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We are expanding our team! MND-SMART is the largest clinical trial for people with MND in the UK with over 850 people randomised from across 22 sites in all 4 nations. As we continue to test new interventions and open new sites we are expanding our central team. Spread the word!

Keep being you Ed Slater The physical and mental battle people with mnd face.

This is what grief is… A hole ripped through the very fabric of your being. The hole eventually heals along the jagged edges that remain. It may even shrink in size. But that hole will always be there. A piece of you always missing. For where there is deep grief, there was

⚽️ #IPSLIV MO SALAH'S #Egyptian teammate Mo'men Zakaria is living with #MND/#ALS, the horrific condition now being tackled by former IPSWICH TOWN striker MARCUS STEWART. MARCUS' brilliant goal for #Ipswich in a memorable win against #Liverpool in 2000... #MND #MoreNeedsDoing!

A massive good luck to the 4Ed Team today who are undertaking a huge 24 hour cycle challenge, ‘Ride Against Time’, for the fight against #MND 🙌 Ed Slater Gloucester Rugby 🍒

Brian and Sandra are the epitome of hope. When Brian was diagnosed with ALS, he turned tragedy into action by launching I AM ALS and leading a movement to find a cure. I’m inspired by these two—and after you hear their story at the 2024 Democratic National Convention, you will be, too.

Please support Billy Twelvetrees Ride Against Time for MND: 350 Miles in 24 gofund.me/f18cb395

I am beyond chuffed to have been shortlisted for this year's #NationalTelevisionAwards! (For Serial Drama Performance) Please vote all things #Corrie! 🙏 National TV Awards Link⬇️ nationaltvawards.com/?s=09

We will be voting for Peter Ash ahead of the National TV Awards 👏 I think we can all agree his portrayal of living with MND has touched so many. Vote here: mndassoc.org/voteforpeter

✨A Million Thank Yous✨ Thank you Billy for putting your body on the line for me and for MND. People don't see what else you and G do for us but now they see what we know. You're a great man with a massive heart. Thank you to everyone who turned out to see the team off and

Check out our latest article on using genomics for drug discovery in #ALS #MND. Fantastic work by Oliver et al Oliver Pain. “Harnessing transcriptomic signals for amyotrophic lateral sclerosis to identify novel drugs and enhance risk prediction.” Alfredo Iacoangeli Ammar Al-Chalabi

Remembering the 'profoundly loved' #Scottish theatre director and radio producer MARILYN IMRIE, who lost her life to motor neuron disease #MND four years ago today, a few short months after diagnosis. Thoughts are with her husband @James_Runcie and daughters Rosie and Charlotte.

We'll be at a couple of local events over the weekend so why not pop along and support us? This is the first one. We'll be selling new, ex-display books as well as a few secondhand ones.

🏉 TEN years ago today the late, great #rugby icon JOOST VAN DER WESTHUIZEN shivered his way through the viral #MND/#ALS Ice Bucket Challenge, nominating the Springboks, the All Blacks and the Wallabies! 😢 WE lost Joost to this hideous disease less than three years later...

ICYMI: Peter Ash is nominated for Serial Drama Performance in the National Television Awards! 🥳 Vote for him here: nationaltvawards.com/vote 🤞

Thanks so much to Tom Morrison MP, MP for Cheadle, for making the time to talk about #MND. We're looking forward to working with you!

Many #MND fundraisers think our questions to MND Association deserve answers. Can you please help MotorNeuroneDisease Patients United2EndMND get them Ed Slater Geoff Burrow Darby Rimmer MND Foundation Ian Flatt Lynn Pritchatt Martyn Clarke Cris Hoskin Challenging MND Stand Against MND Alex Ward MND Angel 💙🧡?

We pre-ordered ours and our grandsons love it! Recommended Xmas gift for any child 🎁

Great morning at Kingsholm for the 4Ed MND Breakfast. Here I am with John Chart who travelled up from London with his wife, Arlene. Looking forward to getting behind George and the team this season. Everyone looking sharp in the build up to Saracens in two weeks. Come on

#ResearcherSpotlight💡 Dr Puja Mehta joined us today at our virtual legacy event to discuss her research. 🔬 Puja R. Mehta 🩺🧠🧪💙 is developing a new gene therapy which could be beneficial for around 97% of people with #MND #ALS. Find out more about her research⬇️ mndassociation.org/research/our-r…