Went for my infusion last month and there’s already talk around the hospital about ocrevus being given as an injection instead of an infusion. Not sure what I think yet 🤷🏼‍♀️has anyone spoken to their neurologist about this yet?

Need advice , I am planning to travel back home as I want to disclose my diagnosis to my parents in person as they are very old and will panic if I share this news over the phone . It’s a long haul flight and travelling alone is making me very nervous. It’s my first travel after the diagnosis and...

Does anyone take any kind of vitamins? I currently take vitamin D3, tumeric, magnesium and omega 3 all high strength. Just wondering if anyone had any suggestions of any more I can add into the mix 😂

Hi, has anyone who has been on Natalizumab for 12+ years successfully moved to another drug? the JCV has been positive for a number of years, so PML risk is up - but trying to find people who have switched, to understand the experience and feedback to the change please. Hope its working for those wh...

Hi , I’ve searched old threads on this topic , and I appreciate every one experiences these symptoms differently . My pins and needles seem to worsen or lessen from day to day. Had them for several months and this week they appear to be intensifying. Is this to be expected ? ( throughout hands ...

Just been diagnosed yesterday with relapsing remitting, think I’m in shock it feels kind of unreal like this all can’t possibly be happening in MY body?. I’ve been told to look over different medications and choose but they all seem to come with side effects …. Do the side effects stop when you are...

I've just got my first year MRI results back and my lesions have decreased I have/ had 2 lesions on my cervical spine. One rather large one and one smaller one. My MRI showed a decrease in the larger one and the smaller one is now invisible. I have only taken year 1 of mavenclad but am optimistic t...

Just finished my second year of Mavenclad treatment and my recent MRI shows no changes which is great because I was told I had very highly active RRMS when I was diagnosed march last year and have between 23-33 lesions on my brain, I’ve been told I don’t need any more treatment for at least 4-5 year...

I’m from Cornwall, anyone else near ish? 😄

Just wondering if anyone else can relate. Been on Tecfidera since 2020 with good effect. My white cells have steadily been dropping though, now at 0.5 so they have cut me down to 1 tablet a day instead of 2. Just a bit worried about the effectiveness if only taking half a dose. Thanks if anyone has ...