This Is MS Multiple Sclerosis Knowledge & Support Community

Hey there, my name is Tracy. I've been a watcher for sometime on this site. I've had diagnosed MS since '98. I've had a great doctor since '99, Dr. William Stuart. I've pinned all my hopes on the drug Tysabri, managed to get a couple doses in last year. However my sight is worsening every week, appa...

I lost my pipeline of informations regarding Tysabri, when my Dr. had by-pass surgery. I am looking ofr any information regarding its re-release. The news I got form my Dr.s RN was pretty discouraging.

Tracy Taggart

I used to be on it. It worked well. I'm noot on it anymore simply because me disease progressed. It is called liquid gold at my infusion center.

:( I been have been diagnosed siince 98. After an incredibly bad experience with Avonex, all interferons were ruled out. I alternate between chemp and steriods (both of which I hate) My last attack left my vision in shreds. I was only doing chemo til Tysabri came out. Now that it is off the market- ...