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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...

A couple of people in another MS group I'm in have been told they can have their next infusion but they will have to self isolate for 12 weeks after. Anyone else had this ?

Hi everyone. Apologies that my question is not MS related but as Psoriasis is also an autoimmune condition I'm hoping someone will have some advice. For the least 5 years, my friend has been struggling to get treatment or even get an appointment at the local NHS Trust because her "condition is not ...

Need to get something off my chest....... so fed up, diagnosed 24th March 2020. Still no communication, phone calls or anything else from any health care professional. I keep reading about asking your ms nurse for advice - think I’m losing it cos I’m still waiting.

This report might upset the bean counters... have a read of this. https://multiple-sclerosis-research.org/2020/06/no-patient-with-secondary-progressive-ms-should-be-left-behind/

...of how all the different MS drugs work. - https://youtu.be/Dr_2F-quv7Y

Hey guys. I hope you are all well. My ms nurse phoned me today to tell me some good news....... I can start ocrevus in 4 weeks time. Whoop whoop. My question is I have a 3 year old daughter and a 2 year old dog (who eats everything he is not supposed to) what advice can you give for me to protect...

Hi all MS trust are in the running for a 5k health lottery grant. Please click here to vote for them (only takes 30 seconds) https://www.easypolls.net/poll.html?p=5ee377f6e4b017b74559f713 Thanks

You may have seen that Mike, Gemma and Zoe have been working through some ideas about building mental resilience with Neuropsychologist Jo Johnson… here’s the playlist in case you’ve missed the videos: https://www.youtube.com/playlist?list=PLm0sRroMtds267oPVxXSAR6bJEZ_Vr__f There are new episodes...

Hi all, first time on this site or any forum for that matter. Hope to make freinds and talk to others about ms, the roller coaster ride to diagnosis, and what happens next. Its taken me five years to get diagnosed and treated and ive been knocked back more times than I can remember. hope I can now...