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*Formally known as the pkDO Foundation

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Unite with us to ensure Generational Health and a PKD-Free Future

Polycystic Kidney Disease (PKD) is a genetic condition that affects 600,000 people in the U.S. It is one of the leading causes of kidney failure. An affected parent has a 50% chance of passing it to their child. The PKD-Free Alliance (PKD-Free) supports proven methods for putting an end to PKD.

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We have a mission to provide IVF funding to families to ensure a PKD-free future for generations.

Featured Story

Utah Jazz General Manager Justin Zanik Shared his support for the PKD alliance

Justin Zanik, the General Manager for the NBA’s Utah Jazz, recently shared comments about his personal journey with Polycystic Kidney Disease (PKD) and his strong support for the mission of the PKD-Free Alliance.

Ending PKD in Your Family

PKD-Free is uniting families, the medical community and organizations to provide information and the necessary resources, including grants for IVF and preimplantation genetic testing (PGT). We are committed to ensuring that PKD is not passed down to future generations. With proven methods, we will change the odds from 50% to 0%. Join us and learn more about how you can end PKD in your family.

PKD-Free News: PKD-Free Spokesmon Natasha Rogina was a guest on the Santa Barbara Nutrients Radio Show and Podcast. She shared important information about how families can have PKD-Free Children and PKD-Free’s grant programs.

The Kellner Family

When we discovered my wife Jo had PKD, we were told there was nothing to do until her kidneys failed.

The Cavallaro Family

My family first discovered PKD more than 30 years ago, with my dad Phil Cavallaro.

The Meyer Family

My wife and I successfully went through the process of PGT (Preimplantation Genetic Testing) and with a team of wonderful doctors we have our amazing son who is PKD free.

 

Molly and Kristi

I call it a miracle that I am healthy today since I came close to needing dialysis.

The Patterson Family

On Halloween 2019 I received the call of a lifetime. It was my transplant coordinator from University of Utah telling me I was going to finally get a transplant from an anonymous donor named Sheryce.

Amy Leininger

I learned about my recipient’s kidney disease via Instagram and saw she was in serious need of a kidney donor.

 

Tim Francis

I was 24 years old when I found out I had Polycystic Kidney Disease.  I went to the radiologist for a lump on my chest. As we were looking at the scans the radiologist said, “Can I show you something?

Scott MacLean

My father, my brother, and I all have Polycystic Kidney Disease. When I was diagnosed, I was told I had 5 years until I’d reach end stage kidney failure.

 

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