of weeks prior but I did not want to see it. I had been taking Daniel to his pediatrician during that previous year because he was falling down a lot, having bilateral knee pain, and limping on his right side sometimes. I got all kinds of answers except what it really was.
On Jan. 30, 2002 We took Daniel in and the doctor said that he wanted us to see a neurologist. This was going to take 2-3 weeks. I told the doctor that I would not leave the office until we were sent somewhere for someone to tell us what was wrong with our baby. Daniel was not quite 3 years old at this time. We were sent for a stat MRI at Washoe Imagining in Reno, NV at 1:00 p.m. that day. They did the MRI and told us it was a brain tumor. I turned pale and nearly fell to the floor. I knew that a brain tumor could be a possibility but quickly pushed that out of my mind.
We were sent to Sacramento, CA for an appointment with a neurosurgeon the next day. We left that night and saw the DR. the next morning. We were told that Daniel had a low grade astrocytoma and that it was most likely benign. We were told to go home for a week and return on Feb. 7, 2002 for surgery. The surgery took almost 6 hours.
When the doctor came to us after surgery, he thought that he had totally removed the tumor because it was all a purplish color and he had scraped very carefully. We were elated until the next morning when the post-op MRI showed that they had only removed approximately 20% and the remaining mass was located in his brain stem, left thalamus, and left pons.
Further surgery was no longer an option. Daniel was in the hospital for 4 days. He was put on decadron even before the surgery and remained on it after the surgery.
We went for another MRI on Mar. 26, 2002 and then back to Sacramento on Mar. 28, 2002 to see the doctor. We were still under the impression that Daniel's tumor was benign. His films were to go to the tumor board that week and we were expecting their call to see what was next.
I called on April 9, 2002 to find out results and what was taking so long. It was at this time that I was told that we were to see an oncologist for a "no big deal" consultation. We went back to Sacramento to see the oncologist on April 17, 2002 and it was a very big deal.
This is where we finally found out that Daniel did in fact have cancer. We were devastated to say the least and very angry about not being told about the cancer sooner. Our trust was very shaky at this point. We were told that Daniel needed weekly chemo for 3 years to delay radiation.
Not knowing any other alternative and not been given any other options by the doctors, I truly believed that the only way to keep Daniel alive was with chemotherapy. We scheduled surgery on April 25, 2003 to insert a portacath so he would not have to have an IV every week and they also planned to administer his first dose of chemo the same day.
We were shown first hand what we had in store for us because we were put into a room with a 7 year old that had over 100 tumors and was on the strongest chemo possible for him and he was way further advanced in his battle. This was absolutely traumatic for Daniel as well as for both of us. We were also given a 40% chance for 5 years as his prognosis. This was even more traumatic for all of us.
So this started the trips back and forth from Nevada to Sacramento every week. We almost moved there because there just was not enough money to continue going back and forth every week and our car was on its last leg.
I got Tim Matson's name from someone who was helping us financially and started to contact him and read the testimonies about the others that were on the PolyMVA and the results they were experiencing with it.
I was already constantly reading, researching, asking questions, contacting others with cancer, and going to the resources that could answer some of my questions. When I read that chemo did not even cross the blood-brain barrier and that the decadron promoted tumor growth I was really confused and lost. (See OUR INSPIRATION PAGE about THE DANGERS OF STEROIDS) It did not make sense to me to do this therapy for such a long time, Daniel having to endure all of the side effects, and me knowing that I was allowing them to poison him. After 5 rounds I listened to my heart and told the doctors that I did not want to proceed any further with the chemo.
The oncologist was flat against us stopping Daniel's treatment and did not want to be held liable. We just wanted Daniel to be a happy little boy running and playing like the rest of the kids. If he did not have a long time on this earth then we wanted him to live it free of the devastating effect that the chemo was causing. We knew it was all in God's hands anyway and we just needed to follow our hearts.
Tim Matson got back in touch with us in June and still wanted to help Daniel. He was convinced that Daniel would get better using the PolyMVA. We were willing to try anything and were already juicing and blending fruits and vegetables that were known to fight cancer and tumors daily as food and medicine. We started the Poly on July 3, 2002 with 3 teaspoons per day and since then, Daniel's MRIs have shown improvement.
At first, his tumor was actually shrinking for about 3 of his MRIs and the last two have shown the tumor as stable, no change. We have gone from 3 to 4 teaspoons per day. Tim also had us add the CoQ10 to his daily organic diet and natural supplements because it gets oxygen to the brainstem.
I was concerned about the tumor being "just stable" but then Tim told us not be concerned about the size because the color is what is most important. He told us about his mother and that their radiation oncologist had shown them how to interpret MRI's and that when the tumor appears "white" it is active and alive cancer but when it turns gray and stops growing it is necrosis.(dead cancer cells) The tumor has continued to turn darker shades of gray which is just great! We are ready to tell absolutely everyone about the PolyMVA. We have shared this news with many people already and if we can only get to one person at a time then so be it but we are spreading the word and will not stop at anything to let the other parents know there is another way, a natural, nontoxic way to help our children and our loved ones.
The cancer resource center has the information here in Carson City, Nevada and is willing to share it with others. Everytime there is a cancer function, we spread the news to all that are willing to listen and take that great step of faith.
Tim Matson and his father Gary Matson have experienced all of this first hand and they have huge hearts and compassion to help others survive the awful battle with cancer. They truly brought hope back into our lives.
We will continue to share our news with you regarding Daniel's MRIs, which are every 3 months. His next MRI is on Oct. 16, 2003 so we will stay in touch and keep spreading the news about this God-sent product.
Best Wishes,
Kelly Barnes Updated Picture September 1, 2004
Paul Weiner
Date: September 17, 2002
Diagnosis: Medulloblastoma
E-Mail: WienerTd@aol.com
3 Updates 2-12-04 – 1-14-05 – 1-08-19
Personal story
Dear Friends,
Beginning in May of 2000 my son, Paul Weiner, began vomiting in the morning unexplainably. After these symptoms became worse, we finally took him to Hershey Medical center on 7/04/00. He was diagnosed with medulloblastoma, a deadly, highly aggressive, brain tumor. He had an operation to remove his tumor the following week.
We were given two weeks to decide what post-surgery treatment option to follow. They wanted to administer chemotherapy and radiation. I wanted to search out my options, having already been predisposed to natural remedies. After searching the Internet, I came across a relatively non-toxic treatment called antineoplastons that was administered in a clinic in Houston, Texas. Antineoplastons were designed to repair the tumor cell so that it would die naturally. In stark contrast, conventional treatments were designed to kill the tumor cells, which also kills good cells thus causing serious side effects.
I soon discovered that FDA mandated that Paul must fail conventional treatment before he could enroll in the clinical trial using antineoplastons. I had no other choice at this point. No other alternative therapies held out much hope to knock out this deadly monster growing in my son's brain (I discovered that two other children with medulloblastoma had gone to Mexico to try laetrile and other treatments only to see their tumors continue to grow.).
On August 1, 2000, I enrolled my son in a clinical trial using high dose chemotherapy, in an effort to avoid radiation therapy. Paul completed this in January 2001. And thankfully he was now in remission. But I knew that medulloblastoma was a highly recurrent tumor. So I continued to look for natural products that would increase his chance of survival.
It was then I read about PolyMVA. When I learned that it also worked on the principle of fixing cancer cells so they would die naturally, I put Paul on PolyMVA in March of 2001.
He has been on it for the last 18 months. I also started Paul on high dosages of CoQ 10 when I saw that there some clinical trials that were done testing this natural substance on cancer patients with encouraging results.
Paul's MRI's(he gets them every three months) have continued to remain clear to this date (9/17/02). He is doing very well mentally and physically. Only God knows what the final outcome for Paul will be. But I have the peace of knowing that I am doing everything I can to give him the best shot of surviving.
Sincerely,
Todd Weiner WienerTd@aol.com
UPDATE: 2-12-2004
Dear Friends,
On January 9th 2004, Paul had another MRI which, thank God, was still clear. This marked the third year since Paul has finished his conventional treatments. Paul has been on the Poly almost three years now. I have used the PolyMVA and CoQ10 as a preventitive. Paul has done extremely well. We continue to want to use things that increased his chances of survival from a very deadly tumor.
Sincerely,
Todd Weiner
UPDATE: 1/14/2005
Dear Friends,
Since my last update of 2/04, Paul has had two MRI's, one in July of 2004 and one today, 1/14/05. Both of these MRI's have been clear and, of course, we are exceedingly thankful to God that he is doing so well and for every day we have with Paul. Feel free to email me with any questions or comments. Todd Weiner WienerTd@aol.com
1-08-2019
Talked to Paul’s Dad, Todd, to see how Paul was doing. Paul was dx in 2000 with Medulloblastoma the size of a golf ball. He had surgery, chemo and stem celll transplant. He was on the Poly aggressive protocol for 2 years. He is now 23 years old and cancer free. When they did his surgery to remove his tumor they nicked his pituitary gland. This stymied his growth somewhat but he is doing great and does weight lifting.
Josslyn McClung
Date: July 19, 2002
Diagnosis: Brain Stem Tumor
E-Mail: jenmcclung@juno.com
5 Updates 5-02-03 – 5-16-03 – 1-24-04 11-05-04 – 5-12-20
Josslyn's Testimonial
Our daughter, Josslyn, was 9 1/2 when she pointed out to us that her left leg had a slight shake or tremor to it. We thought it was a pinched nerve or something. A month later (Dec.11, 2001), the tremor was now in her left arm as well.
A cat scan was ordered, and it showed that she had a brain stem tumor. She was given only a 20-30 percent chance of lasting an extra 1-3 years if she did chemo/radiation. This was not a cure but a poor chance at an extension of life. She was given 4-6 months to live if we did "nothing."
Through much prayer, the Lord directed us to take her to a clinic in Tijuana, Mexico. They immediately put her on Poly-MVA (1 1/2 tsp.) plus some other things. Two weeks into the program, her double vision was gone and her coordination had greatly improved.
We were at the clinic for four weeks in January. In February, she seemed to be regressing so we put her on 5 tsp. of Poly MVA a day. We also started her on CoQ10. We found out a couple months later that this is necessary to help get the Poly-MVA to the brain stem area. God had already impressed upon us in February to start her on this after watching Dr. Sinatra's Video on PolyMVA and CoQ10.
On July 11th, Josslyn celebrated her 10th birthday! We praise God for working a miracle in Josslyn's life. No matter how many days on earth the Lord has for our Josslyn, she has already outlived the doctor's predictions. Josslyn feels great. Josslyn looks great. She is probably the healthiest she has ever been apart from the brain tumor.
To illustrate this she hasn't gotten any of the colds or viruses that other family members have circulated to each other these past months. We go once-a-month to the hospital to have her blood work done and a liver function test done. We had the first one done (since Mexico) in March.
Every thing showed normal, even her hemoglobin, white and red blood cell count. Her third MRI in May showed that the tumor was slightly smaller which meant that it was shrinking and this was all without surgery, radiation or chemotherapy. The oncologist's assistant called to ask what Josslyn was taking. They wanted to discuss her case that afternoon at their doctors meeting. When we go to the hospital to have her blood work done, she looks so healthy and the other children there on chemo look like they are so sad and feel so bad. People tell Josslyn she looks radiant, and she does. Josslyn practicing her bedside manner!
We Give God the glory for her progress but truly feel that God led us to use Poly- MVA for her. She has an excellent out look on life. She feels great.
In February we got a wheelchair for her because of the difficulty in walking long distances. Since the middle of May she has needed it less and less. The only thing that is noticeably wrong with her is that her left side is still weak. We have her in therapy, working to get those muscles working again after months of little use.
Her face muscles are no longer sagging like they were in Dec. and Jan. They have steadily improved to their normal state. We have noticed NO bad side effects from using the Poly. I hope her story will help others.
She leaves for Church Camp next week which we would never have thought possible seven months ago. We give God the glory for her progress but truly feel that God led us to use Poly-MVA for her. She has an excellent out look on life. She feels great.
In February we got a wheelchair for her because of the difficulty in walking long distances. Since the middle of May she has needed it less and less. The only thing that is noticeably wrong with her is that her left side is still weak. We have her in therapy, working to get those muscles working again after months of little use. Her face muscles are no longer sagging like they were in Dec. and Jan. They have steadily improved to their normal state. I hope her story will help others.
She leaves for Church Camp next week which we would never have thought possible seven months ago. God bless you! Jenni and Dale McClung
May 2nd 2003 (A Letter From Josslyn) Josslyn had a cat scan in Oct. 02. It showed that her tumor was relatively unchanged and that she did not have hydrocephalus. The doctors went ahead and put her on Decadron and over dosed her. They put her on 48 mg. The most she should have had is 24 mg.
The next day we felt uneasy about her being on the steroids. We called the doctor's office to have her tapered off of the medicine and found out she was over medicated. It took 2-3 weeks to get totally off the steroids. At the end of the 3rd week, we had her MRI. It showed that the tumor had grown quite a bit. (See OUR INSPIRATION PAGE about THE DANGERS OF STEROIDS) The only difference was the steroids, which we believe caused the tumor to grow. Josslyn was bed ridden from November to January 2003. In January 2003 we took Josslyn to New York City to get her tumor removed. She was originally diagnosed with an "inoperable" brain stem glioma. The New York Surgeon, Dr. Kelly, said it was an "operable" pilocytic astrocytoma.
On January 23, 2003, Josslyn had her golf ball size benign tumor removed through a computer assisted surgery that was very non-invasive. She looked better even right after the surgery. We praise the Lord for directing us every step of Josslyn's journey. She was given a ZERO percent chance of gaining use of her left hand, arm and leg that was left weak from her tumor. She has now recovered use of her left side by 90 percent!! The neuro-surgeon has never seen this happen before. I wonder if the poly had any effect on this miracle happening?
I believe that the poly helped to give us time and prolong her life long enough for us to find a cure for her. It might have healed her totally but we came to a point where we were running out of time. Josslyn is still taking 6 teaspoons of Poly- MVA for daily maintenance. We feel that it is a help to her health and overall recovery.
On April 17th, Josslyn's MRI showed that all the tumor was gone. Extensive blood tests were run and all of her markers were perfectly normal. We thank Gary Matson and Dr. Sanchez for all their support during this time. They truly care and that is why they are in this business. That cannot be said for many companies out there. God bless you all and feel free to contact us if you have any questions for us. We will also be happy to put you on our prayer list. Jenni and Dale McClung - Mailto: jenmcclung@juno.com
Postscript from Gary Matson:
I called Jenni on May 2, 2003 to see how Josslyn was doing. As soon as Jenni recognized my voice she turned the phone over to me to talk to Josslyn. This is sort of a routine for the past nearly year and a half so Josslyn and I have gotten to be pretty good friends. She said, "Gary, guess what," and I said, Tell me Josslyn. She said, "I am learning to play basketball and I can dribble with both hands."
I asked her about school and she said, "I just finished home school for this year and I get to go back to regular school in the fall. "Then after a few more words she said, "Goodbye, Gary" and was off to practice her basketball.
I was left with tears in my eyes as I remembered that she was given just a few months to live in December of 2001. Perhaps this helps everyone understand why we love our work with Poly-MVA. May 16, 2003 E-mail from Josslyn's mother, Jenni McClung
Hi Gary, Sorry it has taken so long to send this. I thought I would type it out since it is a little hard to read and the fax still isn't hooked up. I'll try to send the original by fax when I get it up and running. Noshin is a little girl in Michigan who has a tumor on the brain stem.
The authorities were trying to get a court order to make her parents (immigrants from Bangladesh) have the surgery that didn't offer much hope. They had taken Noshin (2 years old) to Canada for alternative treatment instead. We read about this on Monday 5-12-03.
I had Josslyn read the newspaper article and this is the letter I found that she had written all on her own to Noshin.
--------------------------------------- Dear Noshin,
My name is Josslyn McClung. I'm ten years old. And I had the exact same symptoms you have and I had the same thing you have. I was on Poly Mva (which stands for Minerals, vitamins, and Amino Acids). It worked until my brain tumor started growing, then a friend of mine told me about a Dr. that had done surgery on a little boy who had the same thing only I had found out the Dr. in New York looked at my M.R.I.'S And said I had a different kind. He operated on it and took it out. My eyes don't roll around, my left side is strong again and I am so happy. I thought everyone should have that kind of happiness so I got the idea to raise money to send you and your Mom and Dad to New York to have a visit with Dr. Patrick Kelly to see if he can operate.
By the way mine was smack dab in the middle of my head, and I still have all my hair. (they just shaved a little hair on my hair line). If you want to you can call me some time. You are on my prayer list. God loves you so much. Love a friend, Josslyn McClung
January 24, 2004
Hi! Just a quick note to let you know that we are fine. We just passed the one year anniversary of Josslyn's successful operation on Jan. 23, 2004. I am all too aware of what a miracle God did for our Jossy. There are so many people that we met in the clinic in Mexico that have died. There are a lot of children with brain tumors that we have heard about over the internet with brain tumors that have also died. We give God all the glory and praise for healing Jossy!!!
Josslyn has grown 4 inches in 12 months. She wears a size 7 to 7.5 in ladies shoes. She wore size 4 this time last year. She didn't grow while the tumor was there but almost immediately after surgery she started growing. She loves going to school this year. Her left side that the doctor said would stay paralyzed is 95% back to normal. Her left hand is not quite as strong as the right and she has a small limp in her walk.
Well.....that's about all for now. Thank you for all the many prayers you have prayed for our family and for Joss. We can never thank you enough or praise God enough for all He's done for us.
Love,
Jenni
November 5, 2004
No more do I feel like everything else is happening and I feel left behind. No more do I have to worry about things normal children don't have to. No more do I have to worry in the middle of the night about hospitals and medical hoosawhatsits.
No more do I have to worry about all of my friends worrying about me when everything is okay. There was TOO MUCH WORRYING! It made me mad, it made me sad. It made me ALL UP FRUSTRATED! I could've worried about those things but I knew I didn't have to.
Somehow I knew all God wanted me to do was try to be a normal kid, but not too normal. A Godly normal, but I don't have to worry about worry any more, because my awesome powerful God is in control and I thank Him for it. Now I just go to school, try to do my best and live each day as a normal kid. NO MORE!!!!!!!! written by Josslyn - age 12
May 12th, 2020 Josslyn at 27 Hi Tim. I apologize that this had taken so long. We think the world of your dad and I'm sure you do too. Josslyn was 9 when she was given 3 to 6 months to live. She started polymva the month after her diagnosis. Her tumor stopped growing for 11 months and at about the 5th month it was smaller....
Her tumor started growing again when the doctor accidentally overdosed her on steroids. It was after this we found out steroids can cause tumors to grow. 2 months later she had her tumor removed at NYU Med Center.
Josslyn has been tumor free since then. She is 27 today. A beautiful young lady with a heart for nannying young children. Family Gospel Group She has written 3 books....sings in her family's southern gospel group. She went to China twice with the people she nannies for. Thank you polymva. We truly feel polymva kept Josslyn's tumor from growing. Jenni McClung Kansas City Missouri
Mark Olsztyn
Date: Sunday, July 02, 2000 8:32 PM
Diagnosis: Oligodendro Astrocytoma IV
Email: mark.olsztyn@gmail.com
9 Updates … From 9-07-2000 ........ to 4-07-2010
Personal story
REFLECTIONS ON 15 YEARS OF BEING CANCER FREE WITH POLY MVA IN THE PRESENT MOMENT I sit on my exercise ball which doubles as my chair when I’m at my computer and I am comforted by it and by where I am. I’m 47. It’s 2012. If I had believed the grave statistics that confronted me when I was diagnosed I wouldn’t be here at all. The sun is shining over the San Francisco Bay, it’s 52 degrees here in Sausalito and to top it all off, it’s Friday! 15 years ago things didn’t look so promising. On April 7th of 1997 I underwent brain surgery for the second time in six years for a recurrent tumor. When I received the diagnosis of a GBM I knew my life had taken a radical turn away from anything I had known.
No longer could I take it for granted that I’d live to see my kids (a son at 3 months and a daughter at 25 months) grow up and maybe have kids of their own or that I would even be around for the turning of the millennium just 2 years and eight months away. This time my survival would require strong doses of radiation and chemotherapy and more than a little luck.
Fortunately, that ‘more than a little luck’ was just around the corner, both literally and figuratively. My only shred of hope in all the terror surrounding that diagnosis was my certainty that someone, somewhere had to have survived it. I only needed to hear about this person, a second or third-hand accounting would have sufficed. It would have been all I needed to not just give up the fight and surrender my body to the palliative measures prescribed by my team of doctors to extend my life a few more months, perhaps even a year or two. I asked my primary care physician, a serious and somewhat grandfatherly figure who was nearing retirement, if he had known or even heard of someone who survived this diagnosis.
Unfortunately, he said he didn’t know anyone who survived a GBM for more than a couple of years and added that I was wasting my time talking to him. I should rather, he intoned with severity, be putting my affairs in order and talking to God. The next afternoon I happened to be enjoying the company of our neighbors who had a ground floor apartment next to our building. I told them about my meeting with my PCP and how devastating his feedback had been. Almost miraculously, Dan, an affable software engineer, told me that he did, in fact, know of somebody in his home country of Romania who was still alive after ten years with a GBM. His wife, Adina, confirmed the story of this someone whose cousin’s best friend was alive and well.
This tenuous connection to a survivor, five degrees of separation, was all I needed to infuse me with rapture and great hope. I left their apartment feeling transformed and optimistic. This thing I have, it can be beaten! I knew it! I didn’t ask if I could contact this person in Romania to confirm the story. Part of me didn’t want to know if it was really true but I felt immense gratitude toward Dan and Adina for relaying that information to me at a time when I needed it to simply carry on. Not long after that my first shipment of Poly MVA arrived. My father, a homeopathic physician, sent it to me. Eight brown bottles with a sheaf of photocopied patent diagrams and other arcane information were enclosed in a small cardboard box: an arc of promise.
I followed the dosage instructions even while undergoing 33 rounds of radiation and later, throughout my chemotherapy. I still take one teaspoon per day, every day, and expect to continue with that for as long as I live. I will have taken my 10,000th teaspoon of Poly MVA when I’m 63. EPILOG Being diagnosed with a brain tumor is a terrifying experience. It takes time to simply digest the news that your life will be irrevocably altered. It doesn’t have to mean for the worse.
Cancer can make you aware how precious your time is and how important those whom you love and who love you really are. And I can attest that surviving it is equally magnificent. Nowadays, simply typing a query into your search window can reveal hundreds of cases of people beating the odds against cancer. polymvasurvivors.com is one such site containing the stories of real people, people you can reach out to and talk with for inspiration. Today’s Internet might be the most valuable tool in your arsenal against despair. What I so desperately sought 15 years ago is available now, but I know how it felt to be alone with this prognosis. That is exactly why I’m writing this. For the newly diagnosed brain tumor patient or their loved ones.
I’m here for whenever you need to talk to someone who has made it through 15 years and is still going strong. Write me an email. I’ll write you back. I’ll give you a call if that’s what you’d prefer. I won’t push Poly MVA, but I will tell you (here) that it continues to save my life and it’s entirely non-toxic and that it’s the best anti-oxidant I know of and it costs a lot less than it did when I started taking it in 1997, and that you can take it, as I did, as an adjuvant to conventional treatments and it will lessen the harm done by those treatments.
Chronological History of my Journey
Saint Patrick's Day, 1997 Saint Patrick's Day, 1997. I received the news of my recurrent brain tumor with dread and shock. It had come back after six years, almost to the day, and this time it wasn't a low grade Oligodendro Astrocytoma but a GBM. I imagined what I had before was just a mere Tyrannasaurus, now I had a head full of Velociraptors. The doctors considered my case a medical anomaly, but that was certainly no comfort. I was very despondent. I felt hopeless; the GBM support group I attended (for the first and last time in the basement of Boston's Brigham and Women's Hospital) only magnified my sense of doom.
Although the left-frontal lobe tumor was operable and was resected on April 7th using the latest surgical techniques, the prognosis remained grim. Radiation followed by PCV Chemotherapy was the prescribed post-operative therapy. When I asked the surgeon 'How long have I got to live?' he could only answer "That depends on how you respond to the therapy. We don't know. Right now, all we can do is throw everything at this and hope for the best."
I was desperate to know that somebody had survived this nightmare. My father, a doctor involved in alternative medicine, sent me my first bottle of Poly-MVA only a week after my surgery. I started taking it immediately along with the conventionally prescribed treatments recommended by my surgeon. My first post-op, post-radiation scan was on July 25th and was clean!
I relocated from Boston to Phoenix to continue with part two: chemotherapy, and to be with my family for The End, that I was sure was coming soon. In spite of my clean scan and the fact that the doctors in Phoenix downgraded my diagnosis to an Oligo 4/4 (less of an anomaly but not much less of a threat), I was still given over to the idea that it was just a matter of time before it came back to finish me off. The irony is that I was so certain of my imminent death, that I decided to stop paying taxes. You know that old saying about Death and Taxes being the only sure things in life?
Now I am paying for my doubt in Poly-MVA, but I can't say I mind it at all! I have had clean MRI scans to this day and I consider Poly-MVA - plus my belief in God's great wisdom - to be the cornerstones of my recovery. I used to associate St. Patrick's day with gloom, now I celebrate it as the beginning of my lucky streak! A new chance at life.
2nd UPDATE:
September 7, 2000
I got the results back from last night's MRI. I am still clear and clean. My neurooncologist said I may now space the scan intervals from three to four months! And to think I started out with a scan every two months... Thank You God!!
The immobilizing fear that once gripped me is beginning to lose its hold on my life. Someday, I hope to be free of it entirely. That goal is made possible for me by just two things: my Higher Power and Poly-MVA. I know this to be true.
Keeping The Faith Alive,
Mark Olsztyn
3rd UPDATE:
January 9, 2001 Hello Dear Friends and Family Members, I want to inform everyone who is near and dear to me that I have had my 16th clean scan. Yesterday confirmed what I could only hope was true, there are no changes from the last one that was done last September.
In these cases there is literally no room for "improvement," all you want is that things remain as they are, which for me means no signs of any growth. The physician I spoke with was optimistic. I just need to keep doing what I'm doing. To keep on keeping on.
Love to All
Marko
4th UPDATE:
May 9, 2001
To All Who Seek Hope I am very happy to report that I have had my 17th clean scan since my operation, in 1997, to remove a grade IV Oligodendroastrocytoma of the left frontal lobe. My doctors are very encouraged by my status and I believe that means that they think my prognosis is improved. I just can't get them to actually say that. What matters most is that I think so. I feel very confident that I will reach the ten year mark, a watershed set for me by many gloom- anddoom allopathic statisticians who informed me that only five to seven percent make it that far.
I plan on going at least another 65 years. I want to see my great-grandchildren!
Marko
5th UPDATE:
October 3, 2001
Dear Friends and Family Members,
Yesterday I received news that my latest scan, my eighteenth since my operation, was, once again, clean. I am grateful but not surprised, so I feel more joyful than elated and relieved. Somehow, this time I knew with nearly absolute certainty what the results would be before I saw them for myself.
Over the past few months, with no real concerted effort on my part, I have undergone a subtle but significant transformation that has given me real peace of mind and spirit. I can't say for sure what the catalyst for it was, I only know that I am changed. whether it lasts or not only time will tell, but I feel that I am on a clearly marked path that is leading me to something good.
I would like to acknowledge all of you who have supported me in my struggle with cancer either by praying for me or by wishing me well and thinking of me fondly. It's all good, and I thank each one of you for your contribution to my wellness. God bless you all.
Mark
6th UPDATE Scan Number 19 (February 26, 2002) was Clean (again). It gives me enormous satisfaction to report that my last MRI, performed under the full moon (it's a ritual that comforts me) in Phoenix, Arizona's Barrow's Neurological Institute, was unchanged. No sign of any abnormal growth, just a hole in the familiar gray salmon steak that is my brain when it is viewed on the lateral axis. That makes nineteen now since my operation in April of 1997. It will soon be five years since my diagnosis and I am as cancer-free as I can possibly be. I look forward to the mid-way point and to sharing my progress with everyone concerned with it.
Each day is a gift that I am grateful for, each moment is a fugwalha. -
Mark 7th UPDATE May 15, 2004 Mark and his family enjoying a visit to Heidelberg Castle. May 15, 2004." My last scan was unchanged. So similar was it to the one before and, for that matter, to the one before that and, well, all the scans since about 1998 that my doctor felt I am at the point where I can space them out to one per year. Now, unless you happen to know this man, it is difficult to describe the optimism in my prognosis that his decision conveys. He is, after all, the Chief of Neurooncology and as such doesn't often see cases like mine which go from requiring a scan every two months to one per year within the span of five years.
It was six years, almost to the day, between my first brain tumor in April of 1991 and its recurrence as something considerably more dire in April of 1997. Though, statistically, the odds are still against me I already know that I will be tumor-free this April, six years from the date of my last operation, when my wife and my two children and I will be walking on the pebbly beaches of the Côte d'Azure celebrating those three precious, God given gifts: Life, Health and Family.
Mark
8th UPDATE:
March 18, 2007
I am fast approaching my tenth year without cancer. When I consider that I barely made it past year six when I had the recurrence from which I have been recovering these past ten, I realize what a milestone awaits this extraordinary span of wellbeing and good fortune. And yet, I know that the fight is not over. Despite the prognostications we've all heard almost every week that cancer has finally been cured or that the vaccine has been discovered, it might never be over for as long as I draw breath. Knowing this has not diminished the significance of the day for me or my accomplishment. To survive ten years without a recurrence was my goal. On April 7 of this glorious year I will touch down. My most vulnerable desire will become fulfilled.
It will be a Saturday that marks my anniversary, a day preordained for celebration with family. How perfect. How roseate. How ordinary, just like any other Saturday. As monumental an event as it is to me I have to accept that it will pass without festivity or even a comment from those closest to me. It might have been different if only… (I don't know how to complete this thought.)
I have been blessed and I consider myself extremely lucky to be alive but not everything in my life is as I would like it to be. My wife, my sole partner for over half my life, wants to go her own way now. Our two children, mere infants ten years ago, have grown into two distinct adolescents with their own talents and tendencies. They have demonstrated their concern about our decision to separate but have not displayed anything like opposition to the idea.
Looking back, it is clear that the fissure lines of our relationship were the direct result of my illness. It would be impossible for me to measure the magnitude of shock Belinda felt at seeing me, her partner, a once perfectly healthy 26 year-old man, suddenly writhing in the throes of a grand mal seizure and then, just a few hours later, learning that this horrifying display was caused by a malignant brain tumor. That was in 1991 and it was only the first one, a comfortably low-grade oligo. We were both much more resilient back then. Our ability to withstand and recover from this difficulty would be tested over the next six years until the day we both were informed that it had come back. By that time we were married and I was working full time.
Josephine, the first of our two children, prompted our hasty union in 1995 and our second, Nicolas, was not yet two months old on that black Monday in March. It was St. Patrick's Day and the green shirt I wore to work on that day would be one I would never want to see again. There was no luck for me on that day, only the nauseating, slow realization that some things can't be outrun, no matter how far you've managed to distance yourself from the past.
Mark with his kids, Josephine & Nicolas "What doesn't kill you makes you stronger" is a trite expression but it applies to my marriage and to my life. Cancer killed my marriage but it has made me stronger. It has been my acquiescent companion, in many ways the center of my life. It has given me a purpose, to survive and to tell anyone who will listen that it is weak. It can be defeated, routed or at least pinned down indefinitely until something else comes along to escort it out of your body. I believe this statement applies to Poly MVA.
[By now, you should already know that "Poly" is a thoroughly non-invasive, completely nontoxic treatment specifically formulated to fight cancer and that only we survivors are allowed to say that without fear of federal prosecution.] I have been using it every day since I returned from Brigham and Women's Hospital in Boston on a blustery April afternoon in 1997, to my small apartment in Watertown where my two children, Desmond, our cat, my wife and a box containing six bottles of Poly MVA were waiting for me. I have been scanned regularly and the news is always the same.
"Whatever it is that you're doing," say the doctors, "you should continue it." Most of them really don't want to know what it is that I am doing. I've given up trying to tell them. My message is for you, not for the doubting physicians with their cynicism and blind faith in pharmacology.
My message is for all of you desperate and terrified cancer patients, my extended family. I was once just like you. Hear me! Do all you can to support your immune system. That is the first step. Apply the Hippocratic Oath to yourself: First, do no harm. Your body knows how to eradicate this disease, it just needs your help. You may need to radically alter your lifestyle to achieve this. If so, the benefit will be two-fold. Use Poly MVA. Your body will take notice and try to return the favor.
Treat yourself with compassion and kindness, patience and acceptance. Be tender with your heart. Care. Release your anger. Let go. Ultimately, this is a journey you must take alone so be your own best friend along the way. Recovery is a long journey so bring plenty of water. If ever you need encouraging, consider these words from Edward Abbey: "May your trails be crooked, winding, lonesome and dangerous leading to the most amazing view. May your mountains rise into and above the clouds."
Mark
9th Upate:
April 7, 2010
Dear Friends Old and New,
Many of you have contacted me over the past few years to inquire how I'm doing. This has made me a little self-conscious about how long it's been since I posted my wellness here. The long and short of it is that I am alive and well and living my dreams in Sausalito, California. This day marks 13 years since my operation! That's about 4,700 teaspoons of Poly MVA by my calculations.
I had a routine scan some months ago-notice I'm not obsessing about the exact dates anymore?-and the results were the same. No changes. All's Quiet on the Frontal West. That "trail" Mr. Abbey wrote about is still winding, lonesome (no one can go with you on this journey) and somewhat dangerous, but I really have seen some amazing views along the way.
In August of 2008 I left Germany after seven years of misdirection and moved to Sausalito to begin a new chapter of my life, the happiest and most fulfilling one yet. My chief concern about my kids needing a father was the motivating force behind my having stuck it out all those years, but they were proving to be less and less dependent upon me. Meanwhile, my soon-to-be ex-wife was creating her own reasons to separate and we divorced amicably in 2006.
Freed now to go after the one that (almost) got away, I am living a more purposeful existence doing things that I had put off for so many years. I have a loving companion in Marianna to hike and bike with through the beautiful Marin headlands. I'm painting those hills, too.
I'm still in regular contact with my kids who, in my absence, have turned into beautiful teenagers in Germany. Thanks to the wonders of Skype we are able to see and speak with each other across all those miles free of charge.
Toward the end of 2008 I had two petit-mal seizures within five weeks, the second one on Christmas Eve. My neurologist assured me that these are not unusual or to be worried about. 2010 bodes well.
Mark with Marianna celebrating his 45th Birthday with a dozen or so friends at the Sausalito Summer Jazz Series. July 10, 2009.
Andrea Bockhahn, Chase’s mother
Mrs. Bockhahn’s Testimonial
My daughter, Chase, was diagnosed with osteosarcoma in Oct 2005 at age 7. She began chemotherapy immediately for the remainder of that year, struggling with nausea and vomiting (vomiting up to 10 times during administration). In early 2006, Chase had surgery and her left knee and partial left femur were replaced. Shortly after surgery, we found out about the possible support for her body that Poly-MVA might provide and began the suggested amount for her weight. She began immediately and the highest dose and her energy level was much higher thru the processes and she felt so much better. Her overall well-being was much stronger and she (keep in mind her age) grew 1/2.” Chase is now 12 years old and still taking Poly-MVA (maintenance dose of one teaspoon daily) and CoQ10 and will continue to do so. She is a very active young lady who plays volleyball, cross country skis, golfs and this last spring ran track. We strongly feel that Poly-MVA is supporting Chase’s body and continues to be a part of the supplementation that helps keep her healthy
Andy Koontz
Date:
Mrs. Andy ‘s Testimonial
When I was diagnosed with brain cancer, I was given an opportunity to choose approaches in addition to conventional options. I had heard about the support Poly-MVA might provide from Bill Henderson’s book Cancer-Free – Your Guide to Gentle, Non-toxic Healing, and from a local naturopath. My mother had also done extensive research on therapies that could support my body while I was going through traditional treatments. I had surgery and radiation for the cancer, and when I was just about to start chemotherapy I started taking Poly-MVA, what a difference it immediately made. I know that the support Poly-MVA gave my body is one of the major reasons why I’m still here today. Since my diagnosis, I have completely changed my diet and have added supplements to support my body. I will be taking Poly-MVA for life!
I believe in its benefits at a cellular level and have seen what it can do to help a body’s system that were beat up and in need of help. In my opinion, truly incredible product and such a blessing! I am also told by numerous doctors, nurses and other people on how good I look post-brain cancer – even better than before I was diagnosed, go figure that! I would definitely recommend Poly-MVA to others, along with the CoQ10, two mitochondrial super stars. Additionally, I cannot say enough good about the person that Gary Matson is. He and I have become friends and I treasure the positive impact he has made on my life.
Lou P Cortner
Date: 10/18/23
Cortner‘s Testimonial
I started using Poly MVA after my son was diagnosed with a brain tumor. As I was researching the type of cancer he had, I can across a research paper that recommended the book Radical Remission Surviving Cancer Against All Odds by Dr. Kelly Turner. In her book she covers the 9 factors that can lead to remission of cancers. She also has a website, www.radicalremission.com where survivors share their stories of recovery. On the website you can search different types of cancers and find interview-type stories of people in remission. I found Poly MVA in one of those stories. I went to the website and read all the research and called my son. He was more than willing to try the supplement after sending him the information, especially since it passes through the blood brain barrier.
I decided if he was going to try it, I should as well. Within a few days of taking the maximum dose as recommended he called to say he was feeling great and there was a remarkable difference in his energy levels (he was undergoing radiation and chemotherapy at the time). Thank You God!!
I started on a low dose at the same time (1/2 teaspoon, one time daily). I have Familial Hypercholesterolemia and have been taking Atorvastatin for several years which has brought it down a little. I was due for a blood draw two weeks after starting Poly MVA and to my amazement when I got the blood work back my cholesterol levels dropped significantly!! As a matter of fact…to normal levels!! Thank You again God <3 We both continue to take Poly MVA daily. I recommend it to anyone who is interested. My son has had 2 MRI scans and both have come back clear of cancer. Praise God!
Jean-Philippe Suter
Date: 11/13/2012
Suter‘s Testimonial
I was diagnosed with Oligadendroglioma (brain tumors), Stage 3 in July of 2011, which I had resected. I frst learned about PMVA on October of 2011 from Bob Eslinger of the the Reno Integrative Medical Center in Reno, NV. I started using PMVA in October of 2011 at 4 tsps 4 times a day. later I reduced my dosage to 4 tsps 3 times a day due to cost. Unfortunately due to cost, I have stopped using it completely a few weeks ago. Unfortunately, there’s just no way to know how or if PMVA helped me because due to the seriousness of my condition (brain cancer on top of pre exisitng lyme disease) I began several treatments simultansously with PMVA.
When I started PMVA there was no visible sign (by MRI) of residual or recurring brain tumor, but oncologists insisted that due to the type and stage of tumor, there were almost certainly cancerous cells remaining which would most likely reform visible tumors eventually, but perhapsnot for several years. I’ve been undergoing an MRI every 3 months and the situation has not changed. The doctor who originally suggested PMVA to me recently suggested a new treatment. GC-MAF injections, which I will try but cannot afford financially to take while still on PMVA. So I have stopped PMVA. I really wish PMVA was less expensive for I would have continued to take………. In addition to the cancer not recurring there has been othergood news. Over the last year of alternative cancer treatment, some deficits due to the Lyme disease have been gradually improving.
My ability to read my visual endurance and my activity level have all improved and my OCD has decreased despite these problems having affected me for 25 years. I ttribut these improvements to all th alternative treatments (& life style changes) I’ve used inthe last year. Unfortunately, there;s no way to know what role PMVA played in the improvements. I would recommend PMVA o others. My experience with AMARC employees has been a pleasure. They are always professional and kind to work with.
Chad Schmid
Date: 2016
Chad‘s Testimonial
Hello, my name is Chad Schmid. In 2016 I was diagnosed with a brain tumor after I experienced a seizure while surfing. I shortly after, I had the tumor removed and I was informed that it was a grade 2 astrocytoma. After learning there was no known “cure” for this type of tumor, I began to educate myself on “alternative treatment” options. One of those options was Poly MVA. I immediately began to dig deeper and contacted many people who had experienced long-term success taking it. I began taking it daily in 2017 for about 2 years, and continued to have clear MRI scans . After about 2 years of clear MRI scans, I stopped taking Poly MVA. I felt heathy and I believed that I no longer needed to take it.
My MRIs continued to be clear for about 1 year, however in late 2020, my oncologist informed me that there were early signs of activity. Rather than do the standard of care which included surgery, radiation and chemotherapy, I chose to do a variety of alternative treatments that helped to keep the tumor stable for a couple of years, but the tumor remained. Unfortunately, the cost of these treatments was not sustainable long term and I could not afford to continue. As a result, the tumor continued to grow and my health began to decline. In January 2024, the tumor was removed at UCSF. I also did 6 weeks of radiation. Shortly after having my second brain surgery, I started to take Poly MVA again daily. I continue taking it every day and all scans have been clear!
I plan now to take it for the rest of my life!
Sincerely,
Chad Schmid
Peggy McChesney
Testimonial Date: 2021
Diagnosis: Breast Cancer
Personal story
For 20 years Poly MVA was instrumental in saving and improving my life when the conventional treatments and doctors failed me. I also used Coq10, coral calcium, medicinal mushrooms, Infrared sauna, alkaline water filtration system, organic food.
Benefits I received Poly-MVA include Improved Quality of Life, Energy levels increased, Increased appetite, Less Fatigue, Improved Pain levels along with Improved blood, kidney or liver panels. My life changed dramatically in 2019 with the passing of my beloved husband of 42 years, Curt. He suffered 6 serious surgeries prior to that which was extremely stressful for me and my family. Consequently, my cancer has now come back after 21 years of remission.
One month after my husband's death I slipped on an icy bridge and ruptured the tumor that was growing in my right breast resulting in a very serious infection that eventually came out to the surface. This resulted in a mastectomy, and an increase of PolyMVA to maximum dose.
I refused chemotherapy and radiation since my plate was really full with funeral arrangements and financial concerns. I have continued PolyMVA for over a year and felt wonderful. August of 2020, during the Covid pandemic my legs started going numb resulting from a tumor in my spine. Too dangerous to do surgery so I received 10 doses of radiation treatment which thankfully restored the use of my legs!
I'm very certain that I would not be here today if it weren't for PolyMVA and have referred it to multiple friends and family.
Peggy
Jill Saldana
Date: October 2018
Diagnosis: Breast Cancer
1 Update 6-08-2020
Personal story
They wanted to do double mastectomy, July 26, 2019 of last year. I was scared and wanted a 2nd opinion and at the very least ... another MRI. You can go from lumpectomy to mastectomy but not the reverse. So much fear arises inside you and then to learn that there are many cases that cancer can come back even with a mastectomy. But as of today, June 8 of 2020, I wanted to share my wonderful news with you.
I got my results from my thermogram yesterday and they look really good. I went back to the place that I had gotten them done in October of 2018 and they appeared to be stable to what was done at that time.
I showed the doctor my thermograms from back in January and she could not believe how bad it was then. She said she would never have known that I even have cancer if I hadn't told her and shown her those thermograms from Jan. Praise God!!
The prayers and the poly are working!! I'm SO happy! I know this is just part of a long journey and I am thankful for Lynn Jones, Gary Matson, the staff at AMARC and of course the Poly-MVA.
Jill Saldana
Lynn Jones
Date: February 9, 2017
Diagnosis: Breast Cancer
E-Mail: not available
Personal story
My surgery involved a lumpectomy although when I met with the breast surgeon after diagnosis she suggested I would need a mastectomy. She thought that the chemo would reduce the tumor but did not believe I would have enough breast tissue after surgery so I would need a mastectomy.
I used thermography throughout chemotherapy to monitor the effect of the chemo. By the 3rd of the 6th chemo treatments my tumor was not evident on the thermoscan That changed the surgical prognosis from mastectomy to lumpectomy. I asked the surgeon’s nurse if she regularly changed her mind. She said, “NO!” The radiologist who implanted the surgical “seeds” before surgery told me that they had not seen the likes of my MRI. He could not find my tumor on the MRI so was going to place the seeds where the tumor used to be.
He wanted to know what I was doing and I said that I was ingesting high levels of a powerful immune support called POLY-MVA. He told me that he had not seen results like this and to continue doing what I was doing. I believe that the Poly-MVA directed the chemo, protected my good cells, gave me restorative sleep, regular bowels, increased appetite, and gave me abundant energy before treatment and throughout treatment. This allowed me to continue exercising on a regular basis- good healthy habit.
Treatment Summary:
Chemotherapy start date: 3/23/2017 Chemotherapy Medications: 6 doses every 3 weeks Taxotere, Herceptin, Carboplatin, and Perjeta Radiation Therapy Start Date: 10/16/2017 Radiation End Date: 11/21/2017 Dose received: 5900 cGy in 28 fractions Additional Testing ordered by Integrative Medicine Doctor (Dr. Marcus Cobb) and Thermologist (Dr. Anthony Piana) Pelvic Ultrasound: Negative (Fibroid noted) No problems so no removal Head/Torso Thermogram: Showed inflammation in upper right quadrant of breast, some inflammation in upper left part of my mouth, some inflammation heading for pelvis which is why ultrasound was performed DexaScan: Beginning of osteopenia in left hip SpectraCell Lab testing for vitamin, mineral and amino acid levels Only thing deficient was the amino acid- Serine SpectraCell CardioMetabolic Test Results: Low risk for heart, stroke, diabetes Homocysteine levels still too high Taking Homocysteine Supreme supplement 2x/daily
Genetic Testing for gene mutations: No mutations noted on any of my chromosomes so ovaries were not removed
Pap Smear: Negative Refused Mammography and asked for MRI of both breasts with and without contrast. I will continue with MRI yearly for the rest of my life
Results: 6/4/18 No enlarged axillary lymph nodes, no enlarged internal mammary chain lymph nodes, no liver lesion identified, normal marrow signal, no abnormal enhancement in either breast, no mass lesion identified BEST NEWS EVER!!!!!!!!!!
Lynn Jones
Elizabeth Powers
Date: August 16, 2013
Diagnosis: Breast Cancer Stage I
2 Updates 12-23-13 – 5-15-18
Personal story
I tried to rid myself of cancer naturally and when I failed I looked for products that could protect my body as I went through traditional treatment. I am doing amazingly well for going through chemo. I feel almost normal with the exception that my appetite has diminished. The first few days, after chemo, I am a litter more tired and prone to occasional stomach aches. In a few days though I end up feeling very good and I continue with my life as normal. I have had 3 chemo treatments since taking poly-mva.
My labs test show that my WBC is normal. I have had very few symptoms with my chemo and people are astounded that I am undergoing chemo as my energy is so good and I have few side effects from chemo. I feel unusually good almost normal although my appetite is not as good as it should be as I am very thin.
I do many things to help myself through this process. Acupuncture treatment every 3 weeks plus a lymphatic massage. In addition I do coffe enemas every other day or so to help my liver.
I however feel that Poly-MVA is the main reason I feel as good as I do. I therefore, recommend this product often to others. The staff is great and Gary Matson a God sent: very kind and thoughtful individual. Vivian was great as helpful as well.
Elizabeth
12-23-2013
Spoke to Elizabeth. She did well on the first 4 rounds of Chemo and then had real problems. As a result, her Dr. gave her the ok not to have the 5th round of Chemo because her counts were all good. They still want her to do radiation. She intends to drop the Poly down from 6 tsp to 4 until she starts the radiation.
5-15-2018
Spoke to Elizabeth. She shares Poly MVA info with others. She is not taking Poly at this time.
Tarry Feiss
Date: December 2011
Diagnosis: Breast Cancer
2 Updates 9-25-2014 – 12-29-2016
Personal story
I was diagnosed with breast cancer in December, 2011 and had a lumpectomy in January, 2012 and 5 lymph nodes removed in March, 2012. This cancer was detected by my annual mammogram (ordered by my OB-GYN). My cancer was very small and my margins and lymph nodes were clear. I chose not to receive any radiation and sought the advice and direction from my alternative medicine physician, Dr. Marcus Cobb.
Dr. Cobb introduced me to Poly-MVA and shared the benefits and his expertise and knowledge in dealing with my type of cancer. I started taking Poly-MVA right away. My breast surgeon was not supportive of using Poly-MVA instead of the “normal medical” protocol for treating breast that I was not taking radiation, she would have recommended a mastectomy, which shocked me. I do believe that the traditional surgeons and doctors are doing what they need to do cover their personal liability.
The Poly-MVA is now an everyday thing for me and I have found it to boost my energy level. The Poly-MVA tastes like very strong liquid vitamins and minerals and I take 2 tbs twice a day, every day.
I have had no “side effects” that I am aware of in the 12 months that I have been taking it so far. I really have no evidence that I have had cancer except for the scar on my breast and the scar near my arm pit.
Have had no pain, I have a lots of energy and my last 2 mammograms have showed no cancer. I attribute this to not taking radiation and not needing chemo and those damaging chemicals and that exposure to my body.
I also know that Poly-MVA has enabled me to have strength and energy that those common cancer treatments would have depleted from my system. Dr. Cobb has prescribed custom vitamins and supplements which he has tested me for a formulated for me personally. This combination has been working for me so far.
In May, 2012, Following my surgeries, I entered my competition motor sports season (Truck & Tractor Pulling) as I always have since 1990. In April, 2012 I worked with a therapeutic massage therapist who massaged through my scar tissue and helped me to work with my arm and movement, my left breast was affected and my left arm is my steering arm in competition and my right arm is the throttle arm. I was able to drive my 2500 horsepower two wheel drive truck in competition and never missed an event. I competed in over 30 events last summer and was the “crew chief” for my husband’s 5000 horsepower 3 engine tractor. I am responsible for starting his engines for his 40+ events that we compete with daily thru June, July and August. Needless to say, my performance only changed in that I became more tired earlier in the evening than usual. We finished the season well, I was 2nd in Region 2 and Region 4 and my husband won Region 2 and region 4 as well as the end of season Championship event.
I tell all this, because I believe that the Poly-MVA kept my energy level up and gave me confidence that I was doing the right thing because I had no pain, and no down time. We are preparing for the upcoming season, 2013, and I am happy to report that my very latest testing was negative for cancer.
I am spreading the word about Poly-MVA to my friends with breast cancer that are “ill” from their chemicals. It is hard to convince people that the physicians are not always right and their methods are their standard “protocol”.
Sometimes, thinking beyond the box and knowing what your body needs and what has caused your illness is more important than doing what every one else does. Dr. Cobb had me tested and the result was that my body was not metabolizing my estrogen, hence a breast cancer developed. He formulated my custom vitamins with a supplement that will help me metabolize my estrogen and get it out of my body thru normal body functions.
I feel that the Poly-MVA boosts my system and helps me maintain my busy lifestyle. I am a cancer survivor for 1 year and 3 months and only looking forward from here. I will still receive my mammograms and testing to check for the return of cancer. I do not think about my cancer and dwell on the disease. It is in the back of my mind, but it is not taking over my life. I have had a great life of 58 years and I live my life to the fullest daily.
Poly-MVA gives me extra energy and I feel that I am fighting against the normal and that makes me feel empowered! I am fortunate that I found and believe in my “alternative” physician and his methods and testing. It is all about feeding your body what it needs and finding your deficiencies and supporting those deficiencies with the nutrients and reinforcements your body needs.
The American lifestyle where we live makes it very easy to support unhealthy living and eating. Cancers and diseases develop when you don’t supply your body with what it needs. When you are faced with a problem like cancer, you have to make healthy choices and sadly, it is much harder to do what is right for your body, because the easy foods are not usually the best foods for your body.
Best wishes,
Tarry
9-25-2014
Tarry says she is doing good and feeling well still taking 1 teaspoon of poly daily. Tarry is down to one mammogram per year and will be going in before end of year for her mammogram.
12-29-2016
Tarry is still taking Poly …...
Irene Marshall
Date: September 2, 2011
Diagnosis: Breast Cancer
2 Updates 10-18-16 – 1-14-19
My Poly-MVA Story
Hi! My name is Irene Marshall and I have a simple story to tell you.........Poly MVA works!!
I was diagnosed with Breast Cancer in September, 2002 after going in for a regular mammogram. I was shocked! I was happy, healthy, and active and couldn't believe this could happen to me.
My gynecologist had referred me to a surgeon based on a mamogram they didn't like the look of.....she immediately scheduled me for an ultrasound and when the results came back, she scheduled me for a core biopsy. She gave me the final verdict....it was malignant, and a mastectomy was in my immediate future.
I went home and cried, woke up the next day and cried some more, but by the afternoon, with red, puffy eyes, I did what all of us do these days........turned on my computer and started to research cancer and find out what my options were.
My surgery was scheduled for early in November, but I was determined to take a positive approach to the after care. (I have 3 sons, two of whom were born with a neurological disorder. One thing I learned from working with neurologists over the years is that while medicine has made tremendous breakthroughs in the last 50 years, there is still much they don't know).
I read for hours and then days, taking notes fast and furious. Oddly enough, as thorough as I was trying to be, I didn't find the "Poly" website (that comes later).
What I did discover though, was that using the current protocol: Chemo and or Radiation, the prognosis for survival was 60%. I didn't care for those odds. I had my surgery in November, but the lymph nodes that were removed with my breast also came back malignant, so I went back early in December for a 2nd surgery to remove the remainder of the lymph nodes. I opted to not have reconstructive surgery and have used a prosthesis since then........I'm not sure that was a good decision........my suggestion now would be to talk to women who've had reconstructive surgery and see if there are negative side effects over a long period (10 years at least). Anyway......on with the story!
My surgeon scheduled an appointment for me with an oncologist and he confirmed the survival percentage and answered all my questions quite honestly. I didn't like the answers! I decided to go it alone.......my surgeon was less than pleased and once my follow up visits were over, I really was on my own. I changed to a very healthy diet (something I didn't have before), went through a detoxification program, and then found a doctor who offered alternative health care. He ordered blood work and I had my first CA-27-29 test. I was at the highest end of the normal range........one number higher and I'd have been in the "you're in trouble" range! Enter Poly MVA!!
My son and his wife were vacationing in Santa Fe, NM and struck up a conversation with the people sitting next to them at dinner one evening. The talk eventually wound it's way to life's ups and downs, and the gentleman, told them this story.
He had been diagnosed with an inoperable brain tumor and sent home to put his affairs in order..... he had at most, 4 weeks to live. He went home, booted up, and started researching fast and furious. He found the Poly website and put in his order. That had all taken place 4 years earlier!
My son was so excited, he called me that night and gave me the phone number of their new friend. I called him and he gave me the AMARC information and told me to call Gary Matson. I started taking Poly in October, 2004, two teaspoons, four times a day.
I stayed on that dose for 6 months and then began to reduce the amount. When I had my next CA 27-29 test, I was in the middle of the normal range. Over the next few years, my dose has been reduced to the point of a "maintenance level.......I take one teaspoon a day. My CA 27-29 tests are all in the low end of the normal range.
I'm 68 years old, I work full-time, I play tennis 3 or 4 time week and compete at the USTA 4.5 level and I believe with all my heart that I'm still walking on this earth because of Poly MVA.
I've been to the websites that say Poly MVA is a ripoff and a scam. It makes me both angry and sad. Angry, because it's not true and sad, because I'm afraid people will believe it and not reach out to the people at AMARC.
If you've gotten this far in my very lengthy story, please contact them and decide for yourself. Poly is not a "one size fits all" cure. It works better on some cancers than others, but you need to talk to them and then make the decision that's best for you.
Irene Marshall
10-08-2015
A month ago I had my yearly CA 27-29 test and the result showed an increase of 100% over a 2 year period. It was 19.9 in 2013 and was 38.9 last month. My doctor has scheduled another test in November. I have been on a maintenance dose of Poly - 1 teaspoon a day for several years, but in the last two years I've really fallen off the wagon in terms of diet. Sweets on a regular basis....very regular!
So in the last month, I've gone back to broccoli, sweet potatoes, and other veggies and increased my Poly to 2 teaspoons a day. I know 38.9 is still in the normal range, but I'm heading in the wrong direction.
Irene
10-18-2016
Spoke to Irene. She is doing well and taking a daily maintenance dose of Poly.
1-14-2019
Irene is till taking her daily maintenance dose of 2 tsp per day of Poly which is keeping her markers within the normal range.
Carol J. Roberts
Date: September 2011
Diagnosis: Breast Cancer Stage I
2 Updates 8-29-16 – 8-29-18
Personal story
In 2011, I was diagnosed with Stage I Ductal Carcinoma right breast. It was found on a routine mammogram. I had a partial mastectomy. The lymph nodes were negative so I did not need Chemotherapy. I chose not to have radiation, as that was one of the options I had.
It was suggested that I take Poly-MVA. Everything I read about Poly-MVA was that it is an antioxidant protection from damaging free radicals and nutritional support. After starting to take Poly-MVA, my energy level increased and I was able to do everything as normal. I was active in Church. I went to my organ classes each week. I was able to do my own housework. Went out to lunch with friends. My mammogram in June 2012 was normal after one year of treatment of Poly-MVA.
Whenever, I called AMARC Enterprises, they were always helpful in explaining the benefits of Poly-MVA. Also, they were concerned how I was doing. Carol J. Roberts
8-29-2016
Spoke to Carol and she says that her oncologist said her mammogram came out normal. As a result, he took her off aromodex. Her bone density is good except for her hip.
8-29-2018
Carol said her latest mammogram was negative and she is continuing to take a daily dose of Poly.
Maria “Lupe” Rotunda
Date: April 30, 2010
Diagnosis: Breast Cancer
Update 4-21-20
Personal story
María Guadalupe Rotunda 68 years old in 2020 Poly MVA helped me clear my breast cancer when I first started taking it 4/30/2010. At that time, I was accepted into the QOL Study and I took 2 bottles per week (14 tsp daily).
Currently, I take 1 bottle a month (7 tsp daily) to this day. I believe Poly MVA greatly contributed to my health and recovery. It increased my white cell tremendously even though I chose not to do any conventional treatments, i.e. chemotherapy, radiation, other prescription medications.
I also used the Gerson therapy along with Turmeric, vitamin C IV, B17, melatonin, garlic, selenium. Other benefits from Poly-MVA were: • Increase or maintained quality of Life • Energy • Increased appetite • Cancer support • Improved Fatigue • Less Pain • Improved blood, kidney or liver panels Poly MVA also helped my mom get rid of her cancer after they had gave her only 3 days to live. We were giving her 3 bottles a week (20 tsp daily) and in 15 days she regained conscience and began to walk again!!!
We recommend Poly-MVA to all of our family and friends if they are diagnosed with Cancer. A man that had cancer all over his body and had 6 month to live was given no hope, so he decided to take Poly-MVA in large amounts and has been alive for 10 years and he is healthy.
4-21-20
Lupe has been a real advocate for Poly MVA and has referred many people to the AMARC Enterprise office. She continues to take her daily maintenance dose 10 years since she first started taking Poly MVA.
Yvonne Kirkingburg
Date: August 24, 2009
Diagnosis: Breast Cancer Stage I
2 Updates 9-30-13 – 10-04-17
Personal story
I have used poly-MVA for five years. When I was diagnosed with breast cancer, Dr. Milne of the Milne Clinic in Las Vegas recommended that I be on Poly-MVA. My breast cancer had spread to my lymph nodes and the oncologist strongly urged me to have chemotherapy. I had agreed to radiation but refused chemo.
I believe the poly-MVA has not only given me additional energy, but after five years I am in remission. I am feeling strong and healthy, in spite of lung damage due to the radiation. I give much credit to my life style, diet, and Poly-MVA. Thank you for your continued support. Y. Kirkingburg
9-30-2013
Spoke to Yvonne. She had stopped poly for a few months because she started getting headaches and the headaches stopped. So, she thinks she had an overload of Vit B. However, she said that her energy level went down so she is now back on poly.
10-4-2017
Yvonne continues taking a daily dose of Poly.
Lupe Herrera
Date: November 2009
Diagnosis: Breast Cancer Stage III
4 Updates 8-20-12 – 11-16-12 – 8-06-14 – 1-28-19
Personal story
In November of 2009, I had prior health conditons that kept me bedridden at least until 5:00pm in the afternoons. At that time I was diagnosed with Stage 3 breast cancer.
Knowing that I would possibly die from chemotherapy and surgery, I went to the Century Wellness Clinic in Reno. That is where I was treated and earned about PMVA from Dr. James Forsythe.
I was placed on supplements along with PMVA. After the treatments I stayed on using PMVA when I went into remission. Within 4 months and taking PMVA daily I have been able to get up earlier in the day and remain in remission. I truly believe that with out the PMVA I would not be alive today or be able to get up earlier in the day.
Having severe reactions to chemicals, I couldn't have standard cancer treatments. Were it not for PMVA, there would have been no hope for me. I have hope now and even if people have had standard treatment for cancer, I feel that the PMVA does wonderful things in helping the immune system fight.
I would definitely recommend PMVA to others. AMARC Enterprises has been so helpful and knowledgeable on questions I've had. They are truly caring towards me and all individuals. As I said, I feel that PMVA is a life saver.
Lupe Herrera
8-20-2012
I have been on Poly-MVA for a while now, and because I am on alternative treatments, I never had chemo or surgery. I feel the Poly-MVA is the reason I am in remission and if i stay on it, I feel I will live longer. Thank you so much!
Lupe
11-16-2012
Lupe said that her levels have been steady since 2010. Took Poly and Oracel together. Then after 8 months, she stopped the Oracel since she didn't see good results and started using only Poly, Vitd3 and magnesium.
PMVA has been helping with her pre-existing condition with her ear in 1995. She believes because of Poly she has been able to get up earlier. She was not able to lift her head now she does. This was caused from chemical poisoning with pesticide spray...exposure...
She thinks using PMVA has helped with those systems. Lupe will have another PET scan at the end of the month.
8-06-2014
Lupe recently has had another relapse so will take another round. She has been on Poly for several years and is planning to go to Dr. Fosythe’s again where she will get Poly MVA via IV treatments. She has been taking Poly since 2010.
1-28-2019
Lupe started back on 8 tsp daily of Poly MVA due to another relapse.
Edward Freed
Date: July 24, 2009
Diagnosis: Breast Cancer (Male) Apocrine Carcinoma
3 Updates 5-18-2010 - 7-19-2010 – 5-19-17
Personal story
================================================================== APOCRINE CARCINOMA – Very RARE form of Male Breast Cancer “Apocrine carcinoma of the male breast is an exceptional malignant tumor. It does not have a particular clinical or radiological appearance, but it's microscopically characterized by the presence of granular cells and foamy cells representing over 90% of tumor cells.” ================================================================== When I was diagnosed with cancer, my family was devastated.
First the medical people had no idea what kind of cancer it was but were leaning towards a type called Apocrine. I found out there were exactly 38 people in the world that had this type of cancer before I did and not one of these people had survived.
Next thing I found out was the medical people had no idea how to treat this type of cancer. A decision was made to treat me as though I had male breast cancer and they told me they had no idea how this was going to turn out, all they could do was to cross their fingers and hope for the best.
A Baptist minister from Florida (who I did not know) who heard about me from his daughter who was a friend of my daughter, contacted me and told me about PolyMVA.
He told me that he and 3 other men from his parish all had been diagnosed with different types of terminal cancers and each one was told to get their affairs in order and sent home to die.
He told me that each one of them began to take PolyMVA and now 3 of the 4 are now in remission and the 4th one lived about four years before his cancer finally claimed his life. I made a decision right there that I would use this product for my health. I told a few others about PolyMVA while I was undergoing my radiation treatments.
One of these men also started using the product. Today He and I are both enjoying life. I am convinced this product, PolyMVA, is the reason I am writing the letter to you today. Thank You PolyMVA.
Sincerely,
Edward Freed
5-18-2010
I had the remainder of the tumor removed. My PET Scan showed no new cancer present anywhere in my body. I am convinced that my body being cancer free is all due to the poly-mva. I say this because the other people I met with cancer when I was undergoing my radiation have died from their cancer and here I am cancer free.
Ed Freed
7-19-2010
PET scan no sign of cancer. I am now cancer free. Thank you poly!
Ed Freed
5-19-2017
Ed is still doing well and taking Poly.
Rosario Diaz-Greenberg
Date: August 2007
Diagnosis: Breast Cancer
4 Updates 2-12-08 – 3-24-10 – 12-09-13 9-14-16 – 10-01-18
Personal story
At the end of August I was diagnosed with DCIS. Since I have always used homeopathy as an alternative, I started to research on the net for something that could help me.
There were three products that stood out: a Chinese product, a Canadian homeopathic set of shots, and Poly-MVA. After a lot of reading I opted for the Poly since it was the one that had more testimonies and was locally sold.
I spoke to Gary and told him about my challenge, especially the fact that, if I needed radiation, I felt the Poly might help with my energy level. As a full professor of Education at Cal State San Marcos, I was concerned about the fact that my three hour classes would leave me drained, especially once I started the radiation.
It has been two weeks since I started the Four Corner Protocol. On the first day I thought I was not going to be able to keep it down. I became sick with nausea and was really concerned about the taste. Little by little I found liquids that I could use to make it more palatable and became used to it.
I had a lumpectomy on Wed. Sept 19th, 2007. Amazing as it may seem, my whole family fell asleep by 9 pm that night, while I was up until midnight. Also, I only needed one Vicodin pill that day and have not had another one since then.
My level of energy has stayed high, I am healing properly, my appetite is good, I am sleeping better, and my quality of life is improving. I have not had to take more than two Tylenol pills per day, and my craving for caffeine drinks through out the day is gone.
I guess I did not remember how well one can feel and assumed I was doing very well. Needless to say that after two weeks on the 4C Protocol, I have already felt the difference and have realized I was depending on pain killers and caffeine drinks to feel well.
Tomorrow I am going to get the Pathology results from my surgeon and he will send me to the oncologist. I plan on taking all my bottles with me just in case they ask what I am taking. Hopefully the report will be good. Regardless, I know that the Poly is really working and I am telling all my friends and relatives about it.
I will keep you posted on my progress and will continue to let others know what a good product you have.
Take care,
Rosario Diaz-Greenberg
2-12-2008
Spoke with Rosario. She said she wanted to call before she left for overseas. She also told me she was doing very well. She went in for a mammogram and it came back clear. She is very happy!
3-24-2010
Talked to Rosario. She has been active and feels great. She had her latest mammogram, and all is well. She continues to take maintenance dose of 1 tsp a day of Poly as well as Immuni-2 for immune support.
12-9-2013
Rosario is doing fine, per her Cancer, but is sick due to the flu which has gone to her chest.
9-14-2016
Dr. Diaz-Greenberg will be traveling internationally again soon and is still in good health.
10-01-2018
Rosario is still taking a daily dose of Poly MVA.
Betty Wetzel
Date: June 2007
Diagnosis: Breast Cancer
6 Updates 2-10-09 – 6-06-11 – 5-29-13 1-28-16 – 1-25-17 – 2-07-18
Personal story
Poly-MVA has given me energy and has kept all of my tests (blood) normal and also my breast cancer markers. I was diagnosed with breast cancer, June 2007 and have not had surgery, but have taken faithfully Poly-MVA and I feel wonderful. I am thankful for Poly-MVA.
Thank you,
Betty Wetzel
2-10-2009
Spoke to Betty and she thinks she is doing good. She will be going in for a CTC next week and find out what her markers are and in two weeks she will have a Pet & CAT scan. She asked about eating sugar because she likes to have a little bit of pie or sweet once in a while. We agreed it would be best to restrict her sugar intake but a small amount would be ok if her doctors have not restricted her. She said they haven't but she was reading about how Cancer loves sugar and wanted to be safe.
6-06-2011
Talked to Mr. Wetzel to see how Betty is doing. He said he will have her call me back. Betty did call back and said she is feeling really good and is still taking the Poly. Betty said her thermogram came out very good and she is now seeing an integrative medicine Doctor that says she has no sign of cancer.
5-29-2013
Spoke to Betty and she has started using fermented soy. However, she says that it gives her diarrhea. She said she is just laying low to see if it works for her. She takes a bottle a day of the fermented soy.
1-28-2016
Talked to Betty and she is doing well except she does have a sore on her breast. She is doing 2 tsps a day of Poly and will increase her daily dosing. She said that Neosporin has helped stop the bleeding and that she is going to increase her Poly up to 8 tsp a day and continue on CoQ10 and D3.
1-25-2017
Spoke to Betty about her interest and concerns about stem cells and ozone. She had tried ozone and felt uncomfortable but will do the stem cells and is doing IV Vitamin C. She still has bleeding although the Neosporin and honey she learned about has helped. She will increase her Poly to 8 tsp from 2. We had a great talk about her family.
2-07-2018
Betty had the RGCC test and it shows she should take Poly to continue to target her ongoing cancer recovery. She has been diagnosed with congestive heart failure and said she will take 8 tsp a day plus CoQ10.
Judy Foester
Date: January 6, 2006
Diagnosis: Renal/Breast Cancer
3 Updates 6-28-10 - 11-12-12 – 5-15-13
Personal story
“On my birthday, January 6, 2006, I went for a routine mammogram that was far from routine. A spiculated mass, 2 cm in diameter, was found by ultrasound after the mammogram. Dr. Alison Estabrook, best breast surgeon in the world, did the fine needle aspiration, found the tissue cancerous, and did a lumpectomy on January 26, 2006….
Since I refused chemotherapy (I think it is barbaric and far too destructive), the hospital did a body-wide search for additional cancer. They found a renal cell carcinoma, 1.7 cm, on the outer curve of the left kidney. I had suspected a cancer when I had shingles four times in 1996. I had a full body CT scan and they found a 5 mm. lesion on the left kidney (soft lesion).
To be sure, I had the test repeated in 2002 and they found NOTHING. Now, four years later, they find a large renal cell carcinoma. My radiation oncologist at MSK was Durgesh Hajela. Her fellow doctor, Karen Schupak, ordered the technicians to force the bones of my shoulder into an untenable position for radiotherapy that caused permanent nerve damage in my shoulder. Two more times, they repeated this process. My whole 220 pound body levitated off the table as if jolted by defibrillator paddles. My arm flew in painful jerks in every direction as the nerve remained caught between the bones. I told them and they agreed, that I could not endure such treatment.
I tried to find an integrative approach. The Cancer Treatment Center in Philadelphia offered mammotome therapy (balloon inserted and isotope placed in balloon twice a day) but my insurance would not pay enough of the cost. St. Barnabas Hospital offered mammosite therapy but Alison Grann, radiation oncologist, said the protocol was very strict and it had been too long since my surgery. Scar tissue had already filled in the space where the tissue had been removed.
As soon as I was diagnosed, I began a cancer diet and went on the Mannatech System, with daily Ambrotose, Manna Cleanse, ImmunoStart, omega3 supplements, no white sugar or flour, lots of fresh fruits and vegetables.
My Poly-MVA arrived just in time for the first radiation treatment, on Thursday, June 8th. I have increased from a once-a-day dose of 1 teaspoon to a twice a day dose of 4 teaspoons. I take each teaspoon with 15 drops of LiquSorb CoQ10. I also take Vitamin B 50 mg; calcium gluconate 600 mg. calcium, with 200 iu. Vitamin D2 twice a day; L-carnitine 500 mg.; Mannatech GI Pro; Plus (amino acids); and Arthrosoothe (turmeric) from PNE.
I use Xylitol as the sweetener if I have a recipe that needs one. I also take a multi- vitamin and 1000 mg. of Vitamin C; Vitamin E with selenium food complex 50 iu.; zinc gluconate 50 mg., chromium piccolinate 0.1 mg, Vitamin B12 .1 mg., three tablets of potassium gluconate, one with each meal, 90 mg. potassium; one DHA from Norwegian fish oils, 500 mg; CoQ10, one 100 mg., with lunch. Recently I added Epicor, DIM, serrapeptase (a fibrin digester) and artemisinin (at first I took one a day but recently the Poly-MVA site has recommended nine a day). I just added Vitamin D3 to the regimen, starting at one 1,000 iu capsule a day. I would love to liberate the calcium in all the strange calcifications of the breast and other organs.
Dr. Fleishmann, my pharmacology advisor at Roosevelt Hospital says I probably did not have to have the kidney cancer treated at all. I saw Aaron Katz at Columbia Presbyterian Hospital about having it cryo-ablated. The surgery was successfully completed, with Jaime Landman as chief surgeon, on August 4th, 2006.
Dr. Nader Fahimi met with me again on September 18th and my shoulder reconstruction was scheduled for October 12th, 2006. I saw Dr. Johnson again on July 14th, August 8th and October 3, and once a month since then.
I saw Dr. Estabrook again on July 7th (she said all looked well and scheduled my next mammo for January 8th, 2007). My follow-up visit with Dr. Evans was on September 12th and December 10th. He said all looked well. On January 8th they took NINE films of the right breast. I was furious because this is alpha radiation that they use and very highly ionizing. I told them they missed seeing the tumor altogether for three years and NOW, with the tumor removed, they take NINE films. Each alpha particle strips two electrons from the cell tissue and is highly damaging to DNA. Sure enough, after a couple of weeks, I noticed proliferation of the cells that had remained after the surgery.
I upped my Poly-MVA dose to 20 tsp. a day for a week, added nine artemisinins per day and used the skin cancer cream again for two weeks. I think I clobbered it nicely and it is in its death throes (again). The breast surgeon again pronounced the breast fine, perfect, beautiful. The radiation oncologist was visited on March 13th, 2007 and he said my efforts appeared successful and could find nothing remaining from the latest proliferation. And that's all she (I) wrote! Holding you all in love and prayer.
Judy Foester 6- 28-2010 Greetings all. What a blessing the Poly-MVA Yahoo group has been. From them I learned about the proper 50,000 international units of Vitamin D3 that I should take per week. My mammograms used to show very dense fibrocystic tissue. It was like trying to look through 'old ice' on the surface of a lake. After taking the proper Vitamin D3 and adding iodine (through organic kelp), the view is now as though through 'black ice' (no fishes visible beneath MY ice, however).
With us, every thought and breath is to BEAT it. Poly-MVA and you....perfect together!! Everyone in the group has given me not just hope but confidence. Any newbies out there....this stuff works! It stuns me that doctors and cancer patients can pass by this opportunity.
11-12-2012
I had learned about Poly-MVA originally in the Susan Lark newsletter from my sister's friends who are both doctors. To backtrack, I had been diagnosed with breast cancer in 2006. I had a lumpectomy, radiation. I also had kidney/renal cell carcinoma which was unaffected by Poly- MVA.
In 2012 I had two large and deep skin cancers on my right thigh. I used Efudex on the surface and Poly-MVA. Within about 2 weeks the cancer lesions on my leg were about gone. in fall of 2012, a large patch of skin (4 sq. inches) on my left jaw suddenly turned to mush. I said to myself 'Uh oh! It's a stage of basal cell carcinoma.' I then headed right to the bottle of Poly- MVA. I didn't want to use Efudex or it would leave a large purple/red reaction area for a long time. Three weeks into Poly-MVA there is only a low uninflammed scab left. Hooray!
Poly-MVA's support wins another one for me. There's nothing like it. I feel so blessed to have it available. My current Poly-MVA dose is 2 tsps a day with 15 drops of LiqCoq10 at breakfast. I truly believe that Poly-MVA has contributed to my health and recovery. Every day I recommend Poly-MVA to others. I would tell others" Stop being a disbeliever and try it for a few weeks...then you will know it worth every penny and gives the greatest peace of mind. Have no fear Poly-MVA is here!"
Judy Foester
5-15-2013
Spoke to Judy and there is no indication of cancer in her body. She knows Poly worked. She was taking 2 tsp a day until January and then stopped. However, she said she has some and promised to do at least 1 tsp a day for maintenance. She promised to be more consistent and told me she was so glad to hear from me.
June Black
1st Diagnosed: Stage 1 November 2000
2nd Diagnosis Date: Stage 4 in 2005
Diagnosis: Late Stage Breast Cancer
E-Mail: june1@rconnects.com
4 Updates 3-23-07 – 6-19-09 – 9-04-12 – 8-09-17
Personal story
CANCER ALTERNATIVE vs. COMPLEMENTARY I am writing this to let people know that when you are diagnosed with cancer there are options. It takes time to sort through all the variables and treatments and outcomes and statistics that are given to you by your healthcare providers. However, the providers do not help you recognize that cancer is a life altering experience. This is your wake-up call.
There are a lot of variables on the causes of cancer and these are numerous.
Here is my story:
I was diagnosed with breast cancer late 2000. I was numb and went through the motions. I originally went for a breast reduction and was sent for a mammogram. The nightmare started. There were two lumps and they were extremely small so then we had an ultrasound. The ultrasound could not give a definite diagnosis. The next step was aspiration. I said nope, I am having a breast reduction and if there is anything there they can take it out. Little did I know that the medical protocol has an entirely different approach.
I was then sent back to get a stereotactic biopsy and the pathology report said positive for ductual carcinoma. Now a surgeon becomes involved, oncologist, and plastic surgeon. You run from one appointment to another and the stress takes its toll and you do not even have time to sort out what is happening. You are now a statistic and you are dancing to the tune of the medical establishment.
I had the mastectomy, no radiation or chemotherapy and was put on Tamoxifen. I had a terrible reaction to the Tamoxifen and flushed it down the toilet. I then decided I had enough.
I had an oncologist that was a controller and she was quite upset that I refused further adjuvant hormone therapy and was sending me again for another full body CT Scan. I told her I just had one 3 months ago and it is a lot of radiation. She walked out of the office and the nurse brought in the prescription for the CT Scan. I never went back.
I got another oncologist and this one does not return phone calls when I was asking about results of a chest X-Ray. Took 6 weeks to find out from some office clerk that it was ok and she could not explain this fancy word and said it was just what the pathologist said. I asked to speak to the doctor and two weeks later still no phone call. I was not too impressed. I am now on oncologist number three and not too sure about this one but went along with the program of just being monitored. I went every three months and then every six months for bloodwork and mammograms. So far so good.
By 2005 I was beginning to see a lump forming by the mastectomy scar line. I went to a surgeon and said I needed a biopsy. He felt it was ok and I did not. I was scheduled for an excisional biopsy. The pathology report came back positive for carcinoma. I was upset and could not figure out how cancer could come back on the same site when I had a mastectomy.
I went on line and did a lot of research and did find that sometimes cells drop off during a stereotactic biopsy and cancer can grow back. However, this is a very rare occurrence.
The past five years I did a lot of research on cancer and bought a lot of books on healing and changing your lifestyle and diets. I read up on a lot of people that cured themselves through natural and holistic methods. I changed my diet quite a bit and then slacked off but pretty much stayed with lots of fresh fruits and veggies. I did some meditation and some yoga but working a full time job was quite difficult to maintain a really healthy lifestyle. I knew then that when you are diagnosed with cancer, you have to be very vigilant with your life and maintaining an equitable balance. I worked too many hours to be able to devote much time to healing myself and maintaining a quality healthy lifestyle.
I go to oncologist number three and he did not even have the courtesy to tell me the pathology report, the first words out of his mouth was “I recommend the whole gamut; chemo, radiation and adjuvant hormone therapy.” My answer took a leap of faith “No!” He said “This is your last chance, June!”
I said “ I am sixty years old, I have lived a good life, and I have other plans.” He said “Do you know what dying cancer patients are like? They stink!”
I was pretty upset and then he said he will schedule a CT then changed his mind and said no, a PET Scan. I said ok we can do that but this is what he should have said in the first place. He screamed at me and said he was the doctor. I was pretty upset when I left.
I called the surgeon and said I cannot go back to this man anymore and wanted to cancel the PET Scan. The surgeon said do the scan and we will find another oncologist.
The PET Scan showed negative for further cancers but then it is not sensitive enough to pick up cells, just clusters. The surgeon knew what he was dealing with. I had two subsequent surgeries and the first of the two margins were not clear. I had to go back again and margins were clear but there were two more hot spots which meant the cancer was spreading and now is multifocal.
Oncologist number four said you have to have chemo and radiation and adjuvant hormone therapy. I then said no I will go natural. He was quite upset and felt that he could do no more for me. In essence I was fired. I went back to the surgeon and he said he will monitor me and I went against his advice also but he respected my decision. I asked him what happens when patients refuse further treatment, he said some survive and others go on to die. He did not try to force me into anymore treatments but respected my decision. This was in August of 2005.
By the end of September after spending a month of a very strict diet and enough vitamins and supplements to fill a small shop I realized I was losing the war against this cancer. I was losing weight, I had sweats, I was really weak and it was so bad that I thought death would be a wonderful alternative to the hell I was going through. I was white and had no color and my clothes were really getting loose.
I made an appointment with a homeopathic practitioner who is also a doctor and it took almost two months to get in to see him. The day finally arrived and I sat there while he went through all the reports. He said we know you have cancer, we just don’t know where it has gone and what stage you are now. June and Soki kickin' it on the lanai
STARTING POLY MVA He then proceeded to tell me about some new supplements that are out there and told me of his father-in-law. His father-in-law was diagnosed with liver cancer and was pretty much told to get his affairs in order. The father-in-law did a lot of research and came onto information about Poly-MVA. He started taking this at 14 teaspoons a day along with a very strict diet and lots of other supplements. Of course the doctor felt that his father-in-law was wasting his money.
After four and a half months a liver scan was done and the tumor was shrinking and the gentleman was feeling much better. A year later there was no evidence of cancer. However, he is taking 2 teaspoons a day of Poly-MVA for life. This goes to show that someone actually won this battle.
I felt like a lifeline had been thrown at me. I was put on Poly-MVA loading dose that was to span six months to a year and many other supplements and of course diet.
Insurance does not cover the office visit or any of these supplements. The money was well spent as far as I was concerned. The next day I slept very late as I was very fatigued and started my first 2 teaspoons of Poly. I took another at 4pm. I took another 2 teaspoons at 8pm and really felt fatigued and my brain was washed out and I could not even function or think.
The next day I went to work and looked so bad that I was asked if I could work that day. I had to work, who could support this expensive regime I started. I had no choice. Sunday is day three and I was still exhausted but went into work. By 2pm I felt a shift. I knew something was different and I could not figure it out. I then realize the fevers and sweats were diminishing and my body had calmed down. It was strange as the body that is fighting cancer is really fighting and that is probably the cause of this fatigue also. The calming of the physical being was phenomenal as you have to be at a very bad state to realize what true homeostasis really is. Monday, I had enough energy that I was bouncing off the walls. I had a mystical experience that day.
I was at work and walking to the shed to get sheets for my room when I felt this shimmery feeling overcome me. I stopped to experience this feeling and I felt a sense of peace, love, and I cannot describe the ecstasy I felt, it was beyond words. I then knew that I was going to be ok.
This was six months ago and I am still on the loading dose. I still have some ups and downs and I still tire easily. I also realize that I was seriously ill six months ago and was in total denial. I am still healing and I still need a lot of rest and need to reduce the stress in my life. A lot of people do not realize that the healing path is a long road and recovery is slow. Also faith in the process is a powerful tool on the road to recovery.
I will be having a PET Scan soon and I know in my heart it will show nothing. I also know that I will have to be vigilant and strict about my health and lifestyle. Staying healthy is a fulltime, lifetime job.
I attribute a lot of my healing to a wonderful surgeon that allowed me faith in my choice and encouraged me. I attribute the powerful dynamic of healing choices to a wonderful homeopathic physician that guided me and still guides me. I also thank many of my supporters and my family for their loving support and watching the magnificent experience of my healing take place. I also give first and foremost Poly-MVA the catalyst of dynamically supplementing my body with a tool that helped me with the fight against cancer.
I never say "my cancer" if the reader has noticed, it is not mine, it was not welcome in the first place and never will be. I feel that cancer should not be acknowledged as yours, it is a wake up call to let you know that major changes need to be made in your life. You can choose to heal or you can choose the everlasting comforts of death.
I chose quality of life. I chose to heal myself and not compromise my body with powerful chemicals to destroy cancer and compromise my physical being. I chose a lonely scary road that many have traveled and survived and wrote to live and tell about it, but never met one face to face. I had to rely on faith.
June Black UPDATE: March 23, 2007 BRIEF OVERVIEW OF EVENTS LEADING TO POLY MVA First Diagnosed with breast cancer November of 2000. Modified radical Mastectomy was done Dec. 1, 2000. The cancer was Stage 1 .9cc no lymph node involvement ER/PR+ I did no chemo/rad but tried the tamoxifen and after 10 days pitched the rest of it down the toilet. My system is way too sensitive for chemicals. I had a terrible reaction and the worse of it was my thought processes were not working and I could not communicate or relate to the world around me.
Reoccurred May of 2005. Found a lump along the mastectomy scar line. Margins were not clear. Two subsequent surgeries July 23 margins not clear and August 25th margins clear but a second random site sample indicated the cancer had spread and the cancer had gone into the chest muscle.
A possible involvement of lung mets from chest x-rays done in 2003 that was not diagnosed at the time,just nodules to be watched for changes. A chest x-ray taken June of 2006 showed no nodules. This is after taking Poly for 6 1/2 months. So the supposition was that there were lung mets, no one did any further testing.
After the three surgeries of 2005 I refused further surgery, and an abolute refusal to have radiation, chemotherapy and adjuvant hormone therapy, I told the surgeon I had enough. I will find a way. This was in September of 2005. Staging was not done as I refused further tests and no complementary therapies. Prognosis was extremely poor and given at most a year to live.
I started taking Poly on October 21, 0f 2005. In June of 2006, I had PET Scan, CAT Scan, Brain MRI with and w/o contrast and bloodwork. No sign of cancer. I had some weight gain, more energy and color.
I took the Poly at the beginning 8 teaspoons a day for 6 1/2 months. I then went to 6 teaspoons a day for about 2 months and since then I have been taking 4 teaspoons a day. I also take COQ10 with the Poly, along with Artemisinin,pancreatic enzymes and IP6. This is just the tip of the iceberg of what I am taking. I also take different mushrooms, Epicor, Lugol's Iodine, DIM, Calcium-d-Glucarate. If anyone is interested in my complete list please feel free to contact me.
This list is way to long for my long testimonial. I also eat lots of fresh fruits and veggies. My diet is not of the best, but I do not eat beef, very little chicken, and love seafood. I just had my 62nd birthday March 1, 2007 in Hawaii and gained more weight and feel fantastic. As of now, no signs of illness. I have excellent health and work full time and care for 11 cats.
June
6-19-2009
I am back to the Poly at the high dose. This leap from 17 to 22 on the tumor markers was a real eye opener. This is after I lowered my dose of poly and increased the mushrooms. I do know one thing, the tumor markers do rise when something is going on, EVERY TIME. I have followed the markers very close for quite some time. Hoping increasing Poly will do the trick.
June
9-4-2012
June is still taking Poly MVA and is a regular attendee at the Cancer Control Conference in Los Angeles and helps talk to other Cancer Patients about Poly at the AMARC Booth.
8-09-2017
June suffered a stroke and has started back taking 2 teaspoons of Poly a day.
Trudi B.
Date: October 20, 2004
Diagnosis: Stage 3 Breast Cancer
2 Updates 2-21-11 – 11-20-18
Personal story
To the entire Poly-MVA Team, The first time I noticed the lump in the summer of 2003 in my right breast, I immediately went into the doctor's office and was told after a mammogram and ultrasound that it was benign.
After an additional year had gone by, and I noticed that it was still growing, and even noticed a small pea-sized knot in my left breast, I returned to the doctor's office to find out that I had Stage 3 breast cancer. Only being 40, and overwhelmed with sudden conversation about double mastectomy, aggressive chemo and radiation, I felt that I was in a nightmare and couldn't wake up.
I had surgery on both breasts July 15th, 2004. My follow-up treatment then was defined as aggressive chemotherapy starting August 16th 2004, and consisted of a total of 8 rounds of treatment, every two weeks. The first four treatments were a combination of Adriamycin and Cytoxan, and the last four treatments were Taxol. I followed my treatment schedule religiously, receiving the chemotherapy ever other Monday, referring to each day as #1 through #14. In order to keep my blood count up, I received Neupogen injections days 3 through 10 of each cycle.
Not knowing about Poly-MVA at the point in time I began my chemotherapy, I woke up 3 days after my first chemo treatment unable to get out of bed. I was experiencing unbearable migraine headaches, nausea, all the traditional side effects that one expects from chemotherapy. I fortunately, over the next few days my systems eased a bit, and I was able to get up, move around, and try to distract myself with things to keep my busy. Being the mother of 3 children, that was not hard to do.
Thank god for the efforts of my mother. She ran across an article about Poly-MVA in a Sacramento magazine entitled Comstocks. After receiving the okay from my Oncologist to have me begin taking Poly-MVA as an additional supplement to the traditional medical treatment, I began the heavy dosage of two teaspoons, 4 times a day, on August 20th, 2004 - Day 5 of my first chemotherapy cycle. I didn't notice any immediate results over the next week while I was mentally trying to prepare for my next chemotherapy treatment and inevitable hair loss to come.
Every morning after my second chemo treatment, I did the same thing by waking up afraid to open my eyes to assess how I felt. But when Wednesday morning (Day3) came around that second time, I opened my eyes slowly in bed, looked at my husband, and couldn't believe it.
I felt okay! I was practically skipping and jumping and yelling out that overall, I felt NOTHING like I had on Day 3 of the previous treatment. In fact, I was never 'down' in bed one other day throughout the remainder of the 16 weeks!
I credit my exceptionally high level of tolerance of the chemotherapy side effects to two things - my steadfast adherence to my schedule of consuming the Poly-MVA four times daily as recommended, and my desire to not let the cancer and the treatments get the best of me.
I continued the high dosage of Poly-MVA throughout the rest of the Chemotherapy, and throughout my 6 weeks of daily radiation treatments, and even another month after that. I then slowly reduced my dosage over this last year. I now take only 2 teaspoons every morning - but continue to do that without fail.
My doctor has always been very impressed with my tolerance of the aggressive treatment I received, and ongoing healthy condition. Thanks to the efforts of my mom, and Poly-MVA. Trudi B. Sacramento, CA Breast Cancer Survivor
2-21-2011
Talked to Trudi and she says she is doing well and promised provide an update to her testimonial.
11-20-2018
Trudi is still taking Poly MVA and trying to be consistent with her daily dosing.
Odette Gaud
Personal story
Azores, Pico Island, Portugal
Diagnosed: December 2, 2003
Diagnosis: Invasive Ductal Carcinoma
Phone: 011 351 292 655 209 E-Mail: odette_gaud@yahoo.co.uk
Conventional Therapy: Lumpectomy refused all further conventional treatment Started Poly-MVA April 2004 and is now in remission and following maintenance dosage.
A LIFE CHANGING POSITIVE EXPERIENCE. My Story
How I hope I have beat Cancer and enriched my life for the better. Hi my name is Odette Gaud, I am 36 yrs old and I have 2 wonderful kids a 7yr old boy and a 3yr old girl. My partner and I live in the Azores, Pico Island Portugal. My nightmare began in June of 2002.
The story I am about to tell you could very well be a soap Opera, but it is all very true. In June 2002 we moved to the Azores from Cape Town South Africa. This was done against my will. My folks and friends were left behind. I could not speak Portuguese and I did not understand or even like the culture and I knew nobody. I hated it. Needless to say that for the entire first year of my being here I cried and cried.
In November 2003 I went to the gynecologist for my yearly check up and a check up on the lump that I had carried around with me since the birth of my son. A needle biopsy told me that the lump was not cancerous. HOW WRONG COULD I BE? The Doctor just wanted to make sure so he advised me to have a mammogram, which I did. The Doctor told me that the results were suspicious. I went home in a state and I knew that I was going to follow his advice and have the dam thing cut out. I did this against Graemes advice, but I was listening to nobody. On 2 December I went into hospital and had a lumpectomy. On the 15 December I got a call to go to the hospital and I received my results.
BREAST CANCER - INVASIVE DUCTAL CARCINOMA - DEATH SENTENCE. This had spread past the actual sample that was cut out and used for a diagnosis. His advice, we have no time to waste. The breast has to be chopped the lymph nodes have to be removed to see if it has spread to other regions. Once he had disfigured me and cut away my feminine parts, he then suggested huge doses of chemo and then radiation. With all this information he sent me home and he would wait for my decision.
I have come to realize that the doctors of this world know only that which they have been taught at University. NO THINKING AS INDIVIDUALS ONLY PUPPETS ON A STRING kind of thinking. Please don't misconstrue my words. I believe you need a doctor to fix appendicitis or fix a broken leg. They believe that to fix a problem they have to get the problem out. The most important fact I have learnt about alternative and holistic approaches to curing diseases, DON'T REMOVE THE PROBLEM - FIX IT, NO MATTER WHAT IT TAKES.
My nightmare had begun. But little did I know that huge miracles were awaiting me. The first in a series of events to unfold which would change my life forever, was when a guy from New York knocked on my door, in the middle of the Atlantic, don't forget on an Island that hardly anybody in the world knows about. He was looking for property in the Azores to set up a little health farm. He was a naturopath. We just happen to sell property here too. Not very successfully but we try. We told him what had happened to me and he spent 3 days with me explaining to me what had to be done to change my blood work to a clean slate.
He gave me a protocol, but we were so broke that I could not afford to buy the supplements and stuff on his list. Not only was I penniless but the Azores never had a single health shop on its shores. To make matters even worse I had to consume this raw fresh diet of green Vegetables. All that was available to me was cabbage, wild spinach and parsley. At of course
exorbitant price. I would have to get all my supplements from USA. No money meant no medicines. BUT HE OPENED MY EYES. HE WALKED INTO MY LIFE WHEN I NEEDED A DIFFERENT WAY OF THINKING. The most amazing thing that he did was to take a blood drop and put it on a microscope slide let it dry and he was able to tell me exactly what was happening internally to me. We soon discovered that due to amalgam fillings and a silent infection in one of my root canals and of course the fact that my immune system was non existent from all the stress of immigrating. I had cancer.
I cannot find the words to explain to you the panic, the tears, the thoughts of dying, of leaving my kids to grow up by themselves, the panic attacks and probably the worst, the stress it created between my partner and me. I told my doctor to please give me until February 2004 to make up my mind as to what I wanted to do. He also told me that my chances of survival after doing all of the conventional approach was 50/50. I also did not really understand how and what kind of diagnoses I had. All I knew was that I had breast cancer, I did not know anything else, as I could not really understand what the Dr. was telling me. Little did I know that doctors love to use scare tactics on their patients to push them to make a decision. This was what made me fire my doctors. I decided to take responsibility for my health.
Once I had made my decision my stress was made worse by my wonderful caring family back home sitting on the phone spending a fortune trying to get me to change my mind. It almost worked. But I soon realized that they were just very scared for me and the only way they could make themselves feel better was to try and get me to do the conventional thing that everybody else does. Even if this way led in most cases down the line to death.
I have made everybody around me see things differently. They still think I am crazy especially the people living on my island. But most importantly I withstood the storm and have even got a few people coming up to me to ask me about how I did it. That for me is a success. This began my crusade to knowledge!!!!!!!!!!!!!!!!!!
The Internet. I would spend at least 5 to 6 hours a night on the net. I hooked up with so many wonderful people and groups. I just needed to know that if I decided to go the natural way I had to know how to do this. I spent so much time on the Internet that I basically bankrupted us. I would get a phone bill of two to three hundred Euro a month. This is not too serious if you are earning Euros. We were not. We were still living on the very poor South African Rand, which was 12 to 1 at the time. This also meant that I could not get my medicines. To add to the stress Richard the Naturopath from New York took another blood test and he told me that the cancer had spread to my lymph nodes and to my uterus.
To start the healing process, I had to clean up my mouth. Rid them of amalgams and get rid of the infected root canal. Once this was done Richard could immediately see the difference in my blood sample. I also had to drink 32 oz of green vegetable juice and eat raw live foods. I could not do this! I cheated from almost day one. I new if I did not follow this a painful death was the final outcome???.
But I was still in store for some huge surprises. We had no cash. As I tried to educate myself, I stumbled upon Bill Hendersons web page. I asked him to help me put together a protocol that cost very little cash. He then informed me that he had just interviewed a gentleman by the name of Al Sanchez. Al Sanchez was supplying Poly MVA as part of the research he was conducting.
Bill Henderson gave me contact numbers and before I new it I was part of the tests being conducted on POLYMVA. For me this was a blessing as I would never have been able to afford it as a single bottle of POLYMVA cost at that time $300 dollars, and this for only one 8 oz bottle. For one month I needed 5 bottles. I also became part of the POLYMVA support group. And I found out about the 4 corners Protocol.
Needless to say it took me ages to get my protocol together with a lot of help from a lot a wonderful people. But it happened. Every single tablet has a function within my body. I spent months researching and reading articles as to what the body needs to be balanced. I sort of hope that the balance is a good balance. I often made my decisions based on other peoples opinions. I tried it out and if it did not feel great skipped the supplement. This really was a game of trial and error.
I took the intense protocol everyday for 3 weeks without chewing a morsel of food. I chose not to eat solid foods so as to allow the pancreas to rest and manufacture enzymes so that these enzymes could repair the damaged tissue that had been damaged by the cancer. This was the hardest 3 weeks of my life. I LOVE FOOD. When the 3 weeks were over it had paid off. I will always maintain a diet of NO SUGAR.
When I eat cooked foods it is always steamed vegetables a wholesome plate of broccoli, cabbage, corn a baked potato with olive oil dressing and lemon juice some peas and beans. During the summer it is a lot of salads my favorite salad once a month is sliced organic chicken salad with heaps of fried onions and garlic. Always use extra virgin olive oil. This is my treat for sticking to a no sugar, no meat, no salt, no diary and no white flour diet. In regards to the supplements I will always take the Poly-mva and the 4 corners protocol (finances allowing) but to take all the other supplements on a daily basis is very sore on the throat so I relax and take the other supplements about three to four times a week and not daily. The 4 corners protocol consists of MGN-3, CO-Q10, CORAL CALCIUM, LIVER EXTREME AND MOST
IMPORTANTLY POLY-MVA. The idea behind this protocol is firstly to boost the immune system, to alkalize the body and very importantly to help the liver rid itself of the toxins produced by the die off of cancer cells. And of course to kill the cancer cells and return the damaged DNA to healthy DNA. The rest of the supplements I take are just to balance the body and make sure everything functions right.
I have given up feeling guilty about the way I eat. The stress of worrying about my food intake was worse than the stress I experienced when told I had cancer. I have forgiven myself for being sometimes weak. I enjoy my stolen moments of bliss. The Wonderful result is that I have brought my tumor markers CA15.3 down to 19.09 and my CEA27. 0 down to 0.61. These are all very normal readings.
The hardest part for me is to maintain the diet of raw food and juices. As soon as I don't stick to a good diet I start getting pain on my right hand side by the rib cage. This immediately tells me that my liver is having a hard time dealing with all the garbage I am eating.
Another part of my healing was being able to forgive and let go. I had to clear my inner thoughts that were in turmoil. I had to learn to love the island I lived on, and forgive Graeme for bringing me here. I had to learn how to enjoy my kids I had to learn how to simply enjoy life. That was perhaps one of my hardest lessons to learn.
Cancer for me has been a very positive and rewarding experience. I have learnt a lot and I am really so positive nowadays about my life. For the first time in years I am able to look forward to the future, to know without doubt that I am capable of doing anything that I set my mind to. I have met so many great and wonderful people who are doing what I am doing. When I needed support it was my friends on the net that got me through a bad patch.
I know that the greatest test is still ahead of me, I also know that if I died tomorrow I won't be sorry. I have lived on the edge. And that for me was so much better than living in the confines of what a brain washed society dictates. I felt alive and that for me was so much more divine than being half-alive with no cancer.
ODETTE GAUD
Rhonda Apperson
Date: June 19, 2001
Diagnosis: Breast Cancer w/ mets. to Lungs
E-Mail: not available
Rhonda's Testimonial
Dear Mr. Matson,
Following our telephone conversation of last night I began thinking about my struggle with breast cancer from the beginning. When I first learned I definitely had breast cancer I was devastated and felt so alone. I wondered how I could, as a single mother, tell my 3 children and try to keep my composure. Because in my heart I knew I intended to fight for my life.
My cancer had been diagnosed by the oncologist at a Richmond, Va. Hospital and he recommended chemotherapy and radiation... I went for three rounds of chemotherapy when my hair started falling out, my teeth started to loosen and fall out and I was so nauseated, I decided I just couldn't go ahead with it. However, despite all the side effects from chemotherapy, my cancer had stopped growing.
In the spring of 1999, however, the cancer returned. My breast became feverish and it became painful. But I had decided no more chemotherapy and told my friend and boss Capt. Frank Manson that I was not taking anymore chemo. Capt. Manson said he would not permit me to just let my life go that way. He had a friend, Dr.John Stauch in Atmandale Va., who had some success with alternative therapies and arranged for me to see him. Dr. Stauch gave me a thermogram and found my breast covered with cancer, he said I was in the final stages but he believed he could arrest it. So, I agreed to give Dr. Stauch's alternatives a trial and miraculously they worked for about 18 months. But my cancer refused to give up and I could tell it was coming back.
My symptoms were the same and now I was coughing up grey sputun. I went back to the Richmond oncologist who gave me another MRI. He found the cancer had metastasized to my lungs. The cancer had wrapped around the two top ribs of my left lung. He also found the mass of cancer cells covered my entire left breast. Your cancer has returned with "full fury", he said. You need chemo and radiation immediately. I pleaded for time. "Give me 8 weeks," I said and "if I don't improve I promise to try chemo once more."
Meanwhile I had heard of POLY-MVA from a naturopath friend in Rice, Washington, an expert in herbs. He recommended I download www.polymvasurvivors.com from the internet and try it. I did.
Within 48 hours I could tell POLY-MVA was helping. After 8 weeks of doing as I was instructed by the protocol, I went back to the Richmond oncologist. He found, after another MRI, that my lung cancer had disappeared and the mass covering my breast was now divided into 6 small tumors. "What have you done," the oncologist asked. I told him POLY-MVA, and no other medications. He was astonished and wanted the details which I provided.
Four weeks later I returned to the same Richmond oncologist for a check up. He found my breast cancer was now reduced to 4 tumors and that is where I am at the moment. In contrast with the dreaded chemotherapy side effects of severe nausea, I have had absolutely no side effects from Poly-MVA. Only positive things, more energy, feeling much better as the cancer cells vanish.
I strongly recommend POLY-MVA to anyone with breast cancer. It surely is working for me and this is my third bout with breast cancer following my original diagnosis in 1997 by the Richmond Oncologist who had warned that I had a short life expectancy.
Being a nurse who had treated a number of cancer patients I knew the oncologist had it right unless I could find an alternative which would work for me. Providentially, POLY-MVA is my miracle worker. I am also taking Clodronate to help prevent cancer from spreading to my bones. You have my permission to use this letter so others such as myself may benefit. P.S. Now with God's will and the Poly-MVA I have new hope that I will get to see my Granddaughter, Casey, grow up.
Yours faithfully
Rhonda Apperson
Olivia de Haulleville .
Date: February 2, 2002 .
Diagnosis: Breast Cancer Stage 2 .
E-Mail: solemate@earthlink.net .
Phone: 760-369-7075 .
3 Updates 1-27-04 – 3-16-07 – 9-01-18
Olivia's Testimonial
February 2, 2002 My Stage 2 breast cancer was discovered in the Spring of 1999, after a biopsy revealed two estrogen-receptive DCIS growths in my left breast, one the size of a pea. Radical mastectomy was immediately recommended. Several "second opinions" also recommended that I should have the ‘offending breast’ totally removed, including the lymph node which would determine whether chemotherapy and / or radiation would be needed. I was also prescribed Tamoxifen.
However, I refused all of these options. I immediately changed my diet to eliminate all estrogen foods, i.e. milk & meat products which have received hormone additives; I stayed clear of the microwaves, increased my already mostly Asian diet of seaweed, mushrooms and tofu, and took larger doses of vitamins and supplements.
Being a Holistic Practioner myself, (i.e. Clinical Hypnotherapist) I realized the importance of an integrative approach. My original doctor, Yeshi Dhonden (previous doctor to H.H. The Dalai Lama) supplied me with Tibetan herbal pills, but since I failed to establish a good connection between Tibetan and Western medicine, I decided to forego this initial treatment after my supply was exhausted.
Shortly after, I was lucky enough to be present at a lecture by Albert Sanchez on Poly-MVA. I was so impressed by this man that I failed to take notice of the extensive testimonials he offered on this product. I decided instead to purchase Dr. M. Garnett’s personal journal: First Pulse. I read this book with fascination! Being dedicated to a natural way of life, I was able to discern the power in this substance immediately and immediately had it checked out by my Tibetan doctor who gave me the go ahead.
In July 1999, in order to convince me of the urgency of a mastectomy, my Oncologist requested another mammogram. In fact, the mammogram was done twice… but still could show no suspicious results! My Oncologist seemed nonplussed. He asked me what I proposed to do next; without hesitation I answered: "Continue the Poly-MVA.
UPDATE: 1-27-2004 In 2001, during the course of my follow-ups, I asked my doctor about Thermography since I was not fond of mammograms. I was told that it was not available and ultrasound was recommended. In July 2002 the ultrasound proved "suspicious" and a biopsy revealed malignancy (although the mammogram had showed results as benign!) Once again, my Oncologist recommended lumpectomy, if not mastectomy. I asked for an MRI which then showed suspicion in BOTH breasts! Meanwhile, I started on a loading dose of Poly and after 3 months requested another ultrasound. "Not possible," the doctor exclaimed: "Why should we do that? We KNOW you have cancer."
But I was not convinced and searched out a location where Thermography was available. This is a non-invasive technique, fully approved by the FDA (although NOT reimbursable by HMO's) whereby an infra-red photo is made in a cold room highlighting any areas not affected by the drop in temperature. (i.e. thermo = heat). I understand that this method of diagnosis is 70% accurate with the first result and is 90% accurate with the second.
In September 2003 both these results showed NO abnormality in EITHER breast. I called my Oncologist to explain why I was putting off the operation and asked if she would look at these test results. Upon seeing them she said: "Dear, I cannot trust these results since we KNOW you have cancer." Meanwhile, I continue to feel fine & continue sipping my PolyMVA.
Best to all,
Olivia
UPDATE: March 16, 2007 Even though I had been taking the Poly-MVA for several years, I had been unable to earn me the "cancer free' credential from any Oncologist… maybe because I was not taking large enough dose. However, at this time I have finally been declared "cancer free" by the medical establishment…
Why? Because I underwent a bi-lateral mastectomy in 2005. Why? Because I desperately needed both hips replaced. Why? Because my Orthopedic Surgeon refused to perform this operation unless I got a mastectomy FIRST. So, being in unbearable pain, I agreed. (The mastectomy operation, however, was more debilitating than I had anticipated… but the hip surgery much easier!) When the Oncologist notified me regarding the analysis of the malignancy, he exclaimed "Oh, your cancer was more aggressive than I had believed!" But he never questioned the fact that I had survived comfortably 5 years with no metastis. He continues to urge me to follow up with Femara, etc. but I just continue sipping my Poly-MVA…. and SMILING! God Bless All Survivors -
Olivia
9-1-2018
Olivia has been sharing Poly MVA with other Cancer Patients for 2 decades. Every year she attends the Los Angeles Cancer Control Conference and helps AMARC at the booth.
Imelda Gallardo
Testimonial Date: June 2024
Diagnosis: Breast Cancer
Imelda’s Testimonial
I followed the doctor’s wellness recommendations, but I also knew I wanted to do more. That’s when I remembered Poly-MVA. My husband had started taking it over 21 years ago, and I always kept it in the back of my mind. So I decided to start taking it too.
I don’t remember exactly how much I was taking at the beginning, but it was a higher dose. Now, I take one tablespoon in the morning and another in the afternoon—and yes, I’m still taking it today.
I truly believe Poly-MVA helped me. I was on low-dose chemo, but I didn’t experience the usual side effects. I didn’t lose my hair, and I didn’t feel sick the way many others do. I know the combination of the treatments and Poly-MVA made a big difference for me.
Poly-MVA has been amazing. I do miss the days when consultations were offered for free—it made it easier to ask questions and feel supported—but I’m still grateful for what it’s done for me.
I’m 76 now, and I feel strong and yes, you have my full permission to share my story. If it can help someone else, then it’s absolutely worth it.
Alice Smith
Testimonial Date: Oct 2024
Diagnosis: Breast Cancer
Alice’s Testimonial
My journey began back in 2013, in the most unexpected way—through my dog. She kept nudging and paying close attention to my breast, and that made me stop and think. I felt something thicker in that area, but I didn’t take action right away. It wasn’t until 2015 that I finally started chemotherapy… and it felt like it was killing me. That’s when I made the decision to step away from conventional treatment and turn my focus to Poly-MVA and CC-cream instead.
Before that, I remember waking up in the middle of the night because of this deep, intense itching in my breast. That’s when I knew something wasn’t right and decided to see a doctor. They ran their tests, and I underwent both chemotherapy and surgery—but it only made me feel worse. I wasn’t seeing results, and the doctor eventually told me that if I didn’t go through with radiation, I probably had less than a year to live.
That was a turning point for me. I chose not to follow the standard path. Instead, I started researching alternative treatments. During that search, I found Poly-MVA. My brother had passed away from stage 4 cancer, but I remembered that Poly-MVA helped extend his life by two extra months. That memory gave me hope.
I started taking Poly-MVA shortly after my diagnosis—1 tablespoon every six hours. I paired it with oxygen therapy at night and daily exercise. Today, I’m taking half a teaspoon twice a day and I feel healthy, alive, and free of cancer. By 2017, I was completely cancer-free—and I credit Poly-MVA for being the key part of that transformation.
I’m now 65, and I can say without hesitation that Poly-MVA changed my life. I share my experience on social media and with anyone who will listen, because I believe it can help others just like it helped me. I’m down to my last bottle and will be calling soon for more—because Poly-MVA is something I never want to be without again.
Cudney Marjorie
Testimonial Date: 11/18/2009
Diagnosis: Ductal Carcinoma
Marjorie’s Testimonial
I was diagnosed with infiltrating ductal carcinoma in September 2008. I am so thankful I had knowledge of PolyMVA. I am grateful to have been accepted in the Quality of Life Study. The program that I followed is definitely a benefit and blessing to my quality of life. I plan to continue the maintenance program. I am doing well at this time.
Bonnie Fitzharris
Date: April 2015
Diagnosis: Colon Cancer Stage 2
Personal story
In April of 2015, I was diagnosed with Stage 2 Colon Cancer and decided to go the conventional route with Chemotherapy. After I finished chemo, I started taking PMVA solely along with the complete approach and the following support products.
Grapeseed supreme, magnesium buffer chelate, homocysteine, ultra-mega 3, oxysol, glucosamine chondroitin, vit D 3, vitC, multivitavitamin, irbesartan, hydrochlorothiazide 81mg aspirin I feel that PMVA and the magnesium chelate have been very beneficial in maintaining my quality of life. As I stated, I started using it right after chemo and have maintained using PMVA for 5 years and have not had a relapse.
I would not give up using PMVA because I believe it has been instrumental in keeping my overall health maintained. PMVA is a good support system to have and I believe it has helped me stay healthier, and energetic and stronger. It is worth the expense as your health is wealth. Amarc customer service has been great. Vivien & Gary have been wonderful in support.
Bonnie
Patsy Shea
Date: June 28, 2013
Diagnosis: Colon Cancer
2 Updates 9-07-17 – 4-30-20
Personal story
Initially, I started using 8 tsps per day starting on 06/28/2013. On 04/18/2014, I decreased my daily dosing down to 4 tsps after being on 8tsps daily for almost 1 year. Currently, I am now using 1 to 2 for maintenance per day.
I did not take any other conventional treatments, i.e. chemotherapy, radiation, other prescription medications. Amazingly, I just was using PMVA, NO other treatments. Poly-MVA increased and maintained my quality of Life, Cancer support and improved my fatigue. I believe that the benefits of using PMVA was that PMVA deterred further or any new occurrence of the cancer. It may have cleaned up the cancer that could be left in my body.
By taking Poly-MVA it gave me piece of mind. Toni was wonderful in providing the best customer support possible. She became a very dear friend and I would recommend Poly-MVA to anyone with cancer.
I believe that PMVA gives you piece of mind about any other occurrence. I still take PMVA today to support immunity.
Patsy Shea
9-7-2017
Spoke to Patsy to see how she is doing. She is still taking Poly but has yet to find a new Doctor since Dr. Baughman passed away.
4-30-2020
Patsy is still taking her daily maintenance dose of Poly MVA and doing well at the age of 85 years old. There has not been a reoccurrence of her Colon Cancer.
Roger Orr
Date: September 2009
Diagnosis: Colon Cancer
5 Updates 10-05-09 – 2-10-10 – 6-06-12 10-20-16 – 5-23-17
Personal story
I began using PolyMVA a few weeks prior to surgery (rectum removed) which helps account for my quick recovery and the clarity of mind and a sense of well being that followed. It was as if every cell in my body had received a tonic.
Surely the prayers to and faith in the great physician by my family and my doctors are key to healing. I appreciate the Foundation for researching cancer and its possible cures.
PolyMVA at the very least helped minimize the effects cancer had. I pray that soon it will be assisting others in this fight against this dreaded disease. Thanks to the results from PolyMVA, I plan to continue its use and praise god for its availability.
Thank you!
Roger Orr
10-05-2009
Talked to Roger. He is doing well. His surgeon told him that they believe they got all the cancer during the surgery and the doctor did not recommend chemo or radiation.
2-10-2010
Roger is doing well. He still gets up every morning goes to help out at the convalescent hospital and does bible study with prisoners daily. He will go next week for more blood work.
6-06-2012
Spoke to Mr. Orr and all is going well. He continues to take a maintenance dose.
10-20-2016
Mr. Orr has just turned 80 years old and is still taking Poly MVA. Says he feels good and is doing well.
5-23-2017
Called Roger to see how he was doing. He is still in remission after all these years and still taking 1 tsp a day of Poly. He appreciates our keeping in touch.
Marc Humphrey
Date: March 2009
Diagnosis: Colon Cancer
2 Updates 5-14-12 – 3-29-13
Personal story
The first time I took Poly-MVA it was pleasant tasting and gave me a feeling of energy. I did experience a cleansing effect. This effect came to pass as I was assured. The product was easy to take, no side effects, no nausea, no rashes. The more I took Poly-mva the better I felt.
I believe poly-mva along with the Protocel was a wonderful combination. The poly-mva was easy on my system. I would take this product on a daily bases. I believe it was helpful in my recovery from anemia, and my medical condition brought on by illness.
Addendum Marc said that he is doing well & feeling good. He went back to school. He is still taking 2 teaspoons 3 times a day. He has been on Poly MVA for over a year and has been doing really well since he started poly. We discussed whether he might decrease his dose of poly. He had surgery and has only used all natural methods.
5-14-2012
Called Mr. Humphrey to see how he is doing and spoke with his mother. She said he is still doing well and would let him know I called.
3-29-2013
Called Mr. Humphrey to see how he is doing. Says he is doing great. Admitted he had been off the Poly for awhile due to money but promised to get more soon.
Wanda M.
Date: April 17, 2008
Diagnosis: Metastatic Colon Cancer (Stage 4)
5 Updates 7-14-08 – 5-05-09 – 4-12-10 1-14-08 - 8-08-2011
Personal story
This is my experience in the last 12 months using Poly-MVA. April 17, 2008 I was diagnosed with stage 4 cancer in my colon, uterus , and ovaries. My Doctor first considered surgery but since the cancer had gone to stage 4 he wanted me to go through chemotherapy.
Instead, I began taking POLYMVA on May 21,2008. I took 3 IV’s of Poly-MVA a week plus 12tsp a day on opposite days. This was a total of 48 Poly IV’s.
After 6 months of treatment, a pet-scan showed signs of the colon tumor growing. I began another round of 48 Poly-MVA IV’s. After due consideration I decided on chemotherapy. I started chemo January 8, 2009. I continued my Poly-MVA during chemo.
I had another set of 48 Poly-MVA IV’s during these chemo sessions. I took my last chemotherapy on May 27, 2009. After a pet-scan on June 16, 2009 my chemo doctor told me that I was cancer free.
I continue to take 12tsp of poly-MVA per day orally. I am feeling better now and gaining weight and getting my appetite back. I give all the praise to GOD and the guidance HE gave me.
Wanda
7-14-2008
Spoke to Wanda. She has been feeling really good for the past three weeks. She said the poly has taken the pain out of her stomach and that means a lot to her.
5-05-2009
Followed up with Wanda. She is doing well but still has another round of chemo and then they will do some testing to let her know how she is doing. Wanda said the poly has really helped her get thru the chemo.
4-12-2010
Spoke to Wanda, she is doing very well. She will be going in for blood work on Friday and will see her doctor next Tuesday for the results.
1-14-2011
Wanda says that the new drugs that her doctor has her on seem to be doing ok. However, her doctor asked her to stay off the poly while she is on the new medication.
8-08-2011
Talked to Wanda. She is doing ok but not feeling her best. She will be going on a different series of meds and hopes it will help her. She has been off the poly due to her Doctors request.
Clifford Chan
Date: January 8, 2008
Diagnosis: Colon Cancer W/ Mets to Liver
2 Updates 10-22-2010 – 3-07-12
Personal story
I had colon cancer surgery on January 16, 2008. Tests showed the Cancer had spread to my liver on March 2008. From January of 2008 to March of 2008 I had various side effects from surgery, but I was not pain.
I went in for a colonoscopy in June 9th and was told that I am now cancer free. I had avoided chemotherapy, radiation and drugs. I am amazed that poly-mva cured me so quickly.
Thank you,
Clifford Chan
10-22-2010
Clifford called me back today & told me he was sorry he missed my call and wanted to let me know he just had his 82nd Birthday. He is ecstatic to still be alive! His cancer has not come back and said he is still taking a daily dose of poly.
3-07-2012
Dear Sir,
In March 2008, my cancer was in my liver. I decided to take Poly-MVA, and not chemotherapy or radiation. I have been cancer-free since 2008 and had avoided the side effects of chemotherapy or radiation. I am now 85 years old. Poly-MVA has saved my life. I appreciate the discount of Poly-MVA that has allowed me to continue using it.
Yours truly,
Clifford Chan
L. Jones
Date: February 14, 2007
Diagnosis: Colon Cancer Stage 3C
3 Updates 2-17-12 - 6-14-12 – 3-27-14
Personal story
February 14, 2007
I was diagnosed with colon cancer 2/14/07 at 62 years of age. That same day I visited my primary care physician, Dr. Robert Milne, who prescribed Poly-MVA. After taking Poly-MVA only a few days, I began to feel stronger despite being severely anemic from the colon cancer lesion causing bleeding.
In early March I had a right hemi-colectomy (half of my colon removed) and post surgical pathology report revealed the cancer had permeated my bowel wall and spread to nine lymph nodes, making the cancer stage 3C which I learned statistcally provides 40-45% chance of surviving five years.
My oncologist encouraged me by saying my odds were more like 50% with surgery alone, and that chemotherapy would improve that outlook. I took Poly-MVA throughout all of my treatments, stopping it 48 hours before until 48 hours after each treatment. Each time when I restarted the Poly-MVA, I experienced a rapid recovery from the previous chemo treatment.
I completed eight rounds of chemotherapy, which I tolerated much better than I ever imagined I would, a fact I attribute to the Poly-MVA. In August 2007, I had a PET scan which showed no residual colon cancer.
However, the PET scan did show a small spot on my breast, which turned out to be stage 1C breast cancer, a tumor that my oncologist estimated had been there at least two years and probably longer.
This tumor was HER positive which made it potentially aggressive, yet it was grade 1 (slower growing) and had other favorable reducing its lethality, I had a mastectomy and four rounds of chemo, stopping Poly-MVA 24 hours before until 24 hours after each treatment.
Again, the Poly-MVA helped me recover from each treatment and I tolerated the treatments better than expected. Then I had five more months of Herceptin without stopping the Poly-MVA. I was prescribed an aromatase inhibitor which causes a post-menopausal woman's estrogen to drop to undetectable levels, but I experienced the side effects of episodic arrhythmia and stopped the drug. Now I take only Poly-MVA and a few other supplements.
As I write this testimonial in April 2010, I have had three more clear PET scans. I chose to use all tools available to treat the cancer-Poly-MVA, chemo, lots of veggie juice, daily walking, yoga, and other supplements given to me by Dr. Milne.
I would never, ever have chemo without Poly-MVA. I believe without the Poly-MVA not only would I have had more negative side effects from the chemo; I would not have had the same positive results. I believe the Poly-MVA saved my life.
I have an extensive history of cancer in my family, and I intend to continue taking Poly-MVA indefinitely both to avoid a recurrence of the colon and breast cancers and to prevent a future new cancer.
Sincerely,
L. Jones
Update: 2/17/12 It is now 5 years since I was diagnosed with stage 3C colon cancer, and I have no recurrence of either the colon or breast cancer. While I realize there are never guarantees, I am delighted to have reached the 5 years mark, and I believe PolyMVA has helped me get to this point. Indeed, I believe Poly saved my life.
I still take Poly at a dosage of 2 tsp 3 times a day, but this dosage may be reduced to twice a day when I see my doctor in a few weeks.
I plan to take Poly for the rest of my life since there is a high incidence of cancer in my family and I have been diagnosed with 2 primary cancers. My experience with Poly is extremely positive and I regularly recommend it to family, friends and acquaintances who encounter cancer. L. Jones
6-14-2012
Ms. Jones called and shared with me she is doing well. She has been receiving her Poly MVA from Dr. Milne that has an added Vitamin A. Lynn is a nurse and advocates about Poly to everyone that has a history of cancer in their family and those going through cancer. She expects that she will be on Poly for the rest of her life as her diagnosis in the past was at a 50% chance and at 5 years to live. She has since surpassed that deadline and continues to live a healthy life.
3-27-2014
Lynn is still taking Poly from Dr. Milne and is taking a maintenance dose of 2 Tsp’s 2 times a day.
Mark Carey
Date: August 1, 2003
Diagnosis: Rectal Cancer Stage 1
2 Updates 9-23-2013 – 11-26-2018
Personal story
I began using Poly MVA on 8/3/03 on the advised of a friend. Surgery was successful - no chemo or radiation needed. But I knew that I needed to correct some nutritional issues. Eventually I dropped down to 1 tsp of PolyMVA a day.
However, in February 05. My CEA blood work came back elevated, for 7 months I saw my CEA levels steadily raise. In late August 05, I went back to a full dose 8 tsp a day for 3 months. By November 05 my CEA was normal.
As a result, I backed off my PolyMVA usage again. And again by early 06 my CEA was up slightly. I went back to a full regime until May 06 when CEA levels were normal again.
Since Sept. 06 I've taking 2 tsp 2 times daily of Poly MVA - my CEA levels have remained normal.
Mark
9-23-2013
Mark is on a maintenance which is keeping his CEA levels in check.
11-26-2018
Still using Poly MVA on a daily basis.
Maureen Arnett
Date: June 3, 2003
Diagnosis: Colon Cancer early Stage 3
E-Mail: harriet193@aol.com
4 Updates 2-03-11 - 2-10-14 – 11-17-16 – 4-25-18
Personal story
I have always been most health conscious and had no family history of cancer, yet I was diagnosed with colon cancer in April 2002. I had my ascending colon and right lymph nodes removed at Ohio State University James Cancer Hospital May 17, 2002.
The day after I was released from the Hospital I started regular routine acupuncture sessions with my physician which were a great benefit and speeded my recovery from the surgery. Cancer was also found to be present in one of the thirteen lymph glands; therefore chemotherapy was recommended.
I chose not to follow this process due to my years of studying and following the healthiest, most nutritious program including organic foods, and relying on alternative and natural protocol for healings for myself and family. I was surprised when my surgeon told me the colon cancer tumor had been there for over two years, which I was totally unaware of previous to my diagnosis. I taught First Grade in the inner city of Columbus and had never missed even one day the year previous to my diagnosis.
My surgeon told me if I'd not followed health care practices as I did I may not have done as well as I had. He wasn't aware of alternative means to overcome cancer, but told me he'd support me in whatever I chose to do and continue to be my doctor, which he has.
My family physician, an MD, constantly educates herself on alternative healing and encourages such. After reading about Poly-MVA in one of Dr. Sinatra's pamphlets I immediately called to inquire about it from AMARC. I took the detailed Poly-MVA scientific research booklet I'd received into my doctor who immediately started to read it, spent several minutes reading it, and said, "This doctor is on to something. May I have this to read?" I told her it was hers.
She supported my using Poly-MVA and has encouraged me to continue on Poly MVA. I have been taking Poly-MVA ever since discovering it right after my cancer surgery and am most grateful for Dr. Garnett, AMARC, and all who help make Poly MVA available and pray it will soon be FDA approved. I followed the maximum dosage of 8 teaspoons daily for two months and then dropped down to 4 teaspoons daily until this last month.
My yearly colonoscopy showed no cancer whatsoever. The ultrasounds and CAT scans have revealed no cancer in my body. I am most thankful and grateful that there has not been a recurrence even though I chose not to follow the recommended chemotheraphy. I am continuing to use the maintenance dose of Poly-MVA as well as the immune support program which I have listed as follows: Transfer Factor Plus, Coq10, MGN3, Moducare (sterolins), milkthistle phytosome (with artichoke leaf, dandelion root, and tumeric) for my liver, wheatgrass juice (I grow and juice myself that my doctor told me to do from the time I was diagnosed with cancer), biogenic aloe vera, hyssop (which I attribute to being the main factor helping normalize my red blood count), barley grass powder, quercitin complex, Helix Plus, Risotriene, ester C, garlic, B complex, B12 shots weekly.
I follow eating according to my blood type, rarely ever straying away from such…. At first, growing wheatgrass, juicing it, taking so many things (some added over time), seemed almost overwhelming, but I concentrated on being thankful for discovering things that would help me and persevered on making it part of my daily routine. I have much energy and am very active daily. I am most thankful for regaining my strength and health. I pray others will believe there is hope, have faith, persevere, and overcome.
Maureen Arnett
3-23-2011
Maureen is traveling abroad and continues to take her daily maintenance dose of Poly.
2-10-2014
Maureen is taking ½ teaspoon of Poly daily and said all of her check ups have been good.
11-17-2016
Still doing fine and continues her daily maintenance dose of Poly MVA.
4-25-2018
Continues daily dosing. Check ups are still clear.
Esther Oransky
Diagnosis: Endometrial Cancer
Date: May 16, 2003
E-mail: EstherOransky@aol.com
4 Updates 4-06-07 – 6-23-10 – 8-28-12 – 9-10-18
My Poly-MVA Story
Dear Tim,
Thank you for all the help and support that you continue to give me and your guidance through my use of Poly MVA. I would like to give my testimonial and relate some of my experience to others.
In May, 2001 I had undergone a radical hysterectomy after being informed that a biopsy had revealed a tiny cancerous tumor in the endometrial lining. Unfortunately, although my surgeon had been highly recommended as chief of gynecological oncology at a major hospital, the surgery was not performed promptly as it should have been (I was forced to wait 6 weeks because he was going on vacation).
Also, prior to surgery, I had been given a drug to prevent clotting which caused me to hemmorage severely and I almost didn't make it through the surgery. In any case, I was told afterwards that it was very likely that some cells were remaining and that I would need subsequent radiation treatments for 5 weeks.
I was so sick and weak at the time that I resisted these treatments for several weeks. While I was in the hospital, I had met a nurse who told me about Poly MVA. Her nephew was taking it and doing very well. I kept in touch with her and contacted Gary Matson sometime in June. I was quite frantic by that time and Gary was a virtual blessing. I started on Poly sometime towards the end of June or early July.
In August, I found another doctor to follow up with because I could not go back to the original surgeon who had treated me so badly. She examined me and observed something that concerned her. She did not think that it was cancerous because the cells were flaking off - something that she had never seen before.
I think the flaking off was because the Poly-MVA was starting to kill the cancer. The Doctor sent a sample to the lab for analysis. The result indicated that cancer was present. As I had been warned, during surgery some of the cancer cells had escaped and I was not in the clear. It was decided that I would need five weeks of pelvic radiation followed by several treatments of brachytherapy.
I was frightened and so followed this advice which has created horrible side effects in the cervical area. In total I had radiation treatments for 13 weeks because I was unable to endure consecutive daily treatments and it had to be extended with brief periodic interludes.
All during this time I persisted in taking my Poly MVA although I was discouraged to do so by the doctors. I had read all the data regarding Poly and how it works to destroy the cancer cells as well as preventing new ones from forming .
At this point I am considered to be in complete remission and in spite of great hardship to maintain it I continue to take 2 teaspoons a day. I am convinced that Poly-MVA has made the difference for me.
Poly-MVA is a great breakthrough and if taken in time and in adequate amounts it does indeed keep cancer at bay. I feel that it has improved my chances for survival. If possible, I would like to continue taking it indefinitely.
I look forward to the day when Poly MVA is given full recognition by the medical profession and the FDA for its value in fighting cancer. My thanks to Dr. Garnett, Dr. Sanchez and to Gary Matson for their great contributions.
With gratitude, Esther Oransky EstherOransky@aol.com
UPDATE: April, 6 2007 Started using Poly MVA in 2001. Original dosage : approx. 1 - 2 tsp. 3 X day after surgery for endometrial cancer. Surgery was not entirely successful since there were still some cancer cells present. I started taking Poly and also had 13 weeks of radiation both pelvic and brachytherapy. I continued taking Poly all through my radiation treatments. I have been taking 1 & 1/2 teaspoons of Poly since then. I would like to continue this treatment as long as possible since I do believe that it is a necessary protection.
UPDATE: June 23, 2010 Spoke to Ester and she said she believes that she is still around because of the benefits of poly. She is still taking Poly-MVA on a regular basis and has actually increased her dosage as she is currently dealing with some stressful situations in her life..
8-28-2012
Esther still takes 2 tsp daily. Her husband is bedfast and her daughter has blood pressure problems and autism so she has her hands full. She is a tough lady with a great spirit.
9-10-2018
Esther is still doing well and continues taking Poly daily.
Wendy Jae
Diagnosis: Endometriosis
Date:
Wendy’s Testimonial
Including Poly-MVA for over two years now into my diet and daily nutrition has proven to be a very healing experience. I have taken Poly-MVA for my over all health and I am dealing with endometriosis. My physical pain have diminished. Currently I am tapering and rotating my dosages to 1-2tsp every other day now, I was using 8tsp for 60 days per doctor. I will continue to use this to help maintain my overall health and believe it can help every single human being if allow yourself to be open to this internal healing. I have referred many friends and family to look into Poly-MVA as an option for good nutrition. Thank you very kindly Dr. Llamas and the staff. ……
Terry Goodman
Date: 2014
Diagnosis: Barrett’s Esophagus
(Pre-Cancerous Esophageal Cancer)
5 Updates
4-13-17 – 5-18-18 – 9-10-18
5-02-19 – 6-08-20
Terry’s Testimonial
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Barrett’s Esophagus
Barrett’s esophagus is a serious complication of GERD, which stands for gastroesophageal reflux disease. In Barrett’s esophagus, normal tissue lining the esophagus — the tube that carries food from the mouth to the stomach — changes to tissue that resembles the lining of the intestine. About 10% of people with chronic symptoms of GERD develop Barrett’s esophagus. Barrett’s may have symptoms related to GERD which may increase the risk of developing esophageal adenocarcinoma, which is a serious, potentially fatal cancer of the esophagus.
===================================================================================================
In 2007, I was diagnosed with Barrett’s Esophagus. Barrett’s Esophagus is a precancerous condition. My doctor performed an endoscopy along with a biopsy and found damaged tissue caused by Barrett’s Esophagus.
My doctor stated that, “There is no cure or Barrett’s Esophagus, once you have it, it will not go away.”
At that time there were no treatment options available. My wife and I began to search for something that would help. In 2014, I read about Poly-MVA and began taking Poly-MVA.
In 2016, my doctor ordered another endoscopy, to check to make sure my precancerous tissue did not become esophageal cancer. My wife and I were holding our breaths waiting for the results.
When the reports came in, they showed I did not have esophageal cancer and the results of the scope showed a significant improvement in the damaged tissue.
Had I not started taking Poly-MVA, I truly believe that my Barrett’s Esophagus would have advanced into esophageal cancer.
Terry Goodman
4-13-2017
Contacted Terry and he said he is still taking Poly MVA and feels he is doing better.
5-18-2018
Called to get an update from Terry. He said due to finances he is still taking Poly MVA but sparingly. He is doing ok and said he can really tell the difference without it.
9-10-2018
Terry says he is struggling to keep up with ordering Poly but does feel a difference when he takes it regularly.
5-2-2019
Called and talked to Terry, while he and his wife were in their car traveling. Terry is still very positive about the protective benefits he has received from Poly MVA and tries to it take regularly.
6-8-2020
Poly-MVA, A Boost for a Healthier Life
Poly-MVA has given me a helpful energy boost throughout many years of my life. In one of several ways it has helped me be a little more independent in helping do things for myself. I learned about Poly-MVA, from a friend. It was in 2004, when I first learned about Poly. I have two conditions. The first condition is a rare fat disorder called MADELUNGS Disease. My body grows disfiguring unusable painful body fat that can only be surgically removed.
So,I take a teaspoonful every other day. Poly-MVA gives me a boost in my everyday fight against this disfiguring disease. When I need to have surgery I increase the amount of PolyMVA a few days before and after. My recovery seems to go much better for me.
My second condition is a pre-cancerous painful condition called Barrett’s Esophagus. I’ve had this unsettling condition for years. Along with diet and taking Poly-MVA I feel less stressful. I’m really glad that I have PolyMVA in my corner to help boost my immune system in my fight against MADELUNGS and Barrett’s Esophagus disease
I would recommend Poly-MVA to others and I have recommended it to others. If you are going into surgery use it to boost your system before and after. If you have fatigue use poly to increase your energy. Poly-MVA,gives me such a boost, I do not know how I would get around without it.
The Staff at Poly-MVA and AMARC have been so amazing to me. Throughout the years they have called to check on me to see how I was doing! It has meant so much to me! Thank you Poly-MVA. Your friend Terry G.
Jerry McGlothlin
Date: 08-12-2025
Diagnosis: Kidney Disease
Jerry’s Testimonial
W.J. Perlmutter .
Diagnosis: Chronic Lymphocytic Leukemia .
Date: 9-18-2009 .
E-Mail: WJPerl@embarqmail.com .
3 Updates 10-15-09 – 7-19-17 – 9-04-18
Personal story
Plain and simple, Poly-MVA has saved my life and let me live and pursue my dreams. After over 33 years of active and reserve service with the United States Navy, I retired at the rank of Captain which is equivalent of a full bird colonel in the Army or Air Force and one rank below Admiral or General. For the 33 years, since age 17, the military gave me 100% of all my physical examinations.
One year after retirement, I went to my first civilian doctor, Dr, Harold Pepe who prior to my visit requested a complete blood count also known as a CBC. Upon examination of my CBC he said, “I think you may have something but I want to send you to a specialist to be sure.” I went to the Comprehensive Cancer Center of Nevada which was affiliated with the University of California at Los Angeles (UCLA). Coincidentally I graduated from UCLA back in December of 1973.
When Dr. Pepe got the results, he called me in and said “Coach, the cancer center confirmed my suspicions. You have a rare type of blood cancer called Chronic Lymphocytic Leukemia, or CLL.” He also told me that this type of blood cancer has no cure! You can imagine how I felt being told I had cancer and there was no cure.
He then told me after confirming with his internist partner, Dr, Michael Falvo, that they were at a medical conference recently and sat in on a presentation about a product called Poly- MVA, which was essentially immune system vitamins chemically bonded to the precious metal palladium. Both Drs Pepe and Falvo recommended that I try Poly-MVA.
After looking at my military medical records, they noticed I had had this condition (based on military CBCs) for the previous 6 years and it went unnoticed by multiple doctors, as the condition is so rare. In fact, only about 7,000 people in the United States contact CLL per year.
Looking up CLL on the internet, it states average life expectancy after diagnosis is 8 years and I was in year 7. I did not think I had too much longer to live!
I had been dating a wonderful woman for 7 years as well, and we decided to get married. She also knew of my rare incurable cancer and wanted to be with me, no matter the outcome. We were and still are truly in love.!! Now, for the rest of the story: I called Gary, the Senior Consultant on Poly-MVA at AMARC Enterprises, and he told me they were looking for volunteers who had a cancer diagnosis confirmed, especially with my type, to serve as a test group to see if in fact Poly-MVA would work on supporting the body nutritionally to slow or eliminate the growth of the cancer by natural means, i.e. vitamins bonded to the palladium.
He told me the Poly-MVA product coupled with liquid co-enzyme Q10 (CQ-10) would be absorbed into my body and support my body so to allow my own immune system to combat my CLL. He also suggested I take Extreme Liver, Coral Calcium and Immuni-T tablets… all natural products with no drugs. To this I personally added fish oil, glucosamine, folic acid in a high dose as recommended by Dr. Falvo, milk thistle and a baby aspirin daily.
I then went to get another opinion, after 5 months on Poly-MVA, from one the #1 leukemia centers in the world, M.D. Anderson Cancer Center at the University of Texas, Houston. I was assigned to Dr. William Wierda, M.D. At Anderson they did multiple testing on my body and my blood. I went through CT scans, MRI’s, and a bone marrow aspiration where my hip bone was cut and bone marrow extracted.
Following the extensive testing, Dr. Wierda and his outstanding staff concluded that Dr. Pepe’s initial diagnosis and the Cancer Center of Nevada’s extensive testing and diagnosis were both correct and I did in fact have CLL. Dr. Wierda said that M.D. Anderson was testing a new immunotherapy whereby my bad blood would be taken and after six months of growing and preparing a vaccine utilizing a non-drug therapy which included saliva from a sea snail, that I would be injected on a regular basis to see if the experimental vaccine would have an effect on my CLL.
During the following six months and since diagnosis of my disease, I continued on the Poly- MVA therapy as recommended by Gary at AMARC. I had blood tests monthly at M.D. Anderson for over a year and nearly completed the vaccine therapy when the FDA closed down the program as non-effective.
I never stopped taking my Poly-MVA therapy and in Dr. Wierda’s terms, “we don’t know why your CLL has not gotten worse, but I’d keep taking and doing what you are doing.” All I was doing was exercising regularly, eating health foods consisting of lots of vegetables, chicken and fish and of course using Poly-MVA.
I feel great and look great at almost 58 years of age, and believe it or not I am a Captain of a large logistic aircraft, Boeing f 757’s and 767-s for a worldwide commercial airline. I reported my condition to my aeromedial doctor who initially told me my airline career was over as CLL was a grounding cancer and I would not be able to be issued an airman’s medical certificate…but I felt fine! I was physically and mentally able, I had tons of energy, my lymph nodes were normal, I had little to no bone pain and I spent over 1 hour on an elliptical trainer 4 days or more per week at level 15 of 20!
I wrote a letter to the Federal Aviation Administration’s (FAA) Medical Department, along with letters from the Cancer Center of Nevada, M.D. Anderson and Dr. Pepe. These letters were forwarded to the FAA via my aeromedical doctor, all describing my totally asymptomatic condition and all of NON-DRUG therapy i.e. Poly-MVA and low and behold, a miracle happened and I was granted a waiver allowing me to continue my career. For 2 years I had to go to a cancer doctor every 6 months to ensure I was still asymptomatic prior to seeing my aviation medical doctor for my FAA first class medical.
Recently the FAA issued me a 6 year waiver and reduced to once a year seeing an oncologist. I’m still regularly taking Poly-MVA and as Dr. Wierda said, “keep doing what you are doing.”
I am writing this testimonial in Penang, Malaysia while at a hotel on my 12-day trip throughout Asia. I am living my dream as an Airline Captain, have a great wife and life…thanks in no small part to Poly-MVA!
I can’t thank the staff of AMARC, the FACR, my doctors, friends and especially my family for all the support and love. I hope to see my 100th birthday as an active and healthy individual who is living and surviving and thriving, in no small part due to this great product. Thanks again! W.J.
10-15-2009
WJ says he is still doing great. Working on a speech he is going to give at the Las Vegas Navy ball on Saturday.
7-19-2017
WJ continues his daily dosing with Poly MVA and will be attending the annual Cancer Control Conference in Los Angeles so he can talk to cancer patients at the Poly MVA booth.
9-04-2018
WJ once again attended the Cancer Control Conference in LA and talked to new cancer patients at the booth.
Bob Stegmaier
Date: 2002
Diagnosis: Chronic Myeloid Leukemia
Personal story
In 2002, I was diagnosed with CML (Chronic myeloid leukemia). The oncologist was not very optimistic and told me I would either have a recurrence of the CML or develop another cancer later on.
My Dentist was Dr. Garnett, the scientist that invented Poly-MVA. When I discussed my diagnosis with him, he recommended daily dosing of Poly-MVA. I have taken it for 18 years to fight off the original diagnosis of CML and a later diagnosis of Prostate Cancer.
In April of 2018, I was diagnosed with Prostate Cancer. My daily 1 tsp maintenance dose of Poly-MVA had kept my CML in check for 16 years but was not enough to prevent the onset of Prostate Cancer.
When I received the diagnosis, I immediately started with the maximum loading dose of 8tsp of Poly-MVA daily as well as the complete approach. I am happy to report that I am currently cancer free as of the date of this writing.
I still use Poly-MVA every today as part of my maintenance and good health. Poly- MVA was a very important part of my protocol and I would not have succeeded without it.
I am now a twice cancer survivor. Poly-MVA helped me maintain a good quality of life during both cancer treatments. I went thru bone marrow transplant for CML, high dose radiation and intensity modulated radiation therapy (IMRT) for prostate cancer and used multiple vitamins and minerals. I felt better and was less inclined to get colds.
Amarc Enterprises has a great knowledgeable staff. A great company to do business with and polite friendly caring people. I recommend Poly-MVA to others.
Thank you,
Bob Stegmaier
Brian Mullen
Diagnosis: Acute Lymphocytic Leukemia
Date: June 26, 2001
E-mail: Not Available
Personal story
My Poly-MVA Story God's Miracle Healing of Brian Mullen Using Poly MVA Letter written by Dr. John Mullen (Brian's Father) On Sunday, September 10, 2000, Brian Mullen, age 32, was diagnosed at Emory University in Atlanta, Georgia with Acute Lymphocytic Leukemia (ALL); the Leukemia was present in 98% of his bone marrow.
The doctors gave Brian little chance of surviving through the weekend. During this time Emory University was offering an experimental research study. If Brian survived, he would undergo treatment for the following 2+ years. Even with this treatment, Brian was given a 40% chance of surviving another 5 years.
It became necessary for us to explore other treatment facilities. Based on Brian's critical condition and his aggressive Leukemia, American Biologics, with centers in Chula Vista, CA and Tijuana, Mexico, was the best facility to treat Brian's illness. No other hospital was offering an individualized cancer treatment using integrated medicine that could help Brian.
The physician team at American Biologics chose Poly-MVA as a key ingredient in the treatment protocol to fight Brian's Leukemia. Brian took his Poly-MVA dosages in water with meals; and within a month of treatment, Brian was in full remission - with 0% Leukemia cells in his bone marrow. An amazing recovery - beating all odds.
Brian continues to this day to take Poly-MVA and is doing very well. His blood chemistry is evaluated every two weeks with periodic bone marrow tests. Brian is experiencing excellent health and is living a conventional life with his wife and daughter in Marietta, Georgia.
Sincerely,
Dr. John Mullen
Traci Giles
A Story of Resilience, Awareness, and Cellular Support
Traci is a chiropractor who is currently focused on optimizing her own wellness and long-term resilience. Her personal journey has been shaped by both professional insight and lived experience within her family.
Fourteen years ago, her husband faced significant health challenges following a leukemia diagnosis. During his medical care, Poly-MVA was introduced alongside his treatment plan to support nutritional status and help maintain normal cellular function during a demanding period. His history included significant environmental exposures, including mold and benzene from a family water well. He also followed a mycotoxin support protocol under professional supervision. Over time, his routine blood monitoring reflected positive trends in overall wellness markers while maintaining consistent nutritional support.
Inspired by this experience, Traci has remained attentive to the role that nutrition, detoxification pathways, and cellular energy support can play in long-term health maintenance.
Traci herself has a complex health background that includes environmental exposures, family health history, and lifestyle stressors. She has been attentive to supporting her respiratory wellness, skin health, oxidative balance, and overall vitality. Her family history includes tobacco and alcohol exposure, as well as thyroid-related health challenges in a sibling. Personally, she has experienced multiple episodes of sun overexposure and occupational smoke exposure during a structure fire response.
Recent wellness testing suggested elevated oxidative stress markers, and she plans to retest before beginning a structured nutritional support program that includes Poly-MVA. The proposed plan includes a defined period of consistent daily intake under professional guidance, with the goal of supporting normal mitochondrial function, antioxidant capacity, and cellular energy balance.
Previously, Traci worked with a local wellness clinic where she received IV nutritional support, including glutathione, vitamin C, methylated B vitamins, and hydration during 2022. During several of these sessions, she experienced vasovagal responses, which reinforced the importance of pacing, personalization, and ongoing practitioner oversight in any wellness program.
Today, Traci approaches her health journey with clarity, patience, and respect for the body’s adaptive intelligence. Her focus is not on treating or diagnosing conditions, but on supporting the body’s natural processes — nourishing cellular energy systems, maintaining redox balance, and building long-term resilience through thoughtful supplementation, hydration, lifestyle practices, and professional care.
Her story reflects a growing awareness that wellness is not a single intervention, but a continuous relationship with the body, guided by education, consistency, and informed choice.
John Martinez
Date: May 14, 2010
Diagnosis: Lung Cancer Stage IV
2 Updates 10-26-11 – 1-15-13
Personal story
In May 14, 2010, I was diagnosed with stage IV lung cancer and started radiation oncology on May 22, 2010. I also had six sessions of chemotherapy with the last treatment on July 16, 2010.
After this session of chemo I did not hear from my oncologist for about 2 1/2 months. When I was finally contacted by the doctors they told me the cancer had spread to the esophagus and the liver and they felt I was beyond hope.
They gave me a copy of my CT scan and sent me home. The only thing that could help me was a miracle from God. During the time I was ill and could not attend church I still mailed in my tithe. One day in July I sent a letter with my tithe asking the church for prayers. Pastor gave the letter to Pastor Saeed who gave it the people at TEAM UP! Against Cancer.
They came to see me, prayed with me, provided information on available resources and encouraged me to attend the Tuesday night Prayer Meeting at PFA. I started faithfully attending church, the TEAM UP meetings, the prayer meetings and sitting in the circle of prayer on Tuesday nights believing for my healing.
During that time I gave my CT scan to the people at TEAM UP, and they had a doctor read the scan. He confirmed it was 'stage IV lung cancer with metastasis to the liver, esophagus ('I don’t know how he can eat'), the spine and most likely the brain' – and added, 'He needs a miracle.'
I asked David Bryant what else could I try and he researched and found a support product called Poly-MVA. We contacted the people at Poly-MVA who referred us to Dr. Charles Baughman, a doctor in Peoria, Arizona, and I started on the product on November 17, 2010.
The approach was IV infusion of Poly-MVA three times a week and 8 teaspoons of Poly-MVA liquid orally daily. Dr. Baughman also suggested a specific dietary and supplemental program to go along with the Poly-MVA.
When I started on this approach my CEA blood profile was 16.8 (normal is 4.3 to 5.0). I had faith and God started His work on me; my CEA profile level has come down to 5.7 with our goal being 5.0.
On May 8, 2011, the doctors did a pulmonary procedure on my lungs and took some scar tissue from the lung and ran several tests and they all came back 'Negative.'
I had tests in September of 2011 which proved my liver, esophagus, spine and brain are cancer free and there is no presence of cancer anywhere else in my body.
It has been 6 months since my last tests and I am still cancer free. I give praise and thanks to my God and my Lord and Savior Jesus Christ for my miracle for my healing!"
John Martinez
10-26-2011
Spoke to John and he told me that his doctor haD taken him off Poly-MVA and put him on Vitamin C IV because his CEA marker went from 5.7 up to 5.9. I told John that CEA markers are not just “cancer markers” and these numbers can fluctuate due to other ailments or even an infection. John said he was JUST DOING WHAT THE DOCTOR TOLD HIM. I told him we would get back to him.
1-15-2013
Received an update on John from David Bryant with “TEAM UP! Against Cancer”. John is doing awesome and his latest blood work shows he is clean and clear. He is very active and walks at least an hour a day and looks great.
Howard Parks
Date: January 2009
Diagnosis: stage 3B lung cancer (Adenocarcinoma)
E-Mail: not available
Personal story
Use of Poly-MVA from March 2009 to March 2010 I was diagnosed with stage 3B lung cancer (Adenocarcinoma) in January 2009 and had surgery 1-16-09 to remove the upper and middle lobes of my right lung. In February I went to Santa Rosa to be treated by Dr. Rowen and spent four days in his office receiving a variety of treatments to strengthen my immune system and attack the cancer cells.
In March of 09 I enrolled in the health program and began to take Poly-MVA, three teaspoons four times per day. I continued at this rate through March 2010. I also received IV C, 75 grams twice weekly at Dr. Shaw's office not too far from my home. On the days I received vitamin C, I did not take Poly so I was taking Poly 5 days per week.
I also took carnivore, which is made from the Venus flytrap plant and has a long history of use beginning in Germany more than 20 years ago. My general health remained good overall even though I have diabetes, GERD, and prostate problems. I do suffer with much fatigue.
Each PET scan showed improvement in that the Standard Uptake Value (SUV) of the small nodes in my lungs shrank as time passed, the cancer never progressed anywhere else in my body, nor did I ever have pain or any discomfort as a direct result of the cancer.
I did change my diet, eating no red meat, but having seafood and some chicken. I do consume a good amount of fresh vegetables and fruit. I have reduced my carbohydrate intake and never eat rice or pasta, and very little mushroom pizza. I do have some small desserts such as half a brownie occasionally. I am aware that cancer cells feed on sugar and as a diabetic must restrict my glucose intake.
Overall I deem to be staying ahead of the cancer and winning the war against it. It is impossible to say what part the Poly played since I have been taking Vit C and Carnivora with the Poly in my daily regimen.
I have cut back somewhat on the amount of Poly I take each day, and have cut back on my IV C as well. My next PET scan in two or three months will tell if that was a wise decision or not.
At no time have I had any chemotherapy or radiation. The cancer board at the local hospital forbid my having radiation from the very beginning. I would not have consented to that even if it had been recommended.
The oncologist who is kind enough to order my PET scan said, " it is too bad you are not having chemo because then I could take credit for how well you are doing" I guess that says it all!
Howard
Wilma Brady
Date: November 12, 2007
Testimonial Date: 2011
Diagnosis: Lung Cancer
3 Updates 5-01-08 – 4-27-10 – 7-11-12
Personal story
On Nov 12, 2007, I got diagnosed with Adenoid cystic carcinoma at the upper lobe of my right lung by biopsy. On Dec 19, 2007, Dr. Meyerson removed the right upper lobe of my lung. The tumor was completely removed and surrounding lymph nodes were negative.
I began Poly-MVA on January 27, 2008, and took it daily, 2 tsp a day along with the other supplements. On Feb.2007 I had Asthma & bronchitis treated with prednisone varied doses, Cipro 500mg bid, and Azithromycin 250 mg.
On Mar 17, 2008, Started radiotherapy which ended on Apr 23, 2008. 200 cGy’s per day, total 5400 cGy’s. Upper lobe bronchus stump radiated, approximately 7 ½ cm X 5 cm. Of course my well being declined after the radiation but after two months I was free of symptoms. By Jun 5, 08 the Pet SCAN was negative.
By 11/24/08 showed possible recurrence, areas of suspicion: upper right lobe soft tissue and right lower lobe surface area. No fluid in lung. A lung scan on January 22, 2009, revealed a stable shadow in the right apex lung and consolidation in the right base of the lung. My oncologist thought it was an inflammatory process which was first revealed on a PET/CT scan on November 24, 2008. On January 29, 2009, I received five days of antibiotics (Azithromycin).
On February 11, 2009, a repeat PET/CT scan revealed the same shadow in the right apex lung and consolidation in the right base. There was no uptake of radioactive glucose in either area. The oncologist's conclusion is that the areas were inflammatory processes and benign. The oncologist is having the radiology oncologist review the film to see if the inflammation could be from radiation (2008).
I believe that Poly-MVA has prevented any recurrence of my cancer as well as metastasis. I look forward to following up with you to update my results.
Thank you,
Wilma
5-01-2008
Called to talk to Wilma and she is doing well and still taking the Poly. She is now done with her radiation treatments.
4-27-2010
Wilma is still diligently taking Poly MVA every day and is now cancer free for 3 years.
7-11-2012
Wilma will reach the 5 year cancer free mark in December when she will have her final scan. She called to say hello and discuss whether she should stay on 1 tsp or lower to 1/2. I told her to please stay on at least 1 tsp. She is also still taking CoQ10 and D3 along with the maintenance dose of Poly.
Mary Ellen E.
Date: February 2006
Diagnosis: Lung Cancer Stage 3B
4 Updates 4-15-10 – 4-10-11 – 6-13-12 – 11-14-12
Personal story
In Feb 2006, I was diagnosed with inoperable stage 3B lung cancer. As a nonsmoker and registered nurse I felt I was living a healthy lifestyle. I was given 4-6 months to live and encouraged to get my affairs in order.
A doctor friend, interested in integrative medicine and research, started me on a supplement plan while I was receiving chemotherapy. The goal was to enhance the effectiveness of the chemotherapy. The fatigue associated with cancer and its treatment is very debilitating.
The strength would drain from my body and I felt as though if I didn’t lie down, I would fall down. My doctors suggested I try Poly-MVA and within weeks I had increased energy and felt strong for periods of time during the day. My strength continued to improve and before long friends and family were telling me how healthy I looked.
In Feb 2011, I passed the five-year mark and am grateful to Poly-MVA for restoring my health.
Mary Ellen
4-15-2010
Called Mary Ellen and she called back to let me know she is doing well. She said that she will have a scan 1st part of May and more blood work tests to see where she is at.
4-10-2011
In February this year, Mary Ellen passed 5 years being in remission. She had another scan in the beginning of April and all is good.
6-13-2012
Talked to Mary Ellen and she is going through Chemotherapy again. Unfortunately, the cancer in her lung has started growing again. She said she had Radiation treatments in October of 2011. Her PET scan in March of 2012 still showed some nodules. She has been receiving IV Poly treatments from Dr. Kotowski and has been tolerating her Chemo very well. She still believes strongly in Poly and continues to use it because she says it helps with her energy and recovery after each round of chemo.
11-14-2012
Mary Ellen said she will call back when she is ready to use Poly MVA again. She will have another CT scan to see what her results are and go from there.
Stephen Barry
Date: October 2004
Diagnosis: Lung Cancer
3 Updates 1-17-12 – 5-30-13 – 11-14-14
Personal story
I was diagnosed with lung cancer in Oct 2004. Upper partial left lobe was surgically removed early Nov 2004. One of our physicians, Dr. Robert D. Milne, strongly recommended that I start using Poly-MVA, which I did. I took a daily dose of of 2 tsp, 3 times a day.
I also underwent a 12-dose regimen of chemo. While the dosage has been reduced, I continue the usage of Poly-MVA and remain cancer free. In addition, my brother-in-law was diagnosed with liver and bladder cancer in Jan 2010.
We forwarded a supply of Poly-MVA, which he takes in addition to a very rigorous chemo regimen. He reported to us 2 weeks ago that his doctors had told him that no sign of the tumor were evident on his latest scan. Go Poly-MVA!"
Stephen Barry
1-17-2012
Spoke to Stephen’s wife and was told that Stephen is in ICU. He became ill and septic. She said it was not from the lung cancer but that he was improving day by day and that he may come home within a week. She did say that they were going to have to check with kidney doctors before he can get back on Poly.
5-30-2013
Spoke to Stephen and he said that he is not using Poly MVA at this time. He said he wants to keep his options open but does recommend Poly MVA to others.
11-14-2014
Talked to Stephen. Says he is doing very well and thanked me for calling.
John Flint
Date: July 23, 2000
Diagnosis: Lung Cancer Stage 4
4 Updates 4-12-2001 – 12-03-03 – 7-06-04 – 4-25-16
UPDATES: April 12, 2001 - December 3, 2003 - July 6, 2004
Personal story
On September 1997 I started having difficulties with reading comprehension, I could read a sentence but could not understand what it meant. Within a week I also developed strong headaches. My GP made an appointment to see a neurologist which he scheduled for 2 months in the future and suggested I continue to take aspirin. That same weekend my headaches were so bad that I went to the emergency room of the local hospital.
After a very short examination the doctor concluded that I had a bad set of headaches but "one thing you do not have are brain tumors". I felt reassured that I did not have anything serious and went home. As the headaches kept getting worse and I became more and more disoriented, I managed to obtain an appointment with a young neurologist. After a ten minute examination, she sent me for a cat-scan and within a few hours she gave us the bad news that I had two large brain tumors. She also suggested that the brain tumors were probably not primary and that they probably had metastasised from somewhere else. That day our life changed forever. The quick action of that neurologist might be one reason that I am still alive.
Within a few days they identified the primary as a large lung tumor, non small cell carcinoma, that had spread to the brain. I was rated as stage 4. During the next few weeks I saw 3 different oncologists, they all gave me a prognosis of 3 months to a year at most. All of them suggested I get my affairs in order. They also stated that it would be a waste of time and money to try any alternative methods.
I started full brain radiation which was followed after several weeks of recovery by chemotherapy. This lasted almost six months until the oncologist refused to give me any more treatments as the chemo was having many negative side effects on my system. At that stage the doctors stated that they had nothing more to offer and that I should enjoy life as much as possible. We felt we were left on our own, like abandoned, with no one to help us.
During the long months of chemotherapy, my wife had started looking at possible alternative treatments since my doctors did not seem to think that I had much chance. She called survivors to see what they were doing, cancer organizations to see what they could offer, read books, looked at web pages for the latest that kept on recurring among her various contacts. As we spent more time researching these products we got a clearer understanding of why they worked. Some were being tested in various research laboratories and showed definite signs of reducing cancer. Others dealt with helping the immune system and maintaining the body at its peak condition.
The different cancer fighting products we found attack tumors in different ways. Some prevented the tumors from growing the necessary blood vessels required for growth, these are known as angiogenesis inhibitors. Others attacked the protein membrane that the tumors use to shield themselves from the immune system. Others have chemicals that are necessary for some cancers to grow but also contain chemicals that are poisonous to the tumor - Poly MVA.
Some prevent the small new tumors from attaching themselves and therefore cannot grow. I take them all. To date, most of the data show that no single chemical is 100% effective and that taking more than one product increases chances of survival. Some are probably more effective than others, none of them are harmful. The cost of many of these products is relatively small.
It has been 3 years since I was first diagnosed. To date I have no sign of any visible tumors in the brain or lung. I even have some hair back. We would be glad to send you a specific list of the products I am taking. Also we are always happy to talk to anyone looking for help. We were not able to get help from the medical profession so we took the initiative to do something ourselves. If we can share this with other people, we are happy to do so. Please feel free to telephone e-mail us at jflint@itcanada.com.
John Flint
UPDATE: April 12-2001
Hi Tim, We have written a short paragraph below with the latest on Johns health. As you see, he is still doing very well. We receive at least 5 calls or emails a week asking about poly and the other products that John is taking. We are happy to give moral support and provide any information that we have. Best wishes to you and your father
Judy and John John is doing great. As of April 2001, recent CAT scans could not detect any sign of his earlier brain or lung tumors. He is still taking all of his supplements, including POLY MVA, although reduced to a maintenance level. He also has maintained a diet of at least 7-8 fruits, vegetables daily balanced with protein.
UPDATE: December 3, 2003
Hi Tim, We thought we would let you know that John is still doing great and we are into our 3rd year of cruising on our sailboat. This winter we are off to Belize. John is still following his protocol including polymva.We wish you and your father the best for the holiday season. Please give him our regards.
Judy and John Flint
UPDATE: July 6, 2004
Hi Tim Another 6 months has passed and John still enjoys good health. My mother has been receiving at least 2 -3 requests for John's "protocol" each week. She is happy to forward it to anyone that requests it. John also emails messages to anyone that would like more information. John is still taking Poly MVA as well as other supplements and continues to eat 7- 9 fruits and vegetables per day. Best Wishes, John and Judy
4-25-2016
John and Judy are still taking Poly-MVA.
PASTE THE FULL STORY FOR Maria S. HERE.
Stephen Barry
Date: October 2004
Diagnosis: Lung Cancer
3 Updates 1-17-12 – 5-30-13 – 11-14-14
Personal story
I was diagnosed with lung cancer in Oct 2004. Upper partial left lobe was surgically removed early Nov 2004. One of our physicians, Dr. Robert D. Milne, strongly recommended that I start using Poly-MVA, which I did. I took a daily dose of of 2 tsp, 3 times a day.
I also underwent a 12-dose regimen of chemo. While the dosage has been reduced, I continue the usage of Poly-MVA and remain cancer free. In addition, my brother-in-law was diagnosed with liver and bladder cancer in Jan 2010.
We forwarded a supply of Poly-MVA, which he takes in addition to a very rigorous chemo regimen. He reported to us 2 weeks ago that his doctors had told him that no sign of the tumor were evident on his latest scan. Go Poly-MVA!"
Stephen Barry
1-17-2012
Spoke to Stephen’s wife and was told that Stephen is in ICU. He became ill and septic. She said it was not from the lung cancer but that he was improving day by day and that he may come home within a week. She did say that they were going to have to check with kidney doctors before he can get back on Poly.
5-30-2013
Spoke to Stephen and he said that he is not using Poly MVA at this time. He said he wants to keep his options open but does recommend Poly MVA to others.
11-14-2014
Talked to Stephen. Says he is doing very well and thanked me for calling.
PASTE THE FULL STORY FOR Martha Dalton HERE.
Freda Amway
Diagnosis: Lung Cancer
Date: March 31, 2005
E-Mail: fredaamway@yahoo.com
4 Updates 5-05-11 – 4-02-12 – 5-19-15 – 12-03-18
Personal story
I am a 60 year-young woman that started smoking when I was 14-15 years old and I smoked until I was 36 years of age. I had developed high blood pressure and thought if I quit smoking it would help stop the blood pressure problem, it didn't. My husband still smoked in the house. I was diagnosed with cronic obstructive pulmanary disease in 2000 after having bronchitus two years in a row around the same time of the year. The Dr. put me on inhalers for this.
I was on these for 4 years before I had a breathing problem that caused the Doctor to take a chest x-ray. She was looking for pneumonia and thought the x-ray was good but the radiologist found the shadow that proved to be stage 4 lung cancer that had mestasized to the liver and the adrenal glands.
The oncologist stated I had 6 to 9 months to live if I did nothing, or a year or a little more IF I did the chemotherapy, which I did. I did get sick, lost my hair and became very weak. I had a flu shot the first part of October and a day or two later I became very weak and breathless, we all thought I was having a reaction the flu vaccine, but nobody checked anything.
Eventually my oncologist thought I should have a heart checkup and we found that I had had two heart attacks, the first one I never knew about but the back right part of the heart muscle is dead and does not beat. At first they said the attacks were from my high blood pressure and NOT from the chemotherapy, but later the oncologist stated we couldn't do anymore chemotherapy because of what it had did to my heart.
We were in a hold position waiting for my strength to build up. I didn't like not doing anything so on Oct 23, 2004 I started taking the PolyMVA at 8 teaspoons a day.
My sister had taken me earlier to see Dr. Mary Schrick and had me tested and bought the supplies for me, but my Dr. said I should not take this with the chemo.( I now wish I had earlier). I refused to start up the chemotherapy again.
By Thanksgiving I was feeling good enough to fix the meal and by Christmas I was like a new woman. In Feb. I had a chest x-ray and they didn' t see anything so we had a pet scan done two weeks later and the nurse was so excited she had goose bumps as she said there is nothing on the liver and nothing on the adrenals and the place on the lung is only 2cm. in size where it had been 3 inches in size.
I feel great and have energy to climb the stairs to get to my Sunday school class, I could ride the elevator but why when you feel good enough to climb the stairs!!!
I thank my heavenly Father for His miraculous healing and for the natural product of the PolyMVA that helped do the healing. I will try to send my picture but if I can't get this to work I will mail one to you. Waiting to hear from you and oh, yes I just joined the PolyMVA group on Yahoo.
Freda
5-5-2011
Freda is cancer free and has been taking the maintenance dose faithfully all of these years. In the past two years she has survived a triple bypass heart surgery, surgery for the installation of a pace maker and two aneurisms. She does the Relay for Life Cancer Walk each year in Oklahoma City and hands out literature about Poly-MVA. She welcomes anyone whom she can encourage to contact her. Her new email is: fredaamway@yahoo.com
4-02-2012
Talked to Freda. She is doing great and cancer free. Once again this year, she attended the Relay for Life Cancer Walk in Oklahoma City and handed out flyers about Poly-MVA. She is very pleased to receive an email or phone calls from other lung cancer patients. Her phone number is: (405) 354-9481.
5-19-2015
Freda is still doing well and just had rotator cuff surgery. She will be happy to talk to anyone about Poly. Her son lives in Las Vegas and often refers people with Cancer to her.
12-3-2018
Spoke to Freda who is still advocating for Poly to friends, family and co-workers. She is still in remission and living life to the fullest.
Ronny Rudley
Date: December 7, 2006
Diagnosis: Lung Cancer Stage II with mets to Lymph Nodes
E-Mail: onenevadagirl@aol.com
3 Updates 1-21-08 – 4-08-10 – 9-01-18
Personal story
Here I am ! I am alive....I am healthy and happy !! Life is fantastic !! It wasn't always like this and here's why...2 years ago I was diagnosed with lung cancer....not just one but two. There were two cancers in one tumor.
How lucky can you get ? The names of these cancers are Bronchioalveolar and Adenocarcinoma. I also had 4 lymph nodes that were affected. The sizes of these lymph nodes and tumor is important. The tumor was in Stage 2.... the size was 2.8 the lymph nodes varied from 1.4 to 1.9. I immediately called Amarc and spoke to Gary. That week I received my Poly- MVA and started taking it that day.
In November 2004, actually Thanksgiving week, I had lung surgery. I was Thankful, very thankful. For the 3 months I was on PolyMVA, my tumor with 2 cancers had shrunk from 2.8 to 1.9...Stage 2 to Stage 1 !
Two of the lymph nodes were gone and the other 2 became very small shrinking down from 1.9 to 1.4 and the second lymph node had shrunk from 1.5 to 1.2. The surgery was successful and my cancer markers have gotten lower and lower. In March of 2005 my cancer markers were 1.1. In Sept. 2006 it is the lowest so far at 0.6.
I had refused Chemo and/or Radiation and never suffered any side effects such as nausea, hair loss, and severe weakness. I continue taking the Poly MVA and all the supplements every day. I have tremendous energy and today I am alive and well in Las Vegas. Thank you, Dr. Garnett...for making PolyMVA possible.Thank you POLYMVA for keeping me healthy..!!!
January 21, 2008 Hello Everyone.... I am now 2 years clear of lung cancer. I do get nervous when its time for the Pet Scan and Blood Test..I think all cancer survivors feel the same way. Lung Cancer is one of the few that you can survive - providing you don't do only Chemo or Radiation.
When I was told I had a mass in my lung, the first thing I did when I returned home was to call Amarc - the Poly people..(that's what I call them) PolyMVA saved my life. I had to see an oncologist and I really thought that when I explained everything to him about Poly, he would understand. GUESS WHAT??? Not only did he NOT understand, he told me he would not ALLOW me to take Poly..in fact, he would only allow me to take Chemo and/or Radiation. Can you imagine someone telling you that you can't do something to save your life?!!!
We kind of argued without an argument...you know, agree to disagree... sooo I just said to him ..Why don't I just take the PET Scan and then we can talk about this..... and ...he agreed!
When I left him, I called a very well known Alternative MD on the West side of town. (My town being the Las Vegas area) He gave me the name of an oncologist and surgeon who are sympathetic to Poly use. I don't know if I'm allowed to mention their names - so I won't. I don't want to see anyone so wonderful to have problems.
Well, at that point I had stage 2 lung cancer with 4 lymph nodes.. 2 at 1.9 and 2 smaller. The Lung Cancer had 2 cancers in one tumor..Bronchoalveolar and Adenocarcinoma. My oncologist told me that about 2% of the population had two in one tumor.. It seems as tho I was always in the 2% category of whatever happens..
As soon as the Poly arrived along with COQ10, Liver Flush, Calcium, and an immune booster, I spoke with Gary Matson...and that started our 3 year relationship, so far.. We figured out how to take the Poly because in those days, we had to monitor the food and Poly, as things were a little different than they are now..and believe me it was tough.. Gary introduced me to my Poly friend, Marylin and together we struggled thru the time element of taking Poly, even getting up during the night to make sure it was every so many hours..
It was worth every minute because in 3 months, the stage 2 cancer was down to stage 1, and of the 4 nodes, 2 were "gone", and the 2 larger were now very small.. It was then that I had the surgery.
I must mention that my oncologist was obligated to tell me about Chemo. The Chemo he wanted me to take - Arissa - was taken off the market 2 months later for causing several deaths.
Now he just says, keep doing what you have been doing... Sooo.... Here I am 3 years later.... my blood reading is the lowest it has been, and the PET Scan is as clear as a bell !!!. Thank you again and again for the PolyMVA. - YAY !!!!
April 8, 2010 I recently had my 5 year scan and blood test. Everything is AOK...
Ronny
9-01-2018
Ronny is still living in Las Vegas, Nevada and in remission.
Dickie Russel
Personal story
I can’t quite remember when I first noticed something was going on with my health—it was years ago. I went to my family doctor, who ran a lung test. Based on the results, he sent me to a specialist, and that’s when I found out I had lung cancer.
The doctors did some assessments—I don’t recall exactly which ones—and they advised me to start treatment. But I chose not to go through with it. Instead, I started taking Poly-MVA, and that decision changed everything. The lung cancer went away, and I’ve been taking Poly-MVA ever since.
It was actually my wife who discovered Poly-MVA. She did some research online and gave the company a call. That’s how we found out about it.
I started taking Poly-MVA years ago—can’t remember the exact date—but from the beginning, I was taking 3 teaspoons, twice a day. That’s still my routine today.
Did it help? Absolutely. It made the cancer go away, and I’m still taking it to this day. My experience with Poly-MVA has been very good indeed.
I’m 77 years old now, I hope my story can help others.
Debbie Diaz
Date: February, 2018
Diagnosis: Lymphoma
1 Update 3-31-2020
Personal story
I was diagnosed with early stage Lymphoma on January 15, 2008 but the doctor I saw and the Stanford Doctor said that my case was diagnosed so early that treatment was not needed at the time.
3 Years ago, I learned about Poly MVA from my boss, Ed Sanchez, and started taking 2 tsp daily of Poly MVA. Then, in February 2018, I started taking 4 tsp 3 times a day which I eventually cut back to only 4 tsp daily once I had completed my Chemotherapy treatments.
I had my blood drawn every 3 months and saw my Oncologist every 6 months. In January 2018, my labs showed some changes and a PET scan was done. Due to these changes, I then had chemo once a month (2 times session) for 6 months (March 2018 – September 2018).
I had very few side effects from the Chemo. I believe this was because of the Poly, CoQ10, Coral Calcium, Vitamin D3 and Liver Support supplements. 9 months after increasing my Poly MVA dosing to 12 tsp daily in tandem with completing my Chemo regimen, I had a PET scan in October 2018 – the results to me were awesome!
If I had been shown the previous PET scan, I would have been so much more worried! I continue to take the Poly daily and all of the other supplements I listed before on a daily basis. I continue to have my blood drawn every 3 months and see my Oncologist every 6 months. We are again just watching the Lymphoma because it is small cell Lymphoma and will never completely go away but for now it is in check.
I thank God everyday for meeting Eddie Sanchez because I feel without this meeting and the Poly, my life would be entirely different today!
Debbie
Ronald Sereny
Date: November 27, 2012
Diagnosis: Non-Hodgkin’s Lymphoma
3 Updates 12-02-09 – 7-07-14 – 9-25-18
Personal story
In early 2008, I went to the doctor and they had seen a lesion on my scalp. They had taken a biopsy of the lesion and had diagnosed it to be a cutaneous T cell Lymphoma. I went to Moffett Cancer Center and they had reassessed the outcome to be Non-Hodgkin’s Lymphoma Stage 1A.
I was recommended to have radiation on my scalp. Upon reviewing the information about radiation, I had decided to go a different route. I found PMVA. I have forgotten how I was introduced to PMVA. I have since been taking PMVA since August of 2008. Along with PMVA, I have incorporated supplements in my regimen consisting of Vit D3, Bone Restore (super calcium) Ubi Quinol, Super Mega 3 (olive oil extract, a daily multi vitamin, Super Booster (advanced (k2 complex), Reversatrol, Hawthorne berries, etc.
I am very adamant in my holistic and natural approach. I have found the information given to me by the information packet, web site and the AMARC Staff has been helpful. I often visit the www.PolyMVA.com website to listen to the recordings of the doctors, like Dr. Forsythe, very helpful.
Overall, I feel that PMVA has helped with my overall Quality of Life, Energy, Increase in my appetite and cancer support. I notice that it does help my energy and keeps me active in my life. I often share the information about PMVA and what it has done for me. The proof is in the pudding.
You can only tell someone about PMVA and the ball is in their court. Not all of them pursue PMVA, but those that I have recommended to use PMVA have found it to be helpful in their quality of life.
I am a true believer and advocate of PMVA and I continue to use it and share with others.
Ronald Sereny
12-2-2009
Spoke to Ronald. All is going well, feeling good.
7-7-2014
Spoke to Ron, he is doing well. Still taking Poly.
9-25-2018
Ron is still ordering Poly MVA and doing well.
Joanne Anspach
Date: Summer 2009
Diagnosis: Non-Hodgkin’s Lymphoma
2 Updates 2-24-10 – 3-20-13 – 7-13-15
Personal story
After learning that I was diagnosed with Non-Hodgkin’s Lymphoma, I was directed to Dr. Tierney who recommended Poly-MVA. I used Poly-MVA during my time of treatment of chemotherapy. I was assured the Poly-MVA would not interfere with the chemo treatments. During this time of chemo treatments every three weeks of six treatments my blood counts always remained high enough, so I never had to miss a treatment.
I never had any side effect of nausea, tiredness, etc. I work two days per week and I was able to work and never missed any days. I finished my treatments the end of December2009. I've gone every three months for checkups and so far everything has been good.
People are amazed at how well I have been doing with my chemotherapy treatments. Everyone tells me I look good and I do feel good. Just today, my Dr. told me how well I have tolerated these chemo treatments. I feel very blessed.
I have not told my physician that I am taking the Poly-mva, not sure how she would feel about it. I continue to take 1 tsp. per day of Poly-MVA.
I have recommended Poly-MVA to other people dealing with cancer and some have begun using the Poly MVA. I wish you continued success in finding a cure for cancer.
Joanne
2-24-2010
Anspach, Joanne----She saw her Oncologist and her markers are all normal so she wondered about her dosage level. She will call in 3 months after her next marker test and let me know. Very happy lady.
3-20-2013
I have been able to carry on my life very normally. I feel Poly-MVA helped me grow through this time with little problem from the treatments. I now am down to yearly check ups which will happen in July 2013.
Joanne July 13, 2015 Spoke to Joanne, she is doing very well. She has been released from the doctor for about a year because she is now in remission.
Corrina Reimer
Date: February 2008
Diagnosis: Non-Hodgkin’s lymphoma
3 Updates 12-1-09 - 10-23-14 – 7-8-16
Personal story
I was diagnosed with Non-Hodgkin’s lymphoma. In Feb 2008, I had exploratory surgery because the many tests I had didn’t reveal my digestive problems. Three tumors were found in the small level and removed, since they were positive and I was very weak and had lost twenty pounds I opted out of conventional cancer treatment.
A fiend informed me of Dr. James Forsythe at Reno and I followed his protocol. I had infusions for three weeks and he started me on Poly-MVA for teaspoons twice a day for three months along with CoQ10 and other supplements.
I now take 2 teaspoons daily. I also had an infected root canal tooth removed. Dr. Forsythe says I am in good remission. My markers are in normal range. I have good energy, stronger and active every day. Taking poly-mva has improved my life greatly and I will continue to take it, may God bless you in your work of healing supplements. God has blessed me richly in the journey.
Thank you,
Corrina Reimer
12-1-2009
Corrina is on a maintenance of Poly MVA after having been through Dr. Forsythe's program. Her maintenance dosage is 2 tsp daily and she takes the 4 corners protocol. She will have the 25-Hydroxy Vitamin D test and let us know where she stands. She has been taking 12,000 IU's daily.
10-23-2014
Spoke to Corrina, she is doing ok but has gone to see a neurologist and may have some inflammation in the her brain. She will have some blood testing in a week.
7-8-2016
Spoke to Corrina….. she is doing great and thanked me for my call.
Christine Christie
Date: August 23, 2005
Diagnosis: MALT Lymphoma
2 Updates 2-14-2012 – 2-19-2017
Personal story
I’ve been on Poly MVA for a year and a half for MALT Lymphoma in the stomach. My last blood results in November showed that I am in complete remission. The doctor said I am doing well so I will continue to use the Poly MVA.
I only wish the Poly wasn’t so expensive, as being single and working full-time, it’s hard to pay for Poly. If I weren’t on the Poly Life Study and getting the reduced price for Poly, I would not be able to afford it. Christie C.
2-14-2012
Spoke to client and says nothing has changed since her testimony in 2007; she continues to use Poly-MVA but has nothing new to add.
2-19-2017
Christine is still taking Poly-MVA.
Tralece Sohrabi
Date: Dec 24, 2004
Diagnosis: Non-Hodgkin's Lymphoma with mets to brain & central nervous system
E-Mail: not available
Personal story
Introduction to this story: I just received the testimony this weekend and wanted to share it will all of you. Dr. Mary Schrick has vouched for the truthfulness of this wonderful story. Robbie asked me if he might express his faith journey freely. I told him yes, because it is an important part of their story. I wish that the loving care he and his wife received were always the case where different religions collide. I realize that not everyone reading this has the same belief system. Whatever our spiritual beliefs, I know that we all agree that a spiritual connection can be a very important ingredient in the healing of our bodies, minds and souls.
Date: October 15, 2006
My name is Fakhroddin Sohrabi (Husband) and since it is hard for most Americans to pronounce, I go by “Robbi.” I am 59 years old and was born and raised in the Islamic country of Iran. At an early age, I started practicing the Muslim religion and developed a strong faith in God. In August of 1970, I came to America to pursue higher education and ended up at Bethany Nazarene College where God wanted me to meet one of his beautiful angels named Tralece, who became my wife in September of 1971.
As I grew older, I started studying other religions and it was not clear to me which one was true. I kept searching, and about 2 years ago I had a very vivid dream or vision where Christ in all His radiance appeared to me. I felt it was a sign to me that Christ was very real. I started praying more and more – asking God to guide me in what I believed about Him and to lead me in the right way.
In 2004 my wife started volunteering more at the church, and I would also visit the church occasionally with her. Tralece’s Sunday School class also warmly welcomed me to their functions, but were not pushy. I knew family and friends were praying for me. Then Tralece started having some health problems in September of last year. And when she fainted in the shower on December 24th, I took her to Deaconess Hospital Emergency.
Within an hour the Doctor came and told me that the CAT scan shows a mass has covered her left side of brain and the pressure causing all the problems that she had, which was nausea, headache, loss of memory, loss of vision and control of her right arm and leg.
She was transferred to Midwest Regional Medical Center to be cared for by a Neurologist. In January 15, 2006 she was diagnosed with Non Hodgkin's Lymphoma T-Cell type brain cancer on central nerves system of her left side of the brain.
Since we had Exceptionally great results on all the products by Dr. Mary Schrick, we decided to start POLY MVA and natural products to treat my wife. Unfortunately she got nauseated and we had to take her to the hospital. After 3 months of treatment by Doctors and Poly she did not get any better due to chemo. On April 12, 2006 her condition got worse and on top of all the above problems she stopped breathing.
The Emergency group came to the hospital room and started their procedures to revive her and three times the doctor said we lost her. I knew in my heart that the Lord is not going to let her go. She made it and they took her for cat scan to see what was going on in her brain. It was more swelling that caused her problems. She was in ICU for two and half weeks and she lost all her energy and her muscles were so weak that she could not move or do anything. I asked our Doctor to stop all chemo and other medications and started her on full string Poly MVA.
After a week of Poly she was out of wheelchair and getting normal. To the surprise of all the Doctors and Nurses that treated her, she was alive. If we did not start her on Poly, she would not be here today.
Since Poly treatment in April, she has had two MRI and both were cancer free. Praise the Lord that guided us to Dr. Mary and special thank to Dr. Sanchez who has done exceptionally great job coming up with Poly.
Throughout these past five months of great pain and suffering and multiple trips to the Emergency Room and hospital, I felt God’s presence with me and His signs were all around me. I couldn’t believe all the love we were receiving. We had a Christian nurse who would often pray with us when Tralece was in the hospital. Pastor Phil Hause was so caring and supportive. It wasn’t so much what people said but what they did that helped me discover that Christianity was true.
Then on May 1st Rev. Gene Hulsey came to see my wife for the second time in the hospital. He talked with us and before praying for my wife, he asked me if I wanted to give my heart to our Lord Jesus and I said yes. Since we prayed together, my life has completely changed. I have felt joy, comfort and peace that I have never experienced in all my life.
Vaughn Christensen
Date: January 1998
Diagnosis: Non-Hodgkin's Lymphoma
E-Mail: not available
Personal story
"While driving down the road, my right arm and hand went numb. I couldn't think of the name of the song on the radio, but I knew I had seen it before."
These words were the first sign that something was amiss in Vaughn's brain. A MRI in January 1998 showed four tumors around Vaughn's left ear, the portion of the brain which controls speech. A brain biopsy revealed primary CNS non-Hodgkin's lymphoma. The disease had manifested in the brain; it had not mestastasized from elsewhere in the body-a rare condition.
The first half of 1998 was consumed by a grueling regime of chemotherapy - IV methotrexate, vincristine, and procarbazine, plus an Ommaya reservoir implanted in the skull to deliver direct-brain methotrexate.
The treatment protocol then called for 45 Gy of whole-brain radiation, administered over a five-week period. Fearful of this treatment, we consulted with several doctors, all of whom stated that the radiation was necessary to prevent the tumors from returning. Reluctantly, we followed the protocol.
But the tumors returned anyway. In June 2000 six more showed up. Vaughn underwent five months of Temodar chemotherapy, but when his blood counts dropped too low, he quit. For two years I had been investigating alternative cancer therapies. Most didn't feel right. For example, one therapy called for the ingestion of a chemical that was originally created for jet rocket fuel! But when I read about Poly MVA, I got excited. It made sense. Not only had it been first developed for the treatment of brain tumors, but it was natural and safe.
Vaughn has been on Poly since May 2001. MRIs reveal that most of his tumors are gone, and others are gradually shrinking-something which never happened during the traditional treatment protocol.
Had we discovered Poly MVA sooner, Vaughn would never have undergone the whole-brain radiation, which took a toll on his cognitive functioning. As a computer programmer, he is still able to work, but he is considerably slower.
Nevertheless, Vaughn is well, happy, and lives a normal life. He takes 1 teaspoon of Poly a day, eats a healthy diet, exercises, and stays positive. Rather than nervously waiting for the tumors to return (which is common for lymphoma), then defending against them, Vaughn is taking an offensive approach by taking the Poly MVA. We are very grateful for it, and would be happy to respond to your questions. Please write lchristensen@actslc.com .
UPDATE: February 21, 2004 Vaughn has been on Poly since May 2001. His last MRI in October 2003 showed four remaining tumors. They are neither growing nor shrinking, and the physicians believe they are now calcified and stable. Vaughn feels excellent. He eats nutritious homemade meals, takes daily vitamins, walks four or five days a week, and takes a maintenance dose of ½ teaspoon of Poly per day. He was initially given a 20% chance of living five years. We are happy to report that he just passed the six-year mark!
Had we discovered Poly MVA sooner, Vaughn would never have undergone the whole-brain radiation, which took a toll on his cognitive functioning. Nevertheless, we are very grateful for the Poly now. It enables us to be on the offensive against this terrible disease.
Burt Grice
Date: August 18, 2000
Diagnosis: Lymphoma
E-Mail: not available
Personal story
To Whom It May Concern:
The purpose of this letter is to share our son's cancer treatment experience with you and to share the effects of his Poly-MVA treatment experience. My son's name is Burt, at 24 he was diagnosed with Lymphoma in April of '99.
The Doctors gave us assurance that if you had to have cancer this was the one to have, because it is curable. Of course as you all know that word is something you hope of never hearing, especially your own son, who’s always taken care of himself by watching what he would eat and working out at the gym 6 days a week. He was very dedicated to maintain a healthy lifestyle.
At this time, Burt began chemotherapy (CHOP), then Radiation treatments. In October of 99, everything worked out just like the Doctor had told us it would. In January of 2000, Burt was scheduled for a follow up CT scan. The news was now he had enlarged Lymph Nodes in his Stomach also Chest. The first thing they shared with us was that Chemo did not work.
He should be admitted to the hospital for high dose Chemo. My son at this time spoke with his Doctor. He did not agree with what the Doctor was telling him, and at this time decided he would explore alternative treatment. We did a lot of research only to find Poly-MVA.
This is an answer to our prayers. Burt today has no sign of any enlarged Lymph Node of his stomach and the one in the chest has decreased in size. Thanks to God & Mr. Sanchez. Burt is the owner of Coastal Carolina Landscaping & Maintenance. He has never missed a day operating his business, and also still works out 6 days a week and lives a healthy vibrant life.
We would be more than happy to talk with anyone who is interested in learning more about the experience Burt has had with Poly-MVA. Please feel free to contact me at the address below.
Thanks
Barbara Grice
Jean Kelly
Date: 2009
Diagnosis: Multiple Myeloma Stage
1 Update 5-09-2019
Personal story
I was diagnosed with Multiple Myeloma in 2009 after several years of medical tests and doctor’s visits trying to find a diagnosis. Initially when I was diagnosed it was recommended to me that I take Thalidomide as this was the chemotherapy drug that the oncologist felt was the “gold standard” for this disease. I had heard about this drug before and did not want to take it due to the side effects of this medication.
At that time I knew very little about Multiple Myeloma. I began reading and researching information so that I could educate myself about this disease and the treatment for it.
I sought advice from a friend that had told me that she had Multiple Myeloma. She appeared to be satisfied with her oncologist so I scheduled myself for an evaluation with him. After the evaluation I was not satisfied with his recommendations and I then scheduled an appointment at the Mayo Clinic in Jacksonville, Florida. I was assessed by one of the physicians there who had many years’ experience working with Myeloma patients, so I decided to begin treatment there. He told me that I had stage I MM and he began treating me with Revlimid and Dexamethasone. I began this regimen after having my stem cells harvested and banked at the Mayo Clinic for future use. I was not able to continue the Dexamethasone due to my hypertension and cardiac arrhythmias. I did continue to take the Revlimid alone for approximately three years.
My M-Spike became very low and the doctor decided to try me without any medications. I was able to stop taking the Revlimid in 2012 and was able to stay off any chemotherapy medications until 2018. I first heard about Poly-MVA in 2013 when I read about it on the Internet. I was looking for some supplement to support me so that my condition would remain stable without taking any medication. I called AMARC initially and spoke with Toni there. She was very knowledgeable about Poly-MVA and encouraged me to try it and I am happy that I did. I began taking it on and off initially at 4 teaspoons per day and then 2 teaspoons per day.
I felt that it gave me energy as I was feeling weak at the time, it also gave me a general feeling of well-being, and I was able to take it without problems or conflicts with my other medication and supplements, since I have other medical co-morbidities. During the time that I was taking the Poly-MVA my M-Spike went to 0 and this is the only time that I have had a 0 value for the M-spike since being diagnosed with Multiple Myeloma. My M-spike did climb back to a low value and remained there and I remained stable for the 6 years that I was on and off Poly-MVA. In June 2018 I began to feel weak and ill and my numbers began climbing higher than they had ever been.
I tried vitamin C intravenously but I began having generalized body pain so I discontinued this. I called AMARC and spoke with Toni and began taking Poly-MVA again. I began taking 2 teaspoons per day. I was started on Revlimid again and this time my lab values were higher. My platelets; WBC; HGB.; WBC; and HCT; became very low. I increased the Poly MVA some however; my standard dosage was 2 teaspoons-3 teaspoons per day. I have been able to see an increase in these lab reports to more normal values due to the Poly-MVA. My numbers have declined some and continue to slowly come down. The M-spike is now 1.7 at the last report and I continue to take the Poly-MVA and the Revlimid.
The Poly-MVA has helped me to withstand some of the side effects of the Revlimid since I am unable to take steroids. It has also helped the Revlimid so that my M-spike is now going lower. This is a big help to me. I trust and pray that with Jehovah’s help and Poly-MVA I will continue to improve. Jean
5-09-2019
Called and left Jean several messages and then, she called me back. We discussed her current health status and her dosing levels of Poly. She is doing well and maintaining her Marker levels but agreed that her condition may require a higher dosing of Poly MVA as well as an increase in her daily Vitamin D3 dosing levels. She believes her 25-Hydroxy Vitamin D levels are around 30ng/ml, per her last test. I explained to her that 30ng/ml is severely deficient and referred her to the WHAT YOU MUST KNOW PAGE which shares CLINICAL STUDIES about the crucial role Vitamin D plays in all cancers as well as the chart below that shows she needs to increase her daily dosing levels until she reaches 70-100ng/ml.
Carolyn Huter
Date: December 13, 2011
Diagnosis: Multiple Myeloma Stage 4
4 Updates 9-20-10 – 6-27-11 – 1-12-12 – 10-29-14
Personal story
(My experience using Poly-MVA the last 15 months) I was diagnosed with end stage multiple myeloma in October 2007. I began chemo in November and a stem cell transplant in February 2008. I slowly recovered strength and energy.
In March 2010 lab test began to show a rise in cancer protein in blood and urine. My doctors were encouraging another stem cell transplant, but I felt I would rather take my chances with the cancer rather than go through recovery of another stem cell transplant when stats showed I could expect even a shorter a period of health than before. I did not feel like it was worth the time it took to recover since I was still feeling good.
I started doing a little research on my own and Poly-MVA and friends (other recommended nutritional and detoxification supplements) seemed like the best alternative method I could find but the cost was prohibitive.
So, I kept reading and talking to others about methods perhaps less expensive to fight the disease and not tear down healthy cells in my body. But Poly and friends just kept coming to my attention.
I didn’t actually start it until September 2010; at which time my oncologist insisted I must start chemo at least. I did not want to start chemo either because it made me feel so bad.
I wanted to just try the Poly and friends. He would not consent. I considered removing myself from his care and proceeding against medical advice. But I consulted with Gary Matson, the consultant assigned to me and he recommended I take Poly and friends as a complementary to chemo instead of an alternative. He convinced me that It would most likely prevent the side effect of chemo and it has the tendency to protect my good cells and aid the liver to get rid of all of the cancer cells the chemo was killing more quickly. It did work that way.
My oncologist told me when I started chemo again that I would be on maintenance chemo for the rest of my life. But Poly and friends was keeping me from being as sick as I had felt before so I thought I could follow his advice for a while at least. As months went by, the cancer protein lab tests started coming closer to normal range. My oncologist warned me to not get my hopes up. It would never be 0. But by March of 2011 their tests could not detect the cancer protein.
The tests had the same results in June and the oncologist agreed to let me discontinue chemo. September’s test results were still negative for the cancer protein. I will be tested again this month and I assume every three months thereafter.
I had a wonderful summer(except for a car accident which slowed me down a bit). Even though I did feel better on chemo this last round than originally, I really dreaded the thought of continuing for the rest of my life because the steroids they gave along with it made me very nervous with sleep difficulties and fatigue. But the oncologist predicted that chemo(or another stem cell transplant) were the only treatment options when he started it in September 2010. He had no faith in alternative methods.
Thank you for the opportunity to share my experience with Poly and friends. I have several loved ones who are battling cancer now but I have not been able to convince them to try Poly.
Their doctors, like mine, think there is no other way to fight it except chemo, surgery or radiation. I am sorry that the quality of life studies are not taken more seriously in the established medical community.
Carolyn Huter
9-20-2010
Carolyn is struggling to make a decision about what to do because her numbers are up. She doesn't want to do chemo or Velcade as she knows it only buys a little bit of time. She wanted to prove that Poly could work for her if the Dr. would give her 4 months. He told her she didn't have 4 months. She has decided she is willing to compromise and take his chemo and Velcade to give the Poly more time. She will go on 12 tsp a day.
6-27-2011
Carolyn’s Doctor says she has exceeded all of his expectations so they are stopping the chemo and she does not have an appointment until September. She had a car accident and has a broken sternum but otherwise is great.
1-12-2012
I realize that MM is considered incurable. That is why this is all so amazing. Predictions were for me to be gone this coming October. I don't "feel" like I am going anywhere just yet and the Lord seems to have placed me in a place of learning and teaching. I am content. But I don't want to take a chance for my oncologist to see a need for chemo. Dying doesn't scare me as much as slowly killing myself with chemo.
I did not have the 25 Hydroxy D3 test with the other testing done on 12/19/11. But I will request it for April. I suppose I should request it each time since it is not in the routine orders.
Carolyn
10-29-2014
Carolyn has been struggling with her Doctor about staying on Poly. He insisted she stop it for the time being. She did well for so long but now has a serious problem with her liver. He wants her to stay off of Poly for the time being while he tries to get her liver working properly. She told him that the metals do not stay in her body because they are bonded with the other compounds in Poly MVA….they are not free metals. I told her that she should ask the Doctor about the negative “long term” side effects caused by Chemo and Velcade and whether those drugs are what might be causing her liver problems.
Debra Draves
Date: June 2010
Diagnosis: Multiple Myeloma (smoldering)
2 Updates 11-09-12 - 9-05-13 - 4-07-16
Personal story
In June 2010, I was diagnosed with Multiple Myeloma (Smoldering). After all my lab test and consulting with a specialist at the University of Chicago, my doctor said I didn't need any treatments as of now, because it was (smoldering) just the beginning. I had a hard time trying to decide to do nothing, so after my own research & reading the book "Knockout" by Suzane Somers, I choose to try the PolyMVA.
I started in July 2010 & began the loading dose of 8 tsp a day. I had blood works done in Chicago every 2 months & my levels pretty much stayed the same over the last 6 months. I have reduced my dosage 4 tsp to now 2 tsp a day, my levels are stable & I have continued to have no other treatments.
It (PolyMVA) has helped my energy levels which really helped. I will continue taking PolyMVA and will increase my dose if my levels get too high. I am not 100% sure of the Poly keeping my MM levels down, but I feel very positive its helping some. I'm feeling pretty good and positive it will not let this cancer get me.
At 57 I want to enjoy my 2 wonderful children & grandchildren and be able to help my elderly parents. I've retired after 35 years of employment & enjoying life to the fullest. I would recommend Poly to others!
Thank you.
Debra
11-09-2012
Debra says her levels are the same and has been on a maintenance dose for the last year.
9-5-2013
She let me know that her blood work is the same as 6 months ago.
4-7-2016
Spoke to Debra's husband because she was not in. Her markers have stayed the same; doing okay.
Susan Lannoye
Personal story
Diagnosed August 17, 2008 Testimony Written 3/21/13
Diagnosis: Multiple Myeloma Stage III
4 Updates 11-21-11 – 5-07-13 – 6-10-14 – 3-08-17 My wife, Susan at age 68, diagnosed with stage III Multiple Myeloma Aug. 17, 2008, after being rushed to the hospital with what we thought was a heat stroke, dehydration, and a 104 temperature.
Test results showed she had a life threatening staph infection throughout her system as a result of bone marrow cancer which had destroyed her immune system. That was our introduction to Multiple Myeloma, an insidious decease that we had never heard of.
The Doctors told us there was no cure for MM, but with the latest Chemotherapy treatments followed by either a stem cell or bone marrow transplant, survivability would be 2-3 years. The good news was we were fortunate to live in Seattle because the Seattle Cancer Care Alliance( formally the Fred Hutchinson Cancer Clinic) is one of the leading facilities in the world for the treatment of cancer with stem cell and bone marrow transplants a specialty.
Sue started her treatments with a combination of chemotherapy drugs( Velcade +Revlimid +Dexamethadone) at the SCCA in Dec. 2008. She continued these treatments for the next 8 months with good results as far as lowering her "bad" numbers (Kappa Free Light Chains and the Benz Jones protein) which are the main markers for MM. Aug 7, 2009, one year after diagnosis, Sue underwent an Autogolus Stem Cell transplant at the University of Washington which was expected to give her 18 months of remission. Sadly, she relapsed after 2 months and was restarted on the chemotherapy (Revlimid) for the next 2 months with negative results. The cancer markers continued to increase with each monthly test.
Her Oncologist could only offer to try a different combination of drugs with the hope something would work. We were desperate, but this seemed like not much of an option. Sue was already suffering from neuropathy in her legs and feet from the previous chemotherapy treatments.
I had read Suzanne Somers book, Knockout, about alternative cancer treatments which included Poly MVA. I called Gary Matson and made an appointment to visit him and the staff at AMARC. Sue and I were very impressed with Gary and all the staff at AMARC, with their story and sincere desire to help us.
Sue started taking the Four Corners Protocol on January 20, 2010 at the recommended dosage, in her case, she was taking 1 Tbsp of PolyMVA every 6 hours. Six weeks later, Sue had her first tests since stopping all Chemotherapy and taking only the PolyMVA and Four Corners Protocol. The results were stunning.
I will never forget the moment her Oncologist entered the room with the test results wearing a big smile and proclaiming Sue his " wonder woman." Both the Kappa Free Light chains and the Benz Jones protein had declined dramatically. When I told him about the PolyMVA , his comment was "just keep doing whatever you are doing and I will see you next month."
He could offer no other explanation for the turn around in numbers. Sue has continued this same dosage of Poly mva with her markers declining with each monthly test (presently every other month).
Her cancer markers are still present but at the lowest level since diagnosis five years ago this Aug. She just completed a full skeletal survey(16xrays) last month which showed that the lesions in her thoracic spine and leg have completely disappeared since the last exam 6 months ago.
Sue and I will be celebrating our 52 wedding anniversary in April which we didn't think would be possible after MM diagnosis in 2008. We sincerely believe this was only made possible by discovering PolyMVA. We are looking forward to many more in the coming years.
A special thanks to Gary and all of the caring team and AMARC for allowing us to share this story with others on the same journey. Please feel free to contact us at larrylq@aol.com for more details or questions.
Sincerely,
Larry and Sue Lannoye
11-21-2011
Spoke to Sue, she is doing very well, feels good. Her brother is also taking poly he has liver, colon & lung cancer. When her brother went on poly his numbers came down and he is holding his own. The poly has helped him get thru his chemo treatments. Susan will go back in in Dec. for testing to find out how her numbers are.
5-07-2013
Sue is still taking 1 tablespoon of Poly 4 times a day. She wants to take ALA for her neuropathy. She and her husband are in LaQuinta right now and he is having knee sugery on Friday. They will stay a few weeks and then head back to Seattle What an amazing couple. Her brother, Barry, died, as we feared would happen. She is going to post her story on the Multiple Myeloma blog.
6-10-2014
I had a great discussion with Sue and her husband Larry. She did attend Suzanne Somers dinner and Suzanne read her letter in front of the 2,000 women present at the event. Suzanne Somers had Sue stand and then visited with her afterward. Sue said she was mobbed after by folks wanting to talk to her. She will continue referring patients to Poly MVA. She is doing very well and excited to be a Poly-MVA Survivor.
3-8-2017
Spoke to Larry. Sue is doing pretty well with numbers in good range and still taking 6 tsp daily. They are in Palm Springs and getting ready to home. Sue took Zometa early on and had bad side effects and has not taken any more of it since she went on Poly.
Larry Moore
Date: April 2011
Diagnosis: Multiple Myeloma
4 Updates 7-20-09 – 1-26-15 – 1-06-16 – 3-16-18
Personal story
Poly gave a feeling of well being within a few days. I tool Poly for over 6 months but the cancer was causing severe nerve damage. I got to a point that I could not walk and went to the emergency room. The doctor tested everything they could test but other than the cancer, all my organs were perfect.
The poly was not strong enough to stop the cancer, so I had to go on chemo. When I finished the chemo, I went back on the poly. It started healing the nerve damage within 2 weeks, and has continued to heal the damage much faster that it would have without poly.
I went through this before in 1991, had nerve damage then but was able to stop it by having radiation and changing my diet. The nerve damage was no where near as severe as this time has been, but took years to heal.
That is why I know the poly has really sped up the healing time as well as keeping the rest of my body healthy. Also keeping me in remission so far.
The staff has always been very helpful and the poly is great stuff, I highly recommend using poly. I believe poly has kept my cancer in remission, when doctors told me I would have no breaks, but would continue to get worse until I died. The doctors told me repeatedly there would be no remission.
Each month I went for checkups and bloodwork, the cancer had not started up again. The doctors don’t understand how I have gone so long with the cancer not coming back. I believe the poly is large part of what is keeping me going and healing. I also take vitamins and eat a very clean, healthy diet.
Larry Moore
7-20-2009
Spoke with Laura and she said that Larry’s blood work is coming-back still elevated. I let them know that sometimes it takes a while for the blood work to show improvements because the body is getting rid of the cancer cells but the blood test can’t tell the difference between a live cell and a dead cell.
He is currently on a frequency machine-photon genie-3 hrs a day, to help with his tumors. Cancer has given him nerve damage, the myelin sheeting is taken off his nerves in is feet and hand and when he takes poly they are numb. He is having another blood test in the next couple of weeks.
1-26-2015
Spoke to Larry and all is well and continues his daily dosing with Poly.
1-6-2016
Spoke to Mr. Moore. He said that he has been experiencing diarrhea on 1/2 tsps a day. So, he stopped taking it for a while. The Diarrhea stopped when he discontinued daily dosing of Poly. Told him Diarrhea is a symptom of an immune response and clearing out the debris and die off.
3-16-2018
Larry is still taking Poly MVA and doing well.
James Swelgin
Date: March 15, 2012
Diagnosis: Multiple Myeloma Stage 1
3 Updates 1-14-13 – 3-07-16 – 2-05-18
Personal story
I started Poly in March of 2010 I take 3 teaspoons 4 times a day. Also 10,000 IU of D3, as well as COQ10 and Liver pills.
After a period in which I lost 25 pounds in about 2 months, and was feeling tired all the time, I went to see my Family Doctor in July of 2009 with blood test results. He didn’t like what he saw, and referred me to an Oncologist. After more blood tests, a bone marrow biopsy, and X- rays, I was diagnosed with Stage 1 Multiple Myeloma in January of 2010, and the Oncologist gave me the “most likely scenario” of 6-9 months then I’ll need to take Revlimid, then about 6 months later a possible stem cell transplant. I did not like what I was hearing, so I talked to some folks and checked the internet to find out more about MM.
A friend of mine had been told about PolyMVA and suggested I look it up on the internet. I called Gary Matson and we talked about my situation and the role Poly might play. When he told me the cost for his recommendation, I got myself back up on my chair, and said “Can I get back to you on that?”
My first shipment of Poly arrived in March of 2010. For the next two years, up to and including the current time frame, I take the recommended amount. During all this time, of course, I was visiting my Oncologists every three months, or more often, depending upon their schedule. During that period, I had more, X-rays, and MRIs and CT Scans. Prior to each visit I was getting blood drawn for testing to the necessary parameters to determine the status of my condition. It must have been about November 2010, that, because of my research on the internet, I also cut way back on any sugar intake (Cancer loves sugar). I found that you can’t cut back 100% on sugar, since most foods have some.
My “numbers” stayed steady, out of spec, but steady for the past two years – no Revlimid, no stem cell transplant. About 6 months ago both my Oncologists agreed that I should have gotten worse, but didn’t, so they changed my diagnosis from Stage 1 to “Smoldering” Myeloma. They couldn’t/wouldn’t say why I was so steady and not getting worse, but they did say, “Whatever you’re doing, don’t stop”. So I won’t. I told them I was taking PolyMVA, and they asked for more info in it. I referred them to the web site.
So here I am, 2 years of Poly MVA, my numbers continue to be steady, and feeling fine, getting ready to celebrate the 70th anniversary of my birth in May. I’ll stay with “PolyMVA and friends”, and the no sugar regimen.
I want to give a special thanks to Gary Matson and the ladies who take my monthly orders, for taking good care of me. Gary and I have talked and exchanged e-mails to track my condition, and the Customer Service ladies couldn’t be more friendly and helpful. They are the best!
Jim Swelgin
1-14-2013
Attached is my most recent Blood Results. Note that both my red and white count is below the minimum, but others are still ok. The Igg is down to 5100 range, which is good (probably a bit of noise).
In addition to polymva and the D3 and Liver Pills, I’m taking Curcumin, Fish Oil for Omega-3, Magnesium, COQ10, and Bromelain. WOW, I don’t know if 1 or 2 or what combination is working, but I’m not stopping now. My weight is steady at about 185 average over that last 4- 5 months.
Cheers Jim
3-07-2016
Attached is my blood test results. These results, overall, are the best to date. Need less to say, I'm pleased. It is my plan that if the results were going the wrong way, that I would go to Mexico for another day.
However, it appears to be under control. I understand that it is a chronic disease and I just need to stay on my usual regime. But for now, I'm going to use Mexico as a tune up and I'll be getting monthly to 6 weeks reports to track my status.
Cheers, Jim
2-5-2018
All numbers are in spec. The new/good news is the M-spike. This is a measure of the abnormal protein cells in my blood.. This is one that was 0.5, then 0.1, then 0.5 again.
Well this time the report said "not observed". This means, in lab talk, that there was such a small amount, if any, that it couldn't be measured. I asked for a finer test next time. Next meeting with Kosmo is in March.
Cheers, Jim
Betty Grainger
Date: January 6, 2006
Diagnosis: Multiple Myeloma
6 Updates 11-1-10 – 11-21-11 – 1-16-13 5-17-13 – 2-24-14 – 10-07-15
Personal story
My experience with Poly-MVA has been very positive. I actually heard about the product years ago in a newsletter from Dr. Sinatra. I started taking it, but only small amounts at that time since I did not have actual myeloma, only the markers for it.
In July 2005 my lab tests came back positive for Multiple Myeloma. Because of a family commitment, I did not start treating until February 2006. I was put on Melphalan and Prednisone. I did a series of cycles along with Zometa.
My proteins came down and my oncologist took me off all cancer meds for a number of months. The only side effects I have ever encountered are foot neuropathies and fatigue. There was no hair loss and no nausea(because of Poly-MVA). When my proteins started to go up again, I went back on chemo, this time Velcade and Decadron. I had been on that for a number of cycles, and since last May, I have once again been off all cancer meds.
My oncologist does not say I am in remission, but does say I’m pretty stable. Every six months I have bone marrow punch, full body x-rays, 24 hr urine drop and blood work. When I am in treatment, I have lab work weekly, I will see my oncologist in early February and at that time he may put me back on chemo depending on my tests. This time it will still be Velcade, but by injection once a week. I use Poly-MVA daily and can’t imagine going without it. My family and I believe, even though the cost is high, that Poly-MVA has saved me from serious side effects and very possibly helps keeps my myeloma in check. Thank you Poly-MVA."
Betty Grainger
11-1-2010
Spoke to Betty. She will have a metastatic bone test in December and is still taking her 12 tsps of Poly mva per day. She is taking other supplements as well but is off the MEDS. She has been off of Valcade, Decadron and any other meds for 1 1/2 years. Her counts are still pretty stable so her Doctor is not concerned. She wants to remain stable so is taking this level of dosage.
11-21-2011
Betty is doing well and has not been on any conventional treatments since last May. She will have tests in February to see if she can continue on with the Poly and 4 Corners only. She continues to take 8 tsp of Poly-MVA.
1-16-2013
Betty broke her wrist and is recovering. She weighs about 80 pounds and said she is taking 4 teaspoons of Poly daily but her protein levels are starting to go up. She may be going in for Velcade by IV to try and correct the increase. She may also go back on 8 tsp.
5-17-2013
“I promised to keep you up to date on my myeloma. I am going back in for chemo on June 13th. This time around it will be by injection once weekly with Velcade (and whatever else he puts in). I've been off all chemo for about two years. My oncologist treats it as a chronic disorder and so when my proteins move up (which has been very gradual over this period of time) then he starts chemo again.
So now, here we are. BUT I broke my wrist at Thanksgiving (4 weeks in cast-3 more in splint and then rehab for that). This was followed by one of my morning walks and suddenly I felt dizzy and sat down on the curb until it passed. I forgot all about this for a number of weeks and once again in the market I had the same feeling and hung on to the cart until it passed. Now several things happened at once. Stan got after me to see a neurologist. This I did. I had a CT of my head (and yes, I do have a functioning brain, although my son says the picture is like a brand new brain, but it's never been out of the box).
The neurologist also had this weird test where they grease your hair up and put the electrodes on your scalp. Came out of there looking like Rod Stewart! (The answer to these tests was that there was nothing unusual about them. So then I had my carotids checked--same thing nothing unusual for my age.
At this point I had an appointment with my oncologist and he decided he wanted more tests to assess everything before starting on a round of chemo. He sent me to our cardiologist and I wore the holter? halter? for five days and have also had a Echo cardiogram. I still have to do full body x-rays and a bone marrow punch (these two are yearly tests for my doctor).
I feel fine, I'm always tired because I'm always on the move. I'm actually doing o.k. so far. And Poly, I love you! I take it daily no matter what. For now this is to keep you guys informed and after the 13th when I'm back on chemo, I'll let you know how my tests came out, etc., etc.
BG
2-24-2014
Spoke to Betty and she said her doctor said she was an old frail lady so he is only giving her a mild dose of Velcade. I told her it was best she was and that probably accounts for why she is doing so well. She has not lot any hair and feels good. She will be going for tests in the future so she is going to raise her Poly from 4 tsp to 8 and keep in touch.
10-07-2015
Betty just had chemo yesterday. She has decided she may need to discontinue Poly because she can’t afford the 4 tsp a day. I suggested she go down to 2 tsp. a day rather than stop. She will do so. She also will find out the type of chemo shot she gets and what stage they consider her MM to be and will let me know next week. She called back and told me it is not staged it is IGA and chemo Velcade.
Larry Cunningham
Date: November 2005
Diagnosis: Multiple Myeloma
5 Updates 7-29-08 – 9-13-09 - 10-08-09 5-06-11 - 1-22-13
Personal story
My brother, Larry, was diagnosed with Multiple Myeloma in November 2005 and in researching for answers for support of his body, our family was led to Poly-MVA. He is currently taking Revlemed and Poly-MVA and his numbers are improving. I consider myself a “Cancer Conqueror,” being 6 years cancer-free from colon cancer in May 2006. I decided to take Poly-MVA for daily support and as a preventative measure.
My energy is great, I feel wonderful and I am using Poly-MVA to support continued health. I appreciate AMARC Enterprises and the wonderful work they are doing to support people facing various health challenges; they are always friendly and supportive. I especially appreciate Dr. Llamas and his willingness to answer all my questions. His kind supportive words have been most helpful. Thank you!!
Marilyn Watts
7-29-2008
Marilyn shared Larry Cunningham's latest labs and said he is now off of all chemotherapy agents and continues to be faithful with the Poly MVA. He is doing very well. She is grateful for all of the support.
9-13-2009
My brother has faithfully taken the Poly-MVA since my last report. His M Spike Protein continued to drop while on the Poly-MVA and finally reached 0 on 01-07-08 and has remained at that level since that time. He no longer requires chemotherapy and is doing very well.
He continues his use of Poly-MVA. My husband and I continue taking it as a preventative measure. My husband was diagnosed with Prostate Cancer with a Gleason Score of 8 (March 2007). The doctor wanted to perform surgery, however, we opted to continue with a holistic approach including Poly MVA and other natural methods. He is doing very well - has lots of energy, is able to work full time and enjoy life, with NONE of the side effects common with traditional medical procedures (incontinence, impotence, etc.) Dr. Llamas has been most helpful in our journey to wellness and we are very thankful for him and the entire staff at AMARC. Thank you for all your support and for making Poly-MVA available.
Marilyn Watts
10-08-2009
I personally believe that the Poly MVA is a major contributor to his remission. He did complete the chemotherapy treatment (Velcade & Revlimed) and he believes they were a part of his healing, however, my understanding has been that many Multiple Myeloma patients frequently bring the M-Spike protein down to zero and then it goes back up in a short time requiring further treatment with chemo. So far Larry is maintaining those levels and I attritbute that to Poly MVA. He has not required any further treatment with chemo.
Marilyn
5-06-2011
Marilyn says Larry has stopped using Poly due to the cost...for a short time. He will go back on it some time as there has been a spike in his counts. She said it is hard to say what would have caused his remission, but he may soon be using Poly-MVA again.
1-22-2013
Ms. Watts called in regard to her husband Mort Watts. He had stopped using PMVA as he went to try alternative therapies at this time. She currently has no updates. Her brother Larry Cunningham was also using Poly MVA but has recently undergone a stem cell transplant.
Janice Barsby
Date: June 25, 2005
Diagnosis: Multiple Myeloma Stage 3
E-Mail: buyersoutletmall@earthlink.net
6 Updates 4-7-10 – 7-01-11 – 6-10-13 4-02-14 – 12-28-15 – 3-14-16
Personal story
"Multiple Myeloma is one of a family of diseases known as Plasma Cell Dyscrasias or abnormalities in the blood. Myeloma is a cancer of the white blood cells or plasma cells.These plasma cells are a very important part of the immune system, which in turn helps the body fight bacteria, viruses and fungi. These Plasma cells are found mainly in the Bone Marrow and develop from white blood cells called B-Lymphocytes. When these plasma cells go wrong, it stops the bone marrow manufacturing red and white blood cells and all the cells needed for the immune system. The "sick" plasma cells then form tumors known as Myeloma." Janice Barsby
Janice's Testimonial
I have written on this site before but I am updating my story in July 2008 to let you know how things have gone for me. My original diagnosis was October 2004.
"After reading some of the things others have gone through I feel very fortunate. I am a survivor of Stage III Multiple Myeloma (Bone Cancer). This form of cancer affects the bone marrow where your red blood cells are made. The red blood cells cease to be manufactured and your hemoglobin just drops till you have no red blood cells left. This cancer also eats away your bones. Pain is so intense it cannot be described. I slept sitting in a chair for 2 months (before diagnosis) as I could not bear the pain of lying down on my side or back.
I guess my story started in 2003 when my husband became ill, was misdiagnosed and I had about 3 hours sleep a night for 3 months. He had Diverticulitis, acute, with a bowel blockage, and the pressure caused extreme leg and back pain as it pressed on his femoral nerve. After finding the right doctor, he had 10" of his colon removed and was great. Unfortunately this long of a problem caused his heart to be irregular and we spent 6 months correcting that. It was a stressful time. I was bitten, during this time, by a Brown Recluse Spider, and did not realize what it was and that went untreated till it became infected. (Look up the symptoms of a brown recluse spider bite and they are similar to multiple myeloma)
April of 2004 the discomfort in my legs and back accelerated, but with my husband having to have a second surgery, I put it to the back of the burner. I also had to host a convention of 600 singers (my Sweet Adeline Regional Singing Competition came to Boise) that is stress. By September I could hardly move, constant pain, exhaustion, etc. In July and August I visited the doctor, and on my second visit the doc found really abnormal blood work but just 'kissed' it off as unkown. In September same result only blood work was worse.
I have a long time MD in Nevada so In October, when I had to get around on a rented mobile scooter, I went to see him and he immediately sent me to an Oncologist in Idaho. While waiting, I yelled at my regular doc, and told him I was dying and needed a blood transfusion. His reply " I don't need another doctor telling me what to do!" I did get my blood transfusions and a week later met my Oncologist, a lovely lady called Dr Forsythe. She did a bone marrow test and told me I had cancer (Mulltiple Myeloma) I just sat there and cried. (I will add here I am a retired Registered Nurse. My last position was to work for a world renowned oncologist and open a unit for him in a major hospital. I also gave lots of chemotherapy!)
I agreed to have some radiation, only to Relieve The Pain. I was started on enough pain killer to knock of a horse and was still in agony. This was the last week in October 2004. I was admitted to the hospital the last couple of days of October as I was a little delirious at times, in total kidney failure and just a mess. Well, my dear husband, had just been frantic over my diagnosis and turned to searching for a cure.
He had just re-signed to a MD's natural healing letter, Dr Sinatra, and the following week the doc presented information about POLY MVA. My husband ordered it by overnight mail and as I was leaving for the hospital he gave me 4 teaspoons twice. Then I had a bottle of coca cola (No I did not drink soda's) in the fridge and emptied it and filled the bottle with Poly. I put it in my purse and off I went.
I was prodded, poked, x-rayed, I could not have any procedure where I had to lay down I was so bent, and had a fractures spine that bent me forward, and I was hydrated with IV's and scheduled for dialysis. 24 hours later the doc took another test and noticed my kidneys were better, and decided to wait on the dialysis.. Each day they got better.(The fluids also helped) then she said "Why do you think your kidneys are improving" I said "I don't know" but each hour I was awake I drank 2 - 3 tsps of poly!
(no I did not tell the doctor or anyone as I did not wanted it taken from me) 4 days later I was sent home. They had already informed my husband I would not live. Would not make it to Christmas. At this point I could only walk with help, could not lift my arms, my legs were swollen to 3 times their size and I looked and felt like I was 100…. at that time I was a young 60 years old.
When I went home in 4 days, the doc's were so surprised. I took the 4 corners protocol but mostly took the COQ10 and poly. MY nausea and vomiting was so severe I could not tolerate too many extra things. The radiation was a big cause of the nausea.
Thanksgiving eve was the last time I had blood transfusions as I was starting to regain my bone marrow.The radiation nuked my white cells and platelets so I quit after 3 weeks and said NO MORE! I refused the chemo!!!!
The doc was not too happy but she knew who I had worked for and understood that I knew too much about Chemo. There was no actual chemo that shows it works on Multiple Myeloma, at the time, even though chemo was used for many patients. Several drugs are now used mainly for MM but they only work for a short time. There is no cure for MM at this time. (2008)
I did not eat any sugar and lived on raw juice and cream soups. That was all I could keep down. I lost 60 lbs.(I was overweight but it was scary to have your clothes fall off of you!) Fear was a companion but with help I worked through that and I just knew I was going to get better. My Sweet Adeline group was a tremendous support every day!
I did daily biofeedback and imagery. (That is where you see your cancer cells being eaten up and replaced by healthy cells and bringing in a golden or white light through the top of your head, and spreading it through your body. The cells you see being eaten up you send them to a place where they are destroyed) Each month I improved and gained more mobility. The nausea and vomiting were the worst as It left me exhausted. The hospital personel, who were really good to me, had a big conference to put me on IV pain meds, but I told them that was only for dying people. You could just see the look on their faces, "boy is she in denial"!
Christmas eve I was hospitalized with heart problems (a rate of 200). Turns out the radiation inflamed my heart so badly that it caused it to malfuction, I am still on heart meds but under control. I had some alternative therapy in January, this really gave me a boost, and I knew by spring I would be almost better.
After 6 months of pain and suffering, Thanks to POLY MVA I started to get my strength back, feel better and my blood work greatly improved.(My oncologist still can't believe it) In March my blood tests were normal, my HGB being the best it has been in 5 years.
Yes making my own blood cells like crazy! (You could not test my cancer with blood work or markers, BUT only through A BONE MARROW TEST as I fell into an odd form of Multiple Myeloma -There was a theory thought it was brought on from infection.
A Bone Marrow test in April of 2005 showed NO CANCER and the doc's could not believe what they were seeing.
Now I did loose 6-8 of my thoracic spine disc's to the cancer and lost 5 " in height.(I do not have osteoporosis). When I was able to have an MRI in 2005 it showed cancer lesions still on my spine. By April of 2006 the lesions had disappeared. I still had problems with movement. In the fall of 2006 I went to Curves to try and get more mobility. It helped straighten me up and improved my movement greatly. I get checked every six months and at this time have no signs of my MM. I will not regain the mobility I had but I can walk by myself and sometimes need a light aid (cane) I still have trouble standing by myself. I travel and do what I want to. My doctor told me this week I am "disgustingly healthy" and she just cannot understand why I am alive. Hmmmm
Healthy eating habits and exercise along with spiritual belief of some kind is essential to overcoming this type of illness. I am eternally gratefull to my husband who nursed me night and day and got me through this. To the wonderful people at AMARC for their support and to POLY MVA, without this miracle supplement, I am sure I would not be writing this today. I am grateful to God for sparing my life." Please feel free to contact me at buyersoutletmall@earthlink.net if you need help or information Janice Barsby ORIGINALLY POSTED June 2005 updated July 2008
4-7-2010
"I am still cancer free but had a bump in the road in 2009. My gallbladder had been a "trial" for me all my life and it just kept getting worse. In April of 2009 my doctor was very unhappy with the state of my gallbladder and liver. He suggested I get the gallbladder removed as it was constantly being inflamed, infected and full of stones. I scheduled the operation and about a week before noticed my eyesight was difficult, then I had double vision and then headaches. I went ahead with the gallbladder operation, but 10 days later had an MRI as my face was so painful, it felt like a hundred knives were stabbing me.
The MRI showed an unknown tumor in and near the sinus, unfortunately as so many cranial nerves were involved no biopsy could be taken. I had lost the sight of my R eye and the pain was intense. The radiologist had 2 opinions, 1 it maybe the Multiple Myeloma returning or it was a Sarcoma.
Treatment was started immediately. I had been on 1-2 tsps of POLY MVA for maintenance, but due to my constant gallbladder infections, I believe my immune system suffered. I went on 8 tsps of Poly MVA again and began 8 half dose radiations to my head and that was followed by 10 Tumor specific radiation to my tumor area. It took about 2 months and then I just waited. By November the tumor was gone. I also took 1/4 dose dexamethasone for about 3 months. 10mgs I think.
As I am so sensitive to drugs or radiation they have to cut everything down or I cannot tolerate it. I am on 4 tsps a day Maintenance Poly MVA and CoQ10 plus my other supplements.
Here it is April 2010 and I am still cancer free, doing well and moving about rather well. I wish all who read this to be encouraged. I have a blog www.healingcancernatrually.blogspot.com where I give tips etc on how better to take care of ourselves.
7-1-2011
Janice had surgery on her arm a couple of days ago. The Multiple Myeloma had eaten through the bone of her humus. She takes 12 tsp of Poly daily. She thinks the MM is genetic from her father's side. She was on pain meds from the surgery but sure wanted to catch up.
6-10-2013
Got an update from Janice. The original spot where the MM was in 2004 has recurred. She is back on 14 tsp daily of Poly-MVA. She is using a protocol called magnesium bicarbonate. The Doctor Sircus is the one who has done the recent studies. Janice is sending me the information. She is still helping MM patients as often as possible.
4-02-2014
Janice has had a recurrence of her Multiple Myeloma so she went on low grade chemo in the form of Velcade. She will be going down to see Dr. Milne soon for IV treatments with a new supplement that is designed to target her type of cancer and is compatible with Poly-MVA.
12-28-2015
Janice says that she has mets to kidneys and back. She had been only been taking 4 tsp so now up to 16 daily. She said she is going to increase her daily dosing of Poly, CoQ10 and D3. Will keep me posted as she is determined to beat this once again.
3-14-2016
Janice is still taking Poly MVA and taking her fight day by day.
Susan and Larry Lannoye
Date: 2022
Diagnosis: Multiple Myeloma
Susan and Larry’s Testimonial
My wife, Susan at age 68, diagnosed with stage III Multiple Myeloma Aug. 17, 2008, after being rushed to the hospital with what we thought was a heat stroke, dehydration, and a 104 temperature. Test results showed she had a life threatening staph infection throughout her system as a result of bone marrow cancer which had destroyed her immune system. That was our introduction to Multiple Myeloma, an insidious decease that we had never heard of. The Doctors told us there was no cure for MM, but with the latest Chemotherapy treatments followed by either a stem cell or bone marrow transplant, survivability would be 2-3 years. The good news was we were fortunate to live in Seattle because the Seattle Cancer Care Alliance( formally the Fred Hutchinson Cancer Clinic) is one of the leading facilities in the world for the treatment of cancer with stem cell and bone marrow transplants a specialty.
Sue started her treatments with a combination of chemotherapy drugs( Velcade+Revlimid+Dexamethadone) at the SCCA in Dec. 2008. She continued these treatments for the next 8 months with good results as far as lowering her “bad” numbers ( Kappa Free Light Chains and the Benz Jones protein) which are the main markers for MM. Aug 7,2009, one year after diagnosis, Sue underwent an Autogolus Stem Cell transplant at the University of Washington which was expected to give her 18 months of remission. Sadly, she relapsed after 2 months and was restarted on the chemotherapy(Revlimid) for the next 2 months with negative results. The cancer markers continued to increase with each monthly test. Her Oncologist could only offer to try a different combination of drugs with the hope something would work . We were desperate, but this seemed like not much of an option. Sue was already suffering from neuropathy in her legs and feet from the previous chemotherapy treatments.
I had read Suzanne Somer’s book, Knockout, about alternative cancer treatments which included Poly MVA. I called Gary Matson and made an appointment to visit him and the staff. Sue and I were very impressed with Gary and all the staff and their history and sincere desire to help us. Sue started taking the Four Corners Protocol on January 20, 2010 at the recommended dosage, in her case, she was taking 1 Tbsp of PolyMVA every 6 hours. Six weeks later, Sue had her first tests since stopping all Chemotherapy and taking only the PolyMVA and Four Corners Protocol. The results were stunning. I will never forget the moment her Oncologist entered the room with the test results wearing a big smile and proclaiming Sue his ” wonder woman.” Both the Kappa Free Light chains and the Benz Jones protein had declined dramatically.
When I told him about the PolyMVA , his comment was “just keep doing whatever you are doing and I will see you next month.” he could offer no other explanation for the turn around in numbers. Sue has continued this same dosage of Poly mva with her markers declining with each monthly test( presently every other month) Her cancer markers are still present but at the lowest level since diagnosis five years ago this Aug. She just completed a full skeletal survey(16xrays) last month which showed that the lesions in her thoracic spine and leg have completely disappeared since the last exam 6 months ago.
Sue and I will be celebrating our 52 wedding anniversary in April which we didn’t think would be possible after MM diagnosis in 2008. We sincerely believe this was only made possible by discovering PolyMVA. We are looking forward to many more in the coming years.
A special thanks to Gary and all of the caring POLYMVA team for being on this journey. Please feel free to contact us at larrylq@aol.com for more details or questions.
Sincerely,
Larry and Sue Lannoye
“I was diagnosed with Stage III multiple myeloma on May 1st, 2006. I started on a combination chemotherapy, which I continued for three months. I had heard of the product Poly-MVA at the Cancer Control convention I had attended. I obtained a book about PolyMVA when I returned home from the hospital because I was worn out, tired and needed to do something to feel better. I called Dr. Forsythe to inquire about the product and how best to use it. On May 15, 2006, I started using Poly-MVA and started at 4 tsp/day for 2 weeks, then moved to 8tsp/day and then up to 12 tsp/day until July 1st, 2006. I was feeling better, doing better and markers were dropping. On July 1, 2006, I increased my Poly-MVA to 16 tsp per day as Dr.
Forsythe said that is amount he had used to get his best responses and ensured that blood levels stayed optimum like when he does his IV’s. By August, 2006, I was feeling the best I had in years and my blood tests, liver and kidney function and cancer markers were all better. On November 11, 2006, my reports showed me clear and in remission. I have continued to use Poly-MVA at 4 tsp. per day since. As of June 2014 I am doing very well and all is normal.”
– Doug Wray Passed away peacefully at 77 October 21, 2016
Chase Bockhahn
Date: October 2005
Diagnosis: Osteosarcoma
4 Updates 6-28-10 – 6-01-15 – 5-31-16 – 7-31-18
Personal story
My daughter Chase was diagnosed with Osteosarcoma in Oct 2005 at age 7. She began Chemo immediately for the remainder of that year, struggling with nausea and vomiting (vomiting up to 10 times during administration). In early 2006, Chase had surgery and her left knee and partial left femur were replaced. We found out about Poly MVA shortly after surgery and began the suggested amount of Poly MVA for her weight. She went back on Chemo 3 weeks after surgery and the immediate effect we noticed was her nausea/vomiting had subsided substantially. She might vomit once during treatment or maybe not at all. Her energy level was much higher....the day after treatment she would take it easy and then she would be back to 90%+ within a couple of days. Her overall well being was much stronger and she (keep in mind her age) grew 1/2" during her chemo. treatment which lasted a total of 9 months. This month will be our fifth year since diagnosis.
Five years later, Chase is now 12 years old and still taking Ploy MVA (maintenance dose of one teaspoon daily and CoQ10) and will continue to do so. She is a very active young lady who plays volley ball, cross country skis, golf's and this last spring ran track. I feel that Poly MVA helped Chase have an easier time during Chemo but also helped her body repair itself after Chemo. Chase also had 4 surgeries total to adjust her left femur to accommodate for growth as well as months of physical therapy after. I feel that Poly MVA has helped her system recover each time and continues to keep her healthy. Andrea Bockhahn
6-28-2010
Spoke to Don, both he and Chase are doing very well. Chase was on her way to her annual check up. All of his tests have come back clean. Chase has been taking 12 teaspoons of Pol MVA per day, 9 liver support, 3 Vit D and 3 Calcium.
6-01-2015
Spoke to Andrea, both Chase and Don are doing very well. Chase has passed her 10 year mark cancer free and Don just passed his 5 year mark. They are all doing very well.
5-31-2016
Chase and Don are doing well. Chase will graduate this year!!! Hard to believe. Told Andrea we all are so happy for her.
7-31-2018
The Bockhahn’s are still in good health and continue their daily maintenance dosing of Poly MVA.
Anel Nieto
Date: October 23, 2001
Diagnosis: Osteosarcoma
E-Mail: not available
Personal story
In January of the 2000, Anel started to notice an increase of volume in the left shoulder. The biopsy showed a large tumor mass and the diagnosis was osteosarcoma. When she went to the hospital in Mexico City the doctors said that they could not do anything for her. Life expectancy was zero.
At that time the tumor was proximately 80 x 93mm. Since then she went to different Doctors in cancer medicine. The answer was always the same, there was no chance of survival. In August 2000, she met Al Sanchez, Director of AMARC, and began her treatment with Poly-MVA and clodronate.
The results began immediately, there was significant reduction of tumor and even more important she never presented metastasis to the bone. Before poly-MVA, she used to wear a jacket size 16 due to the size of the tumor that weighted 17 pounds, and she could not raise her arms. Now she can raise her arms without pain, and even more important—she can dance.
At this moment, she is receiving Pallative chemo along with her Poly-MVA/clodronate treatment. The Doctors are evaluating the possibility of the primary tumor resection. “Everyone told me that I was crazy to adopt and assume the responsibility of this young girl. My belief that the impossible is always possible has been reinforced through the trials and tribulations I have suffered with Anel against all odds and I feel vindicated!! Many times I thought that Anel might not make it. Now a shot of adrenaline flows through my veins every time I see and talk to Anel!” Dr. Leticia Maciel Amarc Mexico
Wanda M.
Date: April 17, 2008
Diagnosis: Metastatic Ovarian Cancer (Stage 4) *Also Uterine and Colon Metastasis
5 Updates 7-14-08 – 5-05-09 – 4-12-10 1-14-08 - 8-08-2011
Personal story
This is my experience in the last 12 months using Poly-MVA. April 17, 2008 I was diagnosed with stage 4 cancer in my colon, uterus, and ovaries. My Doctor first considered surgery but since the cancer had gone to stage 4 he wanted me to go through chemotherapy.
Instead, I began taking POLYMVA on May 21,2008. I took 3 IV’s of Poly-MVA a week plus 12tsp a day on opposite days. This was a total of 48 Poly IV’s.
After 6 months of treatment, a pet-scan showed signs of the colon tumor growing. I began another round of 48 Poly-MVA IV’s. After due consideration I decided on chemotherapy. I started chemo January 8, 2009. I continued my Poly-MVA during chemo.
I had another set of 48 Poly-MVA IV’s during these chemo sessions. I took my last chemotherapy on May 27, 2009. After a pet-scan on June 16, 2009 my chemo doctor told me that I was cancer free.
I continue to take 12tsp of poly-MVA per day orally. I am feeling better now and gaining weight and getting my appetite back. I give all the praise to GOD and the guidance HE gave me.
Wanda
7-14-2008
Spoke to Wanda. She has been feeling really good for the past three weeks. She said the poly has taken the pain out of her stomach and that means a lot to her.
5-05-2009
Followed up with Wanda. She is doing well but still has another round of chemo and then they will do some testing to let her know how she is doing. Wanda said the poly has really helped her get thru the chemo.
4-12-2010
Spoke to Wanda, she is doing very well. She will be going in for blood work on Friday and will see her doctor next Tuesday for the results.
1-14-2011
Wanda says that the new drugs that her doctor has her on seem to be doing ok. However, her doctor asked her to stay off the poly while she is on the new medication.
8-08-2011
Talked to Wanda. She is doing ok but not feeling her best. She will be going on a different series of meds and hopes it will help her. She has been off the poly due to her Doctors request.
Nancy B.
Date: September 2007
Diagnosis: Ovarian Cancer Stage 3
4 Updates 8-05-09 – 6-24-10 – 4-30-13 – 4-06-20
Personal story
In September of 2007, I was diagnosed with Stage II ovarian cancer - an 18cm mass, large amount of fluid in the pelvis and abdomen, (Acitis) and right hydronephrosis, underwent a radical hysterectomy, bilateral salpingo- oophorectomy. Postoperative diagnosis: Metastasic uterine cancer with secondary metastasic disease to right ovary.
My doctor recommended 18 months of chemotherapy. Not wanting this chemical and toxic invasion of my body, I did some research and learned about Poly-MVA. I began taking the supplement in December of 2007 [as a part of the Quality of Life study] while I was still recovering from surgery and looking emanciated from about 48 lbs of weight loss due to the cancer.
What happened to my body within 2 weeks of starting Poly-MVA was nothing short of "amazing." My energy level shot up and my appetite increased to where I started gaining back my muscle tone and weight because I was able to eat very well and had no digestive problems. I am continuing with the Poly-MVA program which I use with CoQ10, coral calcium, liver cleanser, vitamin D3, flaxseed oil and organic fruits and vegetables. On 5/1/08 I had a CA-125 test done which came back with a less than 1.0 reading
This product has kept me alive so far, without the destruction of the chemotherapy. I look and feel terrific. I would like to acknowledge Gary Matson with AMARC Enterprises who got me started with the Poly-MVA. I also want to acknowledge the research coordinator, Dr. Jorge Llamas, whom I had the pleasure of speaking with many times when I had questions. He always made time to speak with me. The staff at AMARC was also very helpful and accommodating. My thanks to the manufacturers of this product and those involved in getting it to the patients and monitoring their success.
Respectfully,
Nancy Beckles
8-05-2009
Spoke with Nancy and she says she is doing great. She is still taking poly along with organic juices and she is also taking a lymphatic cleanser.
6-24-2010
Nancy let us know that she is still taking poly once a day, coral calcium, vitamin D3, lymph cleanser, CoQ10, liver cleanser, flaxseed oil, vegetables and fruits and exercises three times a week. She recently had a ca-125 blood test that came back negative.
4-30-2013
Nancy shared her ca-125 test results. I told her it was exciting to see how well she is doing. Her CA 125 is now at 2 which is amazing as a reading below 21 is considered normal. She is still taking 1 tsp of Poly daily plus the 4 corners products and thrilled to be doing so well.
4-06-20
In a nutshell, I am happy to report after 10 years of being cancer free, Poly-MVA saved me from the horrors of chemotherapy and allowed my body to restore to optimum health after undergoing major surgery for cancer.
My body was totally energized, my weight loss was restored, and I felt good at the physical emotional and psychological levels. I am grateful for finding Poly MVA and the experience with the staff was wonderful.
Mary Bonsor
Date: January 2007
Diagnosis: Ovarian Cancer (Stage 4)
5 Updates 4-11-08 – 5-28-08 – 11-12-08 – 9-11-09 8-02-11 – 1-31-13 – 2-25-16
Personal story
I had a terrible diagnosis of stage 4 Ovarian cancer in January of 2007. If I had done the chemotherapy the doctors had recommended, they couldn’t have guaranteed that I’d still be here nearly two years later. Not only am I here, but Praise God! I’m still gaining and intend on sticking around for good.
Your support has been critical in my journey to good health. It has given me the physical support I needed while I fed myself on the Word of God regarding healing and fought the good fight of faith.
Every day I fill my spirit with the Word of God and take my Poly-MVA. I don’t intend to ever let my guard down again! I believe that Poly-MVA has done only good to my body. We’re thankful that you were here when we needed you. Keep up the good work.
Sincerely,
Mary
4-11-2008
Mary was diagnosed early last year with stage IV Ovarian Cancer and only had surgery. She has refused any other conventional treatments and has only been doing 4 tsp daily of Poly MVA for the last year. Her CA-125 was dropping from 30 to 16 but is now going back up to 32. So, she has recently increased her dose of Poly to 8 tsp.
5-28-2008
Due to the recent elevation in her CA-125 marker, Mary has started taking 8 tsp of Poly MVA 2 times a day(16 tsp daily) but it upset her stomach. She has now broken up the dosing into 4 times a day, at 4 tsp per dose, and is taking food with each dose.
11-12-2008
Spoke to Mary and she is excited that her CA-125 test has stopped rising and has dropped from 32, back in early April, to 30 a few months ago and is now down to 22 as of November.
9-11-2009
Talked to Mary and she is doing very well. She and her husband own a camp ground and have been very busy. Mary will have a cat scan done at the beginning of October for her six month check up. She is still taking 8 teaspoon per day.
8-02-2011
Spoke to Mary and she is doing really well. She had tests last month and everything came back clean. She was telling me that NH is fighting to make insurances cover alternative doctors and meds. She said they should know sometime in Sept. if it passed or not.
1-31-2013
Spoke to Mary and her CA-125 markers are still in the normal range. She thanked me for checking in on her.
2-25-2016
Finally talked to Mary again and she is doing wonderful with no problems.
Ilse Boskus
Date: September 2003
Diagnosis: Ovarian Cancer
4 Updates 08-11-15 – 10-16-15 – 02-11-06 6-16-20
Personal story
91 YEARS YOUNG I started using Poly-MVA on November 1, 2003 at 2 tablespoons daily and still using to this day. Used along with conventional treatment protocols. Poly-MVA increased and maintained my quality of Life, more energy with increased appetite. I had less fatigue, pain and improved blood work, kidney and liver panels. Felt stronger with lots of energy.
Hope I can continue taking Poly-MVA. One time I tried to stop and my blood test CA-125 increased and then, dropped after I increased my daily dosing with Poly- MVA. Really feel it gives me a painless life, since I do not have any other illnesses.
Thanks to your product and I would recommend Poly-MVA to my friend or family members.
Thank you!
Ilse
8-11-15
I heard about Poly 12 years ago when I had ovarian cancer and did well for 12 years. Now my CA-125 is going up. After being on 6tsp a day, I have decided I will increase my daily dosing up to 9tsp daily.
10-16-15
Really appreciate your checking up how I am doing. Feeling pretty good, taking poly-mva every day, maybe not enough because my numbers have only come down a little bit. I recently had my checkup with my doctor and he said my numbers are a little high but that he was not concerned because he could not find a tumor. Now I am depending on poly-mva to get the ca125 numbers down a little more, hope I get the results. I will let you know. Thanks for your concern.
Regards, Ilse
2-11-16
Sorry for the delay in providing you with an update. Wanted to wait until I had my new CA-125 test results. Saw a drop of 30 points after increasing poly mva for 6 months at three tablespoons a day (9 tsp daily).
Used poly mva one teaspoon on and off. Then, stopped taking it for some time. My CA-125 was at 98 before I started taking the three tablespoons a day. With the 30 point drop to 68, my hope is that I can bring it down into normal range of 35, my goal. Thanks for your concern and help advising me. Regards, Ilse
Regards, Ilse
6-16-20
Heard from Ilse. She is now 91 years young due to her surviving ovarian cancer for the past 17 years. As of today, June 16, 2020, she is still doing well and continues to take her daily dose of Poly MVA.
Carol Black
Date: June 10, 2002
Diagnosis: Ovarian Cancer
E-Mail: drblack@highstream.net
Personal story
As an addendum to the written program utilized by Carol Black, we have been asked to briefly detail the lab results, the changes and the time frames in which they occurred.
As mentioned in the program write-up, Carol Black was diagnosed with ovarian cancer in February 2001. A CA-125 run at that time was 71. In January it was within normal limits. Surgery was scheduled for March 12th. In the month between diagnosis and surgery, the CA-125 (Bast antigen) had elevated at a rapid rate. We were never told the exact figure of the last test taken the day of the surgery, but were told it had reached "several hundred."
Following removal of the ten pound mass, the Bast antigen dropped over the next two weeks to its initial level of in the seventies. One month later, or six weeks into her program, the antigen had fallen to 17.
In an additional four weeks, it had dropped to 7.5. The oncologist had stated he would be happy with levels from 11 to 13 with 0 to 21 being the range considered normal by the lab we used.
In the next four weeks, the antigen had dropped to 5.5 - a month later it was down to 5.0. During this time, Carol had been very strict with every aspect of her diet and related program.
It has been one year since the surgery as of March 12, 2001. The lab tests continue as a monitoring device. One month the CA-125 was 4.0, another 4.2. In the last five months, the results have varied from the low of 4.0 to 5.0 - never higher.
Carol has had the blood electrolytes and other blood elements monitored every four months. They have always been in range and in good ratio. Better, in fact, than in the years before the cancer.
Carol's success has been due to a combination of factors including a good basic dietary approach, quality products including the Poly MVA, consistency of purpose, good visualization and imaging and a strong conviction that she can heal and survive. She looks better than she has in years and has shed nearly 40 pounds of excess weight.
It has not been an easy road, but she is convinced it has been better than the options presented to her following surgery.
Julia Carter
Date: April 2001
Diagnosis: Ovarian Cancer Stage 3C
1 Update 2-24-2012
Personal story
I was diagnosed with stage 3C ovarian cancer in April 2001. Since then, I’ve undergone several surgeries and chemotherapy. I started taking Poly-MVA in May 2006. In the beginning I felt concerned about the Poly-MVA; what would I expect with this new approach?
I saw the results of my CA 125 (tumor marker for ovarian cancer) begin to rise so I doubled the dosage of Poly-MVA and my CA 125 went back down.
My CT scan in November 2006 showed two metastatic para-aortic lymph nodes. I underwent surgery in December 2006 and something great happened - no malignancy was found during the procedure! It was a miracle and I feel the responsible parties are God and Poly-MVA."
Julia Carter
2-24-2012
Julia is still taking Poly MVA on a maintenance level.
Mary Bonser
Date: 10/17/2008
Diagnosis: Ovarian Cancer
Personal story
I had a terrible diagnosis of stage 3 Ovarian cancer in January of 2007, If I had done the chemotherapy the doctors had recommended they couldn’t have guaranteed that I’d still be here nearly two years later not only I’m here, but Praise God! I’m still gaining and intend on sticking around for good.
Your support has been critical in my journey to good health. It has given me the physical support I needed while I fed myself on the Word of God regarding healing and fought the good fight of faith.
Every day I fill my spirit with the Word of God and take my Poly-MVA. I don’t intend to ever let my guard down again, in the name of Jesus Christ, Amen!
I believe that Poly-MVA has done only good to my body.
We’re thankful that you were here when we needed you.
Keep up the good work.
Sincerely,
Mary
Khleber Van Zant
Date: October 2005
Diagnosis: Pancreatic Cancer
E-Mail: not available
Personal story
Khleber Van Zant was diagnosed with Stage IV Pancreatic Cancer in October of 2005. His surgery was scheduled for November 2, 2005. When his Surgeon began the surgery and saw the size of the mass he realized he could not remove it as it was 9 cm. and to compound the problem the pancreatic tumor was entwined around his aorta. Due to the tumor he also was diagnosed as having Diabetes Type 2 and put on insulin. As a last resort since he could not have surgery his Oncologist gave him 6 weeks of radiation every day trying to shrink the tumor. He was released in January of 2006 and given 6 months to live.
He decided to get a second opinion so Khleber went to Baylor University Medical Center at the end of February. They found the tumor was still 9cm so they put him on chemotherapy and after 4 chemo treatments he was so ill they had to stop. He was having such a problem eating that they put him on a feeding tube. Linda returned home from work one day to find Khleber unconcious and near death so she rushed him to the Emergency Room at their local hospital. They kept him in the hospital for two weeks and then he was moved to a Rehabilitation Center to get him to start eating again. He was not improving so they told him there was nothing more they could do for him. They took out his feeding tube without his permission so they could dismiss him from the Rehab Center. He went home to die.
At this time his caretaker and significant other, Linda Richards, was doing part time bookkeeping for Ashtok Patel MD of Cedar Hill, Texas. Dr. Patel attended the 2006 Spring Meeting of the American College For Advancement in Medicine Conference in Dallas . While there he met the Staff of AMARC and talked to Gary Matson about Poly-MVA.
Here are Dr. Patel's words: "I bought 12 bottles from Gary that would be in April-May 2006. Linda was working part time with me and she heard me talking to my staff-nurse and receptionist about Poly-MVA being used to treat cancer and after that Linda approached me and asked if it helps in pancreatic cancer. I said, yes, any cancer and she bought a bottle the next day and I told her to give Khleber 2 tsp four times a day and within two weeks she bought a 2nd bottle and 2 weeks later she bought the 3rd bottle. That was the time I asked her how he was doing and she said good and I requested that he come in to get his lab done and also establish as my patient. I then gave him supporting nutrients such as CoQ10, Omega 3 fatty acids, Zinc, Magnesium, ImmuneT3, Immpower. Linda was also encouraged to try Poly-MVA from another one of my patients that I started on Poly-MVA who is doing fine now for almost three years with breast cancer.
Khleber started doing all these supplements and continued with POLYMVA. He has now cut his dose to 1-2 tsp daily. He did high doses in the beginning. I follwed him with 2 separate scans as he is doing fine and no need to expose him to extra radiation which will trigger another cancer. It is OK for you to mention my name as I have already talked to some individuals on pancreatic cancer." END OF DR.'S LETTER
Dr. Patel started Khleber on Poly-MVA the middle of May of 2006 and when they did a scan in August the tumor had shrunk from 9 cm to 3 cm. This happened in three months which was amazing. He took 8 teaspoons daily and then stayed on this dosage for 15 months until August 2007. He had a cat scan in February of 2007 and the tumor was stable at 3 cm. Then in August 200, the next cat scan showed no tumor whatsoever. He was in remission after only 15 months on Poly-MVA.
He also was able to get off insulin because the tumor was gone in his pancreas and so he was no longer a diabetic. Khleber takes 1-2 teaspoons a day now for maintenance. He is able to get out and walk and exercise his dogs and mow the lawn." His family feels he is a walking miracle as that six months will soon be 4 years and he is well and strong. They are so grateful for Poly- MVA and for Dr. Patel.
Neal Vallins
Date: April 18, 2018
Diagnosis: Prostate Cancer
Personal story
6 TEASPOONS DAILY I wanted to provide this update on my current status. My PSA is now .06 after levels in the 60's. I had surgery and then 8 weeks of radiation. All went well and I had no side effects from the radiation. I have to attribute that due to taking the POLY MVA and the long term success.
I added at various times DMSO, GRAVILOA, TUMERIC, SODIUM DICHLORACETATE and ONKOBEL-PRO, however the game changer was and is Poly-MVA. As a mitochondrial driver for metabolism and healthy/normal cell function, it was absolutely key to the overall approach. It helped across every aspect of health: Improved Quality of Life, more energy and no fatigue, my appetite was normal, I experienced no pain and all my blood work and panels were right in line each time.
The oncologist was flat out amazed at every test. The online materials, research and customer support and service is outstanding with the group that supports the community. I share this will all my friend and family and it still amazes me that after all I went thru, others are reluctant to try it and follow thru, as they say " YOU CAN LEAD A HORSE TO WATER”, however UNLESS THEY’RE OPEN TO Outside the Box Thinking, AND SADLY MOST PEOPLE ARE VERY CLOSED when it comes to integrative medicine, they don’t think of the rest of the body, they are to focus on the disease.
Thank you!
Neal
Bob Stegmaier
Date: 2018
Diagnosis: Prostate Cancer/CML
Personal story
In 2002, I was diagnosed with CML (Chronic myeloid leukemia). The oncologist was not very optimistic and told me I would either have a recurrence of the CML or develop another cancer later on.
My Dentist was Dr. Garnett, the scientist that invented Poly-MVA. When I discussed my diagnosis with him, he recommended daily dosing of Poly-MVA. I have taken it for 18 years to fight off the original diagnosis of CML and a later diagnosis of Prostate Cancer.
In April of 2018, I was diagnosed with Prostate Cancer. My daily 1 tsp maintenance dose of Poly-MVA had kept my CML in check for 16 years but was not enough to prevent the onset of Prostate Cancer.
When I received the diagnosis, I immediately started with the maximum loading dose of 8tsp of Poly-MVA daily as well as the complete approach. I am happy to report that I am currently cancer free as of the date of this writing.
I still use Poly-MVA every today as part of my maintenance and good health. Poly- MVA was a very important part of my protocol and I would not have succeeded without it.
I am now a twice cancer survivor. Poly-MVA helped me maintain a good quality of life during both cancer treatments. I went thru bone marrow transplant for CML, high dose radiation and intensity modulated radiation therapy (IMRT) for prostate cancer and used multiple vitamins and minerals. I felt better and was less inclined to get colds.
Amarc Enterprises has a great knowledgeable staff. A great company to do business with and polite friendly caring people. I recommend Poly-MVA to others.
Thank you,
Bob Stegmaier
Vernon Carland
Date: June 12, 2012
Diagnosis: Prostate
1 Update 3-25-2016
Personal story
I was diagnosed with prostate cancer in Feb of 2002. My PSA had been monitored and climbing for years prior, but needle biopsy did not find it until 2002. I altered my eating habits, used hyperthermia and chelation for mercury and finally in 2008 went to valley cancer in Los Angeles for hyperthermia and low dose of radiation.
I never felt bad and stopped working, but in 2010 I consulted Dr. Paul Rothwell of Oklahoma City because PSA rose. He put me on Poly-MVA -6 tsp daily. In past 2 years I have taken Poly-MVA every day up to 12 tsp then back to 8tsp. My PSA has fluctuated but all MRI’s show good results. I feel wonderful and do very physical labor at age 70.
I attribute my energy and well being to Poly-MVA and my faith in God. Dr. Rothwell also gave me 100mg IV, and Vitamin C weekly. All things work together for good to him who trusted God. Thank you for helping me with Poly-MVA
Vernon C
3-25-2016
Spoke to Mr Carland and he says he tries to take a daily dose of Poly to stay healthy. However, money has been tight. So, he uses Poly when he can afford it.
James Peters
Date: July 2012
Diagnosis: Prostate
3 Updates 4-07-14 – 10-13-15 – 5-16-16
Personal story
In my mid-thirties I began to suffer clinical effects of exposure to defoliants sprayed around the military bases where I served in Vietnam. Many doctor visits and a two-day battery of inpatient tests revealed nothing. It was necessary to use heating pads to relieve inflammation and discomfort in the rectal area that was diagnosed in 1994 as prostate cancer (Gleason 2+2 via needle biopsy).
External beam radiation that year was unsuccessful, since PSA began to rise again within a few years. In 1999 I began anti-agonist (Zoladex) injections, which generally worked well until 2005, when a double blockade with Casodex began. However, in mid-2010 the malignancy became refractory; PSA velocity averaged a rate of about 10 ug/ml each month. (See the attached charts.) At that rate it appeared that serious health decline would be inevitable within months. I had seen PolyMVA mentioned in Suzanne Sommers’ book(Knockout) on alternative cancer treatments.
In July 2012, after internet research, I began dosing PolyMVA at 40 ml/d (two tsp four times a day). At that point PSA was nearly 50 ug/ml. But within two weeks PSA velocity began to slow, and in another two weeks it stopped completely. It was a real miracle!
Since July 2012, I have used PolyMVA continuously as my main line of defense. I joined AMARC’s Quality of Life Study in October 2012, and markers have remained basically stable in the range of 50s to 60s.
When anti-agonist was discontinued in May 2013, there was a temporary spike in the low 80s. That event could have been an outlier or possibly an indication that some cell lines were still responsive to anti-agonists.
In addition to faith in God, diet, ample clean water, exercise and rest, my health regimen includes PolyMVA and certain dietary supplements and immune system boosters. These supplements have been discussed with AMARC’s excellent health consultants and with my oncologists.
James Peters
4-07-2014
Spoke to Mr. Peters and he is doing well. He still takes 6 tsps of Poly MVA per day. He also shares Poly with his father in law which has helped to lower his PSA. He put his father in law on 10cc of Poly 3 times daily. His father in laws’ PSA was 35 before staring on Poly and after 1 month the PSA dropped to 24. Mr. Peters PSA is steady at 60.
10-13-2015
Since the mid-1970s I suffered inflammation and discomfort and sat on electric heating pads for relief. My condition was diagnosed in 1994 as prostate cancer (Gleason 2+2 via needle biopsy). External beam radiation that year was unsuccessful, since PSA began to rise again within a few years.
In 1999 I began anti-agonist (Zoladex) injections, which generally worked well until 2005, when a double blockade with Casodex began. However, in mid-2010 the tumor became refractory, and Casodex was discontinued.
By mid-April 2011 PSA velocity began to rise at a rate of about 10 ug/dl each month. At that rate it appeared that serious health decline would be inevitable within months. Decisive and effective action was needed and fast!
I had seen PolyMVA mentioned in Suzanne Somers’ book (Knockout) on alternative cancer treatments. In July 2012 an alternative medicine clinic near Dallas recommended PolyMVA. So, after performing internet research, I began dosing PolyMVA at 40 ml/d (two tsp four times a day). At that point PSA was nearly 50. But within two weeks PSA velocity began to slow, and in another week or so, it stopped completely and remained basically stable in the 50s and 60s. It was a real miracle!
When anti-agonist injections were discontinued in May 2013, PSA began to rise again, out of control, reaching almost 120 points within a year. In August 2014 I started a regimen of Zytiga (aberaterone acetate) – a very effective but expensive option usually reserved for metastatic cancer patients. But amazingly, half a dozen CT and other scans of abdomen and chest from 2013 to present have shown no visible metastasis. Clearly, the electrochemical action of PolyMVA, killing circulating tumor cells (CTCs) in the bloodstream has saved my life.
In addition to faith in God, diet, ample clean water, exercise (tennis, weight-lifting and brisk walks) and ample rest, my health regimen includes a triple blockade: PolyMVA three times a day, anti-agonist injections semiannually, and daily Zytiga orally.
The latter two medicines control blood testosterone and adrenaline levels and thus starve the tumor; and PolyMVA kills off CTCs that enter the bloodstream and try to colonize elsewhere in the body. I take certain dietary supplements, as well, and these supplements have been discussed with AMARC’s excellent health consultants and with outside oncologists.
In conclusion, it is clear that PolyMVA is an ingenious, unique, powerful weapon against metastatic cancer—without harmful side effects. PolyMVA’s effectiveness is a modern miracle, providing hope and positive, verifiable, economical results. I continue to co-exist with and manage this disease for the long term and am eternally grateful for PolyMVA and God’s blessings.
James P
5-16-2016
Spoke to James and his wife, Vicky. James is still doing well but they are concerned about James’ 96 year old father in law whose Prostate cancer has progressed. He is not doing well and we discussed dosage and how to best help him. They also asked about some of his current medications and whether they might interfere with Poly. The elderly father in law now has metastasis to his bones and liver.
Jim Miller
Date: 2011
Diagnosis: Prostate Cancer (Advanced)
1 Update 5-08-2019
Personal story
I was diagnosed with prostate cancer in 1999. My PSA was 6 and a biopsy showed cancer with a Gleeson score of 3+3. Surgery was recommended (radical prostatectomy), but I was hesitant due to the main side effects of incontinence and impotence.
I spent the next several years getting second and third and fourth opinions and trying many natural cures. These didn’t stop my PSA from rising, so I finally had the surgery in 2005. My PSA just before surgery was 17. After surgery it was undetectable.
After 2 years my PSA started to appear again. It should have stayed undetectable since I no longer had a prostate gland, so I agreed to have ”salvage radiation” in 2008. Again my PSA became undetectable, but it started to appear again after two years (in 2010). This upgraded my condition to “advanced prostate cancer”, since there is no known cure after surgery and radiation, only delaying procedures.
Throughout my cancer experience I was constantly searching for non-invasive treatments. One of my searches took me to the Poly-MVA site where I read encouraging testimonials, so I gave it a try. At 4 teaspoons a day my PSA seemed to be slowing, so I increased my dosage to 8 teaspoons a day.
Since I never had any symptoms from the cancer and was already feeling good and being very active, I didn’t notice the increase in energy that others have noticed. However, Poly MVA has had an incredible effect on my PSA, slowing the rise to almost no rise at all. This has prolonged my life to the extent that I may never need any additional treatment. Thanks to Poly-MVA.
My oncologist said I don’t have to start any of the delaying procedures (hormone therapy or chemotherapy) until my PSA rises to 10 or a tumor is detected, so I’m trying to slow down the rate of rise. The rate of rise is measured by “doubling time” (the higher, the better) since the PSA usually rises exponentially.
Jim Miller
5-08-2019
Called and talked to Jim to get an update on his status and how he is doing. He provided the following chart and comments that show how well Poly MVA is keeping his PSA levels in check.
JIM’S PSA CHART As you can see by the chart and information below, Poly-MVA has slowed the rate of rise. It seems to be rising linearly instead of exponentially. This has been a great relief, since it appears that my PSA won’t hit 10 for at least 10 years thanks to Poly-MVA.
Doubling time 2011-2012 1 year (no Poly-MVA) 2012-2013 2 years (4 tsp per day Poly-MVA) March-June 2013 6 months (no Poly-MVA) 2013-2019 8 years (8 tsp per day Poly-MVA)
Edwin Stuart
Date: November 2008
Diagnosis: Prostate Cancer
5 Updates 7-01-10 – 5-16-13 – 11-13-15 5-02-19 – 3-13-20
Personal story
I was diagnosed with Prostate Cancer in 2008 and was told about Poly MVA by my daughter in law. In December of 2008, I ordered the product and started taking 4 tsp daily. I have been taking Poly MVA religiously for the past 10 years.
In November of 2008, my PSA had risen to 8.27 before I had started taking Poly. Over the years, it has steadily gone down and now it is averaging around 6.0 some ten years after starting on Poly.
Poly MVA has not only kept my PSA in check but it has given me an improved quality of life as well as improved my Blood, Kidney and Liver test results.
Whenever I hear of someone who has been recently diagnosed with Cancer, I tell them about Poly MVA and what it has done for me. I want to thank the AMARC staff for being so great, which specifically includes Toni and now Vivien. At age 83, I am still alive and well!
Ed
7-1-2010
Spoke to Edwin and he told me he feels great. He told me he never took chemo or radiation so he should be a good testimonial for the PolyMVA. I told him he already is a great testimonial.
5-16-2013
Spoke to Edwin, he is doing very well. Has no questions but said he was happy I called.
11-13-2015
Spoke to Mr. Stuart and he let me know that his wife had blood in her stool and her doctors believes it may be Colon cancer. He will have report next week and will call to let us know.
5-2-2019
When I spoke to Ed, he said he has been taking Poly MVA for 10 years and has not used any other treatment to stop his prostate cancer. He said he has other friends using Poly MVA that he has referred to the product. Most of his friends are people who use poly for prevention.
3-13-2020
Spoke to Ed and he has recently had a hernia operation. He is very proud that he has only used PMVA for the past 10 years and kept his PSA stable. His PSA has not changed. He shared the details of his appointment with his urologist and everything is the same. He is a 10 year Prostate Cancer survivor.
Walter Davis
Date: 2008
Diagnosis: Prostate Cancer
1 Update 2-25-2019
Personal story
I put off updating my testimonial on the effectiveness of Poly MVA for as long as I could. I knew the pain that would be dredged up and tears would come as I recounted my family story with cancer. In the interest of saving lives and assuaging pain and suffering, I am telling my story again.
We have a choice in our fight against cancer: Conventional medicine or integrative medicine. I was the only one in my family to select integrative medicine, a combination of conventional and holistic medicine.
My other family members said I was crazy for my decision. They are all dead now. Poly MVA saved my life. I am a retired navy navigator, Harpoon cruise missile engagement officer and Chemical Dependency Treatment Specialist. I served in the United States Navy from 1975 to 2001. Naval Warfare Operations Specialist Chief Walter Davis, Yokosuka, Japan 1988 Currently I am Executive Producer on the radio and TV show PROGRESS IN THE WORLD. I own an insurance brokerage and for the past 28 years I have been helping people obtain the proper health insurance to protect themselves and family against cancer and other chronic illnesses.
In 2008 I was diagnosed with prostate cancer. My PSA was 6. Poly MVA has been my primary supplement in my fight against cancer. It has saved my life. I have not had ANY conventional treatments. I use the Veteran’s Administration Hospital (VA) in San Diego and The University of California San Diego Hospital (UCSD) in La Jolla for testing and evaluation.
In 2003 while speaking at the Joyce Beers Community Center in San Diego, I was approached after my speech by a lady in the crowd who told me that she had been suffering from cancer. She told me “If you know anyone who has cancer and you love them, tell them about Poly MVA.”
At that time, no one in my family had cancer that I knew of. Soon, things changed. I visited my family in Birmingham, Alabama during this time frame. We took a family picture that was to be our last together. My brother Maurice collapsed a short time afterward on the front porch of my mother’s home. Tests revealed that he had prostate cancer that had spread into his spine. He was paralyzed from the waist down. He died a painful death 15 months later following radiation treatments.
Left to Right, Cedric, Maurice, Mother Rosa, Sandra, Rita, Walter: The last picture of us all together My brother Cedric and I began getting tested every six months after this. Sadly, Cedric’s first test revealed prostate cancer. He elected to get surgery. This rendered him impotent and incontinent.
Maurice died ironically the week that my wife Linda was diagnosed with cancer. She had a lump in her breast shaped like an orange with pits in it. A doctor at Kaiser and one in the private sector told her that she had inflamed lymph nodes and gave her antibiotics for what later was revealed to be cancer. I demanded another test.
It took six painful months to get the conventional doctors to finally diagnose her with cancer at the third test at the Tri-City Women’s Medical Center in Vista, CA. Linda Jordan Davis and our grandson in happier times.
Frantically I searched for the best Oncologist. Fortunately, I had put her on a POS plan through my insurance brokerage. This allowed features of both a PPO and an HMO plan. A primary care doctor at Scripps Hospital took her in and referred her to UCSD to an oncologist that had a good reputation. She saw Linda and she told us that she would let us know after the weekend if she could help us or, if Linda should get her affairs in order.
Maurice’s funeral was that weekend and I had a choice: Go to my brother’s funeral or stay with my wife and help her through this cancer. I stayed with my wife. There was nothing I could do for Maurice. Linda’s mother had passed away from cancer ten years earlier just after she had retired at 66. Linda was falling apart.
We arrived at UCSD early that next Monday morning and the oncologist told us that she could help Linda and that she had stage three cancer. Later tests revealed that she had HER2/NEU positive invasive ductal breast cancer, one of the most aggressive types. A port was cut into Linda’s chest with plastic tubing. The chemo therapy was so strong that it would burn up her veins if put directly into her blood stream.
Each treatment cost $9000.00 or $32,000.00 per month. She had 30 days of radiation and that cost $700.00 per day. Her hair came out and she was bald. Her feet and hands turned as black as my shoes. It was horrible. I had to give her Neupogen shots in her stomach each night to assuage the effects of Chemo as it damaged her immune system. Sex was impossible as her tender flesh tore with any attempt to engage. There were last minute appointments that required me to drive her all over San Diego. My insurance business began to fail and I had to beg for money from charities just to pay my bills.
In successive surgeries, Linda had 30 lymph nodes removed. The cancer was spreading and soon she was diagnosed with stage 4 cancer. I talked to the nurses at the cancer center about all the women I saw getting treatment with no spouses or other support. They confided in me that our chances of having a successful marriage through this was slim. Often, I was the only male in rooms filled with ladies in pick skull caps.
We got a glimmer of hope when my wife was one of the first to get an experimental drug called Herceptin. She was featured on local television. That hope did not last long. After appearing to subside, her aggressive cancer came roaring back. She refused to take Poly MVA and turned to prayer. Linda Jordan Davis during chemo treatment
I kept getting my tests for prostate cancer. My doctors at the VA were foreign born. They were cold and uncaring in their deportment. Finally, I got the dreaded call at about 7:30 AM from a urologist at the VA hospital. In a heavy accent, he told me that my tests had come back and that I had cancer. There was no good morning, no I have bad news, no recommendations, just, “You have prostate cancer and someone will contact you in a few weeks.”
I began to look up prostate cancer options. They all had terrible side effects. I had seen what my brothers had gone through and what my wife was currently facing.
Finally, I got a consultation. I wanted the cancer out of me. I selected robotic surgery. I showed up for the surgery appointment months later at the VA and my surgeon did not show up. The receptionist apologized and said that she was going to set another appointment for me. I told her that would not be necessary because I would not be coming back. The whole waiting room erupted into applause.
I tried to remember what the lady had told me back at the Joyce Beers Community Center. I remembered the word Poly but not the rest. It had been more than four years ago.
I began to search Google. I put in the words Poly and Cancer and Poly MVA came up. I called the people at Poly MVA and they did a consult and I began to take the product. I got a cheaper price by participating in a study while using the product where I shared my treatment progress within the last month. My mother, a nurse, told me to take cancer seriously and to treat it conventionally. My wife said I was crazy as did my brother Cedric. I stuck to my guns and three years later there was no evidence of cancer in my body.
Sadly, my mother died from undiagnosed breast cancer in 2010. Elderly black women are not aggressively tested and treated. My brother Cedric was killed one month later in an accident, never regaining his sexuality.
My wife Linda developed chemo brain in 2011 and thought that I was trying to kill her when I was trying to give her Neupogen shots. She never would try the Poly MVA. We separated. After 10 years of struggle, in 2014 she drowned in her own body fluids after the chemo ravaged her body putting her on an oxygen tank, bald head and black bottoms to her feet and hands.
I stopped taking Poly MVA to save money. Fortunately, now, there are living benefit insurance plans that I offer my clients to pay for integrative medicine treatments. My PSA rose to a 17 then to a 29. At a 4 or above, you have cancer. I took biopsies and the cancer was determined to be nonaggressive. The biopsies were horrible. The urologist inserted a probe into my anal cavity and punctured my prostate through my intestines up to twenty times with needles. I went home wearing a diaper from all the bleeding. The doctors at the VA recommended surgery or radiation. I refused and commenced taking Poly MVA again.
I kept getting primary care and urologist doctors from Africa, India and Cambodia at the Veterans Administration Hospital who could barely speak English. They told me I was going to die. Often, they did not have my most current lab results and they often called me by the wrong name as they had someone else’s chart up on their screen. They often asked me at the top of my appointment “You have cancer, right? I could read your charts but, can you just summarize what has been happening?”
I saw that I had to take charge of my own healthcare. I began to take Poly MVA every four hours. My PSA went down from 29 to 17 in three months. I added cannabis oil and the PSA dropped to 11 in just six weeks. I only see urologists in a supervisory capacity now and I go to integrative medicine centers that understand Poly MVA, cannabis, cleansing and other holistic treatment regimens.
My most recent biopsy was in November of 2018. A fusion biopsy revealed a cancer cell that is .0135 microns is in my prostate. The doctors have recommended that all treatment options be tabled and that I be watched. I continue taking Poly MVA and getting screenings done every six months. If I had listened to incompetent foreign doctors, I would not be enjoying a healthy life today. I would be suffering from the terrible side effects of conventional cancer treatment regimens that my family members experienced. Poly MVA remains the central protocol of my cancer treatment.
As the woman told me at Joyce Beers Community Center in San Diego: If you know anyone who has cancer and you love them, tell them about Poly MVA.
Sincerely,
Walter Davis
Gary Thomas
Date: November 2007
Diagnosis: Stage IV Prostate Cancer
5 Updates 8-25-08 – 3-27-09 – 4-06-12 7-02-13 – 7-10-15
Personal story
Wife diagnosed with Squamous cell carcinoma In June of 2004 my wife was diagnosed with squamous cell carcinoma that had manifested itself in her neck. With an unknown primary she had a modified radical neck dissection and chose not to do the radiation the doctors recommended. She instead found her way to Reno NV. and Dr. James Forsythe MD. He put her on poly and she used it for about 2 years. She has quarterly checkups with her surgeon and NO cancer.
Gary is diagnosed with Prostate Cancer In November of 2007 I ended up in emergency spinal surgery for what turned out to be stage 4 Prostate cancer and had a large tumor removed from my lower spine. My PSA was 1314.
Came home in a wheelchair and was using a walker. Had a catheter and really did not know if I would get any better. Well --- it is now October 2008 - I am walking as I always did, use a catheter once a day to empty my bladder, my PSA is 0.5, my retests in June 2008 showed significant improvement in the bone and lymph node involvement. I have some emotional issues but that may work itself out in time.
Oh did I forget to tell you? I also went to Reno and Dr. Forsythe put me on Polymva and Salicinium, a product that he is working with the FDA to get approved as a Cancer treatment.
I am quite sure without polymva neither my wife nor I would be here to tell you this story. Thank you polymva and your wonderful staff - you have blessed our lives.
Gary and Elma
8-25-2008
Spoke to Elma and Gary and he is doing very well. His PSA is down to 1.4. Gary said, that after the surgery, his PSA came down and his cat scan results showed significant improvement. They are very optimistic and very happy they found Poly.
3-27-2009
Spoke to Mrs. Thomas. She says Gary is doing great and she said his doctors are even surprised how well he is doing.
4-06-2012
Spoke to Gary and he is not doing well. His PSA has shot up and the Lupron he was on is no longer working for him. He called Dr. Forsythe's office, they gave him a protocol that they would use on him however it would cost $31,000.00 dollars and he told me he can't afford it they just don't have any money. His doctor is going to try and get him into a clinical trial testing something called Orteronel Tak 700 this will be the third trial on the drug. Gary is very down and told me he dosen't even feel like eating and just doesn't know what to do.
7-02-2013
Spoke to Gary. He wanted to let me know his PSA seems to be holding. His doctor gave him a choice of three meds or do nothing at this time. Gary has chosen to only take Poly and other Supplements.
7-10-2015
Spoke to Mrs. Thomas, Gary is doing very well and his PSA is still the same as his last report. However, he is having a problem with a tooth will be going into to have it checked next week
Jack Kelley
Date: November 15, 2005
Diagnosis: Prostate Cancer w/mets
E-Mail: not available
Personal story
I was diagnosed with possible prostate cancer on Nov 15, 2005. At this time I was referred to a urologist to verify my condition. I started searching the internet for information and I decided not to have a biopsy with the urologist. At about the same time I contacted CTC of America at Zion, IL. During my research of the internet, I found several alternative and integrative options for treatment and/or support that I decided could be of value in the future, one of which was Poly-MVA.
Before I had my appointment with CTC, my family doctor asked me to have a bone scan to see if the cancer had spread or not. I had this done and found that the stuff had spread to my back and the ribs on the right side. When I went to CTC for my evaluation on Jan 26, 2006 a ct scan that was done revealed a large tumor growing in my mid back.
I was scheduled for an operation to remove this Feb 13, 2006. I spent about 11 days in the hospital and was released for treatment to CTC. I received fourteen radiation treatments over the next 5 weeks and was sent home with follow-up in one month. I was given casodex, avodart, and lupron for the prostate and zometa for the bones. Over the next few months my psa fell to somewhere under 2 but started to climb at the end of 2006.
In May of 2007 the oncologist at CTC wanted me to start taking ketoconozol and hydrocortizone to stop the production of testosterone by my adrenal glands. I decided not to do this because of possible liver damage that could occur.
I decided to start the Poly-MVA Four Corners protocol. I started taking Poly on 7/7/07 with a psa of about 23. The psa readings rose steadily until it was 87.12 in January of 2008 at which time I finally gave in to the doctors recommendation and started using ketoconozole and hydrocortisone. Blood test in February showed a decrease in psa to 48.534. The March blood test showed a psa of 36.27. On 4/12/08 I started Standard Process phyto-nutrient / proto- morphogen protocol to enhance my immune system for cancer treatment because of the very high levels in the liver. In April, the psa was down to 24.99.
Since that time the psa has ranged from about 18 to 22 and the ALT and AST have returned to normal range. I have reduced my use of Poly-MVA to a maintenance dose for the last year and continue the Poly as part of my self administered treatment. All during the time I have had cancer I have been taking supplements recommended by the naturopathic doctors at CTC. I have had no side effects of any sort from Poly-MVA and feel that it has helped me to keep my system strong enough to keep the cancer in check. Thanks to all the folks with AMARC and Poly-MVA that have worked with me during my time of need. I look forward to a long relationship.
Thank you,
Jack
Brian L. Anderson
Date: Summer 2005
Diagnosis: Prostate Cancer
2 Updates 4-13-2011 – 9-28-20
Personal story
I In the mid 1990's my PSA count began to climb above a 3.0 so Dr. Kemire, my regular Kaiser Permanente Doctor did a digital exam of my prostate. He explained that it felt a bit firm and if my next PSA count were to get higher, I should consider having a biopsy to check for any signs of cancer.
Over the following decade my PSA count would increase to as high as 10.5 and then decrease to as low as 6.0. In 2005 I met with Dr, Stewart, a Urologist at Kaiser and we scheduled a biopsy for me. In our meeting after the procedure I was expecting him to say the results were benign and I would leave his office a relieved man. But no, he said, "you have prostate cancer" and I was in a state of absolute shock! After he calmly explained my three medical options, i.e. radiation treatments, chemotherapy or surgical removal of the prostate, I said, "I'd like to take time to consider some other options. "Dr. Stewart also informed me that on the Gleason scale my count was a 7 out of a possible 10which was not good. The best news he shared was my cancer was not aggressive.
After returning home I telephoned my friend, Margaret Walt an RN with Kaiser, whom I knew had attended a cancer convention for alternative therapies in the Los Angeles area. I asked her if she had any information about a product to control prostate cancer. She told me about Poly-MVA and gave me a 800 number to call. I got in touch with GaryMatson at AMARC 2Enterprises and asked him if there were some men currently using Poly-MVA that I could call to hear about their use of the liquid dietary supplement for prostate cancer. He gave me the names and telephone numbers of several men whom I called.
After hearing their testimonies, I knew it was important that I order some Poly- MVA and get started using it on a daily basis. So in 2007I enrolled in the "Quality of Life" program for a year to monitor my usage of the product and provide useful data for the future.
In 2009,because my PSA was at 12.7, my new Urologist, Dr. Chabra, wanted me to have a second biopsy. That made sense to me so I went ahead and had it done. The results were unbelievable to both of us. My Gleason count was a 5, versus the 7 only two years earlier.
The Doctor had the Laboratory check my results twice because he could not believe the lower number. I told him it was due to "the power of prayer, a positive attitude, proper diet and Poly-MVA. I showed him a 8 ounce bottle of the supplement for his information.
Over the past 5 years since 2007I have taken Poly-MVA orally each day (2 teaspoons) and no other products for my prostate cancer. My most recent written report (05/23/11) from Dr. Chabra stated, "PSA is essentially unchanged for the past 3 years at 12.7. Please repeat in another 6 months.”
I have been so impressed with the results of using Poly-MVA that each year I volunteer for 3 days over the Labor Day Weekend at the Annual Cancer Control Convention in Universal City, CA. The conversations I and other "Survivors" have with interested men and women at the Poly-MVA Booth and the sharing of our testimonies at a General Session is a very gratifying personal experience and an encouraging one to our listeners. I plan on using Poly-MVA for the rest of my life and trust I'll have many more years to share its benefits!
Sincerely Yours,
Brian Anderson
4-13-2011
Brian say she is doing well and about to go on an AlaskanCruise. Brian has been a regular attendee to the Cancer Control Convention in Los Angeles where he talks to other cancer patients about his benefits with Poly MVA for his Prostate Cancer
9-28-2020
My husband has used POLY for his prostate cancer since 2007. Over the past 13 years, we have met many cancer survivors who have used POLY and have heard their stories at the National Cancer Conference each Labor Day weekend in the Los Angeles area.
I was so impressed with these stories and my husband's results that I decided to use POLY myself for two main reasons: first, to enhance my immune system and second, to have POLY eradicate any cancer cells that might develop in my body. More than ever I need the immune system support..... I rarely get a cold, flu, or allergy problems, so my immune system is stronger. I also take some other vitamins and Juice Plus.
Poly-MVA has helped both of us with Quality of Life sustaining our nutritional needs, energy levels resulting in less fatigue. It also has also given us a great Peace of mind knowing we have some cancer-fighting assistance.
It has been so great to talk to Gary Matson and have questions answered. He is very knowledgeable, both on the phone and in person. We have developed a wonderful relationship over the years and have visited with him at conferences. Customer service staff have always been cordial and very helpful. Thank you for all of your support!
Rosalyn Anderson
9-22-15 - 2-20-19 9-03-19 - 5-10-20
Michael Muscari
Date: July 4, 2003
Diagnosis: Prostate Cancer
Email: hsp@hspinc.com
Personal story
Prostate cancer has been a part of my family’s medical history for 3 generations on both sides of my family. I do not know of any medical history prior to my grandfathers. My father and his father, my mother’s father and I have all been diagnosed with prostate cancer. Both grandfathers and my father did not survive their diagnosis. Subsequent to their deaths, my mother died in April of 2007 of breast cancer that metastasized to bone cancer. I started having an annual PSA screening in 1995 when I was 42 because the American Urologic Association was offering screenings at a local urologist’s office.
My father had a prostatectomy in 1993 and considering my mother’s father’s death from the disease as well, elected to be proactive. 6 years later my PSA began to rise consistently, and my urologist recommended biopsies beginning in May of 2002 for early intervention. I did not have a sense of urgency to biopsy so I waited while I thought about the consequences and the options that I had learned about and which had been recommended. After turning 49 in July 2002, in September 2002 my urologist completed 6 needle biopsies, 3on each side of my prostate gland. The Gleason score was 6 4 Updates
(3+3) and of the 6 biopsies, the pathology report showed that there was only one core of the 6 which had 10% cancerous tissue. I have elected to forego subsequent biopsies and have had none since. Subsequent to the biopsies I delayed all conventional treatment to familiarize myself with prostate cancer some more and to search for answers that made sense to me. I had been introduced to Mrs. Pat T in 2000 who had survived stage 4 breast cancer having used PolyMVA as part of her protocol, which inspired me and provoked more investigation. Dr.
Merrill Garnet, the dentist/chemist who formulated PolyMVA, and I shared commonalities given my profession in the dental equipment industry, so my confidence grew as I learned more of his history, his dedication to his efforts with PolyMVA, about the resulting formula and the histories of people who had used it to help build their immune systems to address various health challenges they were experiencing. After the biopsy results in 9/2002, I made significant improvements to my diet, drinking filtered water and no soft drinks or any conventional fruit drinks given the sugar levels I wanted to avoid.
I reduced sugar intake from every source possible, eliminated all red meat and began eating mostly white meat hormone free chicken breasts, some non-bottom-feeding fish, no shellfish or bottom feeders at all, quantities of raw vegetables seasoned with spices of all kinds, olive oil, some vinegar, tomato sauce and raw tomatoes, among other raw fresh vegetables, walnuts, cashews and almonds. I have kept to this diet fastidiously since beginning it and have been delighted with my progress and with the variety, flavor and benefits, recommending it often.
In late June of 2003, after a referral from my urologist, I flew to UCSF to be part of an MRI trial to improve the software for prostate imaging, for a consultation with world-renowned urologic oncologist Peter Carroll, MD and for a color doppler sonogram administered by his associate Katsuto Shinohara, MD, which gave me an actual digital image with the x, y and z dimensions, the location and the volume of the tumor within my prostate.
My PSA was 6.3 in early June 2003, almost 4 weeks prior to my appointments at UCSF. I called Mrs. Pat T after my appointment and ordered a bottle of PolyMVA to be shipped to me in Orlando, FL, where I flew for a conference over that July 4th weekend. I started taking the PolyMVA on July 4, 2003, 10 months after the pathology reports of my biopsies in September of 2002 confirmed the Dr's diagnosis. On July 10, 2003 I had a PSA test and the results showed an immediate reduction in my PSA from 6.3 in early June down to 4.6, about 25% after 6 days of dosing with the PolyMVA. July 4th, 2003 started my auspicious journey with AMARC and PolyMVA became apart of my everyday life since.
What a boon to have no dysfunction and be able tomanage life just as well as others who have a variety of other chronic challengeswhich they successfully manage every day for the entirety of their lives In 2009 I began to include vitamin D3 from AMARC in my regimen and I took 15,000 IU daily until I reached 130 in the 25Hydroxy Vitamin D3 test, whereupon I reduced the D3 to 5,000 IU over the next 3 months and saw levels drop to the high 50’s. In August 2009, my 25-Hydroxy D3 tested at 65 and tested in early 2010 at 130. In June 2012, the D3 level hit 90 with 20,000 IU per day so I intend to stay focused on my current protocol since the 130 to 150 range is optimum.
I also chose to regularly test using a meridian technology more regularly, which I initially learned about through Mrs. Pat T who tested me and educated me about her experience with Poly-MVA. By testing for the frequency and electrical charges associated with bacteria, parasites, chemicals, heavy metals and a host of other organic and non-organic foreign matter that can result in toxic or other deleterious situations in one's body, I have found it compliments all of my other protocols that do not use the traditional drugs, radiation, ablation, hormones etc to treat prostate cancer. In terms of the use of the color doppler sonograms, the MD's at UCSF say that they do not rely solely on this technology but promote a
combination of the sonograms, PSA and biopsies. I choose to monitor my PSA with a PSA Free blood test every 6 to 12 weeks along with the Vitamin D with the LabCorp 25-Hydroxy D test and the color doppler sonogram once a year prior to labor day weekend unless I want to schedule another in the meantime. For the record, my PSA still goes up and down, reading as high as 9.3 and as low as 3.2 since the only biopsies from April 2002. The PSA has been consistently around the 6 to 7 range for the last several years with intermittent spikes and drops in the numbers.
The color doppler sonogram showed the tumor measured cumulatively smaller each time since the first appointment at UCSF, even though it changed shape, and the x, y & z axis measurements were always smaller than the initial measure as well, for which I am very grateful. On 9/4/15, there was NO evidence at all of any abnormality or lesion, for the first time since I began having the color doppler sonograms in 2003 and according to the prostate spectroscopy MRI. Between the initial trial MRI in late 6/2003 and my visit to UCSF before Labor Day weekend of 9/2011, I did not have the prostate spectroscopy MRI. However, beginning a couple of days before Labor Day of 9/2012, the prostate spectroscopy MRI resumed and the MRI report indicated NO discernable prostate cancer even as the color Doppler sonogram detected something.
The MRI consistently reported “NO discernable prostate cancer” in 2012, 2013, 2014 and 2015. To finally have the two imaging technologies agree on 9/4/15 that NO prostate cancer was evident is divine intervention, is an answer to prayer, to discipline, to the power of divinely inspired belief, to an attitude of gratitude, to a consistent exercise of verbal acclamation, to the self talk required to redeem me of the consequences of fear and stress that accompanied the pursuit of health over a terminal diagnosis and to the commitment inspired by grace that one can never earn, only choose to receive.
The 8 teaspoons of PolyMVA per day either in 2 teaspoon doses 4 times a day, or more manageable for me in two 3-teaspoon doses after breakfast and lunch and then one 2- teaspoon dose after my evening meal or maybe before bed, with the accompanying dosages of the liquid Co-Q-10, 1 liver support supplement capsule upon awakening and the 4 D3 tabs, 1 each following my wake-up protein shake,
9-22-2015
Istarted taking Poly-MVA in 2003, as part of an overall protocol of supplements, diet, etc, instead of choosing traditional approaches to treating prostate cancer. I continued on a regimen of 8 tsps of PolyMVA and the AMARC-recommended daily protocol.
On 9/4/2015, having received amazingly improving test results for years, no evidence of my previous prostate cancer was evident, something I know is a function of divine intervention – an answer to prayer, to discipline, to the power of divinely-inspired belief, to an attitude of gratitude, to a consistent exercise of verbal acclamation, to the self-talk required to redeem me of the consequences of fear and stress that accompanied the pursuit of health over a bleak diagnosis and to the commitment inspired by grace that one can never earn, only choose to receive. after breakfast a couple of hours later, after lunch and finally after my evening meal or before bed, are standing me in good stead.
As I learn more from people, events and my PolyMVA family, I will continue to adjust and remain diligent with the disciplines that offer and which have achieved the 9/4/15 successful results. To date, since September 2002 after the initial biopsies, I have elected to have no traditional medical therapies of any kind. I see an urologist in my hometown 2 times a year, and 1 time a tear at UCSF, based upon my best discretion. I have PSA Free tests periodically along with other blood pathology as mentioned before and I sincerely appreciate medical science and the testing it provides so well. I have confidence in the doctors and in the choices I have made and will make while experiencing life as a PolyMVA survivor.
I will continue my diet and dosing some PolyMVA and the other supplements as the pathology testing monitors each current snapshot of my health and I’ll continue the imaging as well. What a gift on 9/4/2015, to have received the report of “No discernable prostate cancer, No abnormality, No lesion”, from both of the imaging technologies. There is hope and success even as the world says there is not….. “Be not weary in well-doing”.
As I learn more from people, events and the Poly-MVA family, I will continue to adjust and remain diligent with the disciplines that offer and which have achieved the 9/4/15 successful results. 2-20-2019 Since 9/4/15, God has gifted me with the PolyMVA Protocol and a healthy prostate and I have remained clear of any evidence of the tumors first detected in 6/2003, based upon the Prostate Spectroscopy MRI and the Color Doppler Sonogram administered by UCSF's Urologic Oncology team, including Dr. Katsuto Shinohara, who has examined me with the ultrasound every time since we met in 6/2003. Both the MRI and the Color Doppler Sonogram /Ultrasound have annually been done since that life-improving date 9/4/15, again in 9/2016, 8/2017 and 8/2018 at UC San Francisco. My PSA score goes up and down, as has been the case for several years.
Any infection or BPH, among other health compromises, can actually make it rise. Some research has also shown that it will rise when there is a die-off of cancer cells. This was particularly evident to me when receiving the detailed measurements of the tumor(s) with each Ultrasound, all the while when I was dosing as much as 40ml of PolyMVA per day within the 4 corners protocol, which included the liquid Co- Q-10, Liver Support capsules and 15,000 to 20,000 iu of the Vitamin D3 each day, also divided among the PolyMVA doses). Since 2017 I have been taking 5ml of PolyMVA with the proscribed amount of the Co-Q-10 once a day each morning after breakfast. The other parts of the 4 corners protocol continue as they have always been scheduled and dosed.
Certainly I credit AMARC, PolyMVA, the associated supplements above, my family, the people who have encouraged and befriended me along the way, to so many who have allowed me to encourage and befriend them as they embrace life, and those who I have not yet met, all of whom join those that defy the evil that is cancer, as they embrace the eternal faith that offers eternal life in spite of those who do not.
To victory, healing and wellness on earth as it is in heaven! "Praise Him from Whom all blessings flow!" Michael 05-10-2020 Still, and since September 2002 after the initial biopsies, I have elected to NOT take conventional medical recommendations in lieu of the approaches that have more than proven themselves effective for me. I have confidence in the doctors, and in the choices I have made and will make while experiencing life as a fighter, as a champion of circumstance – something in which I assuredly believe Poly- MVA still plays a vital role. I will continue my fastidious diet, taking Poly-MVA and the other supplements, nutrigenomics and hemp endocannabinoids as I continue to monitor my progress and health status with regular lab work and the most state-of-the-art imaging technology.
My experience shows me that there is hope and success even as sometimes the world says there is not. ‘Be not weary in well-doing.’ 9-03-2019 Subsequent to the death of my wife in May 2019, after a stressful time since Fall 2017, I returned to UCSF in 9/2019 for my annual Prostate Spectroscopy MRI and the Color Doppler Sonogram. The MRI revealed there were 2 lesions on my prostate whereupon I commenced with the implementation of the previous PolyMVA 4-Corners Protocol that resulted in the 9/4/15 discovery of no prostate cancer. The 9/2019 findings invigorated me to focus again on the same effort from before and I am now dedicated to the same result as before until it is achieved.
“Thank you! Thank you! Thank you! You all are our heroes! All of the terrific people at AMARC are heroes and living angels in all survivors' lives. We are so blessed to have one another. We are mindful to be prayerful and grateful every day for the Poly-MVA team, patient family and the way Poly-MVA can provide immune support to those of us with cancer diagnoses. Emotions overcome me as I remember the care we receive from all of you. We are inspired by your dedication and your servant leadership. Love and appreciation to all!” Michael
David Maslow
Date: 2007
Diagnosis: Prostate Cancer
David’s Testimonial
Prescribed by Dr. Forsythe, I have been taking poly-MVA since Dec 2009 as part of his protocol to fight prostate cancer. This is in addition to other supplements including enhanced poly, Pectin, resveratrol and D3. Dr. Forsythe also provides his unique daily supplement assortment pk6 of prostate support items. I have been in a stable remission for nearly two years and know Poly-MVA has made a significant contribution to my success. I feel great, exercise daily, and now “share” the Poly-MVA with my wife.
Ivan Hills
Date: 9/14/22
Diagnosis: Prostate Cancer
Ivan’s Testimonial
He got a bone scan and it shows that his Cancer is in remission. He said that taking the POLY makes him feel good. He is taking average 2 teaspoons a day and wants to go up to 8 tsp. cancer is stable, for 7 years his cancer has not grown, told him he had mets to hip and pelvis 7 years ago, no change for 7 years, attributes it to poly mva, psa went from 6.34 to 5.04, 3 months testing, heard about poly from a book called Outsmart your cancer by Tanya Harter Pierce. Has been taking poly for 6-8 months, Ivan is a great jokester who loves to laugh.
Lagounov, Anton
Date: 3/7/2012
Anton’s Testimonial
I began having on and off headaches back in 2005, since they were not very noticeable at the time I didn’t pay much attention to them and just went on about my days. In 2010, at the age of 26, those headaches which I ignored for some time were now a constant head “pain” which was located in my forehead and other nearby areas. That same year I became very ill and had so many symptoms and very little answers from doctors, as my sickness was progressing I was not sure how much longer I could bare the pain.
Besides the pain in my head, there was pain and pressure in my neck and shoulders, I could not sleep for more than an hour at a time, I had burning pain in my upper arms and upper thighs, red dots on my knees and thighs, dizziness, the feeling of not getting enough air no matter how deep of a breath I would take, I became very intolerant to most foods, my left eye would turn red for no reason, time to time my vision would be blurry, my feet would feel either hot or cold and the list of symptoms goes on and on. By that time I had been to numerous doctors and emergency rooms, I have had cat scans, MRI’s and a spinal tap of which all seemed normal.
My blood work revealed that my White Blood Count was a bit low and so was my Vitamin D levels but other than that everything was showing as normal. But even after I had gotten my White Blood Count up to normal levels along with my Vitamin D, all of these symptoms continued for many months to come. Late 2011, after doing endless research on the internet and trying almost every supplement on the market I came across Poly-MVA and decided to try it. I started with the minimum dosage of 1/2 teaspoon and after several weeks began to feel better. I noticed that my breathing was returning back to normal. What I also noticed was the instant easing of my head pain right after taking Poly-MVA. I increased my Poly-MVA intake up to 3-4 teaspoons a day and noticed even more improvement.
Comparing how I feel now after taking Poly-MVA for more than 2 months, my health and overall feeling of well being is in my opinion up 80% as compared to my condition before using Poly-MVA. I would highly recommend this effective supplement to everyone out there, weather for maintenance use or as a part of a treatment regimen. I want to thank everyone at Poly-MVA for making this product possible and hope that many others out there can benefit from this wonderful medicine. Thank you.
Jones Robert
Date: 3/30/11
Jones’s Testimonial
I started PolyMVA after chemo + radiation but before surgery. Each test or SCAN since then has shown improvements. Last SCAN and sigmoidoscopy could not find any evidence of cancer. The surgeon has finally stopped trying to convince me to have the surgery. The radiation oncologist is amazed. The chemo oncologist stopped asking me to undergo another round of chemo. Follow up visits with all doctors continue. I’m 69 years old + busier than ever.
Walter Davis
Date: February 2019
Walter’s Testimonial
I put off updating my testimonial for as long as I could. I knew the pain that would be dredged up and tears would come as I recounted my family story. In the interest of saving lives and assuaging pain and suffering, I am telling my story again. We have a choice ………. I was the only one in my family to select an integrative approach, a combination of conventional and holistic health. Poly MVA changed my life. I am a retired navy navigator, Harpoon cruise missile engagement officer and Chemical Dependency Treatment Specialist. I served in the United States Navy from 1975 to 2001.
In 2008 my health changed and Poly MVA has been my primary supplement. I use the Veteran’s Administration Hospital (VA) in San Diego and The University of California San Diego Hospital (UCSD) in La Jolla for testing and evaluation.
In 2003 while speaking at the Joyce Beers Community Center in San Diego, I was approached after my speech by a lady in the crowd who told me that “If you know anyone who needs help and you love them, tell them about Poly MVA.”
I visited my family in Birmingham, Alabama during this time frame. We took a family picture that was to be our last together. My brother Maurice collapsed a short time afterward on the front porch of my mother’s home. Tests revealed that he had prostate cancer that had spread into his spine. He was paralyzed from the waist down. He died a painful death 15 months later following radiation treatments.
My brother Cedric and I began getting tested every six months after this. Sadly, Cedric’s first test revealed prostate cancer. He elected to get surgery. This rendered him impotent and incontinent.
Maurice died ironically the week that my wife Linda was diagnosed with cancer. She had a lump in her breast shaped like an orange with pits in it. A doctor at Kaiser and one in the private sector told her that she had inflamed lymph nodes and gave her antibiotics for what later was revealed to be cancer. I demanded another test.
It took six painful months to get the conventional doctors to finally diagnose her with cancer at the third test at the Tri-City Women’s Medical Center in Vista, CA.
I tried to remember what the lady had told me back at the Joyce Beers Community Center. I remembered the word Poly but not the rest. It had been more than four years ago.
I began to search Google. I put in the words Poly and Healthr and Poly MVA came up. I called the people at Poly MVA and they did a consult and I began to take the product.
I saw that I had to take charge of my own healthcare. I began to take Poly MVA every four hours. ……..I go to integrative medicine centers that understand Poly MVA, cannabis, cleansing and other holistic treatment regimens. Poly MVA remains the central protocol for my health.
As the woman told me at Joyce Beers Community Center in San Diego: If you know anyone who needs help and you love them, tell them about Poly MVA.
Judy Foester
Date: January 6, 2006
Diagnosis: Renal/Breast Cancer
3 Updates 6-28-10 - 11-12-12 – 5-15-13
Personal story
“On my birthday, January 6, 2006, I went for a routine mammogram that was far from routine. A spiculated mass, 2 cm in diameter, was found by ultrasound after the mammogram. Dr. Alison Estabrook, best breast surgeon in the world, did the fine needle aspiration, found the tissue cancerous, and did a lumpectomy on January 26, 2006….
Since I refused chemotherapy (I think it is barbaric and far too destructive), the hospital did a body-wide search for additional cancer. They found a renal cell carcinoma, 1.7 cm, on the outer curve of the left kidney. I had suspected a cancer when I had shingles four times in 1996. I had a full body CT scan and they found a 5 mm. lesion on the left kidney (soft lesion).
To be sure, I had the test repeated in 2002 and they found NOTHING. Now, four years later, they find a large renal cell carcinoma. My radiation oncologist at MSK was Durgesh Hajela. Her fellow doctor, Karen Schupak, ordered the technicians to force the bones of my shoulder into an untenable position for radiotherapy that caused permanent nerve damage in my shoulder. Two more times, they repeated this process. My whole 220 pound body levitated off the table as if jolted by defibrillator paddles. My arm flew in painful jerks in every direction as the nerve remained caught between the bones. I told them and they agreed, that I could not endure such treatment.
I tried to find an integrative approach. The Cancer Treatment Center in Philadelphia offered mammotome therapy (balloon inserted and isotope placed in balloon twice a day) but my insurance would not pay enough of the cost. St. Barnabas Hospital offered mammosite therapy but Alison Grann, radiation oncologist, said the protocol was very strict and it had been too long since my surgery. Scar tissue had already filled in the space where the tissue had been removed.
As soon as I was diagnosed, I began a cancer diet and went on the Mannatech System, with daily Ambrotose, Manna Cleanse, ImmunoStart, omega3 supplements, no white sugar or flour, lots of fresh fruits and vegetables.
My Poly-MVA arrived just in time for the first radiation treatment, on Thursday, June 8th. I have increased from a once-a-day dose of 1 teaspoon to a twice a day dose of 4 teaspoons. I take each teaspoon with 15 drops of LiquSorb CoQ10. I also take Vitamin B 50 mg; calcium gluconate 600 mg. calcium, with 200 iu. Vitamin D2 twice a day; L-carnitine 500 mg.; Mannatech GI Pro; Plus (amino acids); and Arthrosoothe (turmeric) from PNE.
I use Xylitol as the sweetener if I have a recipe that needs one. I also take a multi- vitamin and 1000 mg. of Vitamin C; Vitamin E with selenium food complex 50 iu.; zinc gluconate 50 mg., chromium piccolinate 0.1 mg, Vitamin B12 .1 mg., three tablets of potassium gluconate, one with each meal, 90 mg. potassium; one DHA from Norwegian fish oils, 500 mg; CoQ10, one 100 mg., with lunch. Recently I added Epicor, DIM, serrapeptase (a fibrin digester) and artemisinin (at first I took one a day but recently the Poly-MVA site has recommended nine a day). I just added Vitamin D3 to the regimen, starting at one 1,000 iu capsule a day. I would love to liberate the calcium in all the strange calcifications of the breast and other organs.
Dr. Fleishmann, my pharmacology advisor at Roosevelt Hospital says I probably did not have to have the kidney cancer treated at all. I saw Aaron Katz at Columbia Presbyterian Hospital about having it cryo-ablated. The surgery was successfully completed, with Jaime Landman as chief surgeon, on August 4th, 2006.
Dr. Nader Fahimi met with me again on September 18th and my shoulder reconstruction was scheduled for October 12th, 2006. I saw Dr. Johnson again on July 14th, August 8th and October 3, and once a month since then.
I saw Dr. Estabrook again on July 7th (she said all looked well and scheduled my next mammo for January 8th, 2007). My follow-up visit with Dr. Evans was on September 12th and December 10th. He said all looked well. On January 8th they took NINE films of the right breast. I was furious because this is alpha radiation that they use and very highly ionizing. I told them they missed seeing the tumor altogether for three years and NOW, with the tumor removed, they take NINE films. Each alpha particle strips two electrons from the cell tissue and is highly damaging to DNA. Sure enough, after a couple of weeks, I noticed proliferation of the cells that had remained after the surgery.
I upped my Poly-MVA dose to 20 tsp. a day for a week, added nine artemisinins per day and used the skin cancer cream again for two weeks. I think I clobbered it nicely and it is in its death throes (again). The breast surgeon again pronounced the breast fine, perfect, beautiful. The radiation oncologist was visited on March 13th, 2007 and he said my efforts appeared successful and could find nothing remaining from the latest proliferation. And that's all she (I) wrote! Holding you all in love and prayer.
Judy Foester 6- 28-2010 Greetings all. What a blessing the Poly-MVA Yahoo group has been. From them I learned about the proper 50,000 international units of Vitamin D3 that I should take per week. My mammograms used to show very dense fibrocystic tissue. It was like trying to look through 'old ice' on the surface of a lake. After taking the proper Vitamin D3 and adding iodine (through organic kelp), the view is now as though through 'black ice' (no fishes visible beneath MY ice, however).
With us, every thought and breath is to BEAT it. Poly-MVA and you....perfect together!! Everyone in the group has given me not just hope but confidence. Any newbies out there....this stuff works! It stuns me that doctors and cancer patients can pass by this opportunity.
11-12-2012
I had learned about Poly-MVA originally in the Susan Lark newsletter from my sister's friends who are both doctors. To backtrack, I had been diagnosed with breast cancer in 2006. I had a lumpectomy, radiation. I also had kidney/renal cell carcinoma which was unaffected by Poly- MVA.
In 2012 I had two large and deep skin cancers on my right thigh. I used Efudex on the surface and Poly-MVA. Within about 2 weeks the cancer lesions on my leg were about gone. in fall of 2012, a large patch of skin (4 sq. inches) on my left jaw suddenly turned to mush. I said to myself 'Uh oh! It's a stage of basal cell carcinoma.' I then headed right to the bottle of Poly- MVA. I didn't want to use Efudex or it would leave a large purple/red reaction area for a long time. Three weeks into Poly-MVA there is only a low uninflammed scab left. Hooray!
Poly-MVA's support wins another one for me. There's nothing like it. I feel so blessed to have it available. My current Poly-MVA dose is 2 tsps a day with 15 drops of LiqCoq10 at breakfast. I truly believe that Poly-MVA has contributed to my health and recovery. Every day I recommend Poly-MVA to others. I would tell others" Stop being a disbeliever and try it for a few weeks...then you will know it worth every penny and gives the greatest peace of mind. Have no fear Poly-MVA is here!"
Judy Foester
5-15-2013
Spoke to Judy and there is no indication of cancer in her body. She knows Poly worked. She was taking 2 tsp a day until January and then stopped. However, she said she has some and promised to do at least 1 tsp a day for maintenance. She promised to be more consistent and told me she was so glad to hear from me.
John Fox
Date: December 2003
Diagnosis: Renal Cell Cancer (Kidney) with mets to Lungs
E-Mail: not available
Personal story
My name is John Fox. I have been in the Fire Service for 36 years. My story started like most others. One morning I woke up and passed blood, no urine, just blood. I went to an ER. They looked at the blood and said it was kidney stones. I still thought it odd but I went to work and started my shift. Within a few hours, the pain was unbearable, I was transported to the ER (another one) by my crew. Within minutes, my world was shattered! The ultrasound showed a 7cm tumor in my left kidney. I had cancer.
I went through a number of CT and PET scans to determine if it was cancer - all of the scans were positive for cancer. My options were limited, I had the kidney removed in December 2003. Then I was told there was only one reasonably proven treatment that showed promise in 7% of the people, or I could get in a trial study using an unproven manmade DNA. I went for the trial drug with nothing to lose. Through this I had regular scans; they were showing a reduction in the size and number of the tumors. My last scan after the treatment showed that the tumors were gone.
In October 2005 they found a spot on my liver, It was surgically removed and turned out to be dead cells. In July 2007 a scan showed a large nodule that had grown in my right lung. We waited for 2 months and had another scan. This one showed an additional nodule in my right lung and another large one in my left.
With this report, I contacted someone I knew with RCC in remission and asked what he was taking. He indicated he was taking Poly-MVA. I bought an extra bottle he had and started at 8 tsp a day. I called AMARC October 3, 2007 and talked to Gary Matson, who was able to assist me in setting up a proper dose which was 16 teaspoons, start using Coq10 and answered all of my questions.
I took the Poly-MVA for 3 weeks before my surgery to remove the nodule in my left lung. The pathology came back as dead cells, no evidence of cancer. I had a scan 8 weeks later and it showed one of the nodules in the right lung stable and the other one gone.
The only change was taking Poly-MVA. My oncologist does not have an explanation for this but I do! Poly-MVA!! The people at AMARC have been incredible, passionate, and very knowledable - without them I am sure I would not be working in the Fire Department today. They put their hearts in what they do and help save lives everyday! Thank you AMARC for all you do!
Update on 6/24/09 I continued taking 16 teaspoons daily until last month and then I dropped down the dosage to 12 daily as all of my scans are completely clear.
John
Mandy Gonzalez
Date: Jan 2025
Diagnosis: Skin Cancer
Mandy’s Testimonial
My name is Mandy Gonzalez, and I stumbled across POLY-MVA by complete accident not even knowing what its benefits were. A friend of mine had showed me POLY-MVA (she was using it for some health reasons completely different than mine). I have several different forms of skin cancer, and have had several minor surgeries (14 spots removed from my body and still counting at this point). My whole purpose to use POLY-MVA was strictly because I have major stomach problems (hospitalized many many times because of it). I have tried about every product out there to help with little results. Out of guilt because the bottle was given to me I started taking it ( especially when I saw what they cost).
Here I am going about my crazy life the next week. I have a doctors appointment regarding my skin cancer and they now need to cut into my face. A big pimple thing that grew on my jawline came back positive for basil cell and its a big one that needs to be removed. As a woman cutting my face isn’t really an option I am considering. I shared this information with my friend and she tells me to put the poly on the growth. In my head I am like why??? So I do what she said to try. Nothing ventured nothing gained right? So I continue to take my POLY and put it on my growth. Over the next week I notice a remarkable difference with my stomach issues, like they are non-existent. My energy is up like alot! My hair is not frizzy, my skin complexion is like the best I have ever seen. I am getting compliments left and right on the noticeable difference. But the only thing I am doing different is taking POLY…weird.
Third week in I am getting ready for work and putting my makeup on with my make-up brush, going over my jawline where the big cancer beast is lying and I feel something fall of my face. Not paying attention really at this point ( I thought it was a piece of make-up at first) I continue with my make-up and do a once over on my face and notice the cancer beast bump is gone. Like it shriveled up and fell off!!! What I felt fall off my face just a few minutes before was the cancer they want to cut out of my face.
I guess my point was I had taken POLY-MVA for a different reason all together which gave me amazing results for that issue, and to top it off it helped mewith a whole other cancer issue. POLY-MVA will be something I use everyday moving forward.
Janeen Paulsen
Date:
Diagnosis: Squamous Cell Carcinoma
Paulsen’s Testimonial
The year of 1992 proved to be a quiet and uneventful year. At least for the first eight months until we found out my mother was given six months to live due to a metastatic brain tumor. November was another bump in a quiet year when Emery, my husband, was diagnosed with a “possible cancer of the prostate”. When tests proved that, indeed, we were dealing with active prostate cancer, Emery decided to have a prostatectomy after the first of the year of 1993. In March of 1993 we lost my mother and we also learned that Emery’s surgery didn’t help stop the progress of the cancer which was described as a stage three and a PSA which should be less than a <0.01 was now a 3.0 and not going down. Emery insisted on pursuing an alternative medicine approach rather than that of allopathic or traditional medicine. We had agreed to stand together in his choice, pray a lot for wisdom, guidance and healing. My part in this was to plan his diet, do lots of different cooking and do as much research as I could.
Research led me down many paths, reading different kinds of books, cooking differently, trying new things and lots of listening, and following new leads. One of these leads was a sales supervisor recommending a monthly periodical written and edited by Dr. Charles Myers who was the Dean of Medicine at the University of Virginia. This issue was filled with information from the patients who came through the teaching clinic. Dr. Myers would comment on the various procedures, and point out some of the weaknesses and strengths. In an article printed on an 8 1/2 x 11 paper, page 3, middle column, Dr. Myers mentioned that there was a product that showed much promise because it killed the cancer cells but strengthened the healthy cells and enabled the immune system to become stronger.
Ahhhh, there was now real hope if I could only find a doctor who recommended the palladium! That was about 1997. For the next two years Emery had alternative medicine doctors but none of them were familiar with Palladium being used in the fight against cancer. Still hunting, reading and checking things out, a friend who had fourth stage liver cancer called in 1999. I truly thought she had probably passed away but such was not the case. She and her husband had a doctor there in San Diego who had quite a number of cancer patients and who were doing quite well. We might be interested in calling him. We did. We visited with Dr. Crawford regarding his plan for fighting cancer finally asking what was the main product.
He said the main product was called PolyMVA with the main ingredient being that called palladium. We decided to try it out for one month, taking a blood draw for Em’s PSA and then at the end of the month another blood draw to see what the Poly MVA had done and what the PSA had done.
The day of reckoning came. Emery had been a model patient. We went to the urologist who thought the nurse had given him another person’s chart as the results could not possibly be what this was! Could we try again! Of course. The next week we were told that his PSA had gone from 14.67 to <0.01 – the Cadillac!! The doctor said “Whatever you are doing, keep on doing it.” Emery maintained the loading dose for another month and then began tapering down as to his dosage. I have noticed that most people think that if the totals have gone down they don’t have to take PolyMVA anymore. Quite the contrary! You slowly taper down in dosage and Emery stayed on his diet till shortly before he died in 2013. He lived a full life till then thanking the Lord for leading us as He did!
Gary and Elma Thomas
Date: Gary and Elma Thomas
Diagnosis: Squamous Cell Carcinoma
Gary and Elma Thomas’s Testimonial
In June of 2004 my wife was diagnosed with squamous cell carcinoma that had manifested itself in her neck. With an unknown primary she had a modified radical neck dissection and chose not to do the radiation the doctors recommended. She instead found her way to Reno NV. and Dr. James Forsythe MD. He put her on poly and she used it for about 2 years. She has quarterly checkups with her surgeon and NO cancer. In November of 2007 I ended up in emergency spinal surgery for what turned out to be stage 4 Prostate cancer and had a large tumor removed from my lower spine. My PSA was 1314. Came home in a wheelchair and was using a walker. Had a catheter and really did not know if I would get any better.
Well — it is know October 2008 – I am walking as I always did, use a catheter once a day to empty my bladder, my PSA is 0.5, my retests in June 2008 showed signicant improvement in the bone and lymph node involvement. I have some emotional issues but that may work itself out in time. Oh did I forget to tell you? I also went to Reno and Dr. Forsythe put me on Polymva and Salicinium, a product that he is working with the FDA to get approved as a Cancer treatment.
I am quite sure without polymva neither my wife nor I would be here to tell you this story. Thank you polymva and your wonderful staff – you have blessed our lives.
Victoria Castro
Date: May 2019
Diagnosis: Throat Cancer
(Benign Neoplasm mouth Papilloma)
Victoria’s Testimonial
I was diagnosed with cancer (benign Neoplasm mouth Papilloma) and learned about Poly MVA from my brother in law Justin Madison. I started using Poly MVA in September 2019.
My daily dosing has been 3 tsp 3x a day at 10:00 am, 2:00 pm, and 6:00 pm by feeding tube and by mouth.
I was originally diagnosed in 1993 and received chemo and radiation. I had been cleared of cancer for 26 years. However, I was diagnosed a second time in May of 2019 with the same cancer. Same type, same location.
According to my new oncologist, I could not have radiation, because my main veins in my neck were very thin. The 2nd Opinion also said that the radiation was out of the scope of treatment. This was all due to the extensive treatment I received in 1993. I was told I could only receive chemo at this time. I started chemo in June of 2019.
August 2019, I started the Poly-MVA. In the beginning of taking Poly-MVA, I did not feel anything. Within 2 weeks, I got a lot of my energy back and I was able to focus on life and daily chores. I was able to get out of bed at a decent time and I started to craft again. I was making dinner and started to feel like myself. I would eat and take my Poly-MVA 3xs a day and did not miss a dose. I do feel that this product did help and I have made sure I took it 3xs a day.
My last Chemotherapy was October 2019 and my most recent biopsy was negative of cancer. I don’t think the cancer is gone. I think the growth of the cells has slowed. I do have some stiffness in my neck and my upper back. I am still taking the Poly-MVA 2xs a day. I was told to decrease the intake after the positive results of my last biopsy. I feel good and still have energy throughout the day.
My appetite and quality of life is better. I have improved energy and less fatigue, better sleep, increase in appetite – weight has increased.
The one thing that I would say is most notable is I have the best energy and am sleeping better.
Victoria Castro
Robert Willis
Date: 09/19/20
Diagnosis: Thyroid
Robert’s Testimonial
So I was introduced to Poly a couple months into recieving radiation and chemo. I was explained at first from a family member to take full doses. I did that for a few weeks off and on until I just couldn’t take anymore. I took a good 9 to 12 month break from it. Not exactly sure how long that break was but I ended up trying Poly again. This time it came with Ms. Pam. And what an amazing lady she has been. She’s really been like a teacher/dr./mother figure. Ms. Pam and the poly have been a blessing to me and my family. I started the poly for the second time but with instructions to start at a lower dose and progressively move up. It made a big difference with how my stomach acted towards it. It really went alot better than expected.
I ended up having a period where I was having problems with taking my meds at one point but ended up finding out that my thyroid levels were off because of a treatment I take every few weeks. Anyways, after a moth of taking poly I had a scan done and was told that my disease was nearly gone. 3 months after of continuously taking poly I had to get another scan. The results of that scan were that they couldn’t see anymore active cells and the mass is gone. Before I started poly for the 2nd time I had been on a certain treatment that just kept the disease at bay. It wasn’t growing but it wasn’t shrinking either. Within just a couple of months of taking poly it was nearly gone and a few more months of poly cleared it out.
The medicine has really helped me. I believe in my heart i wouldnt be here today if it wasnt for the poly and Ms. Pams guidance/knowledge. I’m going to continue to take it for awhile longer until told otherwise from Ms. Pam. I thank you so much Ms. Pam and Poly for helping me stick around and raise my son, spend time with my elders, family, and friends. You never know what you really have until it’s gone or nearly taken from you. You gave me another chance and I am very much thankful for you guys coming into my life.
Andre Belanger
Date: June 2023
Diagnosis: Pharyngeal Cancer
January 2025
Andre’s Testimonial
In June 2023, I started noticing persistent health issues—a sore throat and a tightening sensation that wouldn’t go away, accompanied by spitting blood. Despite initially being prescribed antibiotics by my doctor, my symptoms didn’t improve. Realizing something more serious was going on, I sought additional medical help.
Further tests and consultations with an ENT specialist revealed that I was facing a significant health challenge. The diagnosis was stage 3 throat and lymph node issues that required aggressive intervention. I underwent 35 radiation sessions and 7 rounds of chemotherapy. While these treatments were necessary, they were incredibly intense, and I knew I needed additional support to help my body cope and recover.
Having worked in the therapeutic industry for 37 years, I came across Poly-MVA in 2023 and decided to incorporate it into my wellness plan. I started with a small dose of one teaspoon and gradually increased it. Currently, I take 2.5 teaspoons in the morning and another dose in the afternoon, consuming about 5 bottles per month.
Poly-MVA became a game-changer for me. The intense treatments I underwent caused significant weight loss—65 pounds in just three months—and left me with severe side effects. However, Poly-MVA helped me maintain energy levels, regain strength, and recover more effectively. I’ve since gained back 12 pounds and started rebuilding muscle.
While I followed my prescribed treatments, I also made lifestyle changes and integrated Poly-MVA into my routine. This decision made a substantial difference in my overall health and well-being. Today, although my body is still in the process of healing internally, I feel closer to normal and am grateful for the role Poly-MVA played in supporting me through this journey.
At 66 years old, I’m sharing my experience to inspire others to take charge of their health. My story is proof that resilience, combined with the right support, can lead to incredible progress. I’m happy to share my story and would love to connect with anyone who may benefit from my journey.
Lee Garoutte
Date: August 14, 2018
Diagnosis: Tongue Cancer
4 Updates 10-10-18 – 11-06-18 5-14-19 - 3-26-20
Personal story
As I write this today on May 31, 2020, it was 21 months ago my husband, Lee, was diagnosed with cancer at the back of his tongue and in his lymph nodes within the throat, at the age of 79.
He required 7 weeks of daily radiation and weekly chemotherapy. The treatments were "brutal" and the side effects were devastating. Knowing he would not be able to swallow as a result of the treatments, a feeding tube was inserted into his stomach so he could get nourishment from liquid supplements.
The doctors were amazed he was strong enough in 5 months to remove it. However, he still has to have all food pureed as his throat muscles are still damaged, but healing.
A couple of weeks into the treatments, a very special and concerned friend, provided him with POLY-MVA, associated supplements, and an advisor to guide him in the use. He is now cancer free and has gained back some of his strength. Initially he was told he could lose 40 - 50 pounds. Ultimately, he only lost 27 pounds and has gained back almost half of that.
He returned to his part time job as an estimator for a construction company after 7 months and continues to take the POLY-MVA on a daily basis. We truly believe that the POLY-MVA strengthened his immune system to help him fight this dreadful disease. Thank you for your continuing support and follow-up.
Julie Garoutte (Lee Garoutte)
10-10-18
Lee was diagnosed earlier this year and his doctors immediately got him started on chemo and radiation. He was only able to take 2 rounds of Chemo before he had to stop. He is still doing radiation and is on a feeding tube because of the damage and swelling from radiation that blocked off his ability to swallow.
He still has 13 out of 35 radiation treatments left that is targeting the cancer on the back of his tongue. Lee was referred to Poly MVA by Ed Sanchez who also bought the Poly for them. I talked to Lees wife, Julie, who said she intends to give him 8 tsp daily and CoQ10 and Four Corners. She said Lee has really suffered a lot from the radiation treatments.
11-06-18
Spoke to Lee's wife, Julie, who said Lee is still taking the Poly MVA through a feeding tube. She is hopeful they will be getting him off of the feeding tube once the radiation treatments have ended.
5-14-19
Called and spoke to Julie. She said Lee is doing better and seems to be slowly recovering from the negative side effects of the chemo and radiation treatments. He had the feeding tube removed but is only able to eat and swallow liquids and pureed foods. He is suffering from a lot of residual problems with his throat due to all of his radiation treatments.
3-26-20
Lee has been told by the Doctor that he is Cancer Free. He is still taking 4 tsps a day of Poly MVA and continues to improve from the throat damage caused by his conventional cancer treatments. Currently, Lee is still only able to eat liquid food sources.
Carol Velazquez
Date: December, 2009
Diagnosis: Uterine Cancer (Stage 3)
6 Updates 2-05-10 – 2-18-10 – 6-14-12 1-30-13 – 1-09-14 – 5-23-15
Personal story
In December of 2009, I was diagnosed with stage 3 uterus cancer. I want to give people hope that are fighting cancer. My Doctors had a meeting about me and said I was a very sick lady, with very low red blood levels.
They started me on radiation after my operation. It was at this time a friend told me about PolyMVA. Soon after starting it, my blood count went up to normal. I was never tired during radiation and was able to continue with life as normal.
My friends and family were shocked at how well I was doing because I did not look sick and remained active. At my 1 year checkup my doctor said I am doing well.
My message to other cancer patients is that when we are losing all grips no matter what we are going through the Lord is our stronghold.
God bless,
Carol
2-05-2010
I spoke with Carol. She is currently taking 4 tsp. of the poly while undergoing radiation treatments. She said she is feeling good, not tired and can eat. Her Doctor has told her that he would like her to do chemo. She wanted to know if we have patients who have only taken Poly and not chemo. I told her we have support members that have done a combination of both. Some of our Survivors have taken Poly MVA and chemo/radiation and some Poly by itself, usually after they have tried chemo before or are told that chemo is not option.
2-18-2010
I called Carol and she is still doing the same and feeling good. She is still receiving radiation treatments and will undergo a total of 28 treatments.
6-14-2012
Carol is cancer free. She takes PMVA once a week now.
1-30-2013
Carol says she is doing really well and is only taking Poly MVA once or twice a week.
1-09-2014
Followed up with Carol. She said that she went in for her check up in December and she is doing well.
5-23-2015
Talked to Carol. She said that she now only takes as a maintenance dose of Poly MVA every now and then.
Ameena Meer
Date: Nov 2009 (testimonial 12-15-09)
Diagnosis: Uterine Cancer
3 Updates 6-09-10 – 4-01-11 – 6-19-2014
My My PolyMVA story
I was in the midst of chemotherapy for late-stage choriocarcinoma when a close friend burst through the door with a bottle of polyMVA. "The only reason the bottle is open is because I had to let them smell it to get it through airport security!" she shrieked, "You HAVE to take this."
That was December 2009 and I’d been having chemotherapy for 2 months. The average treatment time for this particular uterine cancer was a year-and-a-half from diagnosis to "cure". What I noticed immediately was - despite my extremely weakened condition, the fact that I have three young daughters and my tiny apartment is always crawling with children - I didn't suffer any colds or flues that winter.
As soon as I felt something coming on, I took my PolyMVA, coQ10 and effervescent vitamin C, and the symptoms disappeared like magic. Amazingly, everyone else got sick, including my family who was looking after me.
The next thing was that, since I am small boned and likely to have osteoporosis later in life, had decided not to take any more steroids (prednisone) with my chemotherapy. I took only ginger capsules for the nausea. Despite that, sometimes, the nausea was so bad, along with the sores in my mouth, I couldn't eat.
What I found was that, about half-an-hour after my dose of PolyMVA, I was not only able to eat, but I was able to keep the food down. Finally, in February, just 16 weeks after I’d started chemo, my cancer markers were practically back to normal. I told my doctors I’d had enough, I wasn't going to have any more standard medicine.
Admittedly, I was also taking a lot of supplements, eating organic, juicing, and having a sugar/wheat/soy/dairy and peanut-free diet, as well as taking regular palates classes. I was also sleeping on a heated mat of amethyst crystals.
My doctor looked at me and said, "If you walk out of here, you'll be dead in 12 weeks." I said, "If I’m dead, I have nothing to worry about. But if I’m alive, I care about my quality of life."
So I walked out that afternoon and started acupuncture and meditation, kept juicing, eating organic and having 6 to 8 teaspoons of PolyMVA a day. When I came back to my doctor after a month, my cancer marker hormone levels were totally normal. I had no bleeding. I asked the doctor about exercise - and she said, well, most people start slowly.
I told her that, along with the pilates, I was swimming half-a-mile three to four days a week. I just found I needed an occasional nap in the afternoon. Her mouth dropped open.
In three months, they gave me an ultrasound. The tumor was gone, leaving only a scar. The doctor suggested a hysterectomy in case the scar became cancerous. I told her it wasn't necessary. I kept up the juicing, the diet, exercise and the PolyMVA - though I’d stopped acupuncture as it became too expensive. Also, the chemo-induced menopause had completely reversed itself.
At my 6 month check-up, I had another ultrasound - even the scar had healed itself! My financial situation forced me to reduce the PolyMVA to 4 taps a day – divided up in two or three doses.
Now, a year-and-a-half later, people who see me can't believe I ever had cancer, let alone weighed less than 90 pounds and was eggshell bald just 18 months' ago. My hair is thicker than it ever was, I have lush eyelashes and my skin looks better than it did before I got sick.
I recommend PolyMVA to every single person I know who is diagnosed with cancer. It IS expensive, but it works, with or without chemotherapy.
6-29-2010
I had an ultrasound of my uterus and ovaries. the tumor is not only completely gone from my uterus, the previous scar it left on the uterine wall seems to have healed itself as well. there is no sign of any cancer. I do have a small ovarian cyst - a stable echoic shadow - on my right ovary, perhaps from the chemo medicine. we will continue to monitor it.
4-1-2011
I’m so sorry for my delayed response. I was hit by a taxi in february and I’ve just gotten back to things. (that said, the cancer is GONE!)
6-19-2014
Spoke to Ameena and she is doing well and keeping real busy with work...etc... She does have her own blog and she is sharing Poly with others.
Carol Pruzan
Date: August 12, 2008
Diagnosis: Uterine Cancer * Husband w/ Bladder Cancer
7 Updates 11-09-09 – 5-05-11 – 7-26-11 2-26-13 – 6-02-16 – 12-11-18 – 3-13-20
Personal story
During the time I used Poly-MVA, I had 24 radiation treatments following surgery for uterine cancer. Since the end of the treatments I have had 2 follow-up medical exams, 3 and 6 months after the treatment were completed. Besides 2 internal pelvic exams, I had a CT scan of my abdomen and chest. No evidence of growths or metastases were found.
As I continue to feel better and get over the effects of the surgery and radiation treatments, I have been told by my radiologist and gynecological oncologist that I am healing very well. My general health seems improved, although symptoms of health issues I had before, especially irritable bowel syndrome and chronic fatigue persist. My experience had been very good with the Poly MVA program.
I used 2 teaspoons 3 times daily and I am still using Poly as a maintenance today. I started off as a Quality of Life participant and kept a record of my experience and filled out reports. Poly-MVA contributed and supported me thru my cancer.
I used radiation along with other vitamins and minerals plus AHCC. The difference Poly-MVA made is incredible: • Improved Quality of Life • Energy levels increased • Increased appetite • Nutritional support • Less Fatigue My consultant Vivian was and continues to be a source of support, encouragement and help in my journey. She has always been there for me when I needed advice or information, I knew I could depend on her. Even "10" years later she regularly checks in with me and keeps tabs on me.
When my husband was diagnosed with cancer two years ago, I wanted to get him on Poly MVA right away. I discussed it with Vivian and she agreed and worked with both of us to develop a regimen for him. I am happy to say that he is doing well today and that has been a blessing for both of us. I would highly recommend Poly-MVA as my husband Joe is living proof.
Thank you!
Carol & Joe
11-9-2009
Spoke with Carol and she said that she is doing better. At her checkup, the Dr.'s want her to do chemo right after her radiation. So, she decided not take chemo. She was on Poly and CoQ10 while taking radiation. I told her she needs to get the 25-Hydroxy D blood test and we discussed the importance of the 4 corners program. She requested more info on Poly MVA Scientific Research so she can give it to her sister who is a homeopath.
5-5-2011
Carol said she had her cat scan for her chest, abdomen and pelvis with contrast and will have results by Monday. She will see the radiologist on 5/18/2011 for an internal gynecological exam. Physically, she feels fine but she is still scared.
7-26-2011
Carol called to report 2 years of good news about her health. No sign of cancer. Continues to take Poly-MVA but will start to taper down her dosage to reach a maintenance dosage.
2-26-2013
Spoke to Carol. She is still using Poly MVA on a daily basis as a maintenance to prevent a relapse.
6-02-2016
Carol called inregards to Husband, Joe. He has just been diagnosed with Bladder cancer 1A grade 3. The tumor now covers 1/4 of his bladder but has not invaded the muscle. Tests revealed it was an aggressive form of Bladder cancer so Joe had surgery to remove the tumor which was sent to pathology. The recommended treatment suggested by his Doctors is BCG which is the most common intravesical immunotherapy for treating early-stage bladder cancer.
12-11-2018
Spoke to Carol. She said that both her and Joe are doing well. They had a cold during Thanksgiving but are much better now. They continue to remain in remission and are diligent about taking daily maintenance doses of Poly.
3-13-2020
Talked to Carol who said she is currently battling the flu. She is still using Poly MVA for maintenance. Just opened her last bottle and may need more in a month. She said her husband now takes it occasionally with her but he is still doing fine.
Wanda M.
Date: April 17, 2008
Diagnosis: Metastatic Uterine Cancer (Stage 4)
5 Updates 7-14-08 – 5-05-09 – 4-12-10 1-14-08 - 8-08-2011
Personal story
This is my experience in the last 12 months using Poly-MVA. April 17, 2008 I was diagnosed with stage 4 cancer in my colon, uterus , and ovaries. My Doctor first considered surgery but since the cancer had gone to stage 4 he wanted me to go through chemotherapy.
Instead, I began taking POLYMVA on May 21,2008. I took 3 IV’s of Poly-MVA a week plus 12tsp a day on opposite days. This was a total of 48 Poly IV’s.
After 6 months of treatment, a pet-scan showed signs of the colon tumor growing. I began another round of 48 Poly-MVA IV’s. After due consideration I decided on chemotherapy. I started chemo January 8, 2009. I continued my Poly-MVA during chemo.
I had another set of 48 Poly-MVA IV’s during these chemo sessions. I took my last chemotherapy on May 27, 2009. After a pet-scan on June 16, 2009 my chemo doctor told me that I was cancer free.
I continue to take 12tsp of poly-MVA per day orally. I am feeling better now and gaining weight and getting my appetite back. I give all the praise to GOD and the guidance HE gave me.
Wanda
7-14-2008
Spoke to Wanda. She has been feeling really good for the past three weeks. She said the poly has taken the pain out of her stomach and that means a lot to her.
5-05-2009
Followed up with Wanda. She is doing well but still has another round of chemo and then they will do some testing to let her know how she is doing. Wanda said the poly has really helped her get thru the chemo.
4-12-2010
Spoke to Wanda, she is doing very well. She will be going in for blood work on Friday and will see her doctor next Tuesday for the results.
1-14-2011
Wanda says that the new drugs that her doctor has her on seem to be doing ok. However, her doctor asked her to stay off the poly while she is on the new medication.
8-08-2011
Talked to Wanda. She is doing ok but not feeling her best. She will be going on a different series of meds and hopes it will help her. She has been off the poly due to her Doctors request.
C. Petrie
Date: 2005 (testimonial 2013)
Diagnosis: Uterine Cancer
1 Update 5-25-2016
Personal story
My wife had uterine cancer 8 years ago. Dr. Milne put her on Poly-MVA back then. She uses it to this day. Poly-MVA has paid off so far for both of us. We would be afraid to stop, quite frankly. We live a healthy life style going to the gym 4 to 5 times a week, eating organic as much as possible and lots of other supplements along with Poly-MVA part of our daily practice.
The staff at AMARC are fantastic and very supportive. Your order always shows up promptly. Anyone facing health issues should really give it try.
5-25-2016
Petries’ are still taking Poly and cancer free.
#1 Hudson's Story
Poul and Michael
Date: 05/2025
Hudson’s Story
Soon after Hudson’s diagnosis, we began seeing a holistic vet for his treatment. He’s been getting acupuncture everyday weeks for the first year of his treatment, and now he gets it once per month. She also prescribed some Chinese herbs. They include: Dispel Statis in the Middle Palace (Ge Xia Zhu Yu Tang), which are tablets; Concentrated Statis Breaker, which is a poweder; and Onco Support for Pets, which is also a powder. He takes these every day and has been since shortly after his diagnosis. About 4 – 5 months, he started having seizures. The neurologist isn’t sure that they’re related to the cancer but can’t rule out it hasn’t moved to his brain. He’s now on medication for that, which includes high doses of Levetiracetam, brand name Kepra (1,500 mg daily) and high doses of Gabapentin (1,800mg daily). This has definitely helped, but he has had a breakthrough seizure in the past 2 weeks. The last one before that was 11 weeks, so we feel it’s being managed well.
That’s everything that we’ve been doing in addition to the PolyMVA. As Poul must have told you, it’s been about 16 months since his diagnosis and he’s still here, so we feel very lucky to have found PolyMVA and our wonderful vet.
#2 Sinatra-Chewie story
Sinatra-Chewie story
Date: April 2017
Like most pet owners, I really love our three dogs. They are very important members of our family. And just as it is with our children, we get upset when they – the pets – have an upset with one another. Such was the case one day in September of 2005; my two beloved Chow Chows had a vicious run-in with one another over a Milk Bone. The older Chow, Chewie, took the brunt of it. Her mouth was bleeding, and it was the next day before she calmed down enough for me to be able to get a good look at her injury. I felt so badly when I saw that one of her back molars was hanging loose in its socket.
I took Chewie to her veterinarian, who agreed that the tooth would have to come out. As poor Chewie was prepped for surgery that morning, the vet asked if I wanted to be called should there be any unforeseen issues. “Just treat her as you would if she were your dog,” I replied. What could go wrong? Then I headed out for my own office to see my own patients.
When it came time to pick Chewie up on my way home, the vet had bad news for me. Something unforeseen had indeed happened. While Chewie’s mouth was relaxed and open, they had noticed a lesion on her tongue. You see, Chewie’s very ladylike about panting, so we’d never noticed anything. Later, when we scrutinized an old photo of Chewie for a few minutes, we did see that the small round change in color had been there.
Because I had given him permission to use his own best judgment that day, the vet scraped the suspicious lesion on Chewie’s tongue to get a tissue sample ( a surgical biopsy), and awaited my permission to send it out to the lab. Our precious Chewie was in sorry shape that night. Her mouth must have been very sore, because she didn’t eat for days, no matter how we coaxed and coddled her with pureed versions of her favorite foods.
The biopsy of the suspicious lesion was indeed positive for melanoma. The vet explained that because Chows have purple-pigmented tongues, melanomas in that area are not uncommon for the breed. He then suggested a surgical resection that would include an area around the tumor. That would mean literally cutting off a very large portion of Chewie’s tongue. My heart sank. Dogs do so much more than lap up food and water with their tongues; they also express their joy, love and affection with them!
Had I been given the option, I would not have even approved disturbing the lesion for the biopsy. I would have just assumed the worst, and treated my sweet pet conservatively. After all, who knows how long that lesion had been there, how aggressively it was progressing or whether it was progressing at all? Why rip it open and put her through the agony?
There was no big decision to be made. We already knew what we wanted for our dog… We decided against putting Chewie through more pain for a procedure that might ultimately make her unable to enjoy the time we had left with her. I started her on Poly-MVA right away, along with other nutrients to help her immune system keep her melanoma at bay. That was over a year and a half ago.
Our Japanese friend Chizuko takes good care of our dogs when we work and travel, and she follows Chewie’s anti-cancer regimen, too. I get a kick out of how she refers to the Poly-MVA as the “soy sauce for the Chew Chew”. She can’t remember (or pronounce) the name of the liquid dietary supplement that’s been helping Chewie, so the nickname helps us communicate about it with a chuckle and a smile.
We sneak the “soy sauce” in Chewie’s food twice a day. And let me tell you, feeding a Chow is just like feeding a cat; they’re very fickle and very fussy. Just a half teaspoon at each meal has been enough for our 46-pound-runt-of-the-litter. (The first month, I gave her a “loading dose” by giving her four small meals a day, each with ½ teaspoon of “Poly” for a grand total of 2 teaspoonfuls a day in order to get her blood level of Poly-MVA up.)
Chewie was ten years old when her melanoma was diagnosed. A veterinarian friend across the state informs me that he’s yet to see a Chow Chow live longer than twelve years. Our soon to be twelve-year-old Chewie, whose tongue lesion does not appear to have changed since the day it was discovered, is still full of life and still bringing joy into our lives!