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To me it seems truly effortless and pointless to continue knowing I'm going to be a crippled or gimp. No more drive to accomplish things in life,don't see a need to excel through life and career anymore, it's all stupid AF to me. What is the point?? I watched someone with Ms develop bed sores the ...

Not sure about my numbness. Think that I might have ms. Any information is appreciated. Started in my feet and now up to my scalp.

So lets upset everybody. I have Primary Progressive MS, diagnosed 9 years ago so I am officially part of the forum but my ideas are a bit different. I do not think there is a simple cause of MS, like a disease bacterial or viral, which can be treated. Sadly is is very like a lottery, there are milli...

I got ms since 04. It’s hitting me hard these days. Hard stuff!!!!

I think I'm experiencing ms I had symptoms along time ago went and went along time with out them now its come back and have new symptoms I think I had the ms hug like weird sensation like squeezing pressure now along with the hug I'm getting weird pain in my feet and legs sometime legs feal weak asw...

Just been diagnosed with MS after 7months of waiting

Hi guys just wondering when I start lemtrada and have to avoid unpasteurised stuff how long do I need to do that for and does anyone have any food ideas what will be no problem to eat it's all a bit confusing thanks.

I am MS person for 20 years and still suffering from drop leg,spasm

Been of medicine for a year. I found out I had Ms in 2010. I've been on 2 different medications. Now none. I smoke lot of weed and I think it works. I've stop smoking cigarettes for 2 years

Hi! I got diagnosed with MS 10 months ago and my life changed dramatically. I’ve been feeling lonely because no one understands what I have. I cry almost every day and I feel so bad for having this autoimmune disease. Other days are better than others of course, but I can’t help but feel vulnerable,...