Join the GFPD Challenge!

Many of you already know my story. Ashley and I were blessed with four incredible kids including our Warrior, Archer. Our diagnosis journey, without the availability of newborn screening for Archer’s peroxisomal disorder at that time, took until he was 18 months old after a year of testing. The GFPD was quick to welcome us, and today, I am honored to lead this organization that has helped my family so much as the new Executive Director.

In honor of my inaugural year, I am leading a fundraiser for the GFPD. With help from a generous donor, we will match the first $10,000 donated. So friends, I challenge you to meet this match and help the GFPD expand and enhance its programs to help more families across the world.