We are thrilled to announce the launch of Heart to Heart, the very first podcast created by our incredible KDF Youth interns! In Episode 1, the hosts open up about their own Kawasaki Disease journeys – sharing their diagnoses,...
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As we celebrate 25 years of the Kawasaki Disease Foundation, we’re honored to look back on where it all began with one family’s determination to make sure no parent ever faced Kawasaki disease alone. Greg Chin, who founded KDF...
My name is Loren Wheale, and I want to tell you about my daughter Mollie. I am telling this story for the parents who are right now sitting in a hospital room with a sick child, scared out of...
Q. How did you first become connected to Kawasaki Disease and the Kawasaki Disease Foundation? A. My journey with the Kawasaki Disease Foundation began in 2006 when my son, Chance, was diagnosed with Kawasaki Disease at the age of three....
Jamie Dukat’s KD Strong Story | How I transitioned from pediatric to adult cardiology How old were you when you were diagnosed with KD? If you were old enough to remember, how did you feel? What was your reaction...
Chance’s Kawasaki Disease Story Chance was diagnosed with Kawasaki Disease when he was 3 years old. He developed a fever on May 31, 2006, and was treated for a viral infection at a local urgent care clinic. Over the...
Calen Page By: Jennifer Page A committed group of people in Big Rapids, Michigan, are working to raise funds to support KD Research in the Quest for a Diagnostic Test. For many children, having a diagnostic test is the...
My Kawasaki Disease Journey | 26 Years Post KD and Healthy! Written by: Kate Davila My name is Kate Davila, and I had Kawasaki disease (KD) 26 years ago when I was 15 years old. I hope that my...
The Jekums Family: Our KD Story Written by Sari Jekums Orange County, CA We began our journey with Kawasaki disease (KD) when my son was diagnosed four years ago. Even though my husband and I are both Registered...