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?

Has anyone felt being tired of themselves? As I’m tired of being me!! 😢😴. Has anyone felt that feeling before? I’m also tired feel like i want to sleep all day long…

Power yoga this morning then later Pilates after that Aqua Pilates then swimming and jacuzzi 🥰

Just feeling really defeated. Bad drop foot from recent relapse, and I almost feel as if my walking is getting a lot worse. Going to PT and trying to soldier on. Now most days my legs and feet feel like sandbags I’m pushing along. Numb cold, and sometimes lots of buzzing. Had oral steroids for four ...

I’m wondering how everyone deals with fatigue, I’ve tried magnesium and ignoring it for the last 8 years 😅 I’m not sure what to do. My sister said I should try to change my diet but even with that I’m not sure where to start !! Any recommendations would be greatly appreciated :)

Hi all, Just wondering if anyone had been prescribed the generic (cheaper!) version of fampridine privately? My consultant prescribed me Fampyra but I know generic versions are / will be available which will be hopefully much cheaper. Kind regards, Amy

I had my first MRI since starting Kesimpta and eager to hear from the Dr. It’s been a week and a half. I called and emailed this week. Thank you!!

I’m looking to move to a different city and wondering what it’s like to move hospitals or trusts within the uk/nhs as a result of moving cities. My MS nurse says that once I leave here I will have to move my treatment as well since they will not be able to serve me as I’m outside the catchment area ...