The zine presents findings from Dr. Woodgate’s study entitled “Youth Voices: Their Lives and Experiences of Living with an Anxiety Disorder.”
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Arts-Based Boundary Objects Used to Communicate the Results of Health Research
This video series available in English, French, and Cree
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In this article we explore the experience of dyspnea in school-age children with asthma including exploring children’s perceptions of the (1) sensations of dyspnea, (2) precipitants of dyspnea, (3) coping strategies used to deal with dyspnea, and (4) effects of dyspnea on lives of children.
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This paper examines youth’s perspectives of the relationships between health and environment.
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This paper reports on findings specific to fathers’ experiences of caring for their child with CCN and highlights recommendations provided for parents of children with CCN, service providers, and policymakers.
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Dr. Roberta L. Woodgate and her team asked 32 families what they wanted others to know about their lives and the importance of respite care to their families.
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This research study seeks to understand experiences of the use of respite services by families with CYSHCN with the aim to help improve respite services.
Read MoreAn ethnographic study of youth’s perspectives of health and their own health interests.
Read MoreA digital story produced in Norway House and a three part video series.
Read MoreA digital story series based on Dr. Woodgate’s CIHR funded research study entitled “Changing geographies of care: Using therapeutic landscapes as a framework to understand how families with medically complex children participate in communities.”
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Dr. Woodgate developed a video series that brings to life the words, metaphors and visuals from research interviews with youth.
Read MoreMeaningful engagement with young people in research results in richer, more culturally inclusive, and more usable research evidence.
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This article presents our findings on the stigma and discrimination (as well as related themes such as disclosure) experienced by Indigenous people who contracted HIV in their youth and live in urban and non-urban settings in Manitoba, Canada.
Read MoreExploring the perspectives of respite service providers (SPs) and stakeholders (SKs) provides unique insight into families' needs and respite care systems.
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The purpose of this research was to explore the experience of the self in a sample of Canadian youth living with anxiety.
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This paper presents research findings that advance knowledge around the power and agency families with children with complex care needs (CCN).
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Advantages, Challenges and Opportunities in Working with Photovoice as a Qualitative Research Method with Youth and their Families
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The aim of this article is to highlight the ways in which pain is a central experience for young people living with an anxiety disorder.
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