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Hi everyone. I've had M.E. since 2001, but after new symptoms this year the GP thinks it could be M.S. instead after all. Sadly, the current waiting list here for non-emergency neurology appts is over a year (!), so it'll be June 2024 before I see anyone, but that's OK - I'm trying to be glad it's ...

Hi I’m not 100% diagnosed in fact im in the dark, I have suspected I may have ms for around 3-4yrs but put off seeking help things are just getting worse to the point my mobility is now being affected, I made a list of things bother me ie painful spasums weird vibrations and many other things and we...

👋🏼 Hello! I joined Shift.MS when it first began and was very small. I’d forgotten tbh 🫣but having come across the site on FB lately, decided to sign up again. How gobsmacked was I that I HADN’T been forgotten and was greeted with welcome back FoxyLady!🦊 I really would like a few suggestions abo...

Hello newbie here haven’t been fully diagnosed yet but I’ve had a mri and lumber puncher and it’s definitely looking like ms, I’ve got an appointment with a ms nurse in November. Everyone keeps asking me how do I feel about it, I’m happy that I’ve got answers after my doctors wasn’t listening to me...

Casually browsing through the app when I kept thinking... 'where on earth do these people live', 'I've never heard of Mavenclad, Cladribine or Gilenya, Fingolimod' 😅 only after reading an article that I realised it's not really fancy places they live, but DMTs they are on 🤦🏻‍♀️🤷🏼‍♀️🤣 #BrainFo...

Just thought I'd introduce myself, I've not been officially diagnosed yet, the UK NHS has a long waiting period to see a neurologist but as the symptoms I currently have and more keep popping up MS is being looked at as what is happening. I got niggling brain freeze type chronic headache, followed b...

Hi newbie here from Norfolk UK. Finding everything a little overwhelming right now but would love to know if there's groups that meet up or anyone not far from me.

Hi all! I'm a 33yr old Mom of two who was diagnosed with rrms almost 4 yrs ago now. I've been through and am allergic to serval medications. In reality I haven't been on anything solid for almost 2years. I'm starting Mavenclad before the end of this month. Wish me luck.

Hi all! I'm a 33yr old Mom of two who was diagnosed with rrms almost 4 yrs ago now. I've been through and am allergic to serval medications. In reality I haven't been on anything solid for almost 2years. I'm starting Mavenclad before the end of this month. Wish me luck.

Just joined up and read about 30 posts! It’s great to hear both sides of the coin. I can relate to a lot of things that has been written. I’m a newbie with relapse remitting and going through my first relapse and it’s scary as hell! BUTTTTTT I will not let this beat me. Ms nurse and consultant are l...