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.
At the PKD Foundation, we strive to give all types of patient experiences a voice in the community. Recently, an almost un-heard of story came to us from our Orlando Chapter Education Coordinator...
When it comes to finding a living donor, many PKD patients face the same difficult question: how do you ask someone for a kidney? From friends and family to Facebook pages and t-shirts, PKD...
Being a patient takes work and dedication. Depending on our health status, it can feel like a part-time to full-timeRead More
Meet Michal Mrug, M.D., Chair of the PKD Foundation Scientific Advisory Panel (SAP). The Scientific Advisory Panel is comprised ofRead More
At the PKD Foundation, we strive to give all types of patient experiences a voice in the community. Recently, anRead More