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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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Advocacy

Awareness

Education

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PKD Will Not Beat Me
Germaphobe

Germaphobe

Upon becoming a kidney transplant recipient, we must take lifelong medicine that suppresses our immune system to help prevent our body from rejecting the donated organ. At this same time, germs...

PKD Will Not Beat Me
32 Candles

32 Candles

During the silent moment prior to blowing out my birthday candles, I always think of the reality that I was not expected to see my 19th birthday. Also, that it is a true miracle I have turned 32...

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    When diagnosed with polycystic kidney disease (PKD), facing and overcoming challenges are part of the disease. This month, the PKDRead More
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    I was standing with my back toward the wall at Starbucks in the Sacramento International Airport, waiting for my tall,Read More
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    I was in my early 20s when I first met my husband, Noah. We saw each other two nights inRead More
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    Upon becoming a kidney transplant recipient, we must take lifelong medicine that suppresses our immune system to help prevent ourRead More
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    During the silent moment prior to blowing out my birthday candles, I always think of the reality that I wasRead More
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    It is easy to become creatures of habit. Some parts of our daily routine are mundane while others we lookRead More