Institutional and Personal Narratives of Chronic Pain Management: Interrogating the Medical and Social Models of Disability
ISBN: 978-1-83909-144-5, eISBN: 978-1-83909-143-8
Publication date: 25 November 2019
Abstract
Purpose
In this chapter, I explore connections between institutional and personal narratives of treating chronic pain with prescription opioids.
Methods/Approach
I explore how stories told in a Food and Drug Administration public hearing construct moral boundaries around different kinds of pain patients and justify a label change intended to reduce prescribing of opioids to people with chronic pain. I then examine how personal narratives, acquired through interviews with chronic pain patients who rely on opioids, both conform to and challenge the institutional narratives told in the hearing and work as subversive stories. Additionally, I consider how institutional and personal narratives of chronic pain shed light on intersections and conflicts between the medical and social models of disability.
Findings
The “invisible disability” experience of chronic pain highlights the complex entanglement between the struggles associated with impairment emphasized by the medical model, and those stemming from cultural and structural barriers emphasized by the social model.
Implications/Value
I conclude with a discussion of the methodological value of examining narratives such as those of chronic pain and disability at multiple levels of social life. This study contributes to efforts to broaden disability discourse to include experiences such as chronic pain that are poorly represented in disability scholarship.
Keywords
Citation
Wilbers, L.E. (2019), "Institutional and Personal Narratives of Chronic Pain Management: Interrogating the Medical and Social Models of Disability", New Narratives of Disability (Research in Social Science and Disability, Vol. 11), Emerald Publishing Limited, Leeds, pp. 151-167. https://doi.org/10.1108/S1479-354720190000011019
Publisher
:Emerald Publishing Limited
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