Category Archives: Blog
Get to Know 2014 Ilan-a-Thon Honoree Livi Menard
Recently, I had the privilege of interviewing Jen Menard, mother to this year’s Ilan-a-thon honoree,...
May
Pound the Pavement for Peter 5k a HUGE Success!
Congratulations to the Pound the Pavement for Peter team for another successful 5k run in...
Madeline Holt in the News
Sixteen month old Madeline Holt is in the news, along with her mother Meagan. Meagan...
GFPD Family Profiled on CutePotato.com
In honor of World Rare Disease Day, blogger Jennifer Hazard wrote about her nephew Jack...
GFPD Families Celebrate World Rare Disease Day 2014
GFPD families are celebrating World Rare Disease Day by wearing jeans. Here are just a...
Mar
Save the Date for Pound the Pavement for Peter in Atlanta, GA
Save the date for the Pound the Pavement for Peter 5k Race! This year’s race...
Support GFPD with AmazonSmile
Now when you shop at AmazonSmile, Amazon with donate to Global Foundation for Peroxisomal Disorders....
Feb
GFPD Joins Global Genes RARE Foundation Alliance
The Global Foundation for Peroxisomal Disorders has joined with the Global Genes Project in their...
Winter 2013 President’s Letter
Dear Friends, Holiday greetings from The Global Foundation for Peroxisomal Disorders! We have many...
NORD Salutes Congress for Passing Pediatric Research Bill
The National Organization for Rare Disorders (NORD), has announced its support for Congress’ passage of...