I want all my ms sisters and brothers to tell me if you could see any band or group you’d like to see this year if money wasn’t an object. I am a diehard Alice cooper nut, and I’d love to see him this year. Fun fact about me I’m a huge audiophile and I love going to shows. It’s something that keeps ...

I’m currently on Briumvi, but my Dr thinks he saw a new brain lesion on my MRI, and Ive gotten a couple of optic neuritis flare ups/eye pain. Its been about a year now and I have no new symptoms but he thinks I should switch to Zeposia.. Should I stay on Briumvi or switch.. What’s your experience wi...

So I was diagnosed with RRMS "officially" in August of 2025. In April 2026, the Dr told me we were going to try Truxima. It took a month for the insurance to approve. Sadly, I had an allergic reaction. Then we tried Ocrevus and the same thing happened, an allergic reaction. So it's now July and we...

Oh, good. Another man who can't handle that I've got MS.... Brilliant. 😎💪💃🙄

King Midas touched things and they turned to gold. I touch things and they immediately require a warranty claim. Drop a glass? That’s for the gods. Spill something while cooking? Part of the recipe. And my cooking is the stuff of legends. Every spill, drop and minor kitchen disaster adds someth...

I was on Kesimpta for about 9 months. It wasn’t working so my doctor switched me to Mavenclad a month ago. I am not sure if the things I’m experiencing are related to the medication or just my MS. I had some issues when I stopped the Kesimpta. My body was confused not having it. But now I feel the...

Along with 60% of us MSers I’ve been having awful fatigue in the heatwaves we’ve had here in England. This is new to me, I was diagnosed almost 2 years ago and I’ve never suffered with fatigue pre diagnosis. My biggest issue when fatigue creeps in is sensory overload? I’ve zero tolerance to any ba...