Search Results for "Tysabri"

1 - 10 of 1226 Results
I have had RR multiple sclerosis since I was 10 ish diagnosed (finally) in 2008. Had routine MRi of head and neck last month, everything is stable for 2 years now. Thank you Tysabri! My question is the impression of my mri stated T1 and T2 disease bur...


I have been on Tysabri for 7 months and after I had mt first infusion......things started to work again! The closer it got to the second treatment things started to come back, My neurologist said I needed three months of medication to build up a steady lev...


Diagnosed 2/14/13 with PPMS. Neurologist wanted me on Copaxone. Finally started it on 03/12/13. Received a letter from neurologist on Friday(02-15-13) that he would prefer me to be on Tysabri. I am negative for the JV virus so it is something that is possi...


I have had MD for 18 years. Been on Avonex, Betaseron, Tysabri, and now Tecfidera. Unfortunately, I'm also on lots of other medications, mostly due to terrible central pain. My neurologist made me stop the Tysabri after 24 infusions because of safety conce...


Are any of you on Tysabri? My doctor has suggested that I consider starting Tysabri treatment. His neurology practice runs a TOUCH infusion center. I've been on Copaxone for four years and have just had my first flareup. My recent MRI shows progression...


I would like some information/details from anyone who has had (or seen) the rash you can get from Tysabril and/or PML?? I have been on Tysabri 10 years so far without any major issues. I was outside after my treatment for 10 minutes or so. After taking m...


The screening test for the JC Virus for patients considering Tysabri as their tretment was officially approved by the FDA today. The test tells if the person has been exposed to the JC Virus or not. PML on tysabri has only occured in people who are JC po...


My new neuro suggested Tysabri based on increased lesions on Interferon (Rebif). Any persons out there on Tysabri that could share their experience?


Hi All... I was contacted by one of our wonderful Community Leaders to update this thread, since the original one is kind of sparse. (Here's the link to the original post: http://www.medhelp.org/posts/Multiple-Sclerosis/Our-Tysabri-Users---Past-and-Pr...


After my recent visit to my neurologist we discussed changing my dmd. He feels that Tysabri is the way to go. I know that there are others here on it or used to be. I would love some insight on what to expect, how long it takes, etc... Thanks!


Didn't find your question?