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Hello my fellow MSers I have RRMS and one of the permanent issues I have are bladder and bowel control. I've returned to work after a relapse (triggered by work-related stress) and have asked if I could have the ability to reserve a desk near the bathroom (we book desks) as part of my OH workplace...

Hi all, Trying to get info again, as I didn't explain myself well last time... 🙈 Does anyone know how/whether you can easily shift healthcare from the UK to Europe? What is involved? I get a Ty infusion every month - no intention to change - so it's not a case of me just carrying tablets etc... ...

Anyone in the UK completed the Hope Programme - I’d never heard about it until today. It’s an online course with version for MSers to support and help (giving strategies I think - I’m guessing fatigue management etc?) Be interested to hear anyone’s thoughts. Thanks

Just wondering if people have still been able to keep their jobs due to my MS affecting my hands and my legs at the moment I am on sick as I work in charity shop and it’s very very full on physically. I’ve been told by a few people now just to stay on the sick and let them retire me due to ill healt...

I have informed the DVLA of my MS diagnosis. Had a letter today to say they have written to my neurologist to ask her to confirm that I am still fit to drive . How likely is it that they would take her word for it or will I need to be assessed? I honestly feel I am still safe to drive.

I'm not yet diagnosed but I'm pretty sure I've got RRMS and am currently experiencing a flare up of symptoms. I've been on the waiting list to see an NHS neurologist since January, I've got an appointment in December which will be the first time I've been seen by a specialist. I guess I want to kno...