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Hi I’ve been on Tecfidera for about 6 months after moving from Beta interferon injections once a week for the last 9 years, at the beginning of my journey I weighed around 60 kilos which I know at 5 ft is a little on the heavy side, but I find myself now weighing 48.4 :(, with the onset of Covid 1...

Hi all I'm new to the group having only been told I have MS last Thursday although haven't been officially diagnosed but the MS consultant is pretty sure. Bit of a whirlwind following the news bit being as positive as I can. I have an appointment with my specialist nurse in a couple weeks where trea...

Years ago I needed to change my life completely! Why? That was not my choice but my health conditions. I was diagnosed with MS and it felt heavy to carry with me. After 17 years living with MS I feel that there is something more I can do. I`m thinking of creating MS mom needs serving, supportive, a...

Two musicians with MS One in Texas and the other in New York have made something amazing over the last year and a half and never even met in person. This conceptual album is about to change the game. Not only the music but most of the animation and artwork were done by the two musicians with #multip...

Hello everyone, a thought came to me in the dead of last night. Has a diagnosis of MS dramatically affected anyone's car insurance? I presume it has to be declared? Weak legs and twitching eyes are one thing, but if this affects my pocket as well I'll be very unhappy. My car insurance is currently c...

Years ago I needed to change my life completely. Why? That was not my choice but my health conditions. I was diagnosed with MS and it felt heavy to carry with me. I was afraid to dream about the future or even live a day with love, care, and understanding to myself. I felt guilty when I wanted to ...

Hey guys! I hope everyone is enjoying their summer as much as they can. So I always go on a binge search of any documentaries, movies or shows that deal with MS. I would love some recommendations! Only ones I have seen: - Living proof (documentary) - 100 Meters (Netflix movie) so good!

Hi community, Does anyone have experience of neutropenia after Lemtrada? Horrid to have to deal with extra things on top of the MS. If anyone has I would love to hear if it’s reoccurred/needed treatment or went away naturally. Thanks, Sal

https://www.youtube.com/watch?v=ySih1Ef64lU&list=PLVUOB-ZqvZOHIdZD3nrpGPgoSqrOyxoat&index=1 In our new series ‘MS, my Baby and Me’, our MS Reporters are on a mission - to start a conversation about the postpartum period & MS Woman feeding babyBaby In Ep 1, Carla, Rosie & Grace talk surprises, chall...

Are you taking Cladribine for your MS. Turns out it is pretty decent stuff! - Another example of why we need everyone with MS to sign up to the UK MS Register. - https://ukmsregister.org/ - "Over half of MS patients analysed did not relapse or experience disability progression during 60 months of f...