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Hi everyone, I just need some advice. Recently, my MS symptoms have gotten worse, and I find I'm suffering more and more each day. I have seen my MS nurse today, who is now considering putting me on DMT treatment. What experiences have people had with the DMT, and which one has worked best for pe...

Hello, Me again 🙋🏻‍♀️😬 I’m still stuck on what DMT to take. I’m deciding between Mavenclad & Copaxone. I really like the ease of Mavenclad, it’s a pill & the fact it’s a higher efficacy but I can’t work out if there is a less common side effect of PML with Mavenclad? & I’m sure I read the ‘cance...

Hi everyone, I have RRMS and I am currently on Tysabri since my diagnosis in April 2020 but I need to come off it due to PML risk, Dr suggests Ocrevus, just wondering about people’s experience as I have done so well on Tysabri, hope everyone is surviving the heat!

Hi everyone. Just about to start my treatment ofatumumab and i was wondering if anyone could share there experiences. Thankyou

Hey 👋 Just wondering if anyone has experienced a decline in mobility and/or speech after starting DMT's and whether it was a symptom you had before or not? I'm in a local MS Facebook group and a number of people have posted about this and it sounds as if the DMT has made them worse physically but...

Curious about what to expect in terms of outcomes, not side effects. I get that the purpose of a DMT is to slow / hal the progression of MS and hopefully prevent any future relapses and further damage. What I can't see any info on, which maybe answers the question in itself, is the impact of DMTs ...

Hi everyone! Quick question, has anyone switched from Tecfidera to Ocrevus? If so, how long before getting your Ocrevus infusion did you stop taking Tecfidera?

Hi. Just after an idea of how long it takes from a diagnosis to starting a DMT?

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...

Hey everyone, could you help me with advice, please? It’s a hard choice…neurologist offered two options Ponvory or Gilenya. I’m terrified with side effects… does anyone use any of those? If yes, what was your experience like?

Has anyone tried any herbal remedies to manage MS rather than going down the DMT route? If so, how successful has it been?

Has anyone here started straight with high-efficacy treatment (ocrevus, kesimpta or Tysabri) while not yet having accrued any disability and only few lesions in the brain? I am reading quite a few opinions and studies indicating it might be better to hit MS hard and early. In my case (36F) I have 3 ...

I have an irrational fear of meditation. Im not on anything except the two things I was put on when I ended up hospitalized. Just Valium and gabapentin to help manage spasticity. I need help!!! I know I should be on a DMT but just writing this gives me severe anxiety.

Just looking for some advice. Switching from tysabri to Ocrevus and was wondering anyone who switched, did you have a relapse if the switch happened quick? I’m so worried and I’m dreading the summer ☹️

After recently having my yearly MRI scan, today I saw my neurologist. I’ve had stable scan results the last 5 years but today there was a new lesion picked up. He gave me three options going forward.. 1 Tecfidera tablets 2 Brabio injection 3 Extavia injection As I’ve never taken DMTs and only been ...

Hi All, I was just wondering how long DMTs work for? Is it that we change every x amount of years until none of them no longer work? Or can we expect to be on a DMT that’s working for life?

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...

Any advice? Generally I have relapses - one every three years, and I am not on DMT. This year, my left leg slowly fades away. Stairs, walking for a longer period now becomes a challenge.

Just met with my MS nurse for the first time (diagnosed Oct 22). I need to decide on what type of DMT I want... Injectibles or Infusion? Thought I'd ask you all what your experiences have been like?

Hello all, After far too long, starting back on DMT (kesimpta!) and I'm wondering how much people isolated (or not) on b-cell depletion meds? We're going into the holiday season and there's a lot of potential for socialising, but part of the delay in getting back on DMT is that my lymphocytes took...