ACBRD

Experiences of type 2 diabetes stigma in healthcare settings

June 29, 2026June 24, 2026ACBRD

A multi-country review explores what type 2 diabetes stigma looks like in healthcare settings, why it happens, and why it matters

By Emmanuel Ekpor

Can hidden strengths help women manage type 2 diabetes and pre-diabetes?

June 23, 2026June 23, 2026ACBRD

New Australian research suggests resilience, optimism, and a sense of control may help older women manage type 2 diabetes and pre-diabetes

By Sarah Manallack

How can our research keep up, in a changing world?

May 28, 2026May 28, 2026ACBRD

In an era of rapid change, we unpack new and emerging ways to do research and consider what’s next for psychosocial diabetes research

By Eloise Litterbach & Uffe Søholm

Waste not, want… what?

May 13, 2026May 13, 2026ACBRD

How do environmental concerns affect diabetes self-management choices? A recent European study asked people with diabetes what is important to them

By Alison Robinson

More reflections from the Global End Diabetes Stigma Summit

April 30, 2026May 6, 2026ACBRD

Contributions and key insights from ACBRD researchers

By Eloise Litterbach, Meaghan Read, Emmanuel Ekpor, and Sarah Manallack

One month on: reflections from the co-leads on the Global Summit to #EndDiabetesStigma

April 29, 2026April 30, 2026ACBRD

Looking back, moving forward: what it meant to finally be in the room

By Jane Speight and Elizabeth Holmes-Truscott

Mental health, sleep, and social connection: what do they have to do with type 2 diabetes risk?

April 28, 2026May 10, 2026ACBRD

Digital twin study highlights the need to consider psychosocial factors in T2D risk assessment and reduction efforts

By Dr Uffe Søholm

Inside the National Diabetes Summit

April 20, 2026April 20, 2026ACBRD

Key takeaways from a landmark day at Parliament House, Canberra

By Alison Robinson

Centring Lived Experience in Diabetes Research and Care: what helps and hinders meaning involvement?

April 15, 2026April 16, 2026ACBRD

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