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Hey 👋 Welcome to the Shift.ms community! Drop a comment below and let us know where you're from 👇 Whether you've got MS questions, you're seeking advice, or you just want to chat to other MSers, we've got you covered 💚 Take a minute to hear Sarah's MS story and learn how she gets the most out ...

Cambridge Medical and Rehabilitation Center (CMRC), the leading healthcare provider of rehabilitation and long-term care in the GCC, has announced the launch of the Kozia Physician Approach, an intensive neuro-rehabilitation program for patients with cerebral palsy and other conditions. Neurology, a...

So I had my first dose of KESIMPTA yesterday. Injection went well so quick and easy. After effects started 4 hours or so later and were a little more troublesome I had horrendous chills that made my body convulse. Then became so hot and sweaty. Suffice to say it wasn’t a fun first night. Once I’d sl...

We’ve just launched Shift.ms polls! Take part in the first poll below👇 *Bonus points if you can leave a comment and let me know: are you happy with how long it took?

Hi all hope you are coping as best you can, just out of curiosity (and nosiness maybe?) if you’ll take away just 1 of your symptoms permanently which would it be? Mine would definitely be my poor balance, after walking for 15 mins (aided) I’m like one of those wavy blow up things you see outside car...

12th Kesimpta injection done 30 minutes ago. I absolutely love this injection. If I was on Copaxone still, by now it would still be stinging and a big red mark with a big lump in the middle. This injection to me compared to Copaxone is a no brainer. I love it 👍

I’m 37 and cant be bothered to think or do s e x . I know it’s been a while and I want it but there’s nothing I can do to get me in the mood. I have a partner and he’s getting so upset and in his feelings cause he can’t off load his load 🤣but nor can I. I’ve called my ms team and their only suggest...

Hi everybody, hope you're well today. Came across this - https://www.healio.com/news/neurology/20240229/vidofludimus-calcium-linked-to-fatigue-reduction-may-have-longterm-effect-in-ms Looks positive, probably looking at years of research and hope, and who knows in the end - but I thought it might be...

Hi guys, I was just wondering how you all cope with things progressively getting worse? I’ve only Been diagnosed for six years and I am 23. Unfortunately, I have Advanced MS And I am really struggling to deal with not being able to do what I used to do. How do you guys deal with it?

childhood i coulfnt plsy kimdergatden. games vertigo when o play in theme park daignosis 2 optic neuritis poor courfnation i slipped over whhen i played footie with friends slow om staird them limbing sy ini cant manage two stairs veryigo double vesion more than once lost sbility to taste in half ...