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.


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    It’s funny how some moments seem hard to recall and then others have been embedded in our minds forever. I’llRead More
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    With my 10-year kidney transplant anniversary this coming Monday, I thought it would be fun to take a walk downRead More
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    Determination, the “D” in my PKD! Because so many members of my family grapple with PKD, or have died fromRead More
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    Knowledge, the “K” in my PKD! Rather than fear, try and understand! This is what I live by. When firstRead More
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    Last July, I learned that the Renal Support Network was having its 9th Annual Essay Contest. The theme was “WhatRead More
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    Positivity, the “P” in my PKD! The power of positive thinking has no limits! Every morning when we wake up,Read More
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