Today in the UK, six people will hear the devastating news that they have motor neurone disease (MND). In that instant, their world – and the world of their loved ones - is shattered.

MND attacks the nerves, leaving those affected unable to walk, talk, eat and ultimately to breathe. It usually progresses rapidly and there is currently no effective treatment or cure. One third of people with MND die within a year and over half within two years of diagnosis. Despite its devastating impact, MND remains a little understood condition.

The MND Association is here to support people facing that unimaginable diagnosis, as well as their loved ones and their carers. Founded in 1979 by volunteers, our tenacious community has grown considerably, all sharing the same vision – a world free from MND.

The MND Association focuses on funding research, improving access to care and campaigning for people living with or affected by MND in England, Wales and Northern Ireland.

Our support activities for people affected by MND include, a network of multi-disciplinary Care Centres which provides high quality coordinated care from expert professionals. We provide support grants and equipment loans, including communication aids, that improves quality of life for those with the disease. We also have a network of regional staff and volunteers providing support to people with MND.

The MND Association is proud to take a leading role in the global fight against MND by funding ground-breaking research, facilitating collaboration, and raising vital awareness. We fund biomedical research into the causes of MND, the search for a diagnostic test and a cure, we also fund healthcare research to improve the lives of people living with MND. 

We also have the largest advocacy network for people with MND in the country.

Thank you for your support!