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happen. My Lord, my brainfog disappeared. What happened? I  don't know. But if 
it hadn't been for the testimonials I read  in your website, I would not have 
had the assurances that at  least it was worth a try for me. I would not have 
found help  and relief with your products if somebody hadn't talked about  it. 

Dr. Rea put me on what I called house arrest. Avoidance of all  allergens was 
my #1 priority. I'd gotten sick as a result of  second-hand tobacco smoke in 
the workplace--a federal  government agency. I literally could not enter the 
building  where I worked. In order to get disability retirement, my  husband 
and I had to resort to an attorney who told us not to  go for workmen's 
compensation because "the government has more  money than you do." It took him 
a year to get me disability. I  have lived through the mounting medical bills; 
denial by my  gov't insurance because they felt 1) what Dr. Rea was doing  was 
experimental; 2) multiple chemical sensitivity doesn't  exist; the 
life-diminishing pain and agony of really not 
knowing what was going on. The attorney was absolutely kind  and excellent. How 
did I find out about him?? A friend told  me, another patient from this area I 
met at the Environmental  Health Center. 

I've been going through this for 13 years now. There is not a  single physician 
on the Mississippi Gulf Coast, where I live,  who knows the term multiple 
chemical sensitivity and what it  stands for. I am literally without medical 
care for this 
condition because it isn't available. I am an expert in it. I  live. 

And I depend on ethical, decent companies like yours to help  me get through 
every day. And on testimonials/referrals and  information from other lay people 
who have knowledge and  experience. 

I didn't mean to have this email be so long but there are  thousands of us in 
this country in my very same boat. The  medical profession denies that a 
certain condition exists  because they didn't learn about it medical school--we 
all know that. They ignore what's already been published in books even  by 
other doctors--goodness, don't we know all about that. But  there is so much 
more than that--there are people like me who  have no recourse to the medical 
profession because they deny  we exist!! At huge and prohibitive expense we can 
travel to  far-away cities to get some relief. Why are we to be denied  the 
right to find for ourselves what will help us? 

And that's the catch. Multiple chemical sensitivity is so 
diverse, so all-encompassing, so overwhelming to all systems  in the body that 
the professionals throw their hands in the  air and walk away from it. We, the 
ones who suffer this  condition, cannot walk away from it. I said I'm an expert 
in  it. All of us with it are experts in it. Because there are no  medical 
answers except to relieve symptoms--as usual. And  because we try and try and 
try again until we find 
what we finally can take or do. When you go to court, know  that you're 
fighting for me, very personally, not just as  someone who wants to be informed 
in order to buy supplements,  but because that is the only thing I can have. 
There is no  medical answer to my problem. So if medicine is out, where  will I 
go if supplements are limited? My very health, and  life, would be thrown into 
unthinkable despair and further  disability. For what?

You are in my prayers. 
Marta Knowlton  

*********************************** 

Good luck in court. I do not know what I would do without the silver. It keeps 
my bladder infections from killing me. The  doctor could not cure me and tried 
to say I was a 
hypochondriac. After I started taking the CS, I went back to  have my urine 
tested on a routine chec


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