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Morning all! Just a wee reminder about our next virtual meet up, 11am Saturday 19th September for Brunch and a blether about life in general with fellow MSers, since we're still restricted to only meeting 5 households outdoors. Please pm your email address to myself or @watsoncraig for us to send...

Glad to be part of this new group - big hugs to everyone and I hope you’re safe 🙏🏻

Hope I can get some good tips for my ms helo

I am new to this group, but not to MS. I hope you are all staying safe and as well as you can be.

Hello Just wanted to ask the community for any feedback / experience. Redundant 14 months now. Just secured some freelance work 2 days per week, ongoing. In my industry and for a good company. Will not pay the bills but I am hoping it will lead to a full time job and will buy me more time from my...

Hello! I was just wondering if there’s anyone on here that’s started the treatment Tysabri? I’m currently on Copaxone and the neurologist wants me to move over to Tysabri soon. The reason I’m asking is because I’d planned on going travelling next year and am really hoping this new treatment isn’t go...

Nicked this link from a post over on the M S Society forums......................... https://www.youtube.com/watch?v=mlQ9AFjsVK8 Just watched this documentary and I can't believe I have not seen this before. Alright it was first made approx 4 years before MS came into my life but I think it is rea...

Hello All I was diagnosed with MS back in 2003 I’ve had my ups and down I’ve never been on any forums like this before so all new to me after pushing my doctor I’ve managed to have another MRI after 17 years to see how my MS has progressed and awaiting results next week @ 39 now I am worried to be h...

Hello There, Long time no speak. Or type in this case. I just wanted some advice on how to manage work and MS. I have really struggled the past couple of months with my MS and going back to work. I work in hospitality and have been lucky with furlough but also the place I work for has been super bu...

Hello you lovely lot. I was diagnosed with RRMS on July 24 over the phone and have my first phone appointment with my MS nurse next week. I’m not a huge fan of phone appointments - would be so much nicer to meet face to face - but covid means it’s all by phone. Anyway I want to make sure I make the ...