This is us, the MND Association. Renewed, united and driven every day to make change happen. Every day we support people affected by motor neurone disease, campaign for better care and fund ground-breaking research. Because with MND, every day matters.

Tahira loved gardening with her grandchildren. But because of MND, now her hands can't grip a trowel. Help us stop it. Head to mndassoc.org/life-stripped-a…

Jaki is a born performer, taking to the boards as Nancy in Oliver! Now, MND has stripped away the things she loved - like performing. Help us stop it. Visit mndassoc.org/life-stripped-a… .

Before MND stripped away the things she loved, Jaki loved to sing. 🎶 Imagine losing the ability to do something that brings you joy. What's one thing you'd hate to no longer be able to do? #WorldSingingDay

Go Oscar go! 🧡👏 After being inspired by reading ‘Try’, the children's book written by Sir Kev, 7 year old Oscar set himself a challenge to raise money for MND: walking every day for 7 days! And that’s just the beginning - he plans to walk 77 miles before Christmas to continue to raise vital funds. We’re so proud to have you on the team Oscar, thank you for everything you are doing. 🧡 To donate to Oscar incredible challenge, click here. 🔗 fundraising.mndassociation.o…

Steve is a natural born drummer, but now he can't hold his sticks. MND stripped away the life he loves. Help us stop it. Learn more here: mndassoc.org/life-stripped-a…

Go behind the scenes of our new brand campaign with MND Association Head of Brand and Marketing, Siobhan Gray, in our latest blog. 👉mndassociation.org/media/lat…

This party conference season, we met with over 150 MPs, councillors and peers across the political spectrum so people affected by MND are heard by those who can make real change happen. Here's a message from our Director of Engagement, Richard, to say thank you for the part YOU played.

"When a drug shows no benefit, it’s discarded and we go again and again until we hit on something that works." shared Mike Rogers, our Director of Research, following the latest results from the EXPERT-ALS study. The second set of results from the study have shown that the drug ropinirole is not likely to be an effective treatment for people with MND. The researchers will stop testing this drug in new study participants, and people in the study who are currently taking it will stop. You can read more here. 🔗mndassociation.org/media/lat…

Were you successful in receiving a place in the 2027 London Marathon ballot? We need your help! Every day six people are told they have MND. There’s no cure. Not yet. Sign up to be a part of our team and raise funds that will help us with vital work. 🔗mndassociation.org/londonmar…

Motor neurone disease, or MND, strips away the life we love including passions like baking. But what actually is it? Here are the basics. #GBBO

Our Director of Engagement, Richard Evans, talks us through the latest updates on our tofersen campaign in this new blog post. Read now. 🔗mndassociation.org/media/lat…

Feeling inspired by all our autumn events? 🍂 Why not step into spring and take on the 2027 Brighton Marathon? 🏃 Sign up today and help raise vital funds for the MND Association, supporting people affected by MND and helping to make every day count. 🧡 🔗fundraising.mndassociation.o…

Motor neurone disease, or MND, is fatal and rapidly progressing. Here are the facts.

Lorraine is a dancehall queen, but now she can't join in. MND has stripped away those precious moments on the dance floor. #Strictly Learn more. 🔗mndassoc.org/life-stripped-a…

One week on from the end of Sir Kev's 7 in 7 challenge, the team have raised over £1.6 million for MND charities and the messages of support are still flooding in. 👇 @GordonRamsay