On February 12, 2021, the GFPD joined with the TS Alliance and 69 other advocacy...
Dr. Rizzo said several of the diseases are so rare that between 500 and 1,000...
Oct. 5 is a special day for our family as we celebrate Pause for PBD,...
Melissa Bryce Gamble is president and co-founder of the Global Foundation for Peroxisomal Disorders, which...
Melissa Bryce Gamble shares the story of her daughter Ginny's battle with a peroxisome biogenesis...
The Jersey County Journal featured a letter to the editor, from Vicky Maag, about our...
Thomas Thériault, of Saint-Quentin, will celebrate his second birthday on November 24. His community recently...
She's five-years-old, loves all things pink and glitter, and will be sporting a pretty magical...
De Jesus says that it was a specialist in Canada who diagnosed Jaxson with Peroxisomal...
Jaxon’s health has had a backslide lately. The hospice nurses hope he will make it...