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My legs feel numb but I still feel them and when I rub and pinch them I feel them still. But they are feeling numb this happened last night after my shower. I called my neurologist and left a message being it's a weekend I won't hear from him till Monday. Is this normal? I googled but it gave me...

Has anyone had a change in career, or studied to do something different. I am interested in going into mental health or funeral care . Not sure whether it would be MS friendly

Hey all has anyone tried ice baths? I know there are extreme cold and heat sensitivity but I was reading about it “Cold water immersion therapy is proven to provide relief from inflammation and pain, naturally support the immune system, and help to reduce stress. All three are common symptoms for ...

I was diagnosed at 21, been 10 years now, I’ve been in remission for about 7 years now, and I’ve only ever had relapse while not on treatmen, so I am glad to say my treatment (Ocrevus) is working! What is the longest you guys have been in remission? I do occasionally have fears of relapses but ...

Hello, my name is Phillip and I’m new here at this site. A 63 yo male and have been suffering from MS symptoms serious since the 80’s. I blew them off for years, then in 2004 the symptoms started to increase. The would hit all of the sudden and then disappear for a while. First it was muscle cramps...

Hello, Has anybody here changed from teaching career to something else? I've recently gone back full time as I can't afford to be part time but I am *struggling*. I'm tempted to try starting an online tutoring business but I'm nervous about the fluctuations in income and not having the same sala...

My Neuro report came back thankfully but has described some symptoms shortly after my last vaccination as ephaptic transmission in MS. It was a written report so unable to ask what that means? Any of my MS family heard of it? Thanks in advance 👍

https://www.independent.co.uk/news/health/ms-tyruko-tysabri-drug-side-effects-nhs-b2754395.html How widespread is this and is it only Tysabri and (from what I read on another site) possibly Tecfidera affected at the moment? I would hate to be pulled away from Kesimpta and onto a "simillar" drug wh...