After 3 weeks of pain and briumvii reaction, i wake up with a cold. :( This is so not fun. I really hope this is it now. You know cold dissapears then im back to my normal self. I just want to do normal things. Im also extremely nervous to try anything else, its been so difficult. Ofc im sure it ...

I have some cramps in the arches of my feet sometimes when im sleeping and my calves also sometimes. Plus just some overall tightness in other muscles. What other things can I take besides someth8ng like baclofen or anything I'd have to take daily. I dont want anything that has to be takin multipl...

Hi all, I was diagnosed 2001 RRMS tried Avonex for 3 years but could cope with the injections, no further contact with Neurologist and decided just to live life taking LDN. Now back in the system and am SPMS. I use an active manual wheelchair but can't blame the ms entirely for that - I have drop ...

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?

♥️♥️♥️♥️♥️♥️♥️♥️♥️♥️♥️♥️♥️♥️ I am writing to you as a fellow community member from North Africa (Libya). Since I am not fully fluent in English, I often find myself having to constantly copy posts, search on Google Chrome, and switch back and forth just to translate content. It has become quite tire...

Is just me? https://suno.com/s/0gLvhDcb7ZsSK4y7

Just diagnosed in the last week or so (36yo first and only known symptoms Dec 25). I’m feeling OK about it because Drs have basically said “with DMTs symptoms will be minimal” so by all accounts not expecting much to change. Without putting the fear of god in me 😂, how accurate is that? Just wonder...

I couldn't go when I was relapsing but I've started again and forgot how it cheers me up. Not only because gym does that but because I'm well enough to actually go Yayyyy :))))

This summer was supposed to be sunshine, fresh air, and making memories. Instead, I spent most of it fighting my own body, pain, inflammation, spasticity, fatigue, and one thing after another. And now, as we head into fall, I’m still not feeling 100%. I have another MRI coming up, and I’m waiting t...

I think a lot about my diagnosis.. the physical stuff is bad, the mental stuff is bad, people don’t seem to understand. What’s on the top of your list?