Kawasaki Disease Foundation Australia
Awareness. Support. Research
Our History
The Kawasaki Disease Foundation Australia Inc grew from humble beginnings when a number of parents connected following the Herald Sun newspaper in Melbourne publishing a newspaper article in 2002 about Kawasaki Disease.
With a shared quest to raise greater community knowledge of Kawasaki Disease, the combined effort of two parents led to the Foundation gaining its status as an Incorporated organisation in 2007.
From that point on, the Foundation continued to establish itself as an Association to support Kawasaki Disease patients, their parents/carers, families and the community. The Foundation was successful in being recognised as a charitable group and is licenced to fundraise in various States/Territories across Australia and registered with the Australia Charities and Not-For-Profit Commission
The Foundation actively collaborates with various international Kawasaki Disease support organisations and researchers.
Committee Members
Penny Long
President
Tasmania Coordinator
To view Penny and Isaac’s story – Click Here
Cameron Mates
Committee Member
To view Cameron’s story – Click Here
Caitlin Russo
Queensland Coordinator
Shirley Mates
Secretary
To view Shirley’s story – Click Here
Isaac Long
Tasmania Fundraising Coordinator
Joce Turner
Treasurer
Western Australia Coordinator
To view Joce’s story – Click Here
Nidal & Brian Raslan
South Australia Coordinator
Committee Member
To view Nidal’s story – Click Here