‘Mostly accurate with occasional piles of bullshit’: patient ‘boundary-work’ in an online scientific controversy

IF 2.5 2区 医学 Q2 HEALTH POLICY & SERVICES Health Sociology Review Pub Date : 2019-09-02 DOI:10.1080/14461242.2019.1658537
Tarryn Phillips
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引用次数: 3

Abstract

ABSTRACT People with contested illnesses such as Gulf War Syndrome and multiple chemical sensitivities (MCS) have struggled to have their claims to chemical injury recognised as scientifically valid. Patients have thus built on shared experiences and formed ‘embodied health movements’, to challenge mainstream scientific understandings of toxicity and disease causality. Digital technologies have changed the scale and scope of patient sharing and collaboration, yet little attention has been paid to how patients govern each others’ scientific claims. This paper draws from an online qualitative survey of forum users with self-reported MCS (N = 186) to investigate how patient groups internally debate scientificity – in this case over a controversial new ‘neural retraining’ treatment. Despite their own scientific marginalisation, MCS patients conducted ‘boundary-work’ to demarcate scientifically legitimate claims from ‘pseudo-science’ in their analysis of peer theories, and used scientific criteria as a powerful tool to claim and dispute epistemic authority. Moreover, this inter-patient boundary-work had profound social and therapeutic implications in the movement, particularly with respect to the politics of recognition, community solidarity and peer support.
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“基本准确,偶尔会有一堆废话”:网络科学争议中耐心的“边界工作”
患有海湾战争综合症和多重化学敏感性(MCS)等有争议疾病的人一直在努力使他们对化学伤害的声称得到科学有效的认可。因此,患者建立在共同经验的基础上,形成了“身体健康运动”,以挑战对毒性和疾病因果关系的主流科学理解。数字技术已经改变了患者共享和合作的规模和范围,但很少有人关注患者如何管理彼此的科学主张。本文从一项对自我报告MCS的论坛用户(N = 186)的在线定性调查中得出结论,以调查患者群体如何在内部辩论科学性——在这种情况下,是关于一种有争议的新“神经再训练”治疗。尽管他们自己在科学上被边缘化,但MCS患者在对同伴理论的分析中进行了“边界工作”,以区分科学上合法的主张和“伪科学”,并将科学标准作为主张和争议认知权威的有力工具。此外,这种患者之间的边界工作在运动中具有深刻的社会和治疗意义,特别是在政治上的认可,社区团结和同伴支持方面。
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来源期刊
CiteScore
7.50
自引率
0.00%
发文量
14
期刊介绍: An international, scholarly peer-reviewed journal, Health Sociology Review explores the contribution of sociology and sociological research methods to understanding health and illness; to health policy, promotion and practice; and to equity, social justice, social policy and social work. Health Sociology Review is published in association with The Australian Sociological Association (TASA) under the editorship of Eileen Willis. Health Sociology Review publishes original theoretical and research articles, literature reviews, special issues, symposia, commentaries and book reviews.
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