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.
Polycystic liver disease (PLD) often goes hand in hand with PKD. We recently reached out to PKD community member and advocate Jenn Tompkins to share her experience as a PLD patient, how she has...
Being a patient takes work and dedication. Depending on our health status, it can feel like a part-time to full-time job. It is a constant learning process and important to find a balance between...
PKD Foundation appoints past Fellowship recipient Michal Mrug, M.D., new Scientific Advisory Panel Chair
Meet Michal Mrug, M.D., Chair of the PKD Foundation Scientific Advisory Panel (SAP). The Scientific Advisory Panel is comprised of 14 of the most prestigious physicians and scientists in the...
When managing a chronic disease, like PKD, it is important to be your own best advocate. When preparing for aRead More
Summer is coming up faster than you know, and along with it, the 2018 PKD Connect Conference! Formerly known asRead More
Polycystic liver disease (PLD) often goes hand in hand with PKD. We recently reached out to PKD community member andRead More