i don't see how a person that can still use there hands and feet are to bring awareness to a disease that is much more serious than that, like in the early years of this thing nobody really thought is was a big deal. in fact when I retired many thought it was a scam. cause I could still ride a M/c and walk, although my hands & feet had been buzzing for many years. it sounds like another one of those I couldn't do this and was confined to that for a couple of weeks or months thing, like the e deliack thing. I'm almost certain I would be riding a bicycle still if I had not slipped into this stage 4 years ago after GB surgery. it is a another of those 'you can do' inspirational stories. that is not how MS is when it gets to this point. you can do nothing to buck up.