Raise your voice for PKD during Congress’s April recess
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...
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...
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%...
Kate and her dad, Dave My name is Kate Callahan and I’m a 21-year-old college student from the San Francisco Bay Area. My journey with PKD begins when I was...
Lindsay Roper and her family. My name is Lindsay Roper, I grew up in northern California and met my husband Alan while we were going to college in Utah. We...
Rob Herman As many PKD patients know, PKD can often be accompanied by other ailments. Join guest blogger Rob Herman as he shares his and his family’s story about how...