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- I know I keep going on about HSCT. - I know it’s not available or right for everybody with MS -I know you can get info from a variety of sources, including, some Nuero’s (who are dead against the treatment!?). - I know that sufferers are still being misguided by some of those that we’d rightly ass...

🎉 JOIN US FOR A FAMILY FUN DAY IN SUPPORT OF MS SOCIETY UK! 💜 📍 Niagara Leisure Centre, Sheffield (S6) 📅 Saturday 19th July 🕛 12pm – 5pm 👉 https://facebook.com/events/s/ms-society-uk-fundraising-day-/838459067943410/ We’re excited to invite you to a fantastic Family Fun Day packed with fun, f...

Hi I have not been to any events organised by the MS Society, but decided to attend this one on Saturday 20th September in Cambourne Cambridge. I was wondering whether anybody from here coming to this event too? Would be nice to meet other people there! :-) There's a brief event info: http://www.mss...

Hello my fellow MSers, I thought it would be useful to do a MS patient pack. You know my experience has been the NHS leaving me to die and then bully me. No one bullies me & Londrina! So check this out- Listen you are disabled, you have MS and depression lives with us please deny it BUT you are ...

This is hot off the press and has upset people in the medical profession, as well as UK PPMSers. There's already a campaign to contest this decision :- https://signup.mssociety.org.uk/page/30088/petition/1  

Has anyone else seen this video, of one of the top research neuros in the country, talking about using two common drugs (Metformin and Clemastine) to get your own body to rebuild your myelin and repair your nervous system? https://stopms.mssociety.org.uk/annual-lecture.html I asked my neuro (who wa...

Here's something I found on Twitter, I know exactly how he feels, I am made to feel like a fraud when I get out of my chair to walk a few paces. http://www.mssociety.org.uk/ms-support/community-blog/2015/06/misunderstandings

Hi all As if life wasn't already hard enough, here are some potentially very bad news on the range of DMTs available to some of us in the UK: https://www.mssociety.org.uk/ms-news/2017/12/nice-propose-restricting-future-ms-treatment-options?utm_source=Facebook&utm_medium=organic_post&utm_co...

Just wondered what kind of things people do for diet and fitness? I've always really hated the thought of exercising (bad memories of terrible sports lessons at school) and have never been to a gym or exercise class in my life (nor ever would. I'm not a joiner-in or group type person). I did once t...

Thanks to the MSSociety Scotland and The Daily Record I was able to tell my story today about PIP http://www.dailyrecord.co.uk/news/scottish-news/disabled-multiple-sclerosis-sufferer-who-7978372