I AM BIO Patient Story: Eve Dryer, Travere and Melissa Bryce Gamble, Global Foundation for Peroxisomal Disorders

[Available On-Demand]
In 2008, Melissa Bryce Gamble's daughter Ginny was born with a peroxisomal disorder. It took almost two years to get a correct diagnosis for her. It was Ginny's diagnosis that spurred her to form The Global Foundation for Peroxisomal Disorders (GFPD) and get involved in the rare disease space. The GFPD's mission is to improve the quality of life for patients living with peroxisomal disorders and their families through improved access to educational materials and support services, as well as promoting scientific collaboration and funding groundbreaking research.
Speakers
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Executive Director
The Global Foundation for Peroxisomal Disorders
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Vice President, Patient Advocacy
Travere Therapeutics, Inc.