Want to get this off my chest.

I just got put on Zeposia and amantadine. Amantadine is supposed to help with fatigue, brain fog, tremors and muscle spasticity. It’s also prescribed for Parkinson’s and for ulcerative colitis. Anybody have any thoughts or experiences with either of these medication’s?

It doesn’t have to be about MS. It could be about relationships, friendships, confidence, work, or learning to give yourself a little more grace. I’m curious about the lessons life has taught everyone here. 💙

Had my little facial surgery yesterday. The doctor said, “There’ll be a small scar on your cheek.” I said, “Don’t worry about that. I’m telling everyone I got it in a knife fight with a hooker in Vietnam.” 😂 The doctor and both nurses absolutely buckled. Said it was the best answer they’d ever ha...

Been gone for a long time. I think I have the oldest dated membership on here right now 😅. That being said, I’ve been having some issues and I figured who better to ask than the ones who understand the best. Does anyone or has anyone experience stomach issues or has a Neuro tell you if any GI pro...

Im interested to find out how severe your MS needs to be to be granted ill health retirement? Im 50 and full time primary and its getting harder each year.

Hola buenas tardes saludos soy d Jalisco Mexico y tengo ppms, mi vida matrimonial, ya no existe estoy aqui por mi ocrevus q ya va aser cada 9 meses, me toca en Enero y me quiero ir a Mexico y tratar algo en Mexico ya no estoy bien aqui tengo 59 años 8 en ocrevus saludos

How is your body feeling as we wind down? Drop a emoji in the comments that matches your current vibe, whether it's 🛋️, 🔋, or 🌧️. No pressure to be okay.

Since my diagnosis I've fallen 3 times, breaking my ankle, tearing tendons and ligaments in my leg and shattering my humerus. Does anyone have any shoe recommendations for stability when walking around in everyday life? Does anyone find things like splints or AFOs are helpful?