We improve the lives of patients with peroxisomal disorders and their families.
We Provide Worldwide Support and Research to families with Peroxisomal Disorders.
When the GFPD was incorporated and received its 501(c) (3) public charity designation in 2010, we were a small parent support group of approximately 50 families. Nine years later, the GFPD registry connects more than 400 families from 39 countries and we have a Scientific Advisory Board comprised of leading researchers and physicians in the field of peroxisomal disorders. Our biennial Family and Scientific Conferences bring together families and professionals from around the world to meet and collaborate on ways to improve the lives of patients with peroxisomal disorders.
We are Helping Hands
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2017 Scientific Initiatives