I was diagnosed with MS 9/2020 by December I was on ocrevus and took it till December 2023. Life got in the way and It wasn't until June 2025 I went for blood work to start back June 2025 and doc said my immunological (sp?) Was to low . He said let's retest in December for next ocrevus 1/2026. Ha...

I’m 52 have SPMM with rapid progression of disease last 5 yrs. I’m almost wheelchair bound and can barely speak. I live alone in small town but need move city for best treatments but can’t afford. I very discouraged and am start suicidal ideation. Please help me 😢

Even though I was previously diagnosed as having Secondary Progressive, I had a flare up where I woke up one day and my entire right side was numb exactly half all the way down including face. Waited about a month to see if it would subside and then went to the ER. They admitted me and did the 3 day...

Hello everyone! I'm new here I was diagnosed with MMS back in 2022 and progressed to RRMS and I've definitely had some eventful twists and turns through my MS journey so far but I'm glad to be able to find a community of people who are going through something similar to myself. I hope everyone is ...

Numb foot exercises in RRMS

I heard everywhere else about to be cold

https://www.facebook.com/share/r/1DKoQ1TVHP/ Perspective to make everyone think.

Does anybody have an issue with the body not producing sweat no matter intake of fluid