This Is MS Multiple Sclerosis Knowledge & Support Community

Thanks for all the advice. I have, like euphoniaa, done alot of searching for things that work and things that dont. I see, by reading other peoples posts, that exercise is good. It has been hard for me to get moving because it seems to aggravate my symptoms. I wont give up, but I haven't found the ...

I have been reading alot on this forum. I believe I could use all the information that I can get. So I noticed, I didnt write very many of my symptoms. I have had FMS for 11 years. I treated this mostly with heat. It was my natural drug of choice. 2 years ago when things got weird for me, I couldn't...

I dont know very much about MS. but fibromyalgia, i know alot. I have had it for 11 years. Did your Dr do a 18 point nerve pressure test? http://www.webmd.com/fibromyalgia/guide/fibromyalgia-tender-points-trigger-points search alot about FMS before you let a Dr give you that as a diagnosis. I have i...

My name is Jami. I have had issues that have affected my life and my dilemma is: i have no insurance but i have a strong sense that my symptoms are MS. I have a husband on disability and can only work part time. I haven't felt well enough or long enough to get a job to get insurance. When I first ha...