Inaugural ACN Awards Ceremony

Inaugural ACN Awards Ceremony

BE Published on December 21, 2021 | Recently, we hosted our inaugural Advocacy Champions Network (ACN) Awards Ceremony. Together, we honored and celebrated PKD advocates who’ve dedicated significant time to improving the lives of people living with PKD....
Reflecting on 2021, Planning for 2022

Reflecting on 2021, Planning for 2022

Published on December 14, 2021 | Much like 2020, this year had its ups and downs. Challenges and celebrations. At the PKD Foundation, we worked to bring the PKD community the right resources, the right way, and the right time. From continuing our virtual events to...
Helping Your Teens Manage PKD

Helping Your Teens Manage PKD

Published on December 7, 2021 | Since Kari Lusby’s son, Honor, was diagnosed with PKD at age 4, she and her family have managed his disease by focusing on the main tenets of good health. Nutrition, hydration, movement, sleep, mindset, and mental toughness. As Honor...
Holiday PKD-Friendly Blackberry Cobbler

Holiday PKD-Friendly Blackberry Cobbler

Published on November 22, 2021 |  Starting your holiday grocery shopping list? In need of a dessert to wow your family and friends? Give this recipe for a PKD-friendly blackberry cobbler from our cookbook, Cooking Well, a try! It’s low in sodium, low in protein,...
Researcher Spotlight: Melissa Little, Ph.D.

Researcher Spotlight: Melissa Little, Ph.D.

Published on November 16, 2021 | The PKD Foundation’s principal mission is to support basic, translational, and clinical research that will benefit patients with autosomal dominant and autosomal recessive polycystic kidney disease (ADPKD and ARPKD). This mission is...