Abstract
This paper draws on findings from qualitative interviews with queer and trans patients and with physicians providing care to queer and trans patients in Halifax, Nova Scotia, Canada, to explore how routine practices of health care can perpetuate or challenge the marginalization of queers. One of the most common “measures” of improved cultural competence in health care practice is self-reported increases in confidence and comfort, though it seems unlikely that an increase in physician comfort levels with queer and trans patients will necessarily mean better health care for queers. More attention to current felt discomfort in patient–provider encounters is required. Policies and practices that avoid discomfort at all costs are not always helpful for care, and experiences of shared discomfort in queer health contexts are not always harmful.
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Notes
Numbers total more than 19, since some participants identified both a gender identity and a sexual orientation.
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Acknowledgments
Funding for the project was provided by the Canadian Institutes of Health Research and conducted at Dalhousie University. The authors acknowledge the generosity of the participants, without whom the research could not have been conducted. We are grateful to the members of the larger research team (Susan Atkinson, Dalhousie Family Medicine; Mary Bryson, University of British Columbia; Cressida Heyes, University of Alberta; Erin Fredericks, Dalhousie University; and Brenda Hattie, Dalhousie University).
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Harbin, A., Beagan, B. & Goldberg, L. Discomfort, Judgment, and Health Care for Queers. Bioethical Inquiry 9, 149–160 (2012). https://doi.org/10.1007/s11673-012-9367-x
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DOI: https://doi.org/10.1007/s11673-012-9367-x