A late onset for me, I was 52 and lost my ability to walk normally in less than a year. Of course there were other issues and progression that pointed to MS, it took me 3 years to get an official DX in March of 2006.

I spent a lot of time on the internet doing research the first year and a half into my mystery illness, it wasn`t that much of a mystery to me, MS seemed the only logical conclusion, doctors really don`t like patients defining their own illness?

I don`t like it, but is it is following the expected path, so all I can do is deal with it as long as I can?