Peroxisomal Biogenesis Disorder- Zellweger Spectrum Disorder (PBD-ZSD), and the related single enzyme disorders are extremely rare and impact approximately 1 out of 50,000 children, including 5-year-old Max Chapman of Bloomington, IL. The Global Foundation for Peroxisomal Disorders (GFPD) is a 501(c)(3) nonprofit charity founded in 2010 to directly fund medical research and to support families affected by peroxisomal disorders. Tee It Up! For the GFPD! is hosted annually, each year in May, by the Chapman Family. Over the past four years, Tee It Up! For the GFPD! has been the GFPD’s most successful fundraising event, raising over $375,000 for the programs of the Global Foundation for Peroxisomal Disorders.