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Our goal is to achieve the biggest possible impact with our fundraising revenue. We identify and action gaps in funding and support right across the kids' health landscape.

As the only charity in Queensland catering for kids with all illnesses, injuries and conditions, the scope and impact of our work runs far and deep.

Read our latest Impact Report for 2022/23 to discover how your donations fund cutting-edge equipment, vital research and on the ground support for our state's sickest and most critically injured children, throughout Queensland and northern New South Wales.

Our key investments

As the proud philanthropic arm of Queensland Children's Hospital and Children's Health Queensland, we continue to raise our ambitions for children's health to match this world-class institution.

Your support keeps us at the forefront of paediatric healthcare advancements, driving continuous innovation and research – building brighter and healthier futures for our sick children.

Immunotherapy research

For decades, chemotherapy, radiation and surgery have been the mainstays of treating cancer, however these treatments have unwanted side effects, and can leave survivors with chronic health problems, and lifelong physical and intellectual disabilities.

Your donations have supported the establishment of the Ian Frazer Centre for Children’s Immunotherapy Research. By capitalising on the strengths of a multidisciplinary team of experts, the Centre will accelerate the pace of discovery and ensure research is translated into a new era of children’s cancer treatments.

Find out more
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Advanced gene therapies

About 400,000 Australian children currently live with a rare disease. One-third of these children will not live to see their fifth birthday.

With your support, the Queensland Children's Hospital ACTION (Advanced Therapies and Clinical Trials Innovation) Centre opened in May this year to give Queensland children better access to life saving cutting-edge clinical trials and advanced therapies.

Through one centralised statewide hub, the ACTION Centre will deliver hope and promising new treatment options for children with rare diseases and complex illnesses.

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Queensland Children's Hospital ACTION Centre

Brain cancer research

Because of you, we were able to help establish the Children’s Brain Cancer Centre.

Through our multi-year commitment, researchers have discovered that spinal fluid collected in routine lumbar punctures can be used to create a ‘genomic fingerprint’ of a child’s cancer, which can be used to create individually tailored treatments.

This revolutionary discovery could become the standard for treating brain cancer in kids. Research findings like this give kids like Isaac with brain cancer hope for a better future.

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Queensland Children's Tumour Bank

Since 2008, your support has funded the Queensland Children’s Tumour Bank – an openly accessible paediatric tumour tissue bank at the Children’s Centre for Health Research.

Through the collection paediatric tissue samples, doctors have been able to find answers and develop new treatments for children with cancer, including neuroblastoma, leukaemia and brain tumours – supporting research in Queensland and beyond.

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Queensland Children's Tumour Bank

Digital PET-CT scanner

Queensland Children’s Hospital is now home to a state-of-the-art digital PET-CT scanner, thanks to a $2.5 million investment from supporters like you.

This digital PET-CT scanner will provide easier and faster scans for paediatric oncology patients undergoing treatment at Queensland Children’s Hospital. Ensuring kids like Raf can have the right care delivered in the right place at the right time.

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EEG machine

Thanks to you, a high-density electroencephalography (EEG) machine has been funded at the Children’s Centre for Health Research.

This piece of equipment is central to a research study that is monitoring brain waves in children affected by stroke and brain injury. Helping kids like Rowan have a more pleasant treatment experience and giving clinicians a more comprehensive understanding of their brain patterns during recovery.

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Music therapy

Because of you, we have been able to support one of Australia’s largest music therapy programs at Queensland Children’s Hospital for over 30 years, helping sick kids on their road to recovery.

Music therapy is so much more than simply playing music. Research shows the use of individualised musical interventions can improve a child’s emotional wellbeing, help them experience less pain and anxiety during their treatment and support diverse health outcomes.

Last year, the music therapy team at the Queensland Children’s Hospital provided over 1,800 sessions to almost 750 infants, children, adolescents and their families – over 50 hours of music therapy every week.

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Impact programs

Because of you, we can provide our impact programs and services at the Queensland Children’s Hospital to address the needs of families and support the public health system through expanding capacity in a lean operating environment.

From Book Bunker to free meals, bravery beads, craft packs and Cuddle Carers, our programs and services nurture social connection, empowerment and provide safe spaces that kids need to play, learn and be a child.

Each year, we engage in around 120,000 interactions with patients and families during hospital visits and stays.

Impact Programs

Where your dollar goes

When you donate to us, we are transparent about where your money goes.

For every dollar donated 64 cents goes straight to impact like research, equipment and support for patients and families.

10 cents goes towards our future fund. This future fund allows us to make big multi-year commitments to areas of vital importance like immunotherapy, brain cancer and cystic fibrosis.

The last 26 cents goes towards operating expenses and cost of fundraising allowing us to generate more income and operate with good governance.

Multi-year commitments

Children’s Hospital Foundation funds research that’s needed to accelerate breakthroughs and champion the delivery of world-class paediatric care.

Your support helps fund larger multi-year commitments into kids' health.

We’re here to be the difference that really matters.

Raf's story

Nine-year-old Raf is currently receiving treatment for Stage 4 Neuroblastoma - including multiple stem cell transplants – a life changing immunotherapy – to treat his cancer.

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Raf's story

Evie's story

Evie was born with cystic fibrosis – a life threatening disorder that will likely require her to undergo a lung transplant in the future.

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Evie's story

Patrick’s story

Born with multiple joint deformities, five-year-old Patrick has undergone ongoing plaster casting of his torso and legs since birth.

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Patrick’s story

Lachy's story

At an early age Lachy was diagnosed with bronchiectasis and tracheobronchomalacia.

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Lachy's story

Mahalia's story

At just 13 weeks old, Mahalia was diagnosed with a rare condition – Chromosome 22 microduplication syndrome. With little information available the family have faced a journey into the unknown.

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Mahalia's story

Rowan's story

Rowan is living with an acquired brain injury after he was injured during a motorcross event at seven-years-old.

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Rowan's story

Lachlan's story

Lachlan was born with chronic kidney disease and at just four months old, he went into end stage renal failure.

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Lachlan's story

Ash's story

In January 2022 , four-year-old Ash was diagnosed with acute lymphoblastic leukaemia. His treatment will continue until April 2024.

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Ash's story

Eloise's story

Eloise was diagnosed with rhabdomyosarcoma – a very rare type of cancer that forms in the soft tissue. Treatments included 16 months of surgeries, scans, chemotherapy and radiation.

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Eloise's story

Jonathan's story

Jonathan had a rocky start to life, after being diagnosed with hypoplastic left heart syndrome within three days of being born.

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Jonathan's story

Halle's story

At just four and a half months old, Halle was diagnosed with acute myeloid leukaemia.

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Halle's story

Harley's story

Harley was born with hypoplastic left heart syndrome, one of the most rarest and severe heart defects.

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Harley's story

Ava's story

Just a month shy of her eighth birthday, Ava was diagnosed with stage four neuroblastoma. She was given just a 50 percent chance of survival.

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Ava's story

Clayton's story

Diagnosed with dilated cardiomyopathy when he was only one year old, Clayton went into end stage heart failure at just thirteen.

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Clayton's story

Isaac's story

Isaac was diagnosed with brain cancer at only four-months-old. His tumour is inoperable, but he underwent treatment to shrink the tumour.

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Isaac's story

Sarah's story

Seventeen-year-old Sarah was diagnosed with clear cell sarcoma in her knee following an emergency department admission.

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Sarah's story

Tiana's story

In March 2022, Tiana was diagnosed with Ewing sarcoma – a rare cancer of the bone or soft tissue.

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Tiana's story

Together we can be difference every kid deserves

+ Help deliver cures this Christmas
Help deliver cures this Christmas

1 in 3 children with rare and complex diseases will not live to see their fifth Christmas. Help fund research that could save lives today.

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