Our foundation was created after losing our 6 year old son to DIPG. The foundation's mission is to help raise awareness of DIPG and pediatric cancers. We also aim to help support other children and their family who are battling DIPG. 

All over the world, children are diagnosed with DIPG on a daily basis. This affects not only the children, but everyone around them as well. Between medical bills, missed work, traveling expenses, and many other unforeseen costs. Most families are left hopelessly wondering how they will be able to deal with it all. That is where we come in. We strive to provide aid in any way possible to help lessen the burden on these families. Parents should be able to focus on their child instead of worrying about the overwhelming costs of this diagnosis.