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Hi, - This is entirely without judgement and for UK MSers. It involves a few min of your time, no money ;) - I am interested to know who has ever been told about the UK MS Register? - https://ukmsregister.org/ (check this out as well if you like https://www.youtube.com/watch?v=s10osAwugO0&list...

Hi, first post. I was diagnosed almost 7 years ago, in 2013. Initially, I was diagnosed with PPMS, this was changed to RRMS a year later after a big relapse that made it difficult to speak and walk. Almost straight away, I was put on Baclofen and began 2 years of Tysabri. Eventually, I was able to w...

Hi, just thought I'd share my experience of my 1st half doze from earlier today in order that someone else may get some use from it. 1st half doze completed today in Glasgow. So far, so good. I got out about 330pm. I was given lots of advice by lots of people. Seems to have worked well. Few sweets, ...

Hi all, please queue up in an ordinarily fashion and please social distance when you come for my autograph hahahaha 😆 https://youtu.be/n3v_2Bl7fyk

Hi all, I am 22 and was diagnosed with rrms in July after an attack in May. I’ve just started a dmd. Still have some symptoms - fatigue, feeling faint and I overheat quickly. My managers know, but they just don’t get it. My job is so fast-paced and they still think I can do anything and everything...

Hey all, Hope everyone is doing we. I am hanging in there here. a bit run down today. Has been a busy few months and more recently in the last few weeks has gotten insane. Mostly all good things though so there is that at least. Firstly an up date on things with my son. Things are going so am...

Hi everyone For a while now I've thought about purchasing a bike in order to get in some decent exercise. I'm not great at walking long distances (due to my RRMS), so I was looking for another avenue. However, I'm on holiday at the moment and I thought I'd try out my mother-in-law's bike.... the re...

When losing your ability to walk is it possible to overcome that symptoms so you'd be able to walk as if nothing even happen or will it sorta be off (never) the same after getting that? Cause I can walk but not even for 30 mins but prior to having MS I used to walk on highways for my exercise now I ...

I’m returning to work next week after 4 months of furlough. My job entails some lifting of items up and down the stairs and since being off my mobility and strength has deteriorated somewhat. Any advice on how I can speak to my employer about these issues as a little worried about broaching this sub...

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...