Hello! I’m one of the very blessed US patients receiving Mavenclad (and for free!!). I started my first round almost a month ago and start the second (and final for the year) in a week. So far so good and I’m pleasantly surprised by how few side effects I’ve experienced. While I expect that t…
MS Mavenclad
77 conversations about Mavenclad
I always thought the DMTs would be suggested to you and then you’d have a discussion and it would be your choice. Not in the experience I’ve had. I was told I was going on Tysabri, after a faff, turns out I’m JC positive, so it’s too risky. At the internal hospital meeting they re-tabled m…
Hi everyone, I got diagnosed with relapsing and remitting MS just yesterday and I’ve been told we need to start treatment so it’s a good idea to decide what I want to go with. My options have been narrowed down by the MS nurse and neurologist to 3 based on the severity of my MS (I’…
Hi guys, just looking for some advice, insight…Was on Copaxone for 1 year 1/2 but unfortunately not working… my neuro wants me to start Mavenclad. Just wondering if anyone on this medication can tell me their experience, side effects etc…very worried about low immune system
Hi everyone, haven’t been here for a while. But well, here is MS again so I’m back 🙂 For the last 4 years I’ve been taking Gilenya. I’m not suffering from side effects, so I wasn’t complaining. Today I had the results from my check up MRI and turns out I have 2 new,…
Hello, My results from my recent MRI has come through and my current medication isn’t working. I am currently on Gilyena (which is my 3rd, previously been on Tech. and Aubagio) My options are: Cladribine (Mavenclad) Ocrelizumab (Ocrevus) Alemtuzumab (Lemtrada) If you have any thoughts or exp…