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Good afternoon MSers, Hope you are well and having a good week. I did my 3rd MS event last weekend and had a blast. It was amazing to have the same people attend the event. Event not meeting! This isn't business, it's leisure. 😄 3 MSers in The Multiple Sclerosis Club! 😉🥳 In this world if you w...

Good morning MSers, Hope you are well and had a good weekend. Also that your week is going well. I did my 2nd MS event last weekend and had a blast. It was amazing to meet yet another person like me and we had lots in common too. Cheers, new friend. 😁 Now that is 2 fellow MSers in The Multiple Sc...

Hello everyone—just wondering if anyone has any thoughts / tips. I was diagnosed with MS in 2005 and have been on various DMTs since 2012 under the care of a hospital in London (which I felt was good when I first went there). I feel very sorry for them but over the last few years the relevant unit s...

I’ve decided to do the London landmarks half marathon this year in aid of MS After being diagnosed nearly 5 years ago and running actually led to my diagnosis and after a time away from running I’ve slowly eased myself back into it and feel this is a little something I can do to give back so any spo...

Good morning MSers, Hope you are well and had a good weekend. I did my first MS event last weekend and had a blast. It was amazing to meet someone like me and we had lots in common too. Cheers, new friend. 😁 I want to host monthly events. An event does not mean we necessarily will do something...

Hi warriors!! Would love to meet and know more about all of you, to share my journey with ms and meet new people. Hope you are all well. Take care.

I was diagnosed in 1991. My diagnosis was extremely quick as my mother, who also has MS, asked her neurologist to see me. I had an MRI Scan and returned for the positive result. Mum drove me and came to the appointment. She asked me where I wanted to go. I chose to be dropped off at the pub where I ...

Hi MSers, Hope you are well. Happy Friday. Last call for the London meet up happening tomorrow. Anyone is welcomed even if you live outside London. We will be eating Thai food, as it is rich in omega3 food which is better for us :) in central London, near Bond Street (central line), please confi...

Hi all, If anyone is in London, would people be up for a meet up in end of Jan? Would love to meet people and hear everyone's experience and make each other laugh a bit too. There was a post with a funny story about the plane and it helped just laugh instead of always feeling quite down as we are ...

Hello MS warriors ;) Hope you are well. There will be a London meet up on the 28th Jan 2023! Please join me and fellow MSers which will be coming from the original post https://shift.ms/@Yorete/london-meet-up-WHF0XpjxF1DW3V4va21hhttps://shift.ms/@Yorete/london-meet-up-WHF0XpjxF1DW3V4va21h Thi...

I was diagnosed with spms in 2021,still trying to get use to dealing with life with m.s. 😊

Hello, I’m new here. I joined so I could ask whether anyone with SPMS has found a good neurologist in London? I go to the National at Queen Square and my neurologist there turned nasty when I asked too many questions. Thanks in advance

Hi there, I have been receiving infusions at King's College Hospital for the past 2,5 years and I had been - until recently - followed by my MS nurse at St Thomas' hospital. I found out few weeks ago as I tried to email my MS nurse that she was not working in the MS service anymore as I received a...

Just need to try weed again, my pain is overwhelming and I honestly can’t take anymore but would prefer not to go broke either

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‍‍Did you know we're a charity? It costs around £36 for us to reach someone newly diagnosed with MS, this means that every £360 raised will help us reach another 10 newly diagnosed MSers across the world. We have two places left in the Big Half which takes place on 4th September. If you're interest...

Hi all, I am quite sure due to my symptoms that I am likely to have MS (or something like it) and just want confirmation. As none of my symptoms are too bad I can't get an urgent NHS neurologist appointment and therefore have been allocated one in Jan 2023! Obviously want a diagnosis by then. Just ...

Hello all, I’d like to change my hospital and appreciate recommendations Thanks Sarah

I'm currently seeing a doctor at National Hospital for Neurology and Neurosurgery in London but they're always very busy to see their patients(I mean I'm having this dizziness feeling and I wanted to see a doctor but they recommend me to see my GP first). This is not the way I'd like to be treated, ...

I have had a pretty rough time the last few months/year or so not only with relapses but pretty much a lack of support from them. Having had a friend over who has ms too at the weekend was told my care team should be doing a lot more for me especially if i think i had a relapse. so far there was bee...