51 - 60 of 1226 Posts
Hi All I'm back asking advice again! Last week I started my 3rd significant relapse this year, my specialist nurse is now talking about Tysabri. I was on Rebif for about 15 months and wasnt getting on with the side effects so I switched to Copaxone 6...


Got a question for everyone! So the dude has arrived at his 1 year anniversary of living with MS, if such an anniversary is something to celebrate...anyway. During that time he has been taking Avonex. He had 2 flair ups this past year which is a concern...


Hello all... I know "Tysabri" is probably one of those "we see it all the time" posts so I'll try to keep this short and quick. I have a strong suspicion that my doctor is going to recommend that I switch to Tysabri. I've been on all the CRABs. Betas...


I'm just curious .... For any of you who are on Tysabri, I was wondering if your neuros had changed their treatment plans or recommendations because of all the new PML cases and the acknowledgement by Biogen and the FDA that risk goes up after 24 months. ...


Well went to the Dr today and my last mri shows new lesions so my dr is thinking of putting me on Tysabri. Is anyone else on this and how has it worked for you??


Does anyone have information on Tysabri? I haven't been told much on it, although I have been told by 3 different doctors I should take a look at it. I would like to know what others on it experience or experienced while on it?


I am finally set up to take my first Tysabri injection on Tuesday. It has taken a couple of months to get set up because I am in a study. I don't have the paper work on the study in the house and it is COLD outside, so I can post more about the study...


Recently diagnosed with MS (November) and they are starting me with the drug Tysabri. Trying to find out what to expect and if it is helping others with their symptoms? All new to this, really have no idea what I need to know or ask? Just looking for some...


So I just finished my 2nd infusion about a week ago and was wondering what people's side effects were from that. My body felt like I had a severe flu for like 3 days :( . How long also does it take to notice the drug is working for you . Was diagnosed 9/9/...


Well, my neuro called and left a voice mail on my cell. I wish I had heard it when it rang. Basically she left a rather long message about my blood-work. (I saw her about 2 weeks ago, and she wanted to switch me from Copaxone to either Tysabri or Gile...


Didn't find your question?