Empowering better tomorrows through PKD Connect Peer Mentoring Program

Risa Simon At the PKD Foundation, we’re proud to offer support through the PKD Connect Peer Mentor Program. This program is designed to help facilitate and build a strong support...

Join the PKD Foundation for #GivingTuesday

#GivingTuesday is right around the corner, and this year, we’re asking: what can you give? Can you give a donation? Our goal for #GivingTuedsay is to raise $18,000 — the...

PKDF Director of Government Affairs recaps the 2018 ASN Kidney Week

Alexis (left) with the PKD Foundation’s new Director of Research, Elise Hoover This year’s American Society of Nephrology (ASN) Kidney Week took place in San Diego, CA, from Oct. 25...

Successful second Annual PKD Comedy Night brings in major funds and laughs

Carolines on Broadway Just last month, on Nov. 13, the PKD Foundation sponsored its second Annual PKD Comedy Night at Carolines on Broadway in New York City and raised a...

Voices of PKD: Nicole Cardin

Nicole with her granddaughter, Annabelle My paternal grandmother, Helen, is the first that we know of who had autosomal dominant polycystic kidney disease (ADPKD) in the family. We only figured...