Children's Cancer Foundation (Australia)

In 1992, parents of children undergoing treatment at Monash Children's Hospital established KOALA (Kids Oncology and Leukaemia Action) Group. In 2004, the KOALA Group was renamed as the KOALA Foundation and registered as a charity and as a company limited by guarantee. Tony McGinn OAM joined KOALA Group in 2002, was elected President of KOALA Group in 2003 and Chairman of KOALA Foundation on 24 June 2005.[7]

In 1998, parents of children undergoing treatment at The Royal Children's Hospital established the Children's Cancer Centre Foundation. Jeremy Smith, Barrister with the Victorian Bar, joined the board of the Children's Cancer Centre Foundation on 29 March 2009 and was elected Chairman later that year.[8]

In June 2012, the two charities merged to form the Children's Cancer Foundation.

The Children's Cancer Foundation and its sister charity My Room led a capital campaign from 2002–06, raising $23,055,434 to fund construction of a new Children's Cancer Centre at The Royal Children's Hospital and integrated research laboratories at Murdoch Children's Research Institute. The campaign was initiated in 2002 with the support of high profile and influential business leaders; construction commenced in November 2004; and the new facilities were opened on 10 October 2006. The Federal Government provided $10 million (plus interest of $392,000), the Victorian State Government provided $7.3 million and the Children's Cancer Foundation provided additional funding of $5,363,434, which included community, corporate and philanthropic contributions.[9] The Children's Cancer Centre Laboratory continues today hosting several groups funded by the Foundation researching molecular diagnostics, childhood brain cancers, solid tumours and leukaemias.[10]

The Foundation's board of directors, composed of prominent and influential business people, are all volunteers, many of who have been impacted by childhood cancer.[11]

The Scientific Advisory Committee assesses all grant applications and advises the Foundation directors on which funding applications will have the highest impact in cancer prevention, diagnosis and/or treatment, family support and clinical care. The Scientific Advisory Committee and external reviewers are also volunteers.

Curious: We always want to find a better way for every childhood cancer challenge

Collaborate: We know we cannot do this alone, so we seek to partner with the many who can help

Accountable: We strive for the most efficient ways to achieve our ambitions and always provide full disclosure

Advocate: We are the voice for those needing a cure, and are focused on their access to the best possible support today and the promise of complete solutions tomorrow

Belief: We steadfastly believe that we are making a vital contribution to beat childhood cancer for good and the horizon for success is visible

The Children's Cancer Foundation awards grants of $2 to $3 million each year and has distributed more than $52 million to date across clinical care, clinical trials, clinical research and family support.

In 2017, the Foundation expanded project funding to support national projects, including two clinical trials providing access to new treatments to children with cancer across Australia.

A new research initiative launched in 2017, the Hudson-Monash Paediatric Precision Medicine Program, aims to significantly improve treatment for children diagnosed with brain cancers and solid tumours. Scientists at the Hudson Institute of Medical Research have established a living biobank of paediatric brain tumours and solid cancers – including living organoids – to trial and develop targeted treatments and improve clinical outcomes, survival rates and quality of life for childhood cancer patients.[12][13]

In 2019, the Children’s Cancer Foundation partnered with the University of Melbourne, the Victorian Comprehensive Cancer Centre, the Peter MacCallum Cancer Centre, the Royal Children’s Hospital and the Murdoch Children’s Research Institute to fund a new leadership position. The Endowed Chair is a new academic role focusing on clinical care development, paediatric cancer research and the academic development of future generations of paediatric cancer champions.

The Foundation currently has commitments of $15 million across over 30 projects from 2019 through to 2024, funding salaries for 40 hospital and research staff, laboratory consumables and family resources. The Foundation's financials are publicly available, more than $4 million in project funding since 2014 to support children with cancer[1] and shows that over 78% of 2018/2019 of project funding related to clinical research.

• Anthony McGinn OAM, Deputy Chairman - for services to the community in fundraising.
• Mary McGowan, Director, The Victorian Honour Roll of Women 2019 - Local Champion.
• Margaret Zita OAM, The Million Dollar Lunch committee member - for service to the community through charitable initiatives.

The Million Dollar Lunch, launched by Deputy Chairman Tony McGinn OAM in 2005, and supported by a Committee comprising Melbourne's business elite and led by Chairman Jeremy Smith is the annual fundraiser of the Foundation and underpins its project funding.[14][15]

The Million Dollar Lunch 2019, held on Friday, 9 August at the Palladium at Crown raised more than $2.1 million for the Foundation.[16]

In addition to The Million Dollar Lunch, the Foundation raises funds through community fundraising, corporate partnerships, bequests and donations. The Foundation does not conduct public raffles or telemarketing and does not use third party fundraisers.[17]