MNDA

Motor Neurone Disease Association (MNDA)

The Motor Neurone Disease Association (MNDA) is a charity based in the United Kingdom that supports people affected by motor neurone disease (MND), also known as Amyotrophic lateral sclerosis (ALS) in the United States. The MNDA provides care and support to people with MND, their families, and caregivers, while also funding and promoting research into the disease.

History

The MNDA was founded in 1979 by a group of volunteers who wanted to provide support and information to those affected by MND. Since then, the association has grown to become a leading authority on the disease, providing resources and funding for research.

Mission and Activities

The MNDA's mission is to improve care and support for people with MND, their families, and caregivers. The association achieves this through a variety of activities, including providing information and advice, funding research, and advocating for people with MND.

Information and Advice

The MNDA provides a range of information and advice services to people with MND, their families, and caregivers. This includes a helpline, online resources, and local support groups.

Research Funding

The MNDA is one of the largest funders of MND research in the UK. The association funds projects that aim to improve understanding of the disease, develop new treatments, and ultimately find a cure.

Advocacy

The MNDA advocates for the rights of people with MND, working to influence policy and practice at both a local and national level. The association campaigns on issues such as access to care, disability rights, and funding for research.

See Also

• Motor neurone disease
• Amyotrophic lateral sclerosis
• Charity (practice)

References

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