Contributions and key insights from ACBRD researchers
By Eloise Litterbach, Meaghan Read, Emmanuel Ekpor, and Sarah Manallack
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Category: Community involvement
Centring Lived Experience in Diabetes Research and Care: what helps and hinders meaning involvement?
More than 90% of people with diabetes have type 2 diabetes (T2D), yet their voices are often missing from research and healthcare decisions. We partnered with community co-researchers living with T2D to explore what supports meaningful involvement.
By Dr Jo Jordan
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Australians living with diabetes reflect on the 2026 PSAD
2026 PSAD Axel Hirsch Lived Experience Travel Award winners share their thoughts on the 30th PsychoSocial Aspects of Diabetes (PSAD) Annual Scientific Meeting
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PSAD in Australia: ACBRD hosts the 2026 meeting
ACBRD proudly hosted the 30th PsychoSocial Aspects of Diabetes (PSAD) Annual Scientific Meeting in Geelong, Australia
By Dr Eloise Litterbach, Dr Elizabeth Holmes-Truscott, Emmanuel Ekpor, Sarah Manallack, and Alison Robinson
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Smarter diabetes devices – but who owns the data?
Diabetes devices generate and store lots of data to support people living with diabetes. But under current laws, who owns this data is unclear. Researchers from the UK call for greater data protection for the diabetes community.
By Dr Jo Jordan
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