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Hi all I’ve friends who don’t know I’ve MS and they want to go out to the city and walk around few different pubs and nightclub. I won’t be able for that. So I just can’t go. Anything similar happen to you? My close friends know but others don’t and I’m very private about it Thanks xx

I posted the other day about getting hot so apologies but I’m going out of my mind!!! Iv been getting ridiculously hot as well as having hot flashes around my head neck chest and back. It’s almost like my skin is burning, it feels like sun burn. Iv had tonnes of blood tests back and all normal (...

Hi all, the amazing Niamh is taking over our Youtube channel and sharing her tips on managing MS at music festivals - yes she is going out out to the Electric Picnic Festival in Ireland - follow her festival survival guide for MSers over the weekend over at our Youtube channel - also please get invo...

I went to a local gig today and I was thinking how different your priorities are when you have MS. Pre MS days all I bothered about was the price of the booze and that they had good tunes on the juke box. If them the drinks were cheap and there was rock or meal playing, then I was a happy chap. Now...

I signed up to a disabled dating site to find someone who'd understand me and was compatible with me. After one day i got a message from a girl who obviously liked my profile and wanted to meet up! This girl, Jade, was (and still is) perfect for me. She appreciates the same random music as me, h...

Good morning all. For those on Ocrevus, do you avoid social events or going out because of your reduced immune system and chances of picking things up more easily? Asking for my sister who is due to start it in a few weeks. I'm on Tysabri myself. Thanks for any advice you can give 😊

Hi Has anybody had any successful treatment for bladder weakness/urgency? I am on medication which has helped a little but not to the degree where I would feel confident going out walking without a toilet being nearby.

My self-employed, business of 14 years has gone down the drain since I became poorly with MS and I’ve been out of work for about a month and a half. I am literally going out of my head. I’ve worked since I was 16 years old and now I’m 42, so not working is a new and not very pleasant experience for ...

My favorite childhood poem oh how I wish I was just faking now! Shel Silverstein 1930 – 1999 "I cannot go to school today," Said little Peggy Ann McKay. "I have the measles and the mumps, A gash, a rash and purple bumps. My mouth is wet, my throat is dry, I'm going blind in my right eye. My tonsil...

Hi all, I was dx RRMS about 5 years ago and it was suggested I had probably had MS for 25 years based on clinical history. It was a big relapse needing hospitalisation that led to dx. MRI wise am relapse free since dx but the last 2 years have noticed a decline in pretty much everything and Neuro ha...