The Burrow Seven Racing Club have extended their support for the Motor Neurone Disease (MND) Association with a second donation of £50,000 to fund MND research. The unique fundraiser raised £50,000
Research, funded by the MND Association, suggests routine genetic testing should be considered for all MND patients, which could in turn have a positive impact on care and providing more opportunity
Researchers part-funded by the MND Association have discovered a new target for potential drug trials to treat motor neurone disease. Scientists at the Euan MacDonald Centre, led by Dr Arpan Mehta,
One in 300 people will be diagnosed with motor neurone disease. Sadly, more than half of those diagnosed die within two years. Almost a quarter of a million people in the UK alive today will develop
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
Kent resident Sam Bryce-Smith from Cranbook has secured a prestigious PhD Studentship from national charity, the Motor Neurone Disease Association. The Masonic Charitable Foundation PhD Studentship
As a result of the continuing global uncertainty caused by the Covid-19 pandemic, the MND Association has taken the very difficult decision to cancel this year’s International Symposium on ALS/MND.
The UK Motor Neurone Disease Clinical Studies Group (UK MND CSG) is excited to launch the updated clinical research studies section of their website: Visit the website This is a useful resource to