Global Foundation for Peroxisomal Disorders

About the Global Foundation for Peroxisomal Disorders

Founded in 2010 by dedicated parents Shannon Butalla and Melissa Gamble, the Global Foundation for Peroxisomal Disorders (GFPD) unites families impacted by peroxisome disorders, including Peroxisome Biogenesis Disorder-Zellweger Spectrum Disorder (PBD-ZSD). What began as a small support group has blossomed into a global network connecting over 300 families across 30 countries, supported by a Scientific Advisory Board of leading researchers and physicians.

Impact of the GFPD

The GFPD plays a crucial role in connecting families affected by peroxisomal disorders, providing essential educational resources, and funding vital research to enhance patient outcomes.

Why Donate?

Your generous donations to the GFPD directly support critical research and educational programs that benefit individuals and families affected by peroxisomal disorders. Contributions empower families through resources and support services.

Join the Cause

Support the Global Foundation for Peroxisomal Disorders today! Your donation, whether in cryptocurrency or cash, can make a significant difference in the lives of those affected by peroxisomal disorders. Together, we can foster research, education, and community support.