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 lead 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 research opportunities.

Committee Members

Rebecca Wilby

President

To view Bec’s story – Click Here

Meagan Mitchell

Queensland Coordinator

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Simone Staaden

Western Australia Coordinator

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Shirley Mates

Secretary

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Penny Scott & Isaac Long

Tasmania Coordinator/Tasmania Fundraising Coordinator

To view their story – Click Here

Cameron Mates

Committee Member

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Brent Anderson

Treasurer

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Nidal & Brian Raslan

South Australia Coordinator/Committee Member

To view Nidal’s story – Click Here

Melissa Copas

New South Wales Coordinator

To view Melissa’s story – Click Here