Quote:
Originally Posted by AfterMyNap
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.
|
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.
