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 have been asked to speak about how MS has changed my life . From the day of my diagnosis almost 14 years ago, I made myself a promise that I would never let it define me. I was in a very responsible job and could have easily given it all up but no way. If I tell you I have run 14 marathons since d...

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??

There is a Huntsville AL MS information lunching Saturday the 29th. Anyone in here from AL? I plan on attending

Well, they wanted me on Vumerity but insurance put a stop to that so I am now taking the Kesimpta injections. Anyone else on these? How long before any noticeable changes if any? Any one else have some minor-ish side effects?

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 ...

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?

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?