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!
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 🙂
Hello Warriors,
Someone here is currently seeing( or saw) the Netflix show called “apple cider vinegar”. What it’s your thoughts?
Here is mine (without spoilers): food, supplements and sports, as meditation and whatever make you feel calm it’s very important in any disease journey…BUT…. Take the ...
I know that the world can be a not so safe space for us, and how difficult it can be to suffer in silence. When I was diagnosed, the shame and guilt and fear and unkown crippled me for months. Navigating the emotions and experiences was a challenge like I have never experienced before. Combine that ...