The MND Association has received ‘unprecedented support’ from the rugby league community and beyond following the airing of Rob Burrow: My Year With MND. The showing of the documentary at
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Right now, 5,000 people in the UK are living with MND and six more people will be diagnosed with this brutal disease today. There are no effective treatments or cures for MND – yet. The scientific
Inspirational fundraiser Richard Pollins who walked 40km around London on artificial legs, has been awarded a British Empire Medal in the delayed Queen’s Birthday 2020 Honours List, marking his
The Motor Neurone Disease Association has launched its Act to Adapt campaign, calling for more accessible homes and a faster and fairer system for delivering housing adaptations for people with MND.
People who are living with MND in Wales are set to benefit from emergency funding which has been awarded to the Association by the Welsh Government with support from the Wales Council for Voluntary
Children and young people who are close to someone with motor neurone disease (MND) are being given the chance to create, capture and store memories of their loved one thanks to a pilot project