Join me for the GFPD Warrior Walk Run Ride on July 9th -12!

Join me in supporting families impacted by peroxisomal disorders.

Just a small donation will go a long way to helping me meet my goal for The Global Foundation for Peroxisomal Disorders!

My daughter, Shannon, has a rare peroxisomal disorder. After 4 years of many tests and doctor visits we were given a diagnosis to explain what was happening to our daughter. Due to it being such a rare genetic condition the doctor and genetic counselor provided us with little information and suggested we go on social media to try and find someone who had her condition. We felt completely lost. Thankfully, I was able to find the GFPD and it has provided us with so much HOPE and given us a FAMILY of others who understand. The GFPD provides so much support to families like ours. Please consider donating $10, $25 or whatever you can comfortably spare to help others. Thank you!