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Well after a few near breakdowns and a boat load of stress finally been given a solid diagnosis (rrms) last mri shows no signs of activity and also been told I’m going to be starting my Ocrevus treatment in January! Buzzing does not even come close! Today is a good day 🤙🏻

Last month we reached out with an opinion check and asked you if healthcare professionals should discuss progression at diagnosis. While 17% of you said you’d prefer to be told later on, around 75% said yes, you would prefer to be told about progression at diagnosis. In the second of our progressi...

So I was reading my neurologist report on my last visit and instead of rrms he used the name progressive relapsing ms. So just a question cause Google just makes it harder to make sense of, what exactly is that? And anyone here have that diagnosis?

I recently had an appointment with my neurologist, sadly new lesions have appeared for the first time in years (I knew it would happen at some point but still upsetting to hear). I’m currently on Tysabri which I think neutralised the symptoms of a relapse luckily but has anyone else had a similar ex...

https://multiplesclerosisnewstoday.com/news-posts/2025/11/13/ms-drug-fenebrutinib-shows-unprecedented-results-trials/

Hello. Quick questions. Long Post. Sorry. This is my first time posting here. Q1: Can anyone tell me what’s up with PIRA (or Smoldering MS as it’s referred to in some literature). Q2: Has anyone with long term RR MS (I was diagnosed 35 years ago) experienced progression as they age (I’m 62 in a co...