Hello Has anyone in the UK been prescribed Fampridine by the NHS yet ? My sister is paying £360 a month for a private prescription , which seems excessive. Thankfully her walking speed has improved and she is now able to get into the car without having to physically lift her own leg into the car. ...

I’m up to my eyeballs in this thing called life with MS. Sometimes I’m paralysed by fear. Too scared to look down in case I drop the baton. When I look around, all I see are fallen soldiers. Then I look in the mirror and remind myself: I have MS too. I pick up my sword, remembering that strength a...

Living with Multiple Sclerosis has taught me that strength isn’t always about having everything figured out. Sometimes, strength is simply waking up, choosing hope and deciding not to give up, even on the difficult days. Some days are easier than others, and some battles are invisible to the people ...

How did you feel when you found out you had multiple sclerosis? 🤔

Its crazy how im trying to tell my mom how im feeling I get told im being lazy or I complain to much my MS is acting bad today but I have to be told suck it up

"Alchemize their suffering" 💯

Hello, I will be starting Ocrevus next week. I was previously on Tysabri but tested positive for JCV. I’m pretty nervous now. My neurologist said this is safer, but I know there is still a possibility for PML. Anyone have a similar experience?

Whats is peoples opinions on tecfidera that has been on it before are the side effects bad? Any info will be much appreciated

Saw my neurologist yesterday, he told me he was leaving. I’ve seen so many neurologists & he was finally the one that diagnosed me and helped me understand what was wrong with me & now he’s leaving. I gotta start all over with a new one. The heartbreak & hopelesssness you get from dealing with this ...