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New York City Walk for PKD

Three Peas in a Pod

Sadly there are still no treatments or a cure for ARPKD, the recessive form of polycystic kidney disease, the kind that Max and Gabe have. This is our 12th Walk for PKD team and there are still babies dying from ARPKD. Now more than ever we need to raise funds. We need to learn more about this disease and do more research to help find a treatment and give families hope. 

We walk to advocate for our boys. We walk to show them how awesome they are and that we will always support them. We walk to give them hope. We walk to give other families hope. We walk to remember all of the babies (and some children) who have passed away from this horrible disease.....Mia, Brooke, Remi, Emma, Nathaniel, Noah, Alexis, Porter, Devin, Juniper, Thomas, Anna, Timothy, Alex, Harper, Georgia, Eric, Tristan, Jody, Savannah, Colton, Elena, Alexander, Ramsie, Eloise, Greyson, Caroline, Ivy, Molly Mae........ too many to name.

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PKD Foundation

We are the only organization in the U.S. solely dedicated to finding treatments and a cure for PKD to improve the lives of those it affects.

Our vision is that one day no one will suffer the full effects of PKD.

Our home: 1001 E. 101st Terrace, Suite 220, Kansas City, MO, 64131

PKD Foundation is a 501 (c)(3), 509 (a)(1) public charity.
Federal tax ID: 43-1266906

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