Duchenne muscular dystrophy (DMD) is a rare and complex genetic muscle wasting condition, mainly affecting males. It is one of the most severe muscular dystrophies, with muscle weakness appearing in early childhood between the ages of 2 and 5.

Our vision is clear; a world where lives are no longer limited by Duchenne muscular dystrophy.

We achieve this vision through our vital work;
* Funding research for everyone living with Duchenne
* World-class support for families
* Cutting-edge science education programmes


Health Care

Humanitarian

Action Duchenne

Action Duchenne's headquarters in London, United Kingdom

Description

People (3)

Tina Flatau

Helen Keenan

Ravi Mehta

Jobs