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Two musicians with MS One in Texas and the other in New York have made something amazing over the last year and a half and never even met in person. This conceptual album is about to change the game. Not only the music but most of the animation and artwork were done by the two musicians with #multip...

Hello everybody. I just found out about this forum and looking forward to connect and share our experience :) I've been diagnosed a year ago and still learning on how to " collaborate" better with my new friend MS. I hope all of you are safe during this hard period!

Hi , I was diagnosed last nov with MS . I have been on Copazone since jan but after a second relapse I was told it’s not working . I’m starting Tysabri on the 17th July . Just wondering if there’s many side effects . I’m still getting my head around the diagnosis. Sorry just another question , I’m ...

Hi all I'm new to the group having only been told I have MS last Thursday although haven't been officially diagnosed but the MS consultant is pretty sure. Bit of a whirlwind following the news bit being as positive as I can. I have an appointment with my specialist nurse in a couple weeks where trea...

I am wondering if anyone has seen either a geneticist or immunologist in the context of your MS. My brother is encouraging me to go, and he is also encouraging me to eat a keto diet. He doesn't quite articulate what he thinks these other doctors can do for me. My brother reads a lot of books about h...

I don't know if anyone else feels like this, but over the past couple of months I feel lethargic, down and very teary. It's like everything I do, I hit a brick wall and don't want to continue. I've had suicidal ideation, stopped only by the thought of the impact on my family and my partner. I've cri...

Hello everybody. I just found out about this forum and looking forward to connect and share our experience 🙂 I've been diagnosed a year ago and still learning on how to " collaborate" better with my new friend MS. I am based in Romania, Bucharest. I hope all of you are safe during this hard period!

Hi everyone, especially those with PPMS, I watched a video of Prof G via ms society & im sure one of his slides said progressive ms patients should shield. Is that correct? Colette

Hi I’ve been on Tecfidera for about 6 months after moving from Beta interferon injections once a week for the last 9 years, at the beginning of my journey I weighed around 60 kilos which I know at 5 ft is a little on the heavy side, but I find myself now weighing 48.4 :(, with the onset of Covid 1...

Hello everyone, a thought came to me in the dead of last night. Has a diagnosis of MS dramatically affected anyone's car insurance? I presume it has to be declared? Weak legs and twitching eyes are one thing, but if this affects my pocket as well I'll be very unhappy. My car insurance is currently c...