Search and explore digital tools and resources for #multiplesclerosis. A @bournemouthuni project in prototyping. Lead: Keith Pretty @Keefinger #MS. Views own.
We are building a free search tool for digital tools and resources for #multiplesclerosis. We would like input from pwMS, MS carers and health care professionals. Please get involved https://t.co/gYOEh6DPKh
Twitter help!! I've been let down at the last minute and need an awesome Personal Assistant to help me live my life. 18 hours per week. The role isn't just about personal care, you will have a great time too. Please retweet or DM #weymouth#dorset#JobVacancy#help
Heard of https://t.co/kfmy1IFfpW? https://t.co/EBTIk10Rxg volunteer Casey & her colleagues took part in a project to visit attractions, bars, shops & restaurants in Edinburgh to verify accessibility & rate them on the Wheelmap app.
Over 350 places were verified - ace work 👌
The symptoms of #MS can all be part of other conditions, so it can be hard to reach a diagnosis quickly. In this video, Professor Coles explains more about why it can be tricky to diagnose, and what you can do if you suspect you have MS 👇
📽️ https://t.co/IJGO7DNM0l 📽️
Disappointed you missed the deadline to apply for for #MSsessions19?⏰🥺 We don't want you to miss out so...
🚨We've added more spaces to this years festival🚨 so we can bring together even more young people with MS from across Europe 🌍🤝
Apply now ➡️ https://t.co/wLjbxGdY2r
Hearing other experiences of #MultipleSclerosis can help you identify symptoms and manage your condition 👂 👀
Our series 'By MSers' features six people with MS sharing their experience of diagnosis, watch here 👉 https://t.co/DL2duqOuts
What's your MS diagnosis experience?
Looking forward to attending the Disability Benefits Consortium's report launch today in Parliament which shows the real impact welfare changes have had on disabled people like me a person living with #MultipleSclerosis@mssocietyuk#WelfareUnfair
@shiftms I explained MS to a friend once using the analogy of wiring and the insulation of a wire being removed. His response was okay you’ve got mice 😂
Awake, aching and buzzing. So tired. Will shut up about it shortly but so much #teamwork and ingenuity to get me round each obstacle. Started with ‘just’ my friends and upUgo colleagues. Then strangers, volunteers, everyone...
#toughmudder#msawareness#NoTwoTheSame
It's been a busy first day at MS Frontiers - here's Ben, part of our research communications team, showing you our #MSResearch timeline!
From the year 1433 (!) to the present day and what the future holds - there's lots to learn about!
Today is set to be a scorcher! The hot temperatures can affect #MS symptoms. We asked people living with MS for their top tips on staying cool. What's your top tip? #Heatwave
Here's our factsheet with information on coping with hot temperatures: https://t.co/Too5SsOSqu
@porgymonk It's their problem, not yours. Wave and smile or blow them a kiss. It works for me and sometimes they wave back. Mostly they are really confused, trying to work out how they know this drunk looking wobbly man 😊
#MultipleSclerosis#mswarrior#MyInvisibleMS#MSfighter#MS
It's #FathersDay and we want to celebrate all the amazing dads out there!
Tim is one of them! In this video, he talks about juggling MS with being a dad to his daughter Hannah 💙
https://t.co/BwG57qaiJc