MS Digital Tools

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 msdigitaltools.com/get-involved.p…

@Brandon_Beaber @YvetteBrisco @RealTalkMS_jon @tkilgour11 @lomelindi12 @spicyjulesc @MarinaC_Dyb @Tessa_Daye @CathyChes @TheLoreOfHiking Yes please. A PDF would be fine. Thanks

I am going to publish my book about psychological resilience in multiple sclerosis fairly soon. If anyone here would like a free advance review e-book copy, please let me know, and I would be happy to give you one once I have it available.

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 wheelmap.org? Shift.ms 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 👇 📽️ ow.ly/33SZ50v9eM2 📽️

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 ➡️ mssessions.com

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 👉 buff.ly/2lwRTzv 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

Who knew our @bournemouthuni VC @VCJohnVinney and COO @JimAndrews_BU could make such great coffee baristas, supporting @BmthFoodbank with the help of @BUeatanddrink #BUProud #leadingbyexample #Bournemouthfoodbank #ChangingTheNarrative #kindness

It's so easy to miss important things to bring up with your #multiplesclerosis clinician and this can help you prepare for your next #MS appointment.

@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 😂

Great job Mark 👍

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: mssoc.uk/2J51PrZ

@TEasterbrook98 @POWFS Absolutely fantastic news Tom. We all wish you well in the next stage of your personal journey 👍

I'm delighted to say I have agreed to take up a post @POWFS working with the governor's. I'm thrilled to be back supporting a place which gave me & my family great support in the early days of my journey. Can't wait to get stuck in and do my part to support the next generation.

Are you Relapsing? Time to Slow Down, Eat Right and Enjoy Life! buff.ly/2CSWUW2 #livebetter #MultipleSclerosis

@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

is it take the mickey out of cripple day at least 3 car drivers laughing at me while trying to walk. I am glad they are happy and healthy #MS

This is to our brave #MSWarriors who are great father despite the difficulties that come with 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 💙 ow.ly/1FSh50uDiDJ