Brain Cancer Testimonials
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Patient Testimonials |
Poly-MVA Testimonials
The following testimonials
are written by Cancer Patients who have heroically
fought
Brain Cancer. They have offered to share their
stories with you in order to
let you
know that you have OPTIONS, and what some of these options
are.
These testimonials are for information purposes only and we
do not advocate that
this
treatment is for everyone. Prior to changing your treatment
program, please
check
with your physician for recommendations specific to your
symptoms.

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#1 Testimonial |
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Mark Olsztyn
Date: Sunday, July 02, 2000 8:32 PM
Diagnosis: Astrocytoma/GBM IV
Email:
mark.olsztyn@gmail.com
9 Updates
From 9-07-2000 ........ to
4-07-2010 |
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Mark's Testimonial |
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"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.....
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.... |
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......This
day marks 13 years since my operation! That's
about
4,700 teaspoons of Poly MVA by my
calculations.
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.... 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
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Read
Full Report
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#2 Testimonial |
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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 |

9
Years Old
27 Years Old |
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Josslyn's Testimonial |
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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.... |
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.....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. |
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......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!!!
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Read Full Report |
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#3 Testimonial |
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Paul Weiner
Date: September 17, 2002
Diagnosis: Medulloblastoma
E-Mail:
WienerTd@aol.com
3 Updates
2-12-04 - 1-14-05 -
1-08-19 |
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Paul's Testimonial |
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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.... |
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...... 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..... |
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....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 .....
Read Full Report |
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#4 Testimonial |
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Daniel Morrison
Date: September 21, 2003
Diagnosis: Astrocytoma/Glioma
E-Mail:
dennysbutton@gmail.com
Phone: 775-781-9191 |
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Daniel's Testimonial |
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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... |
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....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!
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We are ready to
tell absolutely everyone about the PolyMVA .....
Read Full Report |
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#5 Testimonial |
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Larry Puckett
Date: January 2007
Diagnosis: Glioblastoma Stage IV
3 Update
5-13-13 – 4-08-14 – 3-01-18 |
No
Photo
Available |
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Larry's Testimonial |
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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
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Read Full Report |
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#6 Testimonial |
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Jim Storc
Date:Thanksgiving night, 2003
Diagnosis: GBM4
Brain Tumor
Email:
jcstorc@ameritech.net
2 Updates
2-08-10 -
1-29-19 |
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Jim's Testimonial |
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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.... |
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....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 Poly MVA showed up...
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....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 % ....
Read Full Report
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#7 Testimonial |
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Lynn Rivers
Date: October 8, 2009
Diagnosis: Meningioma (Benign)
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No
Photo
Available |
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Lynn's Testimonial |
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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 .....
Read Full Report |
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#8 Testimonial |
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C. Piazza
Date: April 2016
Diagnosis: Gliomatosis Cerebri Tumors
* Extensively infiltrative diffuse glioma
cells
1 Update
6-29-2020 |
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Mrs. Piazza's Testimonial |
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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.
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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.....
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..... 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 .....
Read Full Report |
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