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

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

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?

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

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? 😂

What type of scan does the dr do to check for lesions on your spin?

Does anyone blame themselves for getting MS like for having an unhealthy lifestyle before

What did you do today?