I don’t know how to explain this but I am in pain I can’t text or doing anything properly 😭😭😭

My consultant has written ahead of us meeting in November to suggest me being prescribed new MS medication Fampridine. Has anyone else had it/been offered it?

When it’s cold or even a breeze and you’re either outside or around a window that’s open … does ANYKNE ELSE have that annoying feeling of using the bathroom we’ve if you did t drink water juice or anything?

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?

Being told that no matter how much you exercise and what you do. Nothing will improve and its gonna slowly get worse and worse is very disheartenin, ain't it

Before my MS diagnosis, I thought I knew myself. I thought I understood what strength meant, what it meant to be brave, and how much I could handle. But life with Multiple Sclerosis has taught me things about myself I probably would never have discovered otherwise. I’ve learnt that I’m stronger than...

Hi, i am loosing my mind!! I emailed my ms team two weeks ago with no reply!! I feel i am having a relapse since my flu jab with new symptoms… i honestly don’t know what to do 😔

I got the cutest picture of my little finch Doris sitting on her treat today and my other two finches, Victoria and Tweety, posing for the camera. 😹