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Hi everyone! I’m new here so just saying hi I’ve been offered Mavenclad and not sure what to do, it seems a bit too good to be true Has anyone taken it?? How effective has it been and how are the side effects?? Tnx, Laura

I have narrowed down to two DMTs and have some questions for anyone who’s ever taken Kesimpta and/or Mavenclad: 1. Did you "feel better" (i.e. did some symptoms become less noticeable) after taking either Kesimpta or Mavenclad? How significant were the improvements? I appreciate DMTs are designed t...

Hi, everyone. I went into a Holland & Barrett health food shop the other day and asked a lady if they sell Vitamin B12 tablets. I told her I have MS and been advised to take B12 by my MS nurses, and that I have been taking 10 micrograms (µg) as I haven’t been advised on any particular dose. My nu...

Hi everyone. Just very worried. I have Relapse Remitting MS. I have tried a few dmd’s (I’ve had tysabri , lemtrada & now ocrevus.) Initially I tend to be ok. But then I have had a big relapse on them. I’m just wondering what if history repeats itself. Where do I go to after having ocrevus? I asked ...

I have a strange story to tell. I got drunk one time, yelled at some kid, said a bunch of horrifying things about my autistic father, and now I think narcissistic people are trying to get revenge on me by dismantling my life and my family. I think that they are trying to imitate me and make my word ...

Hi MS Gang … has anybody on here had stem cell therapy or know anyone that’s had stem cell therapy? if so is it any good? … any feedback or information would be appreciated, thank you 🧡

Hi all, thought I'd share a little about my journey so far! I got my diagnosis at the end of last year, a few months after a hospital stay when I woke up one morning and the entire right side of my body had gone completely numb. Initially it felt like a relief to get the diagnosis, because I'd be...

I’ve been on Tysabri for the last year and found out I was highly JC virus positive in January. I’ve been advised to switch to another high efficacy DMT in the next year. The top choices I’ve been recommended are Lemtrada and Cladribine. I’d like to know from anyone who has had to make a similar cho...

I had my third infusion of Tysabri today and I’m noticing the side effects getting worse than before. Is anyone else on Tysabri? What are your experiences? I was also curious on when they started to feel the full effects of it. Did it take 6 months to a year until you felt the positive change?

Hi, everyone I was wondering if anybody has any information on their cladribine - (Mavenclad) experience and any side effects? What are your experiences/side effects when taking Cladribine(Mavenclad)? How are your long- ter experience//side effects when finishing the course of treatment? Than...