Hi all, I've had MS for 26 years and only took dmds once, on 2023 and 2024 (Mavenclad, so this was the correct way to take them). I have been making more mistakes at work recently though so I spoke to my ms nurse and requested a neuro-psychology assessment which I had on Friday. This has bought i...

Going to a sound bath and a treatment taster session at the hotel me and mum goes to Tonight 🥰.

Whether it helps MS or not, I’d always have some as my body craves it. ☕️

Why does my MS feel like it’s got worse but no new lesions. No active ones either? It’s overwhelming. I’m 32 years old. I just need help to understand it

It's sad that the most relatable narrative about Ms that I've heard came from an Instagram video for a miracle electric foot pad that will repair the nerves

Do you think you’re ms is mean towards other people? Specially if they annoy you etc? Or is it just me with my Ms?!!!!!!

Hi, A question specifically for teachers in England. What things have work put in place to support you? Did you feel the need to get your union involved or were work supportive? Also what do you do when having a relapse? Work as normal on a full timetable or reduced hours?

Are you 👻 Watching scary movies and pretending you’re not scared? 🍬 Hunting for sweets? 🎭 Getting dressed up? 🏡 Happily staying indoors and avoiding all the madness? 😂