DIPG - Diffused Intrinsic Pontine Glioma

Our mission is to help spread awareness of this deadly childhood disease.  Currently there is no cure there is no treatment and the survival rate is less than 1%.  All donations made are given to The Team Cozzi Foundation.  Paul & Cyndi Cozzi started this foundation in memory of their son Camron Cozzi.  Cam fiercely battled this disease and on his 18th birthday received his angel wings.  His wish was to find a cure so no child would have to leave their parents and no child would die of DIPG.  We promised Cam we would continue to battle as one of his warriors.  So we use this platform to help spread awareness of this awful cancer.  Please consider donating.  Every $ is crucial in making a difference.