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OK, Let's try Betaseron.
- Multiple Sclerosis Community
I saw my neuro last week. I'm going through a flair, though not big enough he wants me on IVSM or any thing, but he definitely wants me on SOME sort of immunomodulator. So I'm trying Betaseron, next. The phone calls are flying. I should be on it soon. ...


Should I take Tysabri for my first treatment?
- Multiple Sclerosis Community
I just saw a MS neuro at OSU hospital. He asked me whether I was interested in being in the Tysabri study. I am only 37 and have only had one relapse. I know I will be deciding on a treatment and not sure what direction to go. This neuro is big in rese...


tysabri
- Multiple Sclerosis Community
Hi everyone, I'm new to this community. I'd like to know if anyone on tysabri has ever developed a bad itchy rash. I'm waiting results of antibody test to the tysabri. Good luck to all!


Tysabri - new PML
- Multiple Sclerosis Community
Hey Guys, Just wanted to give you all a heads up, in the interest of us all being informed patients... :) I saw this article this morning, and here's the crux of it: "New Case of PML Confirmed in U.S. A new case of PML, or progressive multifoca...


Question about Tysabri and PML
- Multiple Sclerosis Community
Sorry, I saw it in another post but didn't want to hyjack the thread. Someone said that Jose who died from PML were taking more than one MS medication. Is that more than one DMD or treatment for symptoms?


Tysabri as first line drug?
- Multiple Sclerosis Community
So I went to my first MS appointment since being diagnosed last month in relapse. We discussed medication options and decided that the orals are not a good choice for me because of previous medical problems( ulcers and family history of sudden cardiac deat...


Our Tysabri Users - Past and Present
- Multiple Sclerosis Community
Hi there! Just want to get a count on our Tysabri Users! I know we have a handful now. Having a list of those using it or w/past experiences will be good reminders for all of us as we continue to grow and learn and make decisions. So who? How many in...


Tysabri
- Multiple Sclerosis Community
Does anybody have any experience with Tysabri? I just tested positive for the JC virus and my doc still wants to put me on it for 6 months. He says that the risk of getting the brain infection is very low since I will only be on it for a short period of ti...


Newly diagnosed - straight to Tysabri?!?
- Multiple Sclerosis Community
Hello, I have been very newly (June 6th) diagnosed with RRMS, based primarily on brain and spine lesions with only one round of numbness 4 years ago however with cerebral spinal fluid showing an overwhelmingly positive result for MS. My neurologist has h...


Vitamin d deficit and starting Tysabri
- Multiple Sclerosis Community
Found out yesterday that I have to take 50,000 units of vitamin d to bring that number up. And I'm starting Tysabri. Really don't know what to expect. I would appreciate, anyone who has been on Tysabri, let me know what to expect while on it???? Thank you...


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