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Scott Dad of two, Riley and Georgia. Project community member. Any contribution I can make through community involvement at the Institute is
Nam-Anh Mum of two, Evelyn and Nicolas. Trial participant, project community member. I want to teach my children what it means to be part of a
Congratulations to Alec Truswell, Tamara Veselinović, Anastasia Phillips, and Wenna Lee for being awarded Seed Funding through the Wesfarmers Centre of Vaccines & Infectious Diseases, each valued at up to $25,000, and to Sonia McAlister, the recipient of the 2026 Riley Hughes Memorial Award in Pertussis Research.
A powerful new digital modelling tool is helping tackle an emerging challenge in children’s health – the dramatic decline in walking and cycling to school.
Scientists at The Kids Research Institute Australia are taking their fight against antibiotic- resistant superbugs to the Goldfields working alongside local Indigenous communities and councils.
The Kids Research Institute Australia is returning to Kalgoorlie on 20 and 21 May 2026 to host its second STEM Festival and set off a chain-reaction of fun, with two idea-fuelled days of activities planned for local children and families
As Neurodiversity Celebration Week draws to a close, we are shining a light on an important study underway at The Kids Research Institute Australia, led by Dr Thom Nevill, a Research Officer within our Human Development and Community Wellbeing and Child Disability teams.
Ten emerging researchers took to the stage for our fourth Illuminate PitchFest, where community support helped push the total raised for Illuminate Awards past $1 million.
Rising carbon dioxide levels are being detected within the human body, with new research warning a key blood marker for the gas could near its healthy limit within decades if current trends continue.
In 2026, Rare Disease Day is recognised on 28 February to raise awareness and generate change for people living with rare disease, their families and carers worldwide. This year’s global theme, More than you can imagine, highlights the immense impact of rare disease on families across the world.