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- About MND
- Support and information
Ian and Deanne's views
Ian is living with MND and aged 70. He was diagnosed in 2024 and his wife Deanne is his main carer. They talk openly about the impact of MND as individuals and…
- About MND
- Support and information
David's views
Watch David share his experiences of living with motor neurone disease (MND), including diagnosis, healthcare, and daily life. Includes video clips and…
- About MND
What is Kennedy's disease?
Kennedy’s disease is also known as spinal bulbar muscular atrophy (SBMA) and is a rare disorder of the motor neurones, caused by a genetic mutation. If you are…
Birmingham and Solihull Group
Find out more about the Birmingham and Solihull Group of the Motor Neurone Disease Association.
James's Appeal
Alex lost his life to motor neurone disease in March 2022. He wrote this message to you just before he died.
- News
Cost of Living Support Fund rises to support with household bills
The uplift marks a £150 increase, from £350, and those who have already received the previous amount can still apply for the difference should they need to
Children and young people
Do you know someone with motor neurone disease (MND)? If you are aged up to 18, find out more here. There is also information for parents and guardians,…
- Campaigning
Unlock The Door: Fast-track accessible housing for people with MND
How you can help support the Unlock the Door campaign as an MP.
- Support and information
Benefits, financial support and cost of living
If you have MND, Kennedy's disease or provide support as a carer, you may qualify for a range of benefits or other types of financial support.
BBC Lifeline Appeal
Find out mroe about the BBC Lifeline Appeal