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Hey - anyone else feeling generally worse (more exhausted, more painful limbs, worse sleep etc.) during lockdown? All my normal day to day symptoms have kinda ramped it up over the past 12 weeks. Nothing new to make me thinks it’s new activity, just the same stuff but turned up... Love+solidarity ...

Hi all, hope everyone is doing well. I just have a question...I've had MS for a few years now, rapidly evolving severe, I've had 2 courses of lemtrada but after 1 year of my last course I had new activity so my neurologist put me on copaxone injections. I wasn't eligible for ocrevus as my immune sys...

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...

hey just went to the cafe and work to a get a coffee, and upon trying to pick it up with my right arm i was hit with almost unbearable muscle pain. this isn't one of my usual muscular gripes that we all face day to day, but rather feels like i've torn a bicep or something. super painful and now am ...

Hi All; I am new to the forum and i will be honest in that i have a problem speaking to my GPs due to neglect in the past which lost me my first born.. I have strong symptoms of MS and dared to mention it to 2 diferent GPs but was fobbed of,especially when i mentioned the heat intollerance; all i go...

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 ...

Hello, new to this site. However, I am a 37 year old female with PPMS.

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, 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...