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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 👋 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 ...

Good morning all hope all is well, I will like to know if anyone is struggling with mental health since they was Diagnosed with MS? I am asking because since I was diagnosed my mental health has been off so bad, maybe it is because I seem not to know how to except it fully especially when my little ...

This is my first time posting on here and I'm feeling quite depressed and scared about talking about it. I am 25, have been diagnosed with MS as of the 25th of March. I know its been less than a month since my diagnosis but I still can't come to terms with it. I can hardly say out loud that I have...

Hi, I have been having the Tysabri infusion since Feb 2020, and today just found out that I’m due to swap from having the 2-3hr infusion (monthly) to the subcutaneous Tysabri jab (monthly) in its place….. plus side is it’s a lot quicker and for the first 6 months I just need to be monitored for a...

Morning all, Been together 11 years and have had MS since we met. She now wants a separation that has come completely out of the blue foe me. Can anyone relate to this?