The MND Association was founded in 1979 by volunteers and aims to improve care and support for people with Motor Neurone Disease (MND) and their families. The association funds research, raises awareness about MND, and works towards a world free from the disease. There are various ways to get involved, such as organizing awareness events, using social media for outreach, and supporting fundraising events.
If you are considering volunteering, there are opportunities to support existing fundraising events, attend support meetings for individuals with MND, or become an Association Visitor to provide support and guidance to those affected by the disease. Volunteers play a crucial role in offering assistance and making a difference in the lives of people living with MND.
The story of Mel, a man diagnosed with MND, and Lynn, a fundraising volunteer, highlights the impact of the disease on individuals and the importance of support. Despite the challenges faced by those with MND, the MND Association and its volunteers strive to provide assistance, understanding, and care to improve the lives of those affected by the disease.