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Hi all, - If you take ocrelizumab (Ocrevus) , as I do, and want to participate in a vaccine trial then have a read of this post on the Barts MS blog and get in touch with them via the blog. - https://multiple-sclerosis-research.org/2020/06/mscovid19-covax-or-coronavirus-ocrelizumab-vaccination-study...

Hello MS team! I am an actor writing a play which includes my experiences as an MS warrior. I wanted to know if anyone here has MS counselling experience or can recommend? I would love to have a chat with them by way of researching other perspectives of MS, rather than just my own. I'd also be ...

I am wondering if anyone has seen either a geneticist or immunologist in the context of your MS. My brother is encouraging me to go, and he is also encouraging me to eat a keto diet. He doesn't quite articulate what he thinks these other doctors can do for me. My brother reads a lot of books about h...

Over the last 2 weeks i've started to notice a lot of MS symptoms, like muscle twitching, spasms, weakness, fatigue, pins and needles, numbness. Most of them appeared in the first week and are now slowly getting a bit worse. I wanna know what was your experience of first getting MS symptoms and in w...

Hi all, I'm new to Shift MS, nice to meet you all. I got diagnosed over a year ago, but haven't talked to anyone else with MS before, so just looking to say hi and catch up with someone who might be having a similar experience. How do people deal with day to day stuff? My most annoying thing is work...

Hi everyone, So we used to meet up every month at a gorgeous pub in Victoria, and whilst this has not been possible we have been connecting over Zoom. It's been great to reconnect with old friends who couldn't make the drinks and to meet new people too, including little ones too <3. So, if a...

Hi. I have been searching for information on how MS looks in menopause. I mean for anyone who has/is with experience of this stage of life, can I just say it is difficult. I am finding it hard to pull apart what is symptom of MS vs menopause. I mean cog fog, fatigue, moods, joint pain, dizzines...

During the lockdown I've been binge watching House. They mention MS as a possible diagnosis every other episode, but I'm half way through season 5 and I still haven't seen an actual case... I feel discriminated!

Hello everyone, I've headache which last for a long time. Painkillers can not do anything with it. I really suffer much sometimes like now I do. Does anyone have the same problem and what do you do for coping with it?

I signed a contract for conducting clinical trials of the drug. My relatives did not approve of my decision and each time they scared me with scary stories and the fact that I would be an experimental mouse🤷. In Ukraine, MS treatment is very expensive, and I think that for me this is a chance to ge...