Exploring repeated clinical encounters: an arts-informed participatory project for women and gender minorities living with chronic illnesses

dc.contributor.authorSebring, Jennifer C.H.
dc.contributor.examiningcommitteeMcPhail, Deborah (Community Health Sciences)en_US
dc.contributor.examiningcommitteeWoodgate, Roberta (Nursing)en_US
dc.contributor.supervisorKelly, Christine
dc.date.accessioned2022-07-20T20:03:26Z
dc.date.available2022-07-20T20:03:26Z
dc.date.copyright2022-07-20
dc.date.issued2022-07-19
dc.date.submitted2022-07-20T14:11:19Zen_US
dc.degree.disciplineCommunity Health Sciencesen_US
dc.degree.levelMaster of Science (M.Sc.)en_US
dc.description.abstractBackground: Living with a chronic illness involves frequent interactions with health care professionals and the health care system to manage one’s symptoms. Yet, little research conceptualizes health care interactions as a stressor that may exacerbate or contribute to symptoms. Objectives: This study sought to better understand the health care experiences of women and gender minorities living with chronic illnesses by answering the following research question: Using arts-informed methods, how do women and gender minorities living with chronic illness understand and experience “patienthood?” The project had three objectives: 1) Identify the effects of repeated health care interactions on people living with chronic illnesses and the strategies they use to navigate these interactions and effects; 2) Explore the theoretical concept of “patienthood” through an arts-informed, critical disability lens; and 3) Examine the potential of arts-informed health research as a transformative practice. Methodology: An arts-informed, patient-oriented lens guided the study. Workshops, involving a multi-media collage activity and focus group discussion, were conducted with ten participants. Data analysis included two phases: first, a reflexive thematic analysis to analyze the focus group transcripts, and second, an interpretive approach informed by critical disability studies to analyze the artwork produced by participants. Results: Participants often experienced dismissal or disregard for their concerns during clinical encounters, conceptualized as ‘medical invalidation.’ Experiencing this repeatedly had significant consequences for participants’ well-being, willingness to seek care, and the support they sought and received from their social support systems. We emphasize that medical invalidation is not merely a one-off interpersonal interaction, but influences and is influenced by broader sociocultural ideas about illness and disability. Discussion: Addressing medical invalidation requires a commitment to person-centred, humanist care and critical reflexivity in the medical clinic, as well as a re-imagining of public discourse around illness and disability that affirms and embraces embodied difference.en_US
dc.description.noteOctober 2022en_US
dc.description.sponsorshipCanadian Institutes of Health Research; Frederick Banting and Charles Best Canada Graduate Scholarship-Masters (CGS-M) Research Manitoba; Masters Studentshipen_US
dc.identifier.urihttp://hdl.handle.net/1993/36626
dc.language.isoengen_US
dc.rightsopen accessen_US
dc.subjectarts-based researchen_US
dc.subjectgenderen_US
dc.subjectcritical disability studiesen_US
dc.subjectpatienthooden_US
dc.subjectmedical invalidationen_US
dc.subjectchronic health conditionsen_US
dc.subjectchronic illnessen_US
dc.titleExploring repeated clinical encounters: an arts-informed participatory project for women and gender minorities living with chronic illnessesen_US
dc.typemaster thesisen_US
local.subject.manitobayesen_US
oaire.awardTitleMPN Primary Healthcare Research Partnership Awarden_US
oaire.awardURIhttps://manitoba-pihcinet.com/2019/11/20/building-primary-health-care-research-capacity-in-manitoba/en_US
project.funder.nameManitoba Primary & Integrated Healthcare Innovation Networken_US
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