Colloidal Silver and MS -
What follows is the story of Nancy Delise, who,
over the years, has utilized retail colloidal silver , colloidal
silver made with a basic generator, basic colloidal silver enhanced
with H2O2 ( orally ), and finally IV Silver ( Argentyn 23 by
Natural-Immunogenics - Available only to MD's ).
Condition: MS... before silver I have been on
Betaseron since it came on the market—for 6 or 7 years? I would say
it did as promised; I have had no exacerbation since I began the
injections. However, everyday I hate to get up to see what
additional symptom I have to add to my list to get used to.
My right had is numb, my feet, especially my toes
are numb. When I get hot or tired my right leg does not lift well.
It drags when I walk. After a day at work, I practically have to
crawl to my car. I must hold on to a wall at all times. I really
should use a cane. I cannot even go up a curb without holding on to
someone or something. No way can I climb a ladder.
When I sit for any length of time, my legs
stiffen and get spasms and I have to wait awhile before I can walk.
It appears that I have had too much to drink. I really should use a
cane, but usually I can take my companion’s arm to get to my car.
If I sit on the floor for any reason, like play
with my grandchildren, I must first get on my knees, then on all
four’s, then finally I can get up. Just like a cow. I cannot use
help getting up from the floor, I need more control. I sit on the
floor as little as possible.
When it is hot, I must wear a cold pack vest or I
cannot walk. My feet are hot all the time, and I cannot sleep unless
my feet are uncovered.
I have night paralysis. I must throw my body in
order to turn to another side. My legs are locked in the fetal
position and it is a real chore to get them unlocked and able to
walk. I must use a cane to get to the bathroom during the night. It
is about ten feet from my bed.
Jane Wyman has become my good friend with the
Poise pads. I cannot go out without the Ultra Poise pads. If I know
I will be away from a bathroom for any length of time, I must use
Depends. It goes without saying, I must use the pads at night, also.
Colloidal Silver: Oral Use
I drank 2 oz of Silver water twice a day - in the
morning & at three PM. Day four I begin to drink 8 oz of Silver
water two times per day. I seem to have more energy and the end of
the day seems to come a little later. I do not drag as much to my
Day 12 The night paralyzation seems to be easing.
I can get out of bed with more ease Day 14 thru Day 18 My fingers
and toes are tingling more and more. My toes are aching. As the days
go by my fingertips seem to be aching, also. Day 20 I seem to have
surreal feelings in my fingers. It’s like a far away out of body
feeling. They still ache.
Day 21, I am getting out of bed much easier and
quicker. I climbed a ladder at work, and I am not nearly so tired
when I leave work. I can actually walk to my car without holding on
to the wall. I did some things on the floor at work, and was able to
get up without too much trouble.
Week four, The bottom of my feet are tingling,
and I could feel whiskers on Mike’s face (a surreal feeling). I
could feel cool bathroom tile on bottom of my feet.
My legs ached all night. It was very painful, I
wanted to scream out. My legs hurt a great deal. The next morning I
was able to walk further than I had in years. Mike and I walked
about four blocks that morning. I feel stronger and stronger every
Week five, More and more feeling in both fingers
and toes every day. Less surreal and more natural. Both toes and
finger get cold.
Week 10, Seem to have small changes every day.
Again my toes ached for several days, then I had more feeling in my
toes. It’s as though I have a non feeling pad at the bottom of my
feet, but feeling all the way around. Like an animal’s paw with the
padded bottom. It seems I hurt for a few days, then something feels
Week 12, I feel like a caterpillar in a cocoon. I
wonder if they have pain during the metamorphosis. The bottom of my
feet are no longer numb, the fingers on my right hand tingle only at
the very tips. I don’t even think about lifting a heavy container
with my right hand. For years, I wouldn’t dare lift, or I would drop
whatever I was holding. I poured coffee from a pot without even
thinking about it, until I noticed myself. Doing it. There is NO WAY
I could be working the hours I have this Christmas, if not for the
water. Last year, I had to wear my cooling vest all day every day,
and when I went home I could barely walk to my car. Some days I
literally dragged my right leg to get to my car. I had to hold on to
the building to get around the corner and into my car. When I got
home I actually crawled on my hands and knees to get up the steps.
This year I never once had to wear my cooling vest. I walk normally
to my car at the end of the day, and the steps are not too much of a
problem. I still go up one leg only, but it is stronger. The fatigue
is minimized, also. I’ve worked many more hours this year than last.
Week 14: I started making my own water about
three weeks ago, and I’ve had to send samples to San Antonio for
testing. It seems the probe they sent me was not working to full
potential, and for about a week I was drinking water with very
minimal amounts of silver. After the week I KNEW IT!!! I was
regressing. Things were not working so well, again. I was
regressing. Thankfully we figured out the problem and within a
couple of days I was back on track. Thank God. This set back has
convinced me even more. As if that were possible. I have my life
back. I will never give up silver water. Week 20: Christmas Week. I
had 16 people for dinner Christmas eve. I had 7 people for dinner
Christmas day, I worked 11 hours the day after Christmas, and I had
14 people for dinner the next day. That is four days out of four I
entertained at my house. I can’t remember when I did something like
that. I still have night paralysis, but not nearly as bad as it used
to be, and I have a lot of stiffness still when I sit a long time,
but nothing near as bad as it used to be. My energy level is very
My MS Update 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: Hydrogen Peroxide Added
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: Colloidal Silver IV
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
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
I would be happy to share what I've learned with
anyone. Call me, Nancy Delise, @ 708-442-6229