Greetings, all!

Normally, I don't pass on testimonials. However, this particular one is
certainly an exception to the rule, as it truly is a tribute to the human
spirit.

I became involved in this particular situation due to not-so-great advise
being given regarding IV injections involving the use of saline solution as
a buffer, as well as advising on properly utilizing H2O2 with colloidal
silver to possibily improve CS performance. There is a great void in the
public knowledge base concerning IV use with colloidal silver. Even when
one can find this practice, it is often done with silver proteins or an
unsuitable substance ( like saline solution ) used to buffer the silver.

The following is a copy of the email Denise sent to the eskimo silver list
which chronicles her recovery, which was clinically confirmed, and only
after IV colloidal silver use:

_______________________________________________


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 longe
r 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 a
ttached 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: nancymike@...

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