by Sydney Johnston | Apr 5, 2022 | Advocacy
Published on April 5, 2022 | Launched in 2020, the Advocacy Champions Network (ACN) is an exclusive community of patients, family members, and clinicians dedicated to improving the lives of people living with PKD. The inaugural ACN class consisted of 36 members from...
by Sydney Johnston | Mar 31, 2022 | Education
Published on March 31, 2022 | After a diagnosis, it’s natural to have questions about polycystic kidney disease. How will it affect your daily life? Is there a treatment? How do I manage PKD complications? Finding the right healthcare team can make things...
by Sydney Johnston | Mar 22, 2022 | Advocacy
Published on March 22, 2022 | The PKD Foundation is excited to announce that registration is now open for PKDF Virtual Advocacy Day 2022 taking place on Wednesday, April 27! As the only organization in the U.S. solely dedicated to finding treatments and a cure for...
by Sydney Johnston | Mar 7, 2022 | Awareness
Published on March 7, 2022 | Every March, we recognize the importance of kidney health. It’s a time dedicated to raising awareness, sharing education, and advocating for kidney health equity. For National Kidney Month 2022, we’re sharing resources and...
by Sydney Johnston | Mar 1, 2022 | PKD Foundation News, Research
Published on March 1, 2022 | The PKD Foundation is pleased to announce that Drs. Alessandra Boletta and Albert Ong are the winners of the 2022 Lillian Jean Kaplan International Prize for Advancement In the Understanding of Polycystic Kidney Disease (Kaplan Award)....
