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My neurologist has suggested Ocrelizumab or Mavenclad. He saidBoth are equally effective. Ocrelizumab is 6monthly infusion, while Mavenclad is oral medication-a 2year-course treatment, with 20day-doses over 2year period. Confused? Can I ask members for their experience with either treatments 🤔

Hi all, I’m new to the site, just thought I’d say hello. Bit a about me, I’m a Brit living down under, I have a 10 year old child.....opps I meant 11 (do birthday during covid lock down even count!?! 😂) I love playing hockey and drinking coffee looking out over the sea 🌊 Rx

Hi Has anyone had any news regarding DMT treatments in the UK now? My MS nurse is waiting to hear when they might be able to re-start, and I am on the list for the initial Ocrevus infusion - hoping this will be soon, of course.. Wishing you all well.

Howdy all, I'm new to this site after my MS nurse pointed me in this direction. A little about me: I'm a 34 year old Male. Married with a young son, 7 months old. I Live in Southampton. I enjoy paddle boarding, going out on my mountain bike. I did enjoy the gym but haven't really been since Aug 2...

@msers Hi all Happy Friday...or whatever day it really is in this COVID19 black hole. Just looking for some info on Mavenclad as am over due starting...hopefully soon-ish... Any issues, tips,advice...affects Am kinda a virgin mser...only officially dx since april 1st this year...confirmed by neurolo...

@msers Hi all Happy Friday...or whatever day it really is in this COVID19 black hole. Just looking for some info on Mavenclad as am over due starting...hopefully soon-ish... Any issues, tips,advice...affects Am kinda a virgin mser...only officially dx since april 1st this year...confirmed by neurolo...

📢 Calling all US-based MSers 📢 Do you live in the US? Fancy helping Shift.ms with something? We have a new volunteer role available that is based around the US MS community. If you're interested please email sophie@shift.ms today 📨 Thank you.

I've been on Tech for 4 years and I recently had a MRI scan which showed new lesions (sad and disappointed). Yesterday My Neurologist called to formal tell me of the results. However my brain switched off and I didn't fully listen to what the next step is.

<p>Hi guys has anybody tried this patch it’s called Taipatch. I live in Wales and I believe this has come from USA. It is expensive just wanted to know if it’s any good.</p> <div class="i-support-link"> </div>

<p>Need some advice. I have had health issues half my life. First started when I was about 16. I’ve been trying to find answers for years. Just recently found out that Ms was put in my medical records 2 years ago, although the Dr never verbally told me this. I also have trigeminal, occipital a...</p>