Information for researchers

Part of our mission is to fund and promote research to bring about an end to MND.

We are committed to:

Identifying the causes of MND
Focussing on research of direct clinical and therapeutic relevance
Clinical and healthcare research to improve standards of care and quality of life for people with MND

These key areas are elaborated on in our Research Strategy (91 kb) as well our Research Report (956 kb) and Research governance overview (209 kb)

How to apply for funding

Types of project considered; grant conditions; the application process.

Research we fund

Projects currently funded by the Association.

International Symposium on ALS/MND

The premier conference on ALS/MND for scientists and clinicians.

ALS Young Investigator Meeting 2010

The 8th European ALS Young Investigator Meeting is being held July 28, 29, 30 2010 in London

Utilising our patient register

In collaboration with DeNDRoN we have created a register of people with MND who are interested in participating in research. If you have a study that needs participants with MND who live in England, Wales or Northern Ireland then please visit the DeNDRoN website to find out how we can help.