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...
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KDF See’s Candies Holiday Fundraiser KD Mom, Samantha Encinas, invites you to help raise funds to support the KDF’s mission via this online Yum-Raising Event! What: See’s Candies Holiday Fundraiser When: October 9, 2021 to December 3, 2021 Where: See’s Candies –...
What: UCSD 2021 Virtual Kawasaki Disease Parent Symposium When: Saturday, October 2, 2021, from 9 am to 12 pm PST Who: Jane C. Burns, M.D. Director, UCSD KD Research Center | Adriana Tremoulet, M.D. Associate Director, UCSD KD Research...
What: UCSD 2021 Virtual Kawasaki Disease Parent Symposium When: Saturday, October 2, 2021, from 9 am to 12 pm PST Who: Jane C. Burns, M.D. Director, UCSD KD Research Center | Adriana Tremoulet, M.D. Associate Director, UCSD KD Research...
2019 Kawasaki Disease Awareness Challenge Participant Results The Foundation thanks our 2019 KDAC challenge participants. We are grateful for YOUR support and appreciate the time and energy YOU dedicated to helping raise awareness and funds for Kawasaki disease. Together...
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 6th KD Summit of India/ 1st Annual Conference of the Kawasaki Disease Society of India Written by Dana Bell Fairfield, CA The 6th Kawasaki Disease Summit of India and the First Annual Conference of the Kawasaki Disease Society...
New Rochelle, NY: Bringing awareness to Kawasaki disease During the KDF’s 26 days of Kawasaki Disease Awareness campaign, KD mom, Danielle Foster contacted us for support in raising KD awareness. Danielle decided to host an awareness fundraiser for KD...
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...