Hey all you good people hope you're as well as you can be. Now I've been on Tecfidera since 2021 which doesn't work anymore as new lesions have appeared on my brain and I need to know how effective Mavenclad is??

I’m planning to travel and I’m on Rebif. Since it needs to stay cold, I’m wondering if anyone has experience flying with it. How did you handle the medication during the flight and at the airport?

Hello, I am new to this group and app but I am very excited there is an app like this as I do feel very alone having MS. I was wondering what kind of vitamins everyone takes and what seems to help the most?

I used to feel bad saying no. I used to go above and beyond for others, even when I didn’t have the resources to take care of myself. Now, I don’t feel guilty, if I can’t or won’t show up to certain things, or if I need time away from constant communication. For me, that level of energy output is a ...

Anybody do the yearly Walk? I need assistance but it is a great chance to get together with friends, family and supporters.

For those living with MS or caregivers has NMES been helpful for managing spasticity, muscle fatigue, or mobility? Were there specific settings, devices, or guidance from PTs that made a difference?

Hi all, I thought Id share this for the foot drop sufferers. I much prefer my FES but this has a place. My neurologist said to avoid these if poss as they dont use your actual muscles to lift your foot up. However, if you're just taking the bin out or popping to the shop this is on in seconds and no...

For rrms what pay. Relief do you guys take