I think a lot about my diagnosis.. the physical stuff is bad, the mental stuff is bad, people don’t seem to understand. What’s on the top of your list?

Finally got the diagnosis. Progressive MS. Starting Ocrevus next month. Anyone have any experience with this drug?

Hello! I'm new to all of this, I am not officially diagnosed with MS but it looks like it is... I got numb on my left side last week - right below my eye in the back head area down to my shoulder. Now the numbness is up to my hands. The ER did bunch of tests including a MRI and nothing really came o...

My family not understanding my illness. Hard to convey as not sure what to call it, lanuage barrier wise. If only exercise could fix my back problems I would do it all the time. It doesn’t work. It helps but it doesn’t get rid of it. Or you’re too fat. Don’t get me wrong I am on the heavier side bu...

Dunno what happnemed but Woke up I’m the hospital today guess family found me on the floor snf called 911dpmt rams dd the trip Or anything just Wok up laying on a hospital Bed and they hooked Up all the shit to me. Feel fine besides a headache tho

Had rrms for 25 years now diagnosed with spms. Due to start mayzent/siponimod after being on Tysabri for 20 years. Anyone gone through something similar? And what’s been your experience?

Hi, new here. had MS since 2017, got diagnosed in 2022. Live in Florida so heat and humidity are a killer. Not sure what kind I have yet, got new neurologist. Severe enough can't stand without holding onto somethi9ng. The exhaustion though is what gets me. have to spend most of day in bed. Miss talk...

I thank God that I don't feel like it or look like I've had this illness for 10 years I may not be able to run just yet cause I'm finding out new exercises for my legs 💪and I may have a Rollator but I don't even feel like I have the illness and I give all the glory to God