IMHO we are all looking for/wanting the same thing...a cure!

I feel I have a good doctor (yes he is an MS specialist) and I trust him.

While I do appreciate others concern for me, and I do try to keep up with the latest experiments/treatments, until there is solid widespread evidence of any new treatment of any kind I will think twice before putting myself, physically and emotionally, through the courses of something that is virtually unknown.

My symptoms aren't like everyone else's and the treatment they are recieving may not do a darn thing to help me. But hey, that's just me.

Chris I do wish you the best with the HiCy and while you're at the meeting, maybe you could ask the investors if they could make this treatment available to everyone at a low cost, regardless of insurance...so that we all can benefit from it.