Our Vision is that all people living with PKU, despite their origin, will be able to reach their full potential. Our Mission is to advance PKU as a global health priority and strengthen PKU associations and groups throughout the world. As people living with PKU, our priorities are: - To create a global platform for PKU advocacy that includes ensuring universal access to newborn screening and diagnosis, treatments and comprehensive care; - To mentor like-minded patient associations and groups and offer best practices and support that are sensitive to their experiences, culture, language(s) and laws; - To increase collaboration among PKU researchers, scientists, clinicians and patient groups to move basic science and research forward to accelerate new knowledge, treatments, and a cure.