Had rrms for 25 years now diagnosed with spms. Due to start mayzent/siponimod after being on Tysabri for 20 years. Anyone gone through something similar? And what’s been your experience?

Hello! I’m new to the app. My MS nurse suggested it as I’d said I could just really do with knowing a few people who understand. I have a lovely Instagram community but they’re all over the world and it would be bloody lovely to have a brew with someone local to Bradford/Leeds in West Yorkshire?

Woke up today and it’s a completely different story — Body Battery 74. But the hounds can stay the fuck in the kennel. It’s the weekend, and today that energy belongs to my family. I’m going to watch my 14-year-old son kick arse at rugby, then carry my toddler around—bad leg and all. Because, lad...

I'm starting to get vitamin/supplement fatigue. With which do you all have the best experience? For clarification I mainly struggle with heat intolerance, fatigue, stiff muscles at the moment. Vitamin D high dose is the only thing my neuro recommended.

Hi. Does anyone else suffer from a random dripping nose? No cold or hayfever and just a clear liquid. Just wondering if I need to contact my GP.

What do you avoid eating and drinking now with MS?

I do this every year!!!! I feel like I have a horrible person in me? Don’t know if anyone feels the same? As I don’t talk to my annoying Ms dad for months on end!!!! I just hate annoying people that really irritate me!!!!! I’m not sure it’s me, my Ms or my learning disability needs I can’t help it...

Sorry if this offends anyone, because I know MS hits us all very differently, but I think the wins deserve some airtime too. I went to the gym today after linking my Garmin data to ChatGPT and building my training around what my body was actually showing. Today it basically said: RELEASE THE HOUN...

when the year is progressing like the year before and the year before that and feeling like your life is in a holding pattern?