Being told that no matter how much you exercise and what you do. Nothing will improve and its gonna slowly get worse and worse is very disheartenin, ain't it

Before my MS diagnosis, I thought I knew myself. I thought I understood what strength meant, what it meant to be brave, and how much I could handle. But life with Multiple Sclerosis has taught me things about myself I probably would never have discovered otherwise. I’ve learnt that I’m stronger than...

Hi, i am loosing my mind!! I emailed my ms team two weeks ago with no reply!! I feel i am having a relapse since my flu jab with new symptoms… i honestly don’t know what to do 😔

I got the cutest picture of my little finch Doris sitting on her treat today and my other two finches, Victoria and Tweety, posing for the camera. 😹

Having MS doesn’t give any of us a free pass to be horrible to everyone. Life is hard enough without spreading bitterness around. I’ve been very fortunate to speak to so many talented MSers—a lawyer, a nurse, a chemist, and people from all walks of life. Some have fewer physical limitations; others...

My consultant has written ahead of us meeting in November to suggest me being prescribed new MS medication Fampridine. Has anyone else had it/been offered it?

Hi folks. Do you deal with a dizzy feeling specifically when you move your head too far back or too fast from side to side and up / down? I’ve had some disabling dizziness and vertigo in the past and it’s acting up after a few years off. I’m looking for strategies others have used to lessen the p...

Hi all, I’m in England (I know other countries it seems to work a little differently, that’s what I’ve picked up on this app anyway) I’m curious to know your thoughts. I received a letter today from my MS nurse that states my bloods were done in preparation for ‘potential treatment’ does this mean ...