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I'm struggling to keep my eyes open at some points

I have a really supportive husband. We've been together almost 20yrs and still in love, but MS is becoming a third wheel in our relationship, and I'm struggling to find support for either of us... I'd really appreciate advice from anyone else navigating this. We want to keep our relationship strong ...

I’m currently dealing with a difficult conflict with my mother, and I want to explain why. When I was 13, I had early symptoms of MS. They were noticeable, but they were missed. At that age, I didn’t insist on medical exams because I felt sorry for her and for her financial situation. And her priori...

Hey everyone. I've just been diagnosed with RRMS. I had one episode of optic neuritis in November 2025, which led to numerous scans and a lumbar puncture, with my diagnosis being given on 3rd July. I have one area of demyelination on my brain, and one on my spine - neither of which were accompanied ...

Hi, i just been diagnosed this month after a LP for the final results! I had tingling toes last November, when the whole adiagnosis process stated! I asked before, but didn’t get any answers! I am currently dealing with my legs being numb and tingling all the way up to my hips! I am not sure if the ...

everytime i have a good day i try and use every spoon possible because i don’t know the next time ill feel good. but when i overdo it im sore and in bed for the next 3 days. need help pacing myself

Hi, just wondering if anyone in the UK with SPMS has tried NMN? I’ve bought it but I’m afraid to start it after reading that it can cause Axon degeneration ( none of us need that 🙄)

MS is hard. Some days it asks more of us than we think we have to give. But look at you. You’re still here. You’re still fighting. You’re still finding reasons to smile, hope, and keep moving forward. Progress doesn’t always look like big milestones. Sometimes it’s simply getting through the day,...