Comments on: Interferon Therapy and Multiple Sclerosis http://nothingventurednothinggained.org/2009/12/interferon-therapy-and-multiple-sclerosis/ Health Information and Options Fri, 08 Oct 2010 22:11:07 +0000 hourly 1 http://wordpress.org/?v=3.3.1 By: Karen http://nothingventurednothinggained.org/2009/12/interferon-therapy-and-multiple-sclerosis/comment-page-1/#comment-18 Karen Mon, 21 Dec 2009 21:24:09 +0000 http://nothingventurednothinggained.org/?p=191#comment-18 Hi, Linda, I agree, there is little known about MCS and it's a horrible to health problem to live with. I was also diagnosed with CFS, FM, and MS. The CFS specialist says that MCS is pretty common among CFS sufferers. I had to stop using my gas overn a few years ago because of the MCS, I've had to leave doctors' offices, and countless other situations. It's all a guessing game at to what one actually has. Thanks for stopping by. Hi, Linda,

I agree, there is little known about MCS and it’s a horrible to health problem to live with. I was also diagnosed with CFS, FM, and MS. The CFS specialist says that MCS is pretty common among CFS sufferers. I had to stop using my gas overn a few years ago because of the MCS, I’ve had to leave doctors’ offices, and countless other situations.

It’s all a guessing game at to what one actually has.

Thanks for stopping by.

]]> By: linda http://nothingventurednothinggained.org/2009/12/interferon-therapy-and-multiple-sclerosis/comment-page-1/#comment-17 linda Mon, 21 Dec 2009 21:05:38 +0000 http://nothingventurednothinggained.org/?p=191#comment-17 I wonder how many people with MS also have MCS? Many people with MCS end up tested for MS because doctors know so little about MCS. I have severe MCS and some exposures cause such severe reactions that it is like MS. My Fibromyalgia also becomes severe with some chemical exposures, and from wearing clothing or sitting on furniture that contains traces of chemicals that do not agree with me, but everything almost clears up when the air and my surroundings are free from toxic chemicals. There seems to be a lot of overlap, but most MS and FM docs seem to know nothing about MCS from what I have heard. I wonder how many people with MS also have MCS? Many people with MCS end up tested for MS because doctors know so little about MCS. I have severe MCS and some exposures cause such severe reactions that it is like MS. My Fibromyalgia also becomes severe with some chemical exposures, and from wearing clothing or sitting on furniture that contains traces of chemicals that do not agree with me, but everything almost clears up when the air and my surroundings are free from toxic chemicals. There seems to be a lot of overlap, but most MS and FM docs seem to know nothing about MCS from what I have heard.

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