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.
The UK is set for very hot weather this week. This can increase health risks, so it's important to take extra care.
If you have MND, stay cool and hydrated. Try to drink more fluids than usual. If you have a feeding tube, it can also be used to help increase your fluid intake.
Remembering dad.
1939 - 1994.
Lost too soon to motor neurone disease.
Support vital research @mndassoc to bring the hope of a cure for this brutal disease #mnd#fathersday
In March 2025 my mum was diagnosed with Motor Neurone Disease. She lived for just 245 days but in that time showed remarkable strength and humour. Today is #GlobalMNDAwarenessDay & every day 6 people are told they have MND. They need better support and care. @mndassoc
@mndassoc
On MND global awareness day, Father’s Day and summer solstice, we remember my best mate, Peter Clarke who left us 9 years ago today
Not only today but everyday!
Today marks Father’s Day and Global MND Awareness Day – two truly special days for our community. 🧡
We are thinking of everyone affected by motor neurone disease. We remain here for you every day.
#GlobalMNDAwarenessDay#SpecialDaysMatter#FathersDay
Just 12 weeks to go until our Trio of Thames Challenges!
Whether you're taking on the Thames Path Challenge, Thames Bridges Trek or Thames Moonlight 10 Walk, now is the time to sign up.
Challenge yourself, raise vital funds and help make a difference.
🔗 https://t.co/swhGObumal
Last week, we had the pleasure of attending Louise's 'FUN-eral'. 🧡
"I want to be a part of my life celebrations. Funerals are sad and morbid, but I wanted the occasion to be full of love and laughter and making new memories to treasure." shared Louise.
The event included raffles and craft stalls — raising over £1300. It was a truly special day. Thank you for sharing it with us Louise. 🫶
#GlobalMNDAwarenessDay #SpecialDaysMatter
Motor Neurone Disease takes everything. Which makes the special days all the more special.
Reclaiming his voice through voice banking was Mike’s special day. What’s yours?
#Specialdaysmatter#GlobalMNDAwarenessDay
Have you registered for the next workshop with Dr Ray Owen on 7 July in Loughborough?
During the event, he'll help build confidence & skills to conduct difficult conversations in a compassionate, person-centred way
Book before 26 June👉 https://t.co/LRchjaIAsT
Ahead of #GlobalMNDAwarenessDay this Sunday, Jim — who has MND — has written a song about his life with motor neurone disease. 🧡
Listen now. 🎧https://t.co/iNIVUiTApc
We caught up with fundraiser Will, and asked him why running the London Marathon was a special day that mattered to him.
#GlobalMNDAwarenessDay#SpecialDaysMatter
For our patron, Sir Kevin Sinfield, days spent with the MND community during his 7 IN 7 challenges were special ones that mattered. 🧡
#GlobalMNDAwarenessDay#SpecialDaysMatter