Become a monthly giver
As a monthly giver, you will join a special group of people who believe Queensland kids deserve the best possible health and wellbeing.
Leave a gift in your Will
Leave a legacy and champion world-class care for Queensland kids.
Fundraise for sick kids
Fundraise to fill gaps in funding and support across the kids health landscape.
Charity Raffle
Win BIG and be the difference every kid deserves.
Volunteer
Volunteer to create precious moments in one of the world’s best paediatric hospitals.
Partner with us
We work with partners to engage their stakeholders around a meaningful cause.
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Give sick kids every chance at life this christmas!
This Christmas, give a gift that could give children like Raf every chance to live cancer free forever!
We’re here to be the difference that really matters.
Halle's story
At just four and a half months old, Halle was diagnosed with acute myeloid leukaemia.
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.
Harley's story
Harley was born with hypoplastic left heart syndrome, one of the most rarest and severe heart defects.
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.
Lachy's story
At an early age Lachy was diagnosed with bronchiectasis and tracheobronchomalacia.
Patrick’s story
Born with multiple joint deformities, five-year-old Patrick has undergone ongoing plaster casting of his torso and legs since birth.
Jonathan's story
Jonathan had a rocky start to life, after being diagnosed with hypoplastic left heart syndrome within three days of being born.
Ash's story
In January 2022 , four-year-old Ash was diagnosed with acute lymphoblastic leukaemia. His treatment will continue until April 2024.
Rowan's story
Rowan is living with an acquired brain injury after he was injured during a motorcross event at seven-years-old.
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.
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.
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.
Lachlan's story
Lachlan was born with chronic kidney disease and at just four months old, he went into end stage renal failure.
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.
Clayton's story
Diagnosed with dilated cardiomyopathy when he was only one year old, Clayton went into end stage heart failure at just thirteen.
Sarah's story
Seventeen-year-old Sarah was diagnosed with clear cell sarcoma in her knee following an emergency department admission.
Tiana's story
In March 2022, Tiana was diagnosed with Ewing sarcoma – a rare cancer of the bone or soft tissue.
The difference that shapes their world
Through supporting the Children’s Hospital Foundation, you can improve childhoods and ensure all children and young people have access to treatment - sooner.
