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Forced Into an Ableist Narrative? The Swedish Covid Association’s Quest for Recognition

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Bibliographic Details
Title: Forced Into an Ableist Narrative? The Swedish Covid Association’s Quest for Recognition
Authors: Melander, Stina, Bahner, Julia
Contributors: Lund University, Lunds universitet, Originator
Source: Scandinavian Journal of Disability Research. 27(1):299-312
Subject Terms: Social Sciences, Political Science, Political Science (excluding Peace and Conflict Studies), Samhällsvetenskap, Statsvetenskap, Statsvetenskap (exklusive freds- och konfliktforskning), Sociology, Social Work, Sociologi, Socialt arbete, Other Social Sciences, Other Social Sciences not elsewhere specified, Annan samhällsvetenskap, Övrig annan samhällsvetenskap
Description: During the COVID-19 pandemic, the Swedish Covid Association (SCA) was established to represent individuals with Long COVID (LC). The unique Swedish response to the pandemic, characterized by minimal restrictions, serves as the backdrop for the SCA’s efforts to highlight the specific needs of LC patients, who were largely excluded from pandemic policies and protective measures. Utilizing the Narrative Policy Framework (NPF), this study examines how the SCA advocates for LC patients across micro, meso, and macro levels. Data were collected through analysis of the SCA’s online materials, reports, and interviews with former SCA representatives. The SCA’s narrative positions LC patients as deserving heroes, emphasizing their previous ‘productive’ lives and their entitlement to appropriate healthcare. While this strategy empowers individuals, the focus on the ‘worthy’ patient risks reinforcing ableist standards. Consequently, activists should be cognizant of the potential for their advocacy strategies to inadvertently perpetuate ableist narratives.
Access URL: https://doi.org/10.16993/sjdr.1234
Database: SwePub
Description
Abstract:During the COVID-19 pandemic, the Swedish Covid Association (SCA) was established to represent individuals with Long COVID (LC). The unique Swedish response to the pandemic, characterized by minimal restrictions, serves as the backdrop for the SCA’s efforts to highlight the specific needs of LC patients, who were largely excluded from pandemic policies and protective measures. Utilizing the Narrative Policy Framework (NPF), this study examines how the SCA advocates for LC patients across micro, meso, and macro levels. Data were collected through analysis of the SCA’s online materials, reports, and interviews with former SCA representatives. The SCA’s narrative positions LC patients as deserving heroes, emphasizing their previous ‘productive’ lives and their entitlement to appropriate healthcare. While this strategy empowers individuals, the focus on the ‘worthy’ patient risks reinforcing ableist standards. Consequently, activists should be cognizant of the potential for their advocacy strategies to inadvertently perpetuate ableist narratives.
ISSN:15017419
17453011
DOI:10.16993/sjdr.1234