Hi all, thought I had it sussed this MS after 4 years and permanent symptoms left due to spinal lesson affecting arm and leg sensation. Lockdown has seriously challenged me and deconditioned me, body now reacting. How do you pick yourself up and dust yourself down and stay positive! New treatment ch...
So at the moment I am about 16 months post r2 of lemtrada, and my MRI was due in April, but it has now been postponed until ... further notice...
This gave me immense anxiety and I’ve been having panic attacks for over a month now. I don’t know how to deal with this because even though I appear st...
I was diagnosed with relapse remitting MS in around 2010, and have been very fortunate to only experience 1 relapse since this first attack. It may be coincidence, however since the initial diagnosis and subsequent treatment, I have been experiencing back pain which is worse in the morning. The pain...
Hi all I'm new to the group having only been told I have MS last Thursday although haven't been officially diagnosed but the MS consultant is pretty sure. Bit of a whirlwind following the news bit being as positive as I can. I have an appointment with my specialist nurse in a couple weeks where trea...
Hi everyone I have had RRMS for 15years and have been relatively well but getting worse recently I'm due to start my copaxone treatment with the first delivery Monday and a nurse coming after that but have now been told it wont be with auto injector and I thought it was supposed to be as my hands sh...
Hi
Has anyone had any news regarding DMT treatments in the UK now? My MS nurse is waiting to hear when they might be able to re-start, and I am on the list for the initial Ocrevus infusion - hoping this will be soon, of course..
Wishing you all well.