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  1. Diagramming Disability: A Deleuzian Approach to Researching Childhood Disability.Patricia McKeever, Lindsay Stephens & Sue Ruddick - 2021 - Deleuze and Guattari Studies 15 (1):15-39.
    This article presents diagrams developed from the insights of three middle school children with limited mobility about their experiences navigating social and spatial relations in their home, school and neighbourhoods. The paper explores the concept of assemblage as well as operationalising the Deleuzian idea of the diagram. The diagrams we produce are developed in connection with dominant idealisations of neighbourhood and home range that function in North America to choreograph children's progression from infancy through adolescence. We undertake this diagramming in (...)
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  • Body–drug assemblages: theorizing the experience of side effects in the context of HIV treatment.Marilou Gagnon & Dave Holmes - 2016 - Nursing Philosophy 17 (4):250-261.
    Each of the antiretroviral drugs that are currently used to stop the progression of HIV infection causes its own specific side effects. Despite the expansion, multiplication, and simplification of treatment options over the past decade, side effects continue to affect people living with HIV. Yet, we see a clear disconnect between the way side effects are normalized, routinized, and framed in clinical practice and the way they are experienced by people living with HIV. This paper builds on the premise that (...)
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  • Transforming normative, ableist, and biomedical orientations to living well and quality of life in nursing: Reimagining what a ventilated body can do.Elizabeth J. Straus, Helen Brown, Gail Teachman & Fuchsia Howard - 2023 - Nursing Inquiry 30 (3):e12554.
    A goal of living as well as possible is central to practice and research with young adults living with home mechanical ventilation (HMV). Significant effort has been put into conceptualizing and measuring the quality of life (QOL) as a proxy for living well. Yet, dominant understandings of QOL have been influenced by normative, ableist, and biomedical discourses about what constitutes a good life that, when applied in practice and systems with those living with HMV, can contribute to exclusion and constrain (...)
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