Tysabri ms multiple sclerosis

Common Questions and Answers about Tysabri ms multiple sclerosis

tysabri

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 burden is at least moderate ( written for head and cervical MRI). Also JCV negative this whole time can I stay on Tysabri indefintely as long as I am negative?

//www.medhelp.org/posts/Multiple-Sclerosis/DMD-Users-Past--Present---Copaxone--Rebif--Avonex--Betaseron--Tysabri--other/show/1193746 http://www.medhelp.org/posts/Multiple-Sclerosis/DMD/show/1041491 http://www.medhelp.org/posts/Multiple-Sclerosis/DMDs-experiences-please/show/759170 http://www.medhelp.org/posts/Multiple-Sclerosis/For-those-of-you-on-one-of-the-disease-modifying-drugs/show/471258 You may fair well with side affects.

//www.medhelp.org/posts/Multiple-Sclerosis/Gilenya-Users-Past-and-Present/show/1469412 http://www.medhelp.org/posts/Multiple-Sclerosis/Copaxone-users---past-and-present/show/643683 http://www.medhelp.org/posts/Multiple-Sclerosis/Tysabri-Users---Past-and-Present/show/1569374 http://www.medhelp.org/posts/Multiple-Sclerosis/Aubagio-Users-Past-and-Present/show/1946899 http://www.medhelp.org/posts/Multiple-Sclerosis/Our-Tysabri-Users---Past-and-Present/show/658918 http://www.medhelp.

i had been diagonised with multiple sclerosis in the year 2001. now i am not able to walk. i am also not able to see clearly. my speech is also not clear. i think my type of ms is primary progressive since my condition has worsened gradually. pl suggest some medicines or other alternative therapy.

org/posts/Multiple-Sclerosis/DMD-Users-Past--Present---Copaxone--Rebif--Avonex--Betaseron--Tysabri--other/show/1193746 -Shell

//www.businessweek.

//www.medhelp.org/posts/Multiple-Sclerosis/Our-Tysabri-Users---Past-and-Present/show/658918 http://www.medhelp.

//www.nationalmssociety.org/about-multiple-sclerosis/relapsing-ms/secondary-progressive-ms-spms/how-spms-differs-from-rrms/index.aspx I've always thought the DMD's do help slow progression 'as well' as reduce the number of relapses, the less relapses the longer it takes to reach secondary stages.

For me, Tysabri was more effective then Copaxone, but if you have MS and are thinking of switching, Tysabri is a very dangerous drug, inform yourself before making the decision.

We have a thread here with Tysabri patients discussing their experiences on it. Here is the link: http://www.medhelp.org/posts/Multiple-Sclerosis/Tysabri-Users---Past-and-Present/show/1569374?controller=posts&action=show&id=# If for some reason that doesn't work, just put in "Tysabri users past and present" in the search area at the top and you should find it. I go for my 40th infusion tomorrow. Feel free to PM me if there's any way I can help.

I am currently on the MS treatment Tysabri. Is there anyone on this treatment that have experienced seizures, blackouts or memory loss?

org/posts/Multiple-Sclerosis/DMD-Users-Past--Present---Copaxone--Rebif--Avonex--Betaseron--Tysabri--other/show/1193746 Welcome, and tell us how you feel comfortable to share.

Martin, MDApril 15, 2010 (Toronto) -- Nearly 71% of people with early relapsing-remitting multiple sclerosis (MS) treated with the experimental MS drug alemtuzumab showed no evidence of disease activity four years into a study, researchers report. That's twice the percentage of patients treated with the approved treatment, Rebif, says researcher Alasdair Coles, PhD, of the University of Cambridge.

//fdaac.com" http://www.medicalnewstoday.com/articles/191247.

Recommended