Looking for
something specific?

Like the idea of kesimpta for convenience of subcutaneous administration at home and that it’s highly effective with little risk of PML. How have ppl found it? Does it increase the risk of infections quite a lot? Side effect profiles? Have heard that it can reduce the Ig (immunoglobulin) levels quit...

Hi Everyone ☺️ Im just curious as to what treatment everyone is on and how you've found it?

Looking for people's opinions & experiences with the following DMT's as these are the ones I have been offered. I am doing my own research as well of course. The 4 I have offered are mavenclad, ocrevus, kesimpta and Briumvi. I am in my late forties and am well, work full time and have mild symptoms....

Hi everyone, newly diagnosed but have been having symptoms for 6 years. I'm am choosing a DMT and thinking Tysabri or Kesimpta. Any advice? Anyone a young mum and managing to keep this at bay for a long time?

I signed up for the StarMS Trial yesterday, but I also have to choose a DMT in case I don't get the stem cell transplant (or don't get on the trial based on my test results). I am trying to decide between the 6 monthly infusion(ocrelizumab) or the monthly injection (Kesimpta/ofatumumab) I am leani...

Hi ! Just looking for a bit of advice or opinions on which DMT would be best or people's experience with them, and just to have a bit of a rant I suppose. I'm 29, just been diagnosed with highly active relapsing remitting MS, likely had MS for about 6 years. I've been offered Cladribine, Ocrevus, Ke...

Ive just been diagnosed, i live in the UK and im awaiting being transfered over to the nhs list (i was diagnosed vis private healthcare) the neurologist i currently see has said that i shoud be offered a DMT and mentioned these ones, im not sure which i will actually be offered as need to wait and s...

Hi Everyone, So I've posted on here once before and haven't been very active on here since so my apologies for that and thank you to everyone that replied to me. I think I've been trying to ignore the possible (inevitable) diagnosis heading my way and trying to live life normally while I can. Howev...

Hello everyone! Just got diagnosed with RRMS 1.5 months after a hospital visist where I had (what I'd consider to be) a bad flare. Left leg and left hand were out of commission (numbness, lack of coordination) but after getting packed full of steroids at a hospital and about a month of self-directe...