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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...

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!

I'm newly diagnosed with RRMS. I'm rather young and frightened... can anyone give me advice and support? Thanks

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...

Hi, I was just thinking they say rrms progresses to spms. And it usually is 10 to 15 years after being diagnosed. I would like to know other peoples experiences, if they would like to share. I have been diagnosed since 2010 with rrms, but had symptoms since 2007. Main symptoms numbness from wais...

Years ago I needed to change my life completely. Why? That was not my choice but my health conditions. I was diagnosed with MS and it felt heavy to carry with me. I was afraid to dream about the future or even live a day with love, care, and understanding to myself. I felt guilty when I wanted to ...

Well I'm back to see if anyone knows anything. I've had problems with movement disorder since 2018. - while it's being worse the past few days alongside my spasticity. The thing that confused me is it's like I've got this new tic disorder or maybe it's just worse i dont know. Basically in the pas...

During the lockdown I've been binge watching House. They mention MS as a possible diagnosis every other episode, but I'm half way through season 5 and I still haven't seen an actual case... I feel discriminated!