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Brightening the Future for PKD FamiliesBrianna Rodgers and her family

The spring, for many, signals a new start and a perfect time to set new goals for the rest of the year. For 21-year-old Brianna Rodgers of Grapevine, Texas, 2014 is her year to make a difference in the PKD community. "I just want to take the opportunity to do something good," she said.

Flash back one decade ­­– Rodgers was diagnosed with polycystic kidney disease (PKD) at just 11 years old, making her the youngest person in a family full of PKD patients to deal with the disease.

Read Brianna's Story

What is PKD?

Polycystic kidney disease or PKD is one of world's most common, life-threatening genetic diseases. The PKD Foundation is the only organization soley dedicated to finding treatments and a cure.

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Help give a voice to a widely unknown disease by sharing your story. Your experiences can paint a more powerful picture of what it's like to live with PKD.

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