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Hello, shiftoids, Our Coven of Covid Companionship has ceased to operate covertly, because that was too much alliteration. We're having a public, and, if all goes well, weekly Sunday night Convocation of the Covid Coven of Companionship. 6pm UK time (BST), that's 5 UTC, it should be sunday aftern...

Neuropsychologist Jo Johnson & is LIVE right now with MSer Gemma, who are speaking about mental health & MS. Watch & ask your questions here ➡️ https://www.facebook.com/shift.ms/videos/1564035427092929/?v=1564035427092929&notif_id=1590158895499563&notif_t=live_video

I hate this disease (and I'm trying hard not to fill this with expletives). I have been with my partner 4 years after 16 years in a pretty miserable relationship. We are very much in love and had (and that really hurts me to say) a fantastic sex life. However, my interest in sex had been declining ...

📢 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.

https://www.youtube.com/watch?v=Ueu-jC6cwuY PPE for the mind is a course designed to help develop mental resilience. Launched during #MentalHealthAwarenessWeek 🧠 the course of videocasts is designed to help us stop, notice what's going on inside, realise our values and start following them with our...

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I am not trying to be a party pooper here. Why would I? I wrote a bit about them here https://shift.ms/topic/doms-covid-diary-sat-25th-apr This is an excellent piece from a pharmaceutical market analyst. These folk really don't care about you or me, they are in it for the money. End of. Have a re...

https://www.youtube.com/watch?v=R1RpZtnUrsw&amp;feature=youtu.be Inspired by conversations from right here in the Shift.ms community 💬 'AWAKE' is the latest film that explores the interplay between MS, sleep and mental health 🛌💤😪 THANK YOU so much to all those involved in the filming of AWAKE. A...

Hi I am 10 years in with RR MS, and had 2 very successful doses of alemtuzumab, in January 2016 and January 2017. I responded very well to the alemtuzumab neurologically (despite being highly prone to any virus, cold or infection going in the 1st year) and in 2018 was in extremely good neurologica...

Hi guys 👋 I'm now SPMS and everything is getting decidedly more difficult. Showering in particular is a major hazard in many ways. My right side is good but my left side is affected by spasticity. I'm right handed and can't do a lot with the left due to weakness and proprioception issues. So...