Imagine a terrifying rollercoaster ride that slowly paralyses you. Every turn brings you closer to death and you're forced to ride it. There's no cure for motor neurone disease #MND. We want to change that. Visit takeovermnd.org to find out how and help us #TakeOverMND.

Join us for our monthly social today at The Woodcote, Hooton. 2-4pm.

Great turnout this afternoon for our monthly social! MND Association

"We're all going to die, right... It's just happening that bit quicker for me." Joe Hammond has motor neurone disease and has decided to write his two young sons birthday cards for every year until they turn 21. #5News | Claudia-Liza Vanderpuije | MND Association | @theenditwasokay

Always enjoy hearing from Debbie at MNDA Wirral Group on the work they do there. Debbie’s a brilliant campaigner, and always pushes local services there to improve and build on #MND Care. Great to hear their social group is growing in strength.

It's officially #ChocolateWeek and we want to give a shout out to Amelia, who earlier in the year, gave up chocolare for a month to raise money for the Association 💙 who else fancies the challenge? #TeamMND #MondayMotivation x.com/mndassoc/statu…

Will you contact your MP today and help ensure all people with MND can use the Special Rules process so they can access their benefits quickly and sensitively? Find out how: bit.ly/S6Msocialmedia - you can also add a picture or video to share your personal message about MND.

Today marks 1 month until the 2nd reading of the Access to Welfare (Terminal Illness Definition) Bill. Please get in touch with your MP as soon as possible and ask them to support the #Scrap6Months campaign! Email them here: bit.ly/S6Mdropinevent

The Disability Benefits Consortium (DBC) has launched a #UniversalCredit survey so that we can find out more about the experiences of disabled people and people with long term health conditions. Take the survey here: surveys.parkinsons.org.uk/s/DBCBigBenefi… #UCandMe

"You can lay down and die, or you can stand up and fight" Glenn was diagnosed with #MND a few days before his 45th birthday. Since then, he's ran the #LondonMarathon and plans to do so again in April. You can run for #TeamMND 🥇 visit bit.ly/FundraiseTakeO… to start!

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Please watch and share Jack and Rose’s story to show why the #Scrap6Months campaign is so important for people with #MND and other terminal conditions. Join 11,000 others, and sign the petition here: bit.ly/S6Mpetition

This incredible woman was still going to raves four months after being diagnosed with motor neurone disease liverpoolecho.co.uk/news/liverpool…

I know Debbie works really hard with the group to build local connections, the list of wins she’s made with health folks in Wirral and much more is to be admired. As the MND Association - Manchester & District Branch branch chair, I give her and MNDA Wirral Group huge credit for their hard work as volunteers.