Looking for
something specific?

Hello all, So I have been on Copaxone for 3 years. 1st year all good no relapse or new MRI lesions. Second year I got one new lesion but since it was also small my dr said let’s stay on Copaxone. Now my latest MRI showed one new lesion but at the same time I got lipoatrophy on my thigh from the Cop...

Hi everyone Can anyone recommend anything for the horrible itchy, crawly sensation. I have been dogged with them for days & they also stop me from sleeping. Would be grateful for any advise? Thanks

Hi there, I would like to ask, have anyone ever had eye twitching and sound in ear like water(not blocked just sound) and do you think it’s related with the MS? It lasts nearly a week and I’ve started to be really worried now as I’m thinking even if something else like stroke or I don’t know but ju...

Hello there, I've moved from London to Brighton in November, and at the time I decided to keep my neurologist in London, but now going back and fourth for MRIs etc isn't ideal. Does anyone have any experience of ms doctors/nurses in Brighton? Any recommendation? Cheers, g

Good afternoon everyone. My name is Rachel, a 33 year old mum to a very energetic 7 year old boy. I have very recently been diagnosed with MS and after having my first call with my hospitals MS specialist today they put me in touch with this very special and unique site. I am very new to this an...

MS I feel worse when it's wet weather

Hi. My name is Cara & I have had MS for 15 years. I started a company, The SwitchVR, 3 years ago. Our purpose is to develop holistic therapeutics (i.e. meditation, mindfulness, Qigong) using technology so that we can offer complementary practices for MS patients, like myself. Our first product i...

Hello, have you been able to check out the new shift ms site? it's pretty nice.

Hey Peeps. Spoke to the consultant yesterday, my yearly follow-up which went ok apart from mentioning about armpit, arm and neck and shoulder pain. I was referred to the breast clinic in March which they checked me over and just said lumps were normal and having no history in the family was a good...

I tried to draw some sketches to describe how my MS felt to me and people thought I was depressed. I'm really not. I just wanted to show how badly the sickness gets sometimes. Soon after, I stopped drawing about the negative impact of my MS and started making a fairytale out story out of it. 💪🔥