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I don't know if anyone else feels like this, but over the past couple of months I feel lethargic, down and very teary. It's like everything I do, I hit a brick wall and don't want to continue. I've had suicidal ideation, stopped only by the thought of the impact on my family and my partner. I've cri...

Hello everybody. I just found out about this forum and looking forward to connect and share our experience 🙂 I've been diagnosed a year ago and still learning on how to " collaborate" better with my new friend MS. I am based in Romania, Bucharest. I hope all of you are safe during this hard period!

Hi everyone, especially those with PPMS, I watched a video of Prof G via ms society & im sure one of his slides said progressive ms patients should shield. Is that correct? Colette

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...

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...

Hi there, Ive had MS (relapse and remittance) for 15 year now. I was just wondering whether anyone has heard of 'Soursop' or have tried the herbs/ drink. If so, How did you find it? The reason why I am asking is because I have heard from a number of people (people who don't know each other) that ...

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 ...

Hi Has anyone had any news regarding DMT treatments in the UK now? My MS nurse is waiting to hear when they might be able to re-start, and I am on the list for the initial Ocrevus infusion - hoping this will be soon, of course.. Wishing you all well.

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...

Well I'm back to see if anyone knows anything. I've had problems with movement disorder since 2018. - while it's being worse the past few days alongside my spasticity. The thing that confused me is it's like I've got this new tic disorder or maybe it's just worse i dont know. Basically in the pas...