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/

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...

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. ...

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 ...

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

I was diagnosed in Nov 2020 as having MS by two MS experts. Unfortunately, they never considered mold toxicity. About 3 months ago, at the advice of two functional medicine doctors, I finally was tested for mold toxicity and my numbers were off the charts. The recovery is slow, but I am making pr...

Hi, I posted before about meet ups or im also happy to chat as a group or whatever I'm in central South East London (SE1) I was diagnosed late 2022. all the info is in my bio, we don't have to chat about MS but its nice to connect with people nearby that have similar experiences in this MeSsy diseas...

Anyone on kesimpta bit of help needed I no when they give you the information packs it says possible infections we could get and I've come out with a cold sore I used to always get them and would never worry, but atfer I saw the ms nurse before I first started she made out if I get any infection I'm...

Hi everyone, I’m not sure if anyone has experienced this but I have a friend who has been experiencing some pretty intense neurological symptoms for the last couple of years and is currently dealing with what I would describe as a relapse. (He’s been told that he either has a brain tumour, MS or bra...