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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

Action Duchenne Questions

Katie Endacott is the CEO of Action Duchenne.

14 people are employed at Action Duchenne.

Action Duchenne is based in Bristol, England.

The NAICS codes for Action Duchenne are [621, 624, 6241, 62, 62419].

The SIC codes for Action Duchenne are [832, 80, 83, 809].

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