All my friends on the list....so many of you have been extremely helpful with
my quest for my "cure". So many of you have answered many of my questions with
great patience. I have learned more in the two years I have been on the silver
list then I believed I learned in the last 30 years. You have opened my eyes
to so much, and have been very instrumentla in helping me get my life back from
MS. You must all be commended
Nancy
August 2002
My MS Update
I am sending this to all who have inquired about my original MS journal or
helped me along the way.
This is the second anniversary of my long, but wonderful journey with colloidal
silver (CS).
I am a 59-year-old female who had relapsing remitting MS for 31 years. About
1995 it changed to secondary progressive MS. Thus began my long road of
decline. Everyday I got worse. When I discovered CS I could barely walk. I
was beginning to use a cane. I could not even go up on the curb without aid.
My prognosis was grim. I had some knowledge of the great properties of silver,
so the idea of CS intrigued me. I researched CS. What did I have to loose?
I began drinking 16 oz per day. In about three weeks I began to
notice a difference. You already have a log of my first year's progress. I
seemed to reach a plateau about this time. I did not improve, BUT I never got
worse.
I have since had an MRI and it showed that at this time Aug 2001, I
no longer had MS. I have had no new lesions for well over a year. What I was
working on at the time is to now repair the damage. Since the damage is to the
myelin and not the central nervous system, I was quite confident I could
improve.
1 year-6 months: I have researched adding hydrogen peroxide to the CS. One
drop of H2o2 per 2 oz of CS. I learned this would cause the tiny silver
particles to break up into even more minute particles. After 15 minutes, the
peroxide was evaporated out of the CS, so it is not harmful to the body, but
the tinier particles of silver got into the blood stream quicker. All this
time it was a slow process because by the time the silver got to the myelin
where it was needed, it was so diluted, it couldn't penetrate the lesions and
kill the mycoplasma (MS virus) Within a week I began to feel old symptoms
again. This is what I call a healing crisis: I would get symptoms of the MS
as the virus was dying and the dying pathogen aggravated the nerves, so for 2-4
days I would feel like I was having varying degrees of exacerbation. After a
short period, it would end and I was improved again.
If I had known about this earlier, I am convinced my recovery time would have
increased a great deal.
1 year-9 months: I am sure there is a way to go even quicker... I began to
research IV drips. There are cases of HIV-AIDS infected patients going into
complete remission after three infusions. I worked on this project for about
six weeks. I finally found someone with a protocol of infusing CS
intravenously. I also found a doctor willing to work with me and give this a
try.
1 year-11 months: First IV: I had my first IV. By that evening I had my first
healing crisis; my legs became extremely heavy (like they were 2 years ago).
My fingers tips were still numb, but the numbness was extremely exaggerated.
All was better at day four
Second IV a week later: My legs are again aching a great deal, the numbness
in my fingers is very intense. It almost feels like they are not attached to
me. All better by day three.
Third, fourth, fifth IV: Each time I experienced a reverse of some symptoms I
had either forgotten about over the last 40 years, or didn't realize over the
years were actually MS symptoms. I've practically no problems at all. I feel
better then I have in 15 years. I will have no more IV's, but I will NEVER
stop drinking CS.
If I had known about the IV's I probably would have had full recovery even
sooner. I am quite sure the old lesions are going away. I am anxious for
another MRI to prove this also.
TWO YEAR ANNIVERSARY: No more MS, no more symptoms. Most myelin repaired.
PS: My friend, also an MS patient is on the IV drip. She also no longer has MS
(By her MRI), but she was sores than me, and not able to get out of her wheel
chair. Since IV's she has given up all her spasm medication and has begun to
take STEPS ON HER OWN.
I would be happy to share what I've learned with anyone. Call me 708-442-6229,
snailmail me: Nancy DeLise, 380 Blachawk Road, Riverside, Il. 60546, or email
me: [email protected]
I am completely convinced this will help anyone with any autoimmune disease.
Traditional medicine vs
colloidal silver
Cost: minimum $1000. per month $80 per
month
Method of injection minimum 1x per week drink 16 oz. per
day
Delivery:
Side effects page after page
NONE
Prognosis learn to cope and expect to
kill all MS virus within 6 - 8
Continue to deteriorate
months. Repair damaged
Myelin and regain most functions 6 - 12 months
