Maria McCarrick, mother of Katherine McCarrick, contributed this article in the most recent newsletter for...
Follow the link below to read the GFPD’s year-end update letter from President Shannon Butalla:...
Follow the link below to hear a 2011 presentation by researchers from the University of...
Aspen Pollock, a thirteen-year-old girl with a Peroxisome Biogenesis Disorder, won first place at the...
First ever multi-cellular model of rare disease developed at the University of Alberta. http://www.med.ualberta.ca/Home/NewsEvents/News/article.cfm?ID=2288...
Pound the Pavement for PBDs is the official Run/ Walk Fundraising Event for the Global...
Jennifer Murphy and her son, Clayton were featured on the news in San Antonio to...
We had an amazing first conference in Omaha, Nebraska July 31 – August 2nd! Thanks...
Thanks for visiting the online home of The Global Foundation for Peroxisomal Disorders (GFPD). We...
Thanks to all who have taken the time to visit our website. There has been...