#ENDPKD YOU HAVE THE POWER TO Join the ADPKD Registry Introducing the ADPKD Patient Registry Patient registries are a critical component in the advancement of medical research, especially with rare diseases like autosomal dominant polycystic kidney disease (ADPKD). That's why the PKD Foundation has created the nation's first network of individuals affected by ADPKD. LEARN MORE AT PKDCURE.ORG/REGISTRYhttp://www.PKDCURE.ORG/REGISTRY