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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...

I am switching from Tecfidera to Ocrevus. I'd been waiting since the beginning of the year and then the coronavirus came into play. So now I am still waiting. It seems that I had new lesions on my last MRI scan even though I'd been on Tecfidera for the last five years. I just hope this thing starts ...

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...

Well I'm back to see if anyone knows anything. I've had problems with movement disorder since 2018. - while it's being worse the past few days alongside my spasticity. The thing that confused me is it's like I've got this new tic disorder or maybe it's just worse i dont know. Basically in the pas...

New here and not sure how to find friends. Is this like FB for MS?

Time to get campaigning again folks; NICE have rejected Siponimod for SPMS in the UK https://www.mstrust.org.uk/news/siponimod-active-secondary-progressive-ms-rejected-nice Might have to get my battle hat on again.....

From the International MS Federation. June 2020 - https://www.msif.org/news/2020/02/10/the-coronavirus-and-ms-what-you-need-to-know/ - Just the latest, that is all.

Hey all, Hope everyone is well. Been not doing to bad here the last little while. Excluding today. But the last I don’t know 5 weeks or so now been feeling pretty good. Been getting stuff done outside that hasn’t been able to get done in the last 3 years. So was a lot of work. Also had to move ...

Hi all, I am seriously new to all of this, My RRMS journey has been a whirlwind. I had the MRI and got diagnosed literally overnight. Multiple MS occurences all at once. After a huge course of steriods Methylprednisolone 1000mg 5 days. My flares have calmed down. Not gone away, I my hands are numb a...

Hi all, I wondered if anyone could help answer some questions/give their experience.... I was diagnosed in May this year with rapid RRMS following loss of sensation/power in right leg/Side in December 19 and then optic neuritis in April 20. First MRI was in March 20. I was originally told I would r...