Looking for
something specific?

...about MS. - This is v short notice for this afternoon - Wed 2nd September. I was only asked last night. - It turns out my GP is also the director of this program - https://www.ox.ac.uk/admissions/undergraduate/courses-listing/medicine-accelerated - and I have been roped into giving a last-minute...

I am Patrick and I am badly disabled by Multiple Sclerosis to the extent that my balance is atrocious and must use a walking frame. I threw my walking sticks away a few years ago, they were no good. Instead I use a walking frame because it’s better at keeping me upright with my feet on the ground. ...

Has anyone never had a days rest?. Always something with my MS spasms pain bladder optic nerve inflammation in the nerve so on so forth never-ending since I was diagnosed I was wondering is this common with MS

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...

Hi im new to all this, i got diagnosed with MS last year and have just tried my best to carry on. I have had many of the symptoms for years and a rather big relapse but didn't seem understood back then lots of different tests. In the end just carried on dealing with it all, then i got optic neuritis...

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

So I was at my Neurologist and her assistant stated to me that I should be a lot worse than what I am! My neurologist agreed.. so this of course got me thinking of the future. I have decided that I do not want to get bad, I know some people r and are happy and that’s their choice and right. I have t...

I have recently developed neuropathy across both soles of my feet (before, it was more localised). I havent notified my doctor or the DVLA as it's fairly mild but I am attracted to doorframes more frequently. I have slow burn SPMS. I'm not sure whether to keep this to myself or do the honourable thi...

Still in the throes of diagnosis. I was prescribed Baclofen for my left leg but reacted badly including losing all balance and having double vision. Then moved to Gabapentin. My left leg has now swollen and I cannot wear my trousers let alone shoes... What next? Your experience please…