Share how GFPD has impacted YOUR loved one with Peroxisome Biogenesis Disorder
The Global Foundation for Peroxisomal Disorders has reached over 200 families around the globe who have come to know the harsh realities of Peroxisome Biogenesis Disorders.
Do you know a friend or family member whose child has a Peroxisome Biogenesis Disorder (also called Zellweger Syndrome, Neonatal Adrenoleukodystrophy, and Infantile Refsum Disease)? If so, how has the GFPD community benefitted them? What else could be done to help these individuals/families?
Share your stories, photos, videos, and suggestions of how GFPD has helped and what more can be done to help.
Supporters are now helping to
July 1st, Sam Butalla will celebrate his #11 birthday! His life has been significantly impacted by the devastating effects of Peroxisome Biogenesis Disorder. Sam's life inspired The Global Foundation for Peroxisomal Disorders (GFPD), which provides support to families and children impacted by the disorders and the professionals who study & treat those affected.
Show your support for families impacted by Peroxisomal Biogenesis Disorder-Zellweger Spectrum Disorder (PBD-ZSD) by donating to the GFPD Conference Scholarship Fund. The conferences hosted by the Global Foundation for Peroxisomal Disorders (GFPD) are the most important and influential gatherings for families affected by PBD-ZSD and the medical and scientific community that treat and…
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