The swiss organization CHIP was founded in 1988 by parents whose children have PKU. Today it is an independent organization with 125 members representing parents, young adults with PKU, partner organizations and sponsors. The main objective is to unite all persons and institutions involved in PKU and other disorders treated with a low-protein diet and organize meetings for information exchange, courses, camps and other activities.

Go to www.chip-pku.ch to inform you more about the organization and event dates and details.