Living with PKD During COVID-19
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...
About
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.
Advocacy
Awareness
Education
Research
Fundraise Your Way: Kansas father runs in honor of son to raise money for PKD research
Our Fundraise Your Way program is one of the best ways you can help create a future without PKD. When you turn your hobbies and passions into creative fundraisers, 100% of the money you raise...
PKD Foundation CEO reviews major accomplishments for 2018
This year, we hit some incredible milestones as an organization and community. I’d like to thank patients, caregivers, volunteers, researchers, physicians and staff for all their time and efforts...
Important memo for PKD community regarding the Affordable Care Act
Our Director of Government Affairs, Alexis Denny, recently provided the following memo on a federal district court judge's decision in the case of Texas vs US regarding the Affordable Care Act...
Coconut Angel Food Cake from Cooking Well
It's the most wonderful time of the year! As a holiday treat, we're sharing our Coconut Angel Food Cake recipe from Cooking Well. When you whip up this delicious treat, you won't have to worry...
Voices of PKD: Nicole Cardin
My paternal grandmother, Helen, is the first that we know of who had autosomal dominant polycystic kidney disease (ADPKD) in the family. We only figured it out when others in the family started...
Successful second Annual PKD Comedy Night brings in major funds and laughs
Just last month, on Nov. 13, the PKD Foundation sponsored its second Annual PKD Comedy Night at Carolines on Broadway in New York City and raised a grand total of $121,159.88! Carolines on...
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Only a few new drugs for chronic kidney disease (CKD) have been approved in the last several decades because drugRead More
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Our Fundraise Your Way program is one of the best ways you can help create a future without PKD. WhenRead More
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Our Fundraise Your Way program is one of the best ways you can help create a future without PKD. WhenRead More
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This year, we hit some incredible milestones as an organization and community. I’d like to thank patients, caregivers, volunteers, researchers,Read More
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Our Director of Government Affairs, Alexis Denny, recently provided the following memo on a federal district court judge’s decision inRead More