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Hi, I have rrms, diagnosed in 2010, symptoms since 2007. I started copaxone in 2018, had MRI new lesions. So started tecfidera in February this year. I just wondered as i have not been on dmds for 8 years after being diagnosed. Whether the dmds would be less effective going forward, I know t...

Hi i am new to this site i am 53 and was diagnosed with RR ms when i was 19 only got told about this site recently nice to find people in the same situation and now what its like hope everyone is fine and safe at this unsure time. I am at the moment ok just sat waiting like some of you to start new ...

Hi all, I've was diagnosed almost 10 years ago now and was just wondering how do you know once you've gone to SPMS/PPMS? Sorry if this sounds a silly question.

Hi all, what’s the lowdown on stairlifts? Is the consensus to get one? I am very fortunate to have enough rooms in my house to make a bedroom downstairs & we are having our large utility/ cloakroom converted into a wetroom. I’m undecided whether to get a stairlift as well to prolong my sleeping ...

Sorry long post!! Finally got a diagnosis in March this year. Been a long haul from 2013. In the last 4 days I've had excruciating pain in my face and a banging headache. Back in 2013 it was optic neuritis I was diagnosed with but I ended up with more symptoms and everything got worse over the years...

Hello everyone, hope you are all well.......... It looks like I am/ have been starting to relapse. For a few weeks now my legs are heavy and numb and I am waking up in the morning needing almost 30 minutes to get my legs moving before I can get out of bed. My vision is going hazy throughout the day...

Hello everyone, as the title suggests I'm new here. Although, I've been lurking for some time. I got diagnosed with MS last week after a lot of barking up the wrong tree. I'm a Police Officer and in 2016 I decided to apply to transfer to firearms. The fitness test is a bit harder for this but didn't...

Daniel & Kevin are live on the Shift.ms Facebook page talking about diagnosis, MS and relationships. Tune in and ask them your questions here: https://www.facebook.com/shift.ms/videos/969374456852750/?v=969374456852750&notif_id=1590677836563640&notif_t=live_video

Long story..had mri Feb 2 non specific liasions on my brain and 2 non specific liasions on spine. My left leg and foot numb since Jan. My right leg and foot and my right toes numb last 4 weeks..so my mobilty gradually deteriorating last 14months..dreadful burning night pain in legs and feet burning ...

Can anyone tell me if Tysabri infusions are free I have been recently been diagnosed with RR MS and will be starting this infusion soon. Are they free if you only have private health insurance 😊