I can't seem to get back to a good place with my wife. I feel like shes turned into a flatmate and honestly, im scared im pushing her away. She keeps trying to give me (bad) advice and gets upset when i say im not going to try it. Or she thinks im making an excuse when i cant do something. Its exhau...

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 🙄)

Having mild infection signs and signs of hipothermia (temperature below 35). AI is driving me nuts with its: "you have to seek emergency services immediately" talk. What are your experiences with Sepsis/ infections? I'm still new to being immunosuppressed (Mavenclad Y1W15). How do you monitor yourse...

How do yall deal with this just soul deep exhaustion? I don’t have the option of taking off work … even when I can’t make it to the physical office I have to do Telehealth … so I’m really not able to rest … any tips? Tricks? 🧡🧡

'MS Hug' be renamed 'MS agonising pain not unlike being crushed to death by an invisible titanaboa'. That is all

does anyone one here get more answers from ChatGPT than their neurologist?

Hey, my MS team have referred me to start Sativex as nothing else has helped ease the spasms or muscle pain. Have you been on this? What’s your thoughts, did it help, did you have any side effects? It’s a new one for me so it would be great to hear your experiences. Thanks so much, Diagnosed 202...

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,...

Hi, I have been diagnosed with relapsing remitting MS. I often have static noise in my head. I also suffered trauma and it did seem to appear after that but it has remained. Just wondering if anyone else gets this with MS or if it is trauma related?

Past two weeks or so my feet feel like they are burning. It gets so much worse when I’m back home after working for 10 hours. This is a new symptom for me and I’ve recently switched to Briumvi from Ocrevus. I was on ocrevus since 2019 and I was very stable, some flaring of old symptoms but never a...