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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!

Hi all, I'm new to Shift MS, nice to meet you all. I got diagnosed over a year ago, but haven't talked to anyone else with MS before, so just looking to say hi and catch up with someone who might be having a similar experience. How do people deal with day to day stuff? My most annoying thing is work...

Hi! I<code>m not usually the one to write and ask, but there come moments like this when it</code>s just a natural action. So to the point...I understand your questions, life challenges, your ups, and down days. I`m an MS mom and have the disease for 17 years now. So the first time I met MS as a dia...

Hello Lovely People.... I have RRMS, late diagnosis at 55, after 20 years of misdiagnosis. I’m on Tecfidera. I am experiencing more and disabling issues. I have to use walking sticks and by the end of the day, a mobility scooter. I have extreme pain in both feet, some evening spasms and string elect...