Hi,
Here are two reports from two of my clients, and one
from a doctor friend. The first one is a man who just
recently started buying CS from me. This is an email
he sent me last Friday:

today is friday...
 
wednesday evening ate out at a lobster pigout and i
used a lower molar, that had had serious work done
earlier this summer, without regard, and even though
it was a little sore, just kept at it till it hurt...
 
thursday morning i woke up with my face swollen up and
running a little temp...did the last of my cs and
called my dentist...
 
told him i used a little cs and he didn't dis it but
said he would call the pharmacy with a script for
clindamycin....
 
so i went to get it, and a thermometer.....but while
at the shopping mall went to natural foods and got a
couple bottles of your cs.....
 
by the time i got home i was running a real fever,
37.8 [about 100 deg. F - Terry]
 
and here's where the but comes in...
 
i didn't even open the bottle of clindamycin.....the
first line of warning on the info sheet that came with
it said it was to be only used on the most serious
infections, and that severe intestinal problems,
including death, were a possibility.....
 
that scared me much more than the fever i had and i
opened the cs bottle and started holding in my mouth
by the tooth, as long as i could  .....
 
kept this up all evening and even when i woke a couple
times in the night i did the same....used about 3/4 of
the bottle [16 oz] in 10 hours....
 
thursday morning temp down to normal, pain gone,
swelling down 70% and by this morning, friday,  all
gone......
 
and to think i was supposed to assult my body with the
most powerful antibiotic man could invent four times a
day for 10 days......
  
whew....if i didn't know about cs, i would have taken
all that poison in my already challenged system....
 
which is improving daily by the way


The second report comes from a woman in the US who
called me to tell me about her experience with CS and
her MS. It wasn't my CS she used. This is her journal:

August 2000
My MS
I have been on Betaseron since it came on the market 6
or 7 years ago. 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 hand 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.

I drank 2 oz of Colloidal Silver water twice a day -
in the morning & at three PM.

Day 4: 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 car.

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 4: 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 the
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 day.

Week 6: More and more feeling in both fingers and toes
every day. Less surreal and more natural. Both toes
and fingers 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 better.
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 Colloidal Silver 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: This is amazing. I have my life back. I will
never give up Colloidal 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 high. 

Week 24: It seems I was at a standstill for the last
several weeks. I didn't see much improvement, but then
I saw NO back sliding - Just status quo. This is OK
with me if I don't improve much. I've come such a long
way back. However, the stiffness & night paralysis
could improve. I drink at least 16 oz of Colloidal
Silver water per day. Some days when I have a lot to
do, or am especially busy I will drink 24 oz.

Week 28: I have been drinking 24 oz of Colloidal
Silver water almost every day. The night paralysis is
lessening. It is not taking as long for my legs to get
moving in the night or in the morning. More of the
numb parts of my body have feeling. 

Week 30: It's hard to believe, but I can still feel
better. I can walk almost instantly when I get up from
sitting a long time in one place. In the morning my
legs are not nearly as stiff as they used to be. I can
get moving much quicker then before. I think the
newest miracle is the raw cilantro pesto I have been
eating the last 1 1/2 weeks. 

Week 52: It is now a full year and I would say I am
about 70% improved. I have not improved much again,
but I have not gone backward either. I can be
extremely happy if I stay this way. I feel better than
I have in several years.

1 year 4 weeks: Some of my email friends have been
discussing drinking Colloidal Silver water with
Gatorade. They seem to believe the electrolytes in the
Gatorade will get the silver into the blood stream
quicker. It will not have to go through the entire
digestive system to get to work. What have I got to
lose.

1 year 8 weeks: They were right. I have been drinking
Gatorade two parts to one part Colloidal Silver water.
It has truly helped. I cannot believe the change. I
can't remember ever feeling this good in my entire
life. I have some numbness in the very tip of my
fingers and the incontinence is still there to some
degree, but then again I drink over 48 oz. of liquid
everyday. The morning stiffness is still there to some
extent, but it is not at all serious. I can get out of
bed fairly quick, and it takes only a short time for
me to begin walking. If I over do it during the day my
legs do get heavy and tired, but compared to not being
able to walk at all a year ago, it is wonderful. 

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 lose?

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 35% 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 of CS. 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. I
would be happy to share what I've learned with anyone.
Call me 708-442-6229, snailmail me: Nancy DeLise, 380
Blackhawk 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/mo        $80/mo 
Method of Delivery: injection, minimum 1x per week,
drink 16-24 oz. per day

Side effects: page after page      CS: NONE 

Prognosis: Traditional: learn to cope and continue to
deteriorate

CS: Expect to kill all MS virus within 6-8 months.
Repair damaged Myelin and regain most functions within
6-12 months      
                                                      

Last year a medical doctor I know and introduced to CS
called me to report that she had resolved an ulcer
using CS. She had been advised by a pharmacist friend
of hers (he orders CS from me) that he had resolved
his ulcer using CS. She drank one ounce every 2 hours.
When she called me it was to report that it was the
end of the 4th day, and all symptoms were gone. A
month later she called back to report that she had 4
patients with ulcers doing the same therapy, and two
them had already reported remission of all symptoms.
She was waiting to hear back from the other two. She
told me that antibiotics don't work anymore where she
lives, they have become immune to antibiotics - but
not CS!

Terry Chamberlin

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