Information about our next meeting. Please come along and join us! 🧡💙

The @Opti_cals clinical trial explores the impact of tailored nutrition of people with MND, aiming to boost quality of life and survival.

Currently seeking participants in the UK, learn more about this innovative intervention and how to get involved!
mndassociation.org/research/get-i…

We would like to say a big thank you to everybody that was involved. 🧡💙

Shoutout to the incredible #TeamMND who have dived into #Swim6kinMay !

Your dedication has already raised a staggering £100k for the MND community. Let's keep making waves 🏊

Did you watch BBC Breakfast this morning?

Thank you for highlighting how important psychological support is for people living with #MND .

Read the latest pioneering study here mndassoc.org/commend 💙

We have to be neutral when it comes to the football, but it’s great to see the MND Association and #MND gaining some awareness…

Liverpool FC 🤝 Everton

🎯 #PLDarts Luke Littler

A newly launched Irish language school has been named after a woman whose family were forced to fight to inscribe her headstone in Gaelic.

This month Coventry Irish Soc announced that their new Irish language school will be named after Mrs Keane.

irishpost.com/news/irish-lan…

2 years ago today we lost our friend and co-founder Chris Rimmer, yet his fight and determination is still at the heart of everything we do.

You are still inspiring us all. We all miss you mate ❤️

#attackmnd
#darbyrimmerMNDfoundation
#MNDresearch
#ChrisRimmer

Please go along and support, you're more than welcome to take your bakes to donate so they can sell them to make money for this much needed cause 🧡💙

You can also donate here:

justgiving.com/page/kimberley…

We are running a virtual peer-to-peer support programme for informal caregivers of individuals with #MND at risk of becoming or currently technology-dependent. Read more here rb.gy/scyv6s or email [email protected] #RCT #peersupport

My friends at the Motor Neurone Disease Merseyside branch are fundraising for Motor Neurone Disease Association. Check out their JustGiving page and please donate if you can. Thank you! #JustGiving justgiving.com/page/motor-neu…

Man embarks on B-road coast-to-coast challenge for MND charity bbc.in/43GS7VN

Denying access to ( #Tofersen ) a life-saving drug is beyond unforgivable. Imagine telling people with MND/ALS and those who’ve poured their hearts into its development and clinical trials that, despite its effectiveness, UK regulators NICE have halted its reach. It would

On 25 April, join us online for The Walton Centre #MND Special Interest Group's study day. Hear attendees will hear from a range of expert speakers, focusing on the care of people living with MND. Sign up for this free event at mnd.eventsair.com/the-walton-cen…

We will be live on BBC Breakfast at 8:45 am for the start of the March of the day walk, from Valley Parade, Bradford. DON'T MISS OUT

#MARCHOFTHEDAY ATTACKMND

(subject to anything overrunning)

This weekend the football community comes together to tackle #MND .

Led by Stephen Darby & Marcus Stewart both living with the disease, teams will walk from Bradford City AFC to Liverpool FC stopping at 17 grounds along the way.

Watch them set off live on BBC Breakfast just before 9 📺

Would you like to abseil down this magnificent building and raise money to support people living with MND? Please let us know! MNDA Merseyside

This decision by NICE is utterly wrong and is likely to deny a life-saving treatment for people with SOD1 #ALS #MND that is already approved in Europe and the US. A terrible, wrong-headed decision that must be changed.
Department of Health and Social Care MND Association My Name'5 Doddie Foundation MND Scotland

On this #InternationalWomensDay2024 we are so proud to share that Coventry Irish Soc are launching the ‘Margaret Keane Irish Language School’ what an amazing legacy for mum, the woman who raised us and made us!

Celebrating all women today 💚

We are hoping to speak with a few more friends/family members of people living with MND. If you provide any level of support to someone living with MND, we'd be very grateful for your input.