We can give HOPE to GFPD Warriors!

As most of you know DJ and I had a little boy, Ezekiel, born almost 3 years ago with a Peroxisomal Disorder. It was called Zellweger Syndrome. I became connected with The GFPD shortly after he was born. THIS group was and still is today a HUGE support for our family. In fact this group was almost more helpful than local doctors. We have a yearly event coming up called WALK, RUN, RIDE, followed by Pause for the GFPD to help show support and raise funds to help this group continue to help other families like ours. This group helps provide many connections, a panel of doctors and scientist, among many other things to help direct and support PBD families. Please consider helping me by donating to this organization. We also ask that you join us on Saturday, October 1 for our own walk, run, ride event. We will do a 3ish mile walk leaving from our house at 9:00 am. Please help us celebrate Ezekiel and all the other families and children who have been affected by a Peroxisomal Disorder. God bless and thank you so much

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