'You'll never walk alone' Special messages from Jurgen Klopp, Alan Shearer and more for Stephen Darby and Marcus Stewart, who are both living with MND, as they begin a walk of over 175 miles called #MarchofTheDay with the football community bbc.co.uk/sport/av/footb…

What a wholesome day yesterday was! A look back at #MarchOfTheDay in aid of Darby Rimmer MND Foundation ❤️ Hear how Jamie Raynor is feeling right now by tuning in to coverage of Harrogate Town vs Bradford City on all our frequencies! 👀 #BCAFC | #BBCFootball | #AttackMND

Joining March of the Day on the Bolton to Bury leg of the walk - raising awareness and money for Darby Rimmer MND Foundation to help in the fight against MND ✊🏻🚶‍♀️#MarchoftheDay #attackMND

3.5 hours in and still smiling ❤️✊🏻 Darby Rimmer MND Foundation #attackMND #MarchOfTheDay

What an incredible weekend, the support has been outstanding and all the walkers are the superstars of the weekend. Stephen, Marcus and all the team associated with Darby Rimmer MND Foundation cannot thank you all enough THANK YOU 😁 #MARCHOFTHEDAY #ATTACKMND #PROUD

'We're really fortunate to have a good support network but many families don't have that' Steph Houghton, whose husband Stephen Darby is living with MND, spoke to #BBCBreakfast after hundreds of people completed a 3 day 178 mile walk to raise awareness bbc.co.uk/news/uk-englan…

Cheering crowds greeted former Liverpool player Stephen Darby at the end of a 178-mile trek to raise money for research into MND and support those living with it. Darby, forced to retire after his diagnosis in 2018, led #MarchOfTheDay to Anfield after passing 17 grounds en route.

Absolutely thrilled to hear that March of the Day has smashed the £200,000 barrier for Darby Rimmer MND Foundation Absolutely delighted for Stephen and Marcus — and imagining how proud Chris Rimmer would be. Incredible work by them, the heroic Mike Wilson* and many others #marchoftheday #MND

We have had over 400 signings and messages so far supporting Darby Rimmer MND Foundation Rob Burrow CBE Ed Slater Marcus Stewart, partners and Geoff Burrow - Open letter to the Mirocals consortium. See all the messages here and perhaps add your voice? united2endmnd.org/2024/04/30/wou… #united2endmnd

This is so important - Please show your support and sign #attackMND #united2endmnd

Everyone at Darby Rimmer MND Foundation is heartbroken and devastated to hear the sad news that our great friend Rob Burrow has passed away. Our thoughts are with lindsey, Macy, Maya, Jackson and family. Rest easy Rob x

'By the time that you watch this I will no longer be here' A poignant final message from the Leeds Rhinos legend and MND campaigner recorded before his death for a special BBC documentary 'There's Only One Rob Burrow' BBC One BBC iPlayer

We’ve received a lot of messages in the last 24hrs, sorry I couldn’t reply to everyone but I’m sure you understand why. Thank you for your kindness and support, it means a lot. Teddy my 7 yr old daughter was at the horrific incident in Southport yesterday. She went in with

Not good enough. Falls way short of what people battling mnd need and deserve. It’s embarrassing. Regardless of the results serious lessons need to be learned to make sure we don’t see a repeat of this disastrous situation.

Agree - nowhere near good enough ! WHY can’t MND sufferers have access to IL-2 🤷‍♂️ the drug used in clinical trials ? IF ILTOO are seriously delaying publication of Trial Data until “they” have an alternative version, then WHY are media companies not helping with publicity ?

.MND Association Many in #MND community think our questions are REASONABLE N.b. for #Mirocals trial funded by OUR donations & taxes. Pls can you answer them? Can you help Claire Ryan lan Byrne MP APPG on Motor Neurone Disease Ed Slater DHSC Media Centre Wes Streeting Fergus Walsh richard horton

Our Chief Exec Tanya Curry has written in Conservative Home to encourage the new Conservative leader, as Leader of the Opposition, to ensure that the needs of people with MND are given the consideration that they deserve. Read more here: conservativehome.com/2024/08/26/tan…

The MNDA need to look at patients’ needs when it comes to #MIROCALS and give us some answers that patients and fundraisers deserve.

Former England international footballer, Steph Houghton, is taking part in the AJ Bell Great North Run!🙌 Steph is running to support the Darby Rimmer MND Foundation, which aims to raise awareness of MND, fund research and support. Good luck Steph Houghton MBE!🤩

This clearly shows #Mirocals results expected by end March 23. WHY the delay? We're not demanding access to #Proleukin We know we need results. TRANSPARENCY is a MUST for CHARITY funded trial. MotorNeuroneDisease, pls ask MND Association for answers to our 6 questions united2endmnd.org/2024/09/02/is-…