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Peter Speaks with Jo Eames at the Action Duchenne Conference

January 16, 2018

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Muscle Owl Talks Ep73: Understanding the Clinical Trial Process for Rare Diseases

October 11, 2017

Watch our latest episode of Muscle Owl Talks! We are joined by Action Duchenne CEO Diana Ribeiro, and Lynnette Ellison, as Diana answers our questions on the clinical trial process for families with a child who has a rare disease.



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