Thanks Cheryl, for your report. I'm glad it went well for you and I hope, right along with you that the Touch program runs a little more smoothly, in the future.

BTW, what are the positive reports. How does Tysabri seem to be working for PwMS. Are they reporting good results or not?

Good work, FG, it's great to have representation from someone who isn't busy organizing their own raises in pay.

Sal, most, I'd guess 90% of those I've heard from on Ty have had a lot of positive experiences with it. I can think of only two out of about 25 who feel it's not working. I haven't heard any directly negative reactions to it. Mind you, this is just from a small handful of patients with whom I communicate.

Sally

This wasn't that kind of conference. It was a conference to discuss RiskMAPs in general. So, I cannot really comment on that.

Kudo's to you FG!!!! I shouldn't be surprised that you went to the conference.... Just like you to always be a front runner on trying to help others... I take my hat off to you!

Hey, who took my hat???? Hugs to ya Cheryl!

Well done!!!!! So proud of you!!!!

Thanks, Cindy. I appreciate your answer. I just haven't heard too much since Tysabri started back up. I heard wonderful stories, when it was first out and now...not much.

I assumed that the hype was bigger than the bite. In other words, Tysabri is just another MS Modifying Med. and not any closer to a cure than the rest of them.

Considering all this, the expense is rediculous and sinful. They should be ashamed. I hope that in the near future, a cure or at least something to stop MS in its tracks, will be found.

I've given up, for it to happen in my lifetime, but I hope it will happen in yours.