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Two musicians with MS One in Texas and the other in New York have made something amazing over the last year and a half and never even met in person. This conceptual album is about to change the game. Not only the music but most of the animation and artwork were done by the two musicians with #multip...

Are you taking Cladribine for your MS. Turns out it is pretty decent stuff! - Another example of why we need everyone with MS to sign up to the UK MS Register. - https://ukmsregister.org/ - "Over half of MS patients analysed did not relapse or experience disability progression during 60 months of f...

Over the last 2 weeks i've started to notice a lot of MS symptoms, like muscle twitching, spasms, weakness, fatigue, pins and needles, numbness. Most of them appeared in the first week and are now slowly getting a bit worse. I wanna know what was your experience of first getting MS symptoms and in w...

Hi all, - If you take ocrelizumab (Ocrevus) , as I do, and want to participate in a vaccine trial then have a read of this post on the Barts MS blog and get in touch with them via the blog. - https://multiple-sclerosis-research.org/2020/06/mscovid19-covax-or-coronavirus-ocrelizumab-vaccination-study...

Hello to everyone, I have just joined you. I was initially diagnosed in 2009 with ADEM & thought it was benign MS. I have had ongoing symptoms over recent years which led to a recent MRI showing multiple lesions. The Consultant has diagnosed MS and referred me to Queens Square in London. I ...

I have a conflict of interest to declare: I am on the UK MS Register committee. - The MS Register here struggles to get more sign-ups. Everything you share is to further the cause of MS research. Your data is secured properly and never ever shared, outside of the anonymised research data. - The Fre...

Today is a good day. Going to write some words to see how they're classified. Like Lemtrada...... It actually needs more text than this and we're going to make it content that talks about medical diagnosis of multiple sclerosis.

Hi all, I am seriously new to all of this, My RRMS journey has been a whirlwind. I had the MRI and got diagnosed literally overnight. Multiple MS occurences all at once. After a huge course of steriods Methylprednisolone 1000mg 5 days. My flares have calmed down. Not gone away, I my hands are numb a...

Hello I am new to this site and hope to make some connections with others with multiple sclerosis. Hope to be helpful to others. All best