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What is KD?

Kawasaki disease (KD), also known as Kawasaki syndrome, is a serious illness characterized by inflammation of blood vessels throughout the body that primarily affects young children and infants. Symptoms include prolonged fever, rash, red tongue.

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The Kawasaki Disease Foundation is supported entirely by unpaid volunteers and individual and corporate donations.

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Looking to get involved? Volunteer?  Fundraise?  Or maybe you just want to connect with other KD Families.

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About The Kawasaki Disease Foundation

Our Mission

Kawasaki Disease Foundation strives to be at the forefront of Kawasaki Disease issues by uniting the personal insight of families with the expertise of medical professionals. KDF’s mission is based on three basic principles.

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Kawasaki Disease By The Numbers

1

Cause for Acquired Heart Disease

15

Board Members

1600

KD Cases Annually

2546

Parents and Doctors Reached

100% of your Donation goes toward the Mission of The Kawasaki Disease Foundation: Awareness and Research.

KD Donation

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Kawasaki Disease History

Kawasaki disease (KD), also known as Kawasaki syndrome, is a serious illness characterized by inflammation of blood vessels throughout the body that primarily affects young children and infants. Kawasaki disease is the leading cause of acquired heart disease in children. Although about 80 percent of patients are under five years of age, older children and teenagers can also get KD, but this is uncommon. KD is more common in boys than girls, and the majority of cases are diagnosed in the winter and early spring. It is not contagious.

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Overview

The KDF Bridges program matches families currently facing Kawasaki Disease with trained Support Volunteers. The volunteers are generally parents of children who have Kawasaki Disease, or adult patients who have recovered from Kawasaki Disease. The volunteers are screened and trained by experienced support professionals. The role of the support volunteer is to provide personal insight that may be helpful in coping with Kawasaki Disease.

The program evolved as a method of accomplishing one of the Foundation’s basic goals: providing support to families dealing with the diagnosis of Kawasaki Disease.

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Kawasaki Disease Research Center at University of California San Diego

A very informative site with an overview, parent guide, photographs, and multi-language fact sheets. Find out about research being conducted at the University of California San Diego. Participants in important promising studies are urgently needed.

https://www.pediatrics.ucsd.edu/kawasaki

Kawasaki Disease Research Center at UCSD enrolling young adults (age 15 or older) with a history of KD in childhood in study of health outcomes. Contact adultkd@ucsd.edu to learn more

Kawasaki Disease Research Center at UCSD enrolling families in study of KD genetics. To learn more, contact kdgenetics@ucsd.edu

 

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