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
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Katie Endacott is the CEO of Action Duchenne.
13 people are employed at Action Duchenne.
Action Duchenne is based in Bristol, England.
The NAICS codes for Action Duchenne are [6241, 624, 62, 621, 62419].
The SIC codes for Action Duchenne are [809, 832, 80, 83].