The Motor Neurone Disease Association (MND Association) focuses on improving access to care, research and campaigning for those people living with or affected by motor neurone disease (MND) in England, Wales and Northern Ireland. MND is also known as amyotrophic lateral sclerosis (ALS) or, in the United States, Lou Gehrig's disease. The Association is the only national charity in England, Wales and Northern Ireland that funds and promotes global research into the disease and provides support for people affected by MND.

Activities

Research

The MND Association funds and promotes research to understand what causes MND, how to diagnose it and, most importantly, how to effectively treat it so that it no longer devastates lives. It does this by: The Association organises the International Symposium on ALS/MND, an annual event which brings together leading international researchers and health and social care professionals to present and debate innovations in their fields. The Association funds research that includes animal testing.

Care and information

Fundraising

Awareness and campaigns

The Association has a campaigns network that helps shape a better future for people with neurological conditions such as MND. It does this by:

Patrons and ambassadors

Current patrons and ambassadors for the organisation include:

Past patrons