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something specific?

Anyone on here over 65ish and still receiving treatment (DMT’s) or had treatment stopped due to age? I’ve been informed that progression/new symptoms tend to decrease after your mid/late 60’s and that can affect what treatment is available/offered.

The media announced yesterday that the junior doctors and the consultants will strike on Monday 2nd October here in the UK. My infusion date is the same date 😢. I guess I’ll get cancelled, unless the strike is called off because needs are met. Does anyone know what happens if they are cancelled. Ho...

I got officially diagnosed on my 27th birthday last month.. anyone of a similar age from the UK on here that is interested in forming a friendship? I don't have any social media so I feel so alone, and as much as this app has helped me realise I'm really not alone - I still feel it as I haven't had ...

Hi all. Been keen to meet up with similar folk with similar symptoms in my area (West Sussex). Lots of the sites and groups just look so old fashioned or staid and this one just had a bit more buzz. Bit nervous about joining a group full of very different people to me but would love to share a beer,...

Hi I'm based in the UK and have been on a long waiting list to see a neurologist, I'm due to see them in January but as I have extreme fatigue and can sleep anywhere at anytime I've been referred to a sleep clinic also, the sleep clinic's appointment came and it's under neurology as this is in Novem...

Hello All, I work at Manchester Airport UK and have recently joined the Neuro Dissability forum. I am looking for any stories (good or bad) travelling through an airport with MS, any advice/tips you find would be useful for anyone else travelling 😊 Many Thanks

recently saw this after participating in a similar type of study...would love to hear any thoughts and wished to share. shorturl.at/LPWX5

Afternoon all. I have RRMS and live in the UK. Does anyone have any travel insurance provider recommendations?

to train Soldiers. Now I am here. No MS Worries, it is A freaking war 20km away. Daily a nightly shelling. So why worry over MS. 🤪

I thought I’d post something, that when I was originally diagnosed, would have definitely helped me dealing with the whole sh*t show that is life with MS, and how to at least make it at least a little bit easier. Don’t get me wrong I’m no MS suffering martin lewis (the irony been by nature Im very...