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Just back from infusion #5 of tysabri and doesn’t seem to be making any difference at all...... Still original symptoms and new symptoms Anyone In same boat...? Also whilst I’m on, anyone got recommendations on CPD vapes?

Hi everyone, even though I’ve had MS for over ten years I’m pretty new to the forum scene. I haven’t really spoke or sort advise on anything like this? I’m thinking of purchasing an electric wheelchair as my mobility over the last couple of years as become worse. Can anyone make any recommendations,...

Hi I’m looking for some advice if poss.... I have been on copaxone for 10 years and the sight reactions are much worse which has made me seek alternative DMTs. I’ve chosen Tecfidera and got the green light so just waiting on starting. My issue is I work in public facing role for civil service and h...

I’ve had to come off Gilenya because it caused me to have deranged LFTs and since being off it I’ve had a a new lesion form on my spine. I just don’t know whether to start Tysabri or Mavenclad. I don’t know if I want to have to get infusions every month but I could go straight back to work once I st...

Hi all, I’m looking for some inspiration - I think I need to change career to something that’s more suited to a slower pace of life and a bit less demanding (I’m a digital product manager - which is kind of like a project manager, quite fast paced and demanding). Has anyone retrained to do somethin...

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 I was diagnosed with MS in 2018 by a general neurologist after all the tests and on and off symptoms for years, I have 5 lesions on brain 1 on the spine, since then been with a MS specialist who did not want to put me on disease modifying drugs as he wanted to watch me further he believes it's M...

Hi! I’m Aimee and I’m new to Shift.ms, I’ve just joined the team as the Community Intern. I’m here to listen to your stories and hopefully share some of them through various media across the site. If you’re up for a chat, please feel free to drop me a message- it would be great to get to know you ...

Hi everyone, I'm currently planning on moving to Dublin, Ireland within the next 6 months and I'm starting to think about changing neurologists. I will obviously have to get a referral from my GP to see a neuro. I've been told that it can take up to 6 months to get an appointment!! Does anyone ha...

More of the type of research we can all support ;-) https://multiplesclerosisnewstoday.com/news-posts/2020/06/30/boosting-mitochondria-cellular-energy-at-myelin-loss-sites-may-stop-ms-progression/