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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/

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

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...

Hey guys going on your 36 hours without sleep I only sleep about 20 to 30 minutes at a time when I can sleep usually maybe four hours every other day I work out when my body will let me try to eat right but still no sleep anyone have some advice?

Hi there! Is anyone else struggling with your relationships after the diagnosis? I personally feel that Ms changed me a lot and my wife seems to miss the person I was… and that I will never be again. Also, sometimes I feel “flat” like my emotions are not fully out, I think Ms changed that too. Very...

Hey 👋 Welcome to the Shift.ms community! Drop a comment below and let us know where you're from 👇 Whether you've got MS questions, you're seeking advice, or you just want to chat to other MSers, we've got you covered 💚 Take a minute to hear Sarah's MS story and learn how she gets the most out ...

Does anyone else suffer from excessive dry mouth at all?. I have read some articles saying that this is not an MS symptom but, I don't recall ever experiencing it this bad before. I drink plenty of water during the day so it's not a dehydration issue.

I have been in a relationship with my partner for 9 years, we were together for about 1.5 years when the MS hit bad, he stuck through it, not without upset, but here we are 9 years later, when we get into arguments it always reverts back to “I stuck with you through your illness” which I take on bo...