PAEDIATRIC MENTAL HELP FOR CHILDREN OF DEFENCE PERSONNEL, VETERANS AND FIRST RESPONDERS Psychosocial research translated into teaching resources
Filmed in Armidale, New South Wales | November 2024
Dr Marg Rogers is a Senior Lecturer in Early Childhood Education at University of New England (UNE) in Armidale, New South Wales. She is a prominent figure in early childhood education New South Wales, and is also a Post Doctoral Fellow at the Manna Institute, a mental health research organisation within the regional university network across Australia, that is building place based research capacity to improve the mental health of regional, rural and remote Australia.
Dr Rogers has taught across all areas of education: early childhood, primary, secondary and tertiary. She researches marginalised voices within families and education, especially in regional, rural and remote communities.
Many Australian Defence Force (ADF) members reside in rural, regional, and remote (RRR) communities, creating significant challenges for their families regarding mental health service access. With 30% of current ADF members living in these areas, families often endure waiting lists for specialised care, which is typically located in metropolitan settings. As a result, children in these families frequently witness trauma, leading to potential mental health issues.
Australian Health Journal spoke with Dr Rogers on her research focusing on paediatric mental health, specifically developing early intervention psychosocial resources for children from veterans, defence families, and first responders.
Dr. Rogers emphasises the need for increased support and resources for these families, advocating for flexible, accessible care that moves with them, including telehealth options. Her work includes developing printed and digital storybooks based on children’s narratives to help families cope with issues like moral injury.
The impact of her work, has also garnered interest overseas, in collaborative efforts with Canadian and UK institutions who are further enhancing these resources for affected families in their own countries.
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Persistent pain also has debilitating personal costs – negatively impacting quality of life and the ability to engage in meaningful work and life activities.
Despite the enormity of this problem, very few effective treatments exist with most showing only small to moderate improvements. New treatments are desperately needed. The group believes the best way to create impactful change is to work with people with lived experience of persistent pain to devise solutions with them, not for them.
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