I have heard all kinds of stories about telling employers about MS and I really don't know what the answer is. I am a private person, but I have found support by talking to fellow MSrs in the community.

I plan to live to be 120!

I take one of the interferon therapies, Rebif.

Someday they may cure MS, that idiot thing. It gets in there and they can't get it out.

When you hear the word 'disabled,' people immediately think about people who can't walk or talk or do everything that people take for granted. Now, I take nothing for granted. But I find the real disability is people who can't find joy in life and are bitter.

I think eventually they're going to find out that MS is like 10 different things. I have a neurological disease something like MS, and it's MS, so let's take medicine for it

I've always been this insane. Isn't that interesting?