The AADC Foundation is a non-profit organization dedicated to raising awareness and funding for Adenylate Deaminase Deficiency (AADC), a rare genetic disorder. The foundation aims to support research efforts, improve diagnosis, and provide resources for affected families. In addition to funding research, the AADC Foundation offers educational materials and connects families with medical professionals. They work to create a community for those impacted by AADC, fostering collaboration among researchers, healthcare providers, and families to enhance understanding and treatment options for this condition.