Looking for
something specific?

You know that thing with MS where they tell you not to overdo chores ETC? Well I think I have over done it...BLAHHHH :o/

Does anyone follow/recommend any sort of special anti-inflammatory diet for those with MS? I'm pretty healthy don't drink, don't smoke and practice very low impact yoga. I just wondered if anyone on here swears by a specific diet. Thank you x #diet #workandplay #nystagmus #tremor #yoga

Anyone else get a dreaded brown envelope arrive on the doormat and think 'great another fight to face!' I think the endless reviews of Personal Independence Payment for those of us with MS is absolutely disgusting! I mean did I miss something? Or is there suddenly a cure for Multiple Sclerosis that ...

Hello fellow MSers Nice to meet you all. Newbie MSer here. I am usually nervous when joining group but I came across Shift MS by chance and appreciate I found a place where others have questions and worries that I also share. It's refreshing since those around me sympathise but don't understand. ...

My MS journey started in 1989 with what transpired to be optic neuritis. Living in London in a bachelor pad that resembled a scene from the movie Animal House after a major relapse and a dose of steroids life went on. Yes rugby was a non starter but the chaos of a 20 year old continued at a ridiculo...

In anticipation of our brand new Women & MS video series (launching later in the autumn. Watch. This. Space), we’re taking the needs of female MSers directly to healthcare professionals next month at ECTRIMS, Europe’s biggest MS conference. We’ve already had an amazing response to two previous Wome...

Yesterday was my 12 month check up with Neurology. I was told she can’t decide if I have CIS or RMS but I’m being given information about my local MS nurses. So does this sound like I do have MS? Still in limbola d I think

I've been given an informal diagnosis of MS by my GP based on my recent MRI. He said I'd need to see a neurologist for a formal diagnosis and maybe more tests. I've had my letter through for my neurology appointment but its not until January. Safe to say I'm feeling down about it. 4 more months of s...

I’m still waiting on neurology appointment since February for a diagnosis of MS. Ended up back in hopsital all day today due to losing control of my bladder. Worst thing is it was at work and I don’t think I’ve her been so embarrassed. I didn’t realise I had wet myself until it was too late. I’m so ...

I want to hear everyone's little frustrations that come with life with MS. Laughter is the best medicine so I thought this would be therapeutic 😂 I'll start in the comments, add yours below! 👇