Published May 12, 2020 | In these unprecedented times, families across the globe are adapting their way of life to stay safe and healthy. Living with PKD during the COVID-19 pandemic can be even more challenging. Whether you're a transplant recipient, currently on...
The PKD Foundation Blog is contributed to by PKD Foundation staff and members of our incredible community. Focused on bringing you important PKD and Foundation updates, our blogs cover advocacy initiatives; awareness events; education for patients, caregivers, and health care professionals; and updates from and for our researchers.
Have you ever used an app to help manage living with PKD? There’s an app for everything these days! Why not use an app to help make the best nutrition choices while shopping at the grocery store...
Hello, and Happy Father’s Day to all the dads! My name is Ed McVey and my daughter Meredith has PKD. When I was asked to tell our story for this blog post, I realized how important it is to talk...
In honor of today being Best Friends Day, we reached out to our friends Liz Casperite and Maria Weaver to learn more about how their transplant journey brought them closer together. Philadelphia...
Please join the PKD Atlanta Chapter as we welcome Dr. Rahbari-Oskoui, MD, MS, FASN to discuss JYNARQUE™ (Tolvaptan), clinical trialsRead More