Multiple Myeloma Testimonials
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Cancer Testimonials |
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Poly-MVA Testimonials
The following testimonials
are written by Cancer Survivors who have heroically
fought
Multiple Myeloma. 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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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 |
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| Janice's Testimonial |
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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).
...... 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..... 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 unknown. In
September same result only blood work was
worse.
....... 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.....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 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 want 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......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!!!!
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.
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| #2 Testimonial |
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James Swelgin
Date: March 15, 2012
Diagnosis: Multiple Myeloma Stage 1
3 Updates
1-14-13 – 3-07-16 – 2-05-18 |
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Photo
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| Jame's Testimonial |
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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.....
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.
My “numbers” stayed ........ 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.
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| #3 Testimonial |
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Susan Lannoye
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 |
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| Susan's Testimonial |
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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.....
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.......
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.....
I had read Suzanne Somers book, Knockout,
about
alternative cancer treatments which included Poly MVA......
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."
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