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.
Fundraise Your Way: California man gathers family and friends to raise funds with beer and bocce ball bash
Our Fundraise Your Way program is one of the best ways you can help create a future without PKD. When you turn your hobbies or passions into creative fundraisers, 100% of the money you raise goes...
As Kidney Month starts winding down, keep up the momentum by raising your voice for PKD! Both the House and Senate will leave Washington, D.C. from April 15-26, 2019, and many will be back in...
There are some truly fascinating techniques in the research field being used to help increase our understanding of PKD. This week, our Chief Scientific Officer, Dr. David Baron, shares how the...
Earlier this week, I joined over 200 people from pharma, biotech, patient advocacy, regulatory agencies and patients at Patients as Partners 2019 in Philadelphia, PA. It was great to hear about...
If you follow us on social media (Facebook, Twitter, Instagram and LinkedIn), we hope you’ve already heard about our excitingRead More
My name is Lindsay Roper, I grew up in northern California and met my husband Alan while we were goingRead More
Our Fundraise Your Way program is one of the best ways you can help create a future without PKD. When youRead More
As Kidney Month starts winding down, keep up the momentum by raising your voice for PKD! Both the House andRead More