Melissa Bryce Gamble is the executive director of The Global Foundation for Peroxisomal Disorders (GFPD), an international 501 (c)3 nonprofit, public charity focused on funding groundbreaking research on peroxisomal disorders as well as supporting families impacted by the rare, devastating, terminal childhood illnesses. This cause is especially close to Melissa's heart as her oldest child, Ginny, was born with a peroxisomal disorder and sadly lost her battle with the disease 3 years ago. The work Melissa does for the GFPD is in her memory, so that, hopefully, someday kids born with a peroxisomal disorder will live longer, happier, healthier lives.
I AM BIO Patient Story: Eve Dryer, Travere and Melissa Bryce Gamble, Global Foundation for Peroxisomal Disorders
In 2008, Melissa Bryce Gamble's daughter Ginny was born with a peroxisomal disorder. It took almost…