I find that I need to tell my wife and others what I am feeling when I say I have MS. I try to tell them that I feel like pins and needles on my legs and arms. I explain that it is like walking on balloons. I tell them that when I lower my chin to my chest I feel like elastic buzzing in my body. D...

This is kinda an annoying symptom and a bit embarrassing. Just wondering how many people also deal with this? It doesn't effect me all the time. It's like I had to pee a little when I was leaving work and I probably would have been fine to make it home. but I figured I'd go to the bathroom and the m...

I've noticed that whenever I feel stressed, I start losing my voice. It starts breaking and talking starts to take so much energy, I have to really push the words out. Does anyone else experience this?

They don’t know what type of ms I have yet…And they said Tysabri infusions are good for me because I’m “otherwise healthy”. I’m 27 diagnosed 2 years ago, how do I become certain of what we’re doing if they don’t know what kind? How did they chose your med and admin style? I heard not everyone infuse...

“To anyone fighting MS: you are not alone.” “Bad days don’t mean a bad life.” “Your story is powerful—keep going.”

I have my first ever treatment scheduled for Wednesday, my doctor and I feel that my best option is infusion. I'm not going to lie, I'm a little scared. What should I expect afterwards?

I may be new to this journey with MS, but I refuse to let it define my life. I’m learning, adapting, and staying strong.

What do you wish others knew about MS?

Is anyone taking anything for this?