Just bought tickets for Womad Glasgow in July. My life has become very insular since my diagnosis in 3023 so I made a spur of the moment decision and bought the tickets so I'll heading to a festival in July 😊. Fortunately it's not a camping festival so there'll be a nice apartment to return to at ...

Not sure if I'm looking for support, commiseration or advice. I was told during my first trimester of pregnancy that I most likely had MS but wasn't formally diagnosed until after my daughter was born in Aug of 2025. After battling insurance for months to get started on treatment, pretty much any e...

Sometimes it’s just the little things in life that make you really grateful. I have only recently been diagnosed and have had a flare of symptoms since the end of December. I would say this is the first day since then that I have felt a bit more like my old self again. I didn’t realise how much ...

Hey i been finding trips out more difficult. Like my ankles feet,legs,stiff and hurt having to think, being slower at places and difficulty with steps. Im 37. I try my best to stay active. Its difficult when in crowds as people just rush or try push past me. Alsocfinding trains hard to deal with as ...

My neurologist has said my options are very open in terms of treatment at the moment because I’m 26 but he has said he would prefer me to start with the higher full on options KESIMPTA or OCREVUS. I’ve seen a lot of people mentioning things to go alongside this treatment in terms of vitamins etc bu...

Where is the best country to live with MS in terms of daily living and climate?

Hi. I have recently been diagnosed with RRMS and will be taking Tysabri after finding a new doctor and making a mutual decision together for the best treatment option. Since I am scheduled to take my first dose of Tysabri next week, I am not sure of what to expect since this will be my first DMT. Ar...

Hello, everyone, question. Well, let me start by saying I use to drink and I stopped as well as smoking weed, stopped. But, I am having difficulty time with cigarettes. 😔 my questions is, does anyone else have this issue?

So I am approaching 10 year anniversary of having MS this month and the last few weeks I have been hit with a wave of grief - how do you explain this feeling to your friends and family? In many ways it seems like it's been so long I really should be "over it" by now...is anyone else in the same boat...