Looking for
something specific?

Just joined and thought I’d say hi 👋 I was diagnosed with ms in April 2008 , after I had my eldest son. My relapse effected my eyes and my face and mouth where numb, I was given a course of intravenous steroids and that seemed to make a difference, but within 4 weeks I had another relapse that al...

Can this happen I lost so much weight it ridiculous first it was mouth ulcers got rid of them with zinc and vitamin c.hair loss, now weight loss l'm loosing muscle not fat scary. No ms nurse here seeing gp/ neurologist soon.

Hi, feeling fed up. I'm just about to move on to my 4th DMT in 5 years. So far I've done Tecfidera, Gilenya, Aubagio and now on to Ocrevus. Any positive stories anyone can throw at me would be gratefully received right now!

started one month ago and having some stomach/digestive issues. Posted list of side effects says this should pass in two weeks. Not my experience and asking others if they’ve experienced anything similar. thanks

Hi, I'm interested in knowing your experience on hair loss with Aubagio

2001 Optic neuritis. Go blind suddenly - and fortunately temporarily - in one eye. Ophthalmologist sends me to neurologist. The neurologist tells me in a jovial tone to say that I have had optic neuropathy to insurers - if I say optic neuritis they’d put me down as having MS. MRI done. No follow up...

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...

Just wondering what peoples experiences are on Aubagio, as a little scared. Copaxone caused a massive allergic reaction and I ended up in hospital, and tecfedira made me feel so ill. Been off meds a few years but need to get back on something. What was your experience on aubagio? Thank you xxx