I live in the north west england UK and I was diagnosed with RRMS in 2022. Since then I have been denied DMTs despite requesting every time I see my Nuerologist. Since diagnosis I have decorated ALOT I have had quite a few attacks (each has gave me a lovely new symptom). But when ever I see my neuro...

I have SPMS but for the last few years I've also had worsening arthritis and my hips have been terrible, so I bought an electric wheelchair - a Drive Autofold power chair. It has been great, comfortable and easy to drive and use, but in the last year I've had both hips replaced and now I don't need ...

Around my diagnosis is when this one popped up. I'm older hah

What’s one little thing you do for yourself to find a bit of joy while managing MS? For me, it’s watching a funny movie or comedy special — laughing always lifts my spirits. I’d love to hear about your little joys.

I got a couple things that bother me cognitively. for example, I cannot just make a damn decision about anything, which bothers me. Also, sounds crazy but i feel like MS has kinda made me dyslexic, sort of. Anyway, just asking. Thx.

Where are you joining from while living with Multiple Sclerosis? 🌍

What is your experience with strength training and exercise? I noticed when I lift heavy my gate is good for that day and the next and I have a little bit more balance, but I also am having a hard time defining that red line where if I go any further, I’ll push myself over the edge and pay for it w...