For National Kidney Month, we challenge the PKD community to take action to spread the word about polycystic kidney disease (PKD). PKD is a chronic, genetic disease that causes fluid-filled cysts in the kidneys that often lead to kidney failure. There is no cure. In 2018, the very first ADPKD treatment in the United States was approved by the FDA, but we still have so much to do!
Use your social media to raise awareness of polycystic kidney disease.
Use our cover image
Share PKD fact graphics
Share your PKD story
World Kidney Day
Help us bridge the knowledge gaps to better kidney care and bring Kidney Health for All on World Kidney Day, March 10. Make sure to tag PKD Foundation and use #NationalKidneyMonth.
Virtual PKDCON 2022
Connect with PKD patients, caregivers, health care providers, and researchers at our free virtual conference in June.
Join over 2,000 individuals with ADPKD in advancing research by contributing to the first national, secure, patient-powered ADPKD Registry.
Newly diagnosed? Find everything you need to know about ADPKD and ARPKD with our free, downloadable patient handbooks.
From diagnosis to dialysis, explore expert-created information and tools created for patients, caregivers, and health care providers.
Feeling overwhelmed? Our Peer Mentor Program and HOPE Line are here for you. We also have financial assistance resources and information about local events.
You can make a difference during National Kidney Month! When you give to the PKD Foundation, you further our mission to give hope by helping us fund research, advocate for patients and build a community for all impacted by polycystic kidney disease (PKD).