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I had totally forgotten about it, and did not even correlate it at the time ,

but I also had painful distending gas back in 1991, when I had my first mold

attack. The MCS was so disabling that I had forgotten the other symptoms I had

at that time. At that time, my dr new less than nothing, and nothing she gave me

helped the asthma or MCS. Living in the mountains and the mega vitamin regime

seemed to cure me then, but my exposure had been so short, after the moldy

couches had been taken out, I was only re-exposed to mold when more moldy stuff

was brought in on a rotating base. I feel so sorry for people like Janet who

have had long term exposure. My recent exposure was more long term, but I am

recovering after 5 months away. I am so grateful to not be as sick as the people

on this site. Years of migraines , arthritis, and almost loosing my business

seem small in comparison. My sister literally saved my life by taking me in and

treating me like one of her children, I was sterilized, fed, kept on a good

diet, taken to a homeopath who understood, bought new clothes, housed in a safe

room with an air filter. That and getting on Cholestramine early on, I think

everything together saved my life, because I really felt like I was dying. My

only advice to people who are sick is to get out by any means from the place

making you sick, and do everything you can to save yourself. I am so lucky, I

think I have little permanent damage.

Good luck,

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