Peg,

None of us want to "spook" anyone when it comes to providing as much info as possible about Tysabri or any other MS medication. But when providing this information you have to provide as much as you can, whether it be good or "not so good". That's the only way a person can determine what decision is best for him/her.

I'm sorry to hear that the Tysabri doesn't appear to be helping you at this time. Perhaps a little more time may change things. Like all drugs for MS patients, some help and others don't. MS patients have reacted differently to medications out there for years and I doubt Tysabri will be any different. Let's hope things turn around for you soon.

Take care.

Harry