Articles on Aboriginal health services
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Aboriginal people in remote Australia have no choice but to live in homes too small for their families and face long waits for plumbing and washing machine repairs.
First Nations women face almost twice the risk of stillbirth compared to non-First Nations women. Much of the inequity can be linked to the ongoing impact of colonisation on birthing women.
Lupus is two to four times more common among Aboriginal and Torres Strait Islander people. It’s also tends to be more severe, with higher rates of kidney failure than non-Indigenous people with lupus.
A transactional mental health system fails to accommodate consumers’ needs for human connection and understanding. Elders in Perth are helping to transform this system.
People who menstruate in rural and remote Indigenous communities face a unique set of challenges, and have a particular need for better access to period products.
Children as young as ten don’t have access to Medicare if detained. And they’re dying of largely preventable diseases.
Here’s where we could lift our game to ensure reliable, equitable and culturally safe telehealth for First Nations people in Australia, whether living remotely or in our cities.
Government health organisations need to provide better support for Indigenous people suffering from musculoskeletal conditions.
Birthing on Country services acknowledge First Nation peoples’ continued ownership of land and unique birthing practices.
Many Aboriginal community controlled health services are already running urgent vaccination campaigns within their existing resources, but more needs to be done.
A Western Australian study, one of the first of its kind, reveals the complex experiences of those living at the intersection of being Indigenous and part of the LGBTIQ+ community.










