*Formerly known as the pkDO Foundation
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.
We have a mission to provide funding to families to ensure a PKD-free future for generations.
Patty's Story: How Her Family Ended PKD
Living with Polycystic Kidney Disease had a big impact on Patty's life and her daughter's life too. Fortunately they found a solution to end it before it affected her granddaughter Juliana. Learn how they did it with support from PKD-Free Alliance, and how you can too.
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.
1/21/26: Alliance Celebrates One Year Since Rebranding
Over the past twelve months, we focused our mission by prioritizing access to grant funding for preimplantation genetic testing (PGT-M) and in vitro fertilization (IVF), so families impacted by polycystic kidney disease could stop the disease from being passed on to the next generation.
"Our team established meaningful connections with patients and providers, expanded outreach, and helped parents achieve their dreams of having healthy children free of the burden of PKD," said Alliance Founder Richard Kellner.
“It’s emotional, especially for us.”
Marcus and Callie Payne of Whitestown, Indiana, made a courageous decision to break the cycle of PKD that has affected generations of Marcus’s family. Through IVF with preimplantation genetic testing, they ensured their child wouldn’t inherit the disease that has required Marcus to undergo two kidney transplants.
Read About Affected Families
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.
PKD-Free News & Events

