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?

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...

Hey, can anyone give me anything I can do to deal with spasms down my arm and hand? 🙏

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...

Do Ms make you think about killing yourself

I had my tysabri monthly injection yesterday, and being single hit hard. Some days I wonder if I’ll ever find someone patient and kind enough to support me through this journey but I trust the right person will come when the time is right. Anyone else feel this way?

Hi everyone, how are you all doing? I was diagnosed with MS in 2024, when I was 22, and I’m 25 now. As I mentioned in the title, I’ve been feeling really lonely since my diagnosis. I know MS is considered a relatively common disease, but I don’t know anyone my age who has it. Sometimes it feels li...

Edit: Thanks to everyone that has signed up for this! I’ve sent out a Google Meet invite (it’ll come from Amber Plant - that’s me!) Looking forward to chatting with everyone on Monday. 💚 Hey everyone, Amber from the Product Team here. Martin, El and I are hosting our first Product Development Town...

My Doctor has talked about potentially moving to an infusion treatment. Is anyone willing to share any side affects they have experienced after infusion? Heard 2 weeks of flu like symptoms, head exhaustion...wondering what others have felt.