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Hi there im just wanting some advice and help really. In a nut shell I am 25 years old and had this illness since just shy of my 16th birthday (great gift that was) anyway last year after my birthday i suffered a miscarried (first time pregnant as well) and that sent me down a dark dark hole anyway ...

I’m struggling at the moment. As we went into lockdown, my partner of 11 years decided to tell me he effing hates living with me and dumped me, the same week as I had to have my 19 year old dog put to sleep. He knew from the outset of the relationship that I had ms and it is a degenerative disease...

Hello Shifters, I will performing some standup comedy "live" over the internet, as per the New Normal. Starts tonight at 8:20 (20:20 - get it? Cause it's the year? see what they did there? ) FB: https://www.facebook.com/events/306540333735425/ YT: https://www.youtube.com/watch?v=7RsMJtmmqOI Tha...

Facemasks are not for me, they are for YOU should be the new slogan

Just back from infusion #5 of tysabri and doesn’t seem to be making any difference at all...... Still original symptoms and new symptoms Anyone In same boat...? Also whilst I’m on, anyone got recommendations on CPD vapes?

Hi! I’m Aimee and I’m new to Shift.ms, I’ve just joined the team as the Community Intern. I’m here to listen to your stories and hopefully share some of them through various media across the site. If you’re up for a chat, please feel free to drop me a message- it would be great to get to know you ...

Hello I've been recently diagnosed, I'm still getting my head round it, fed up with the chronic pain, I'm working mum with two kids. My MS Nurse is coming to see me next week. I feel like people that don't have MS don't really get it. If I say I'm tired they say oh I am too, erm it's not the same!!...

Hi I’m looking for some advice if poss.... I have been on copaxone for 10 years and the sight reactions are much worse which has made me seek alternative DMTs. I’ve chosen Tecfidera and got the green light so just waiting on starting. My issue is I work in public facing role for civil service and h...

Hi all, thought I had it sussed this MS after 4 years and permanent symptoms left due to spinal lesson affecting arm and leg sensation. Lockdown has seriously challenged me and deconditioned me, body now reacting. How do you pick yourself up and dust yourself down and stay positive! New treatment ch...

So I was diagnosed with MS in 2018 by a general neurologist after all the tests and on and off symptoms for years, I have 5 lesions on brain 1 on the spine, since then been with a MS specialist who did not want to put me on disease modifying drugs as he wanted to watch me further he believes it's M...