Read all the latest news from across the Association. You can select a specific category from the drop down list and click 'find' (using the magnifier icon) to see all news for that category. We've also include the option to search by keywords. Again, select your category, enter the key word (s) and click find.
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
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
Almost a year ago former Leeds Rhinos player Rob Burrow announced he had been diagnosed with motor neurone disease. Now he is laying bare the last 12 months of his life in a BBC documentary Rob
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
In July 2019, the Department for Work and Pensions (DWP) announced a review of how well the benefits system works for people who are terminally ill. The announcement came in response to campaigning by
We are delighted to announce our successful accreditation through the Patient Information Forum (PIF), following their assessment of our information process. This means our resources for people with
The journey of Dr Peter Scott Morgan who has pledged to ‘thrive’ while living with MND is being featured on a Channel 4 documentary being shown at 9pm on Wednesday 26 August. Peter: The Human
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