Literature DB >> 18418983

Electronic support groups, patient-consumers, and medicalization: the case of contested illness.

Kristin K Barker1.   

Abstract

This article illustrates the role electronic support groups play in consumer-driven medicalization. The analysis is based on an observational study of a year in the life of an electronic support group for sufferers of the contested illness fibromyalgia syndrome. The analysis builds on and extends scholarship concerning the growing influence of lay expertise in the context of medical uncertainty by showing how the dominant beliefs and routine practices of this electronic community simultaneously (and paradoxically) challenge the expertise of physicians and encourage the expansion of medicine's jurisdiction. Drawing on their shared embodied expertise, participants confirm the medical character of their problem and its remedy, and they empower each other to search for physicians who will recognize and treat their condition accordingly. Physician compliance is introduced as a useful concept for understanding the relationship between lay expertise, patient-consumer demand, and contemporary (and future) instances of medicalization.

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Year:  2008        PMID: 18418983     DOI: 10.1177/002214650804900103

Source DB:  PubMed          Journal:  J Health Soc Behav        ISSN: 0022-1465


  41 in total

1.  Interpreting genetics in the context of eating disorders: evidence of disease, not diversity.

Authors:  Michele Easter
Journal:  Sociol Health Illn       Date:  2013-11-28

2.  Generating a Social Movement Online Community through an Online Discourse: The Case of Myalgic Encephalomyelitis.

Authors:  Olaug S Lian; Jan Grue
Journal:  J Med Humanit       Date:  2017-06

3.  Narrative change, narrative stability, and structural constraint: The case of prisoner reentry narratives.

Authors:  David J Harding; Cheyney C Dobson; Jessica J B Wyse; Jeffrey D Morenoff
Journal:  Am J Cult Sociol       Date:  2016-07-06

4.  Social networks of experientially similar others: formation, activation, and consequences of network ties on the health care experience.

Authors:  Elizabeth A Gage
Journal:  Soc Sci Med       Date:  2012-09-12       Impact factor: 4.634

5.  Disentangling the exposure experience: the roles of community context and report-back of environmental exposure data.

Authors:  Crystal Adams; Phil Brown; Rachel Morello-Frosch; Julia Green Brody; Ruthann Rudel; Ami Zota; Sarah Dunagan; Jessica Tovar; Sharyle Patton
Journal:  J Health Soc Behav       Date:  2011-06

6.  Living kidney donors and their family caregivers: developing an evidence-based educational and social support website.

Authors:  Laura A Taylor; Nasreen Bahreman; Matthew J Hayat; Frank Hoey; Geetha Rajasekaran; Dorry L Segev
Journal:  Prog Transplant       Date:  2012-06       Impact factor: 1.187

7.  The devil you know: parents seeking information online for paediatric cancer.

Authors:  Elizabeth A Gage; Christina Panagakis
Journal:  Sociol Health Illn       Date:  2011-08-19

Review 8.  Culture, science and the changing nature of fibromyalgia.

Authors:  Frederick Wolfe; Brian Walitt
Journal:  Nat Rev Rheumatol       Date:  2013-07-02       Impact factor: 20.543

9.  The process of deciding about prophylactic surgery for breast and ovarian cancer: Patient questions, uncertainties, and communication.

Authors:  Robert Klitzman; Wendy Chung
Journal:  Am J Med Genet A       Date:  2010-01       Impact factor: 2.802

10.  Degrees of Medicalization: The Case of Infertility Health-Seeking.

Authors:  Arthur L Greil; Katherine M Johnson; Michele H Lowry; Julia McQuillan; Kathleen S Slauson-Blevins
Journal:  Sociol Q       Date:  2019-06-27
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