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At 6 weeks old David was diagnosed as having cystic fibrosis. His parents say that his involvement in research offers them their greatest hope for his future.
Kojonup couple George and Trish Church ensured their legacy of generosity and kindness lived on, by including The Kids in their will. Read more.
Read the 2024 edition of the Together Magazine
News & Events
Introducing Illuminate PitchFestAt The Kids our greatest asset is our people. We are strongly invested in the future of child medical research welcoming, nurturing, and encouraging the best and most innovative Australian and international researchers.
News & Events
Paediatric clinical service delivering critical health needs to Indigenous childrenComplex health needs of Indigenous children are being fast-tracked by a unique project designed to reduce red tape and deliver timely paediatric services.
You are so valuable to us! Not only can you help fund our research into what makes kids healthy and happy, but you can also raise awareness of how important that work is.
Meet the Friends of the Institute, a very impactful group of volunteers whose Friend-raising efforts have supported The Kids for more than 25 years.
Parental Experience of Information and Education Processes Following Diagnosis of Their Infant With Cystic Fibrosis Via Newborn Screening. Abstract
Conditionally reprogrammed primary airway epithelial cells maintain morphology, lineage and disease specific functional characteristics The study of
Airway surface liquid pH is not acidic in children with cystic fibrosis Modulation of airway surface liquid (ASL) pH has been proposed as a therapy