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Building research where it matters most: a new opportunity for regional, rural and remote Australia
A new grant opportunity from the National Health and Medical Research Council is supporting locally led research grounded in community need and informed by lived experience.
The critical role of interpreters in patient care
Many clinicians think booking an interpreter or using an AI translation app is enough. New Australian research shows why this approach falls short.
You know where you feel safe: trauma-informed and aware health care for Stolen Generations survivors
Trauma-informed care need not be a specialist model. For Stolen Generations survivors, it must be embedded in every healthcare interaction — especially in each GP, dental and aged care interaction.
Health care's plastic paradox: from life-saving innovation to public health concern
Insights from Australia's Senate Inquiry into Microplastics and Human Health.
Putting people at the centre of cancer care
Cancer survivorship reminds us that cancer care is more than caring about cancer. It is caring about people.
Does POTS need a new name?
There’s a lot of mis- and disinformation about postural orthostatic tachycardia syndrome (POTS) online. Experts say a new name would clear up some of the confusion.
What would I know: on brain injury, advocacy and the comfort of consensus
People living with acquired brain injury are being let down by a lack of data, siloed specialities and closed feedback loops.
New clinical practice guidelines for suicide and self-harm in children
The evidence-based guidelines demonstrate what lived experience can tell us about the current state of the mental health system.