A multi-country review explores what type 2 diabetes stigma looks like in healthcare settings, why it happens, and why it matters
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Tag: T2D
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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What do people want to hear when they’re diagnosed with type 2 diabetes?
A US-based qualitative study highlights the emotional and informational needs of people with type 2 diabetes at diagnosis
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Are rural communities forgotten in diabetes research?
This ACBRD-led study explored ways to increase research participation for people with type 2 diabetes living in rural Australia
By Dr Jo Jordan
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Why reducing weight stigma may be key to healthy behaviours in type 2 diabetes
New ACBRD research highlights the link between weight self-stigma, healthy eating, and physical activity among Australian adults with type 2 diabetes
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Can parents’ behaviour and the foods available at home influence children’s food choices in families at high risk for type 2 diabetes?
A European study shows children’s food choices are dependent on parenting patterns
By Aashi Chhatiawala
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Does stigma impact how adults with type 2 diabetes manage their weight?
US research finds people with the double burden of diabetes and weight stigmas perform fewer weight-related health behaviours
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What are the expectations and experiences of non-insulin injectables among adults with type 2 diabetes?
Reducing diabetes distress: Can cognitive behavioural therapy (CBT) help?
