Most people know Lou Gehrig’s famous words from his 'Luckiest Man' speech. Days after his ALS diagnosis, Lou stood before a packed stadium, too weak to hold his trophies but still strong enough to lift others up with gratitude. He’s the reason we choose to Live Like Lou. 💙

Well- tried to have dinner at the Ivy at Wimbledon, but they won’t allow Lulu into the restaurant- so plan B

The Bayeux Tapestry is to be displayed at the British Museum, London, next year. The 70 metre long Eurppean medieval masterpiece, depicting the Norman Conquest of England, was created by a team of highly skilled women artisan embroiderers in the 11th century #WomensArt

You still have time to sign our #PrescribeLife petition! Your support will help to urge the government to make #tofersen accessible to people living with SOD1 #MND. You can sign here: act.mndassociation.org/2025-prescribe…

You still have time to sign our #PrescribeLife petition ⏲️ Your support will help to urge the government to make #tofersen accessible to people living with SOD1 #MND. You can sign here 👇

A fitting tribute to an incredible man 💙💛

Truth 🧡

A huge congratulations to our co-director Ammar Al-Chalabi! We're thrilled he has been recognised for his vital work in #MND and focused approach to collaborative research.🎉

Bereavement changes all aspects of life including holidays, which can be difficult to plan and navigate post-loss. How have you managed holidays after being bereaved? ow.ly/akCu50WoaP4 #soloparentholidays #widowedtravel #holidayingalone

Marcus is so honest & open about his experience of living with MND. Football, friends & his beautiful family help to keep him positive. He shares his own experiences & uses his platform to help others diagnosed with MND be seen & heard 💙 Jayne Halhead bbc.co.uk/sport/football…

A new chapter starts for Neuroscience Institute! 🧱 A bricklaying ceremony marks a major milestone for the expansion of the institute which will double the research capacity of the world-leading research facility, accelerating the progress of breakthrough treatments for degenerative

🧠💤 Have MND/ALS? We need your voice. Sleep is more than a symptom, it reflects underlying disease processes, affects quality of life, and may offer clues for new treatments. Take part in a 15-min King's MND Centre survey to guide future care and research. 🔗 surveymonkey.com/r/D8SYJPQ

COMPETITION TIME! 🦁🎁 Want to win the ULTIMATE prize bundle worth £250+ from OddBalls, My Name'5 Doddie Foundation & @LionsOfficial? 🤩🎉 ENTER HERE: myoddballs.com/s/LionsCompX 🙌 PLUS, LIKE and RESHARE this post to enter our BONUS bundle giveaway! ✨ GOOD LUCK! 🤞 #Lions #Lions2025

One Irish man. One concert. One world. #Bobgeldoff

Eric was diagnosed with MND/ALS on the 7th July 2010. He was 44. A strong, fit man until in 2009 he noticed weakness in his left hand. It took 9 mths to diagnose + Eric had self diagnosed months beforehand once he’d noticed the fascinations in his arm. Picture taken Aug 2010.

This week, we’re hosting our 4th #MNDEnCouRageUK event! This event supports and celebrates the work of early career researchers working in #MND #ALS 🔬 We chatted to 3 early career researchers who came to the very first event to see what they’re up to now. Read our blog 👇

We will be on the BBC Breakfast red sofa at 8.15am today to talk about life saving changes being made to the school curriculum in England

Aug 2010. This was our penultimate holiday to our beloved Cornwall. Eric had just received the diagnosis that he had MND/ALS. We lived every moment of that holiday with every fibre of our souls. When we went to bed at night we held each other and cried. Knowing what lay ahead.