I've recently been talking to someone at work who's newly diagnosed. He remarked about the support he's getting from other MSers
Going to test an @ and # by saying @Sclerobro#ocrelizumab
Hello there.
I have just joined the group as I have MS. I was diagnosed in 1994 and it's been a rollercoaster journey since. I'm feeling a bit miserable at the moment as my memory has gone on a go slow. I thought that things would improve when the heat reduced but I'm so forgetful. I went to an opt...
Hi I'm new to this group, I was diagnosed June 2020. My first symptoms started 2hrs ago as Carmel tunnel syndrone. My right arm would go numb for a few minutes and I would shake it off. January 2020 I went to ER with symptoms of right sides numbness and when I bend my forward I feel an electric ting...
Hi!
Recently just officially joined the MS gang and thought I would say hello. I have been looking around on the site and it looks really great and it's pretty awesome that something like this exists and is so accessible for people that have MS.
I went from thinking I had Transverse Myelitis w...
I was dx (RRMS) over the phone on July 24th, a year after the symptoms which led to initial referral by GP to Neurology. Consultant said he was 'anxious to start treatment'. I was given two weeks to decide between Aubagio and Tecfidera. Told if I chose not to have treatment I'd be discharged back in...
I was dx (RRMS) over the phone on July 24th, a year after the symptoms which led to initial referral by GP to Neurology. Consultant said he was 'anxious to start treatment'. I was given two weeks to decide between Aubagio and Tecfidera. Told if I chose not to have treatment I'd be discharged back in...
I was dx (RRMS) over the phone on July 24th, a year after the symptoms which led to initial referral by GP to Neurology. Consultant said he was 'anxious to start treatment'. I was given two weeks to decide between Aubagio and Tecfidera. Told if I chose not to have treatment I'd be discharged back in...
Looking for some advice please. Before I was diagnosed with MS I smoked for almost 10 years. I did stop about a year before I was diagnosed and was using a vape which I stopped using after diagnosis.
My question is most of the people I live with still vape and regularly do so indoors. Could this s...