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13 years ago today I was officially diagnosed with MS. I acknowledge this day every year for two reasons. The first is so I can say a massive thank you to the friends and family who have been there since the beginning (or joined me on the way) in supporting me on my journey living with this disease....

I'm Camilo, diagnosed with MS in November 2023. On this journey of reconnecting with myself, learning day by day. Excited to join, share, and find support in this amazing network. Ready to hear your stories!

Any one from Ireland on this I'm Tipperary

I've been diagnosed since 2006 and been through 4 different drugs and currently on tysabri and thinning on switching over to ocrevus,any sugestions?? Would be really helpful

Recently diagnosed and just had my 3rd OCREVUS IV. Reaching out to see if anyone else experiences brain squeeze headaches and emotional outbursts, memory loss, ear tingling. Since my 3rd IV I've rapidly deteriorated

Hello warriors I am about to make my very first post about MS which is going to be pretty long as I have a very long story to rant about!😂 I just wanted to check how many people can see it. So please drop a ❤️ if you guys can see my post, and I'll share the tea with you all!! Best, Srushti

I am newly diagnosed with MS and single. My question is are you all still dating or do you keep this a secret? Is it the end of finding my “nurf gun partner?

Hey my fellow warriors, Just wondering if there are any other veterans out there going through this? I served 22 years as a British Army Medic, leaving in 2019. Would be great to connect 🙂