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Hello from Calgary,Alberta ,Canada. I am Scott, diagnosed May 10/2012 Primary Progressive Multiple Sclerosis. Poet with 8 books in print(2017 release "Imaginative Spasms". 5 YouTube videos(Scott Alderson Poetry). Life is good, just different. Still human, simply modified. Hope for today is that y...

Hello, everyone. Due to complications, I am forced to take monoclonal antibodies. I am still to take Aquaporin 4 to see if I'm supposed to be on Nataluzimab or Rituximab. However, both medicines have to come from abroad as I live in the Philippines and is not covered by insurance. Can anyone please ...

Hello all, So I have been on Copaxone for 3 years. 1st year all good no relapse or new MRI lesions. Second year I got one new lesion but since it was also small my dr said let’s stay on Copaxone. Now my latest MRI showed one new lesion but at the same time I got lipoatrophy on my thigh from the Cop...

Hello there, I've moved from London to Brighton in November, and at the time I decided to keep my neurologist in London, but now going back and fourth for MRIs etc isn't ideal. Does anyone have any experience of ms doctors/nurses in Brighton? Any recommendation? Cheers, g

Hello, have you been able to check out the new shift ms site? it's pretty nice.

Hello everyone! I was recently diagnosed with optic neuritis (and what apparently has been MS for several years now) and after long consideration I finally decided to opt for steroid pulse therapy (5 x 1000 mg methylprednisolone). The first few days were fine, I didn't experience any euphoria, slee...

Hello all, I'd like some thoughts from you knowledgable folk plz. I was diagnosed rrms in September 2017 and have been on tec since March 2019. I have remained stable, however my most recent MRI last month (delayed from March) has shown 4 new areas of inflammation. I have not had a noticable relap...

Hello all, I'd like some thoughts from you knowledgable folk plz. I was diagnosed rrms in September 2017 and have been on tec since March 2019. I have remained stable, however my most recent MRI last month (delayed from March) has shown 4 new areas of inflammation. I have not had a noticable relap...

Hello all, I'd like some thoughts from you knowledgable folk plz. I was diagnosed rrms in September 2017 and have been on tec since March 2019. I have remained stable, however my most recent MRI last month (delayed from March) has shown 4 new areas of inflammation. I have not had a noticable relap...

Hello! I was recently diagnosed with PPMS. Ever since I have had usually heartburn and swallowing issues. I visited gastroenterologist some months ago and according his review I had no visible problems when swallowing. The question is that can MS cause problems with swallowing? Whenever I try to sw...