Hey. I am working with a practioner who suggested making friends with other MSers with either bowel or bladder urgencies (I seem to have both). Sharing stories. Normalise the topic. Understanding each other. And so on. Anyone?

Hey friends. I’m newly diagnosed, starting my treatment on Monday and overall I’m really positive and optimistic about my future. I’d love to meet others to connect and exchange knowledge, experiences but also to just connect on a human level. My friends are great but just don’t understand at times....

Just wondering how common it is in ms patients to constantly have an outbreak of shingles?

I have a start date for 10th sept for my first briumvi infusion. Im really nervous about it.

Just saw my neurologist & he is telling I can change my DMT to Zunovo. Is anyone else on it? Is it better than Ocrevus?

I was diagnosed at 42 I’m 46 I have drop foot. Just wondering has anyone recovered from drop foot. I walk at least 5000 step/day, workout and wearing AFOs for about a yr. I’ve noticed improvement in my cadence just wondering is it all in my head or if recovery is possible

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.