Non-profit organization designed to promote awareness and support for those who have been affected by Kawasaki Disease.
Creates and maintains a support and information exchange for patients and families dealing with Kawasaki disease.
Parent lead support group, creating awareness of KD in Canada. Includes a forum, KD information and a pamphlet.
A partnership of parents, patients, and professionals. Includes fact sheets, support, parent guide, forum and resources.
Site dedicated to a young boy in the UK who had KD in March 2005.
Independent and active forum on Kawasaki disease without adds.
Thanks to DMOZ, which built a great web directory for nearly two decades and freely shared it with the web. About us