{"title":"Contested illness, contested identity: How women with fibromyalgia construct legitimacy online","authors":"Jenna M. Kerr , Carey DeMichelis","doi":"10.1016/j.socscimed.2025.118251","DOIUrl":null,"url":null,"abstract":"<div><div>This research explores the lived experiences of women with fibromyalgia (FM) and the various ways they go about legitimizing a contested medical condition. Through ethnographic observation in a private online community, “<em>Fibro Women Canada,”</em> and in-depth interviews with its members, we explore how women work to be seen as legitimate pain patients in the eyes of their healthcare providers. We argue that FM produces a dilemma of legitimacy, a dilemma of identity, and a dilemma of morality for its sufferers. In the face of these dilemmas, <em>Fibro Women Canada</em> functions as a backstage environment that supports two distinct, yet interwoven, forms of legitimacy building: (1) <em>illness literacy</em>, and (2) <em>identity work</em>. In particular, we attend to the moral stakes of seeking biomedical recognition, illuminating the every-day strategies that women use to construct themselves as deserving of care.</div></div>","PeriodicalId":49122,"journal":{"name":"Social Science & Medicine","volume":"381 ","pages":"Article 118251"},"PeriodicalIF":5.0000,"publicationDate":"2025-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Social Science & Medicine","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0277953625005829","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH","Score":null,"Total":0}
引用次数: 0
Abstract
This research explores the lived experiences of women with fibromyalgia (FM) and the various ways they go about legitimizing a contested medical condition. Through ethnographic observation in a private online community, “Fibro Women Canada,” and in-depth interviews with its members, we explore how women work to be seen as legitimate pain patients in the eyes of their healthcare providers. We argue that FM produces a dilemma of legitimacy, a dilemma of identity, and a dilemma of morality for its sufferers. In the face of these dilemmas, Fibro Women Canada functions as a backstage environment that supports two distinct, yet interwoven, forms of legitimacy building: (1) illness literacy, and (2) identity work. In particular, we attend to the moral stakes of seeking biomedical recognition, illuminating the every-day strategies that women use to construct themselves as deserving of care.
这项研究探讨了患有纤维肌痛(FM)的女性的生活经历,以及她们将有争议的医疗状况合法化的各种方式。通过对私人在线社区“Fibro Women Canada”的人种学观察,以及对其成员的深入访谈,我们探索了女性如何在医疗服务提供者眼中被视为合法的疼痛患者。我们认为,FM为其患者带来了合法性的困境、身份的困境和道德的困境。面对这些困境,加拿大妇女纤维组织作为一个后台环境,支持两种截然不同但又相互交织的合法性建设形式:(1)疾病扫盲,(2)身份工作。特别是,我们关注寻求生物医学认可的道德风险,阐明女性用来构建自己值得照顾的日常策略。
期刊介绍:
Social Science & Medicine provides an international and interdisciplinary forum for the dissemination of social science research on health. We publish original research articles (both empirical and theoretical), reviews, position papers and commentaries on health issues, to inform current research, policy and practice in all areas of common interest to social scientists, health practitioners, and policy makers. The journal publishes material relevant to any aspect of health from a wide range of social science disciplines (anthropology, economics, epidemiology, geography, policy, psychology, and sociology), and material relevant to the social sciences from any of the professions concerned with physical and mental health, health care, clinical practice, and health policy and organization. We encourage material which is of general interest to an international readership.