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So my wife of 31 years was diagnosed with RRMS in 1995. In that time she has tried many many medications. Nothing has stopped or even slowed her progression into secondary progressive MS. We travelled to Poland 2010 for CCSVI treatment. Still her MS progressed. She has been using a wheelchair now fo...

So dealing with RRMS, symptoms are in check as of today. I have used psycotropic drugs to rid my brain of the plaques in a timely fashion then use high dose of vitamin D3 to keep me going. No serious excerbation since 2015. Even that was minor compared to my event in 1996, THAT SUCKED! Do some readi...

Hi there, I was wondering if anyone in this community has used or heard about using RSO to treat MS, this is an oil derived from marijuana, I’ve heard a lot about it, just want some feed back the MS community, thank you.

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 ...

I would like to ask can doctor(s) be sure in the beginning that I have PPMS 100 %? I was taken basic magnetic photos and likvor sample. I had lots of inflammations (lesions) in spine and brain for years according to doctor. By those I was given PPMS sentence. Can it really be true?

Hi all, I am new to this site. I am currently in limbo. I do not have a diagnosis, although the neurologist felt it probably is MS. Limbo is difficult because I do not fit in with any group. One minute I am up, and then I am down. This is uncertainty. I guess a lot of people out there have experienc...

Hey guys, So I was diagnosed in January and after recovering mostly from my first noticeable relapse I thought I was doing just fine. In the last month or so I've been having some bowel and bladder problems such as urgency and hesitation etc it's making me scared to leave my house or walk far or go ...

Hi Everyone - I am newly diagnosed. I go in next week for my prescription. I am curious...is this it? My memory and brain are not functioning very well...is it just always going to be like this? I don’t think working anymore will be an option for me if I am unable to improve. My physical abilities h...

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...

I have been feeling so crappy. I am diagnosed with RRMS since 1998 at age of 28. No real problems until 2017! When I had a flare up main symptom dizzy and fatigue - severe. I recovered nearly complete, went on my first dmt copaxone. Annual mris were fine, a couple of small lesions even disappeare...