Motor Neurone Disease Association

Motor Neurone Disease Association
Founded 6 October 1979 (1979-10-06)
Type Charitable organisation
Registration no. England: 294354
Focus Motor Neurone Disease, health policy
Location
  • David Niven House, 10–15 Notre Dame Mews, Northampton, NN1 42BG
Area served
England, Wales and Northern Ireland
Members
8000
Key people
David Niven
Employees
140+
Volunteers
3000
Mission A World Free of MND
Website www.mndassociation.org

The Motor Neurone Disease Association (MND Association) is a British charity, operating in England, Wales and Northern Ireland, established in 1979 by a group of volunteers to coordinate care, support, and research for people affected by amyotrophic lateral sclerosis, which is a form of motor neuron disease (MND) (and also as Charcot disease or, in the United States, Lou Gehrig's disease).

The Association's Chief Executive is Sally Light. Its President is neuroscientist Colin Blakemore. The Patrons of the Association are HRH The Princess Royal, neurologist and four-minute mile record breaker Roger Bannister, entrepreneur and philanthropist Joel Cadbury, palliative medicine consultant Baroness Finlay, neuroscientist, broadcaster and author Baroness Greenfield, world-renowned cosmologist Stephen Hawking (who is living with MND), former Chief Inspector of Schools Sir Chris Woodhead, challenger and entrepreneur Richard Noble OBE, Jamie Niven (Senior Vice President at Sotheby's art dealers in New York and younger son of actor David Niven, who died from MND), former English cricketer and current official Chris Broad, and American businessman James Sherwood.[1]

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 Motor Neurone Disease. It is a membership organisation with nearly 8,000 members forming a national and local network that provides information and support alongside fighting for improved services. It has over 3,000 active volunteers in England, Wales and Northern Ireland and 140-plus paid staff, who are dedicated to improving the lives of people affected by MND.

Activities

Benedict Cumberbatch has been an ambassador of the Motor Neurone Disease Association since 2004.[2]

Research

The Motor Neurone Disease 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 MND 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 MND Association funds research that includes animal testing.[3][4]

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:

External links

References

  1. Archived September 27, 2008 at the Wayback Machine
  2. "Press Office - Hawking Benedict Cumberbatch". BBC.co.uk. 2014-09-24. Retrieved 2015-05-20.
  3. "Models of MND". MNDassociation.org. 2015-05-16. Retrieved 2015-05-20.
  4. "Health Charities and Animal Testing". Animalaid.org.uk. Retrieved 2015-05-20.
  5. Archived March 8, 2013 at the Wayback Machine
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