Relevant bibliographies by topics / Contested illness

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Contested illness'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Contested illness"

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Armentor, Janet L. "Living With a Contested, Stigmatized Illness." Qualitative Health Research 27, no. 4 (2016): 462–73. http://dx.doi.org/10.1177/1049732315620160.

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This study focuses on the negotiation of relationships among women living with the chronic illness fibromyalgia. Twenty in-depth, semistructured interviews were conducted with women diagnosed with fibromyalgia. Drawing from interactional and constructionist perspectives, the analysis focuses on participants’ approaches to communicating with others about their illness, the reactions of others to their experiences, and participants’ strategies to manage stigma. Participants attempted to describe their illness experience to others through direct and educational approaches. Often, in the managemen
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Aronoff, Gerald M., Steven Mandel, Elizabeth Genovese, et al. "Evaluating Malingering in Contested Injury or Illness." Pain Practice 7, no. 2 (2007): 178–204. http://dx.doi.org/10.1111/j.1533-2500.2007.00126.x.

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Fair, Brian. "Morgellons: contested illness, diagnostic compromise and medicalisation." Sociology of Health & Illness 32, no. 4 (2010): 597–612. http://dx.doi.org/10.1111/j.1467-9566.2009.01227.x.

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Bülow, Pia H. "Sharing Experiences of Contested Illness by Storytelling." Discourse & Society 15, no. 1 (2004): 33–53. http://dx.doi.org/10.1177/0957926504038943.

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Ballard, Dustin. "The Medicalization of Human Condition and Contested Illness." Emergency Medicine News 33 (January 2011): 1. http://dx.doi.org/10.1097/01.eem.0000393506.71508.cc.

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Cable, Sherry, Steve Kroll-Smith, Phil Brown, and Valerie J. Gunter. "Illness and the Environment: A Reader in Contested Medicine." Contemporary Sociology 32, no. 1 (2003): 78. http://dx.doi.org/10.2307/3089861.

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Johnson, Branden B. "Illness and the Environment: A Reader in Contested Medicine." Risk Analysis 23, no. 1 (2003): 238. http://dx.doi.org/10.1111/1539-6924.t01-1-00303.

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Tanaka, K. M. "Contested Histories and Happiness: Leprosy literature in Japan." Health, Culture and Society 5, no. 1 (2013): 99–118. http://dx.doi.org/10.5195/hcs.2013.133.

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At the turn of the twentieth century, the Japanese government passed a series of laws targeting people diagnosed with Hansen’s Disease (leprosy). As a result, many patients were quarantined in public leprosaria, often for life. In order to cope with both the diagnosis of a heavily stigmatized illness and a lifetime in isolation, patients began to write. The works produced by sufferers became so popular that by the mid-1930s their writing was referred to as a distinct literary genre, “leprosy literature.” Studies of leprosy literature have focused on its depiction of human rights violations, st
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E. Shriver, Thomas, and Dennis D. Waskul. "Managing the Uncertainties of Gulf War Illness: The Challenges of Living with Contested Illness." Symbolic Interaction 29, no. 4 (2006): 465–86. http://dx.doi.org/10.1525/si.2006.29.4.465.

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Thomas, Carol. "Negotiating the contested terrain of narrative methods in illness contexts." Sociology of Health & Illness 32, no. 4 (2010): 647–60. http://dx.doi.org/10.1111/j.1467-9566.2010.01239.x.

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Dissertations / Theses on the topic "Contested illness"

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Volkmann, Anna-Maria. "Making meaning of contested illness : medical uncertainty and fibromyalgia." Thesis, University College London (University of London), 2018. http://discovery.ucl.ac.uk/10042145/.

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The work presented in this thesis aimed to investigate the way in which individuals who have been diagnosed with fibromyalgia make meaning in the face of medical uncertainty. Medical uncertainty in fibromyalgia has been found to be a defining feature of the condition, as much as specific clinical symptoms. The argument is supported by evidence from the literature as well as through empirical studies presented here. A review of the history and review of current medical literature on fibromyalgia established that little consensus exists among experts about the condition, creating uncertainty. Bi
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Welch, Melissa Jane. "Decreased Visibility: A Narrative Analysis of Episodic Disability and Contested Illness." Scholar Commons, 2018. https://scholarcommons.usf.edu/etd/7378.

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In the United States alone, disability touches the lives of a tremendous amount of people. An increased prevalence of chronic illness, coupled with an aging population means it is likely and perhaps inevitable that everyone will experience disability in one way or another over the course of their lifetime. However not everyone who is disabled is recognized as such. Culturally, the narrative of “the healthy disabled person,” – or someone who is healthy, permanently, predictably, and visibly disabled renders many people with chronic and episodic pain, fatigue, and illness as unrecognizable as
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Bülow, Pia. "Making sense of contested illness : talk and narratives about chronic fatigue /." Linköping : Univ. : Dept. of Communication Studies [Kommunikation, Institutionen för Tema], Univ. [distributör], 2003. http://www.bibl.liu.se/liupubl/disp/disp2003/arts280s.pdf.

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Cooper, Lesley. "Contested knowledge, constructed illness? : a critial examination of the ME controvesy." Thesis, University of Essex, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.265021.

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Ouimette, Monique Y. "Common Scents?: Regulating the Use of Fragrances in Workplaces." Thesis, Boston College, 2017. http://hdl.handle.net/2345/bc-ir:107526.

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Thesis advisor: Juliet B. Schor<br>Fragrances in consumer products have become a contested topic in daily life. Workplace fragrance policies problematize fragrances, which, for many people, are normal aspects of consumer products. This mixed-method dissertation focuses on employees in a large non-industrial workplace with a fragrance-free policy. It examines employee reactions to a policy that requests behavioral changes based on claims that everyday consumption of fragranced products may be harmful to employee health. In order to develop an understanding of how and to what extent fragrances a
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Sweeney, Elizabeth. "Defining Reality: How Biomedical Researchers Determine the Existence of Pain." University of Cincinnati / OhioLINK, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1258480141.

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Moretti, Chiara. "Il dolore non legittimato : un’analisi della sindrome fibromialgica." Thesis, Strasbourg, 2018. http://www.theses.fr/2018STRAG016.

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Ma thèse doctorale vise à analyser la fibromyalgie en tant qu’entité prise en charge et traitée par des savoirs et des pratiques biomédicales contemporaines et localisées. Tout en prenant en considération une vision biomédicale transnationale du syndrome, mon terrain de recherche est situé dans le contexte italien. La première partie de la thèse est consacrée à l’analyse de la vision médicale de la douleur chronique sans lésion, également entendue comme la « douleur-maladie » ; elle propose aussi une analyse de la manière dont les formes douloureuses chroniques complexes sont encadrées au nive
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CLEMENTI, SILVIA. "IL PEER SUPPORT IN CONTESTI SANITARI: UN'INDAGINE ESPLORATIVA IN TRE REPARTI OSPEDALIERI." Doctoral thesis, Università Cattolica del Sacro Cuore, 2018. http://hdl.handle.net/10280/50317.

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Questa ricerca esplorativa qualitativa si è posta l’obiettivo di comprendere il funzionamento del peer support in ospedale e le ragioni che spingono alcuni pazienti a diventare peer supporter. È stata realizzata un’ osservazione di tre reparti ospedalieri italiani in cui il peer support è praticato e successivamente sono state condotte 27 interviste agli attori coinvolti (peer supporter, pazienti, operatori). Uno sguardo internazionale si è avuto con la realizzazione di due interviste a peer supporter del King’s Hospital di Londra. I dati raccolti sono stati analizzati e interpretati alla luc
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Dieudonne, Maël. "Une société pathogène ? : les hypersensibilités environnementales au prisme de la sociologie cognitive." Thesis, Lyon, 2017. http://www.theses.fr/2017LYSE2134/document.

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Depuis une décennie se rencontrent de plus en plus nombreux des malades d'un genre particulier. Présentant des symptômes variés et souvent invalidants, ils en attribuent la responsabilité à des facteurs environnementaux très spécifiques : produits de la chimie de synthèse pour les personnes hypersensibles chimiques multiples (MCS), rayonnements électromagnétiques artificiels pour les personnes électro-hypersensibles (EHS). La définition, l'existence même de ces maladies font l'objet de controverses autant politiques que scientifiques, que la littérature sociologique a déjà bien décrites. L'exp
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Horn, Amanda J. "An exploration of diagnosis and illness experiences of women and men living with Celiac Disease." Thesis, 2017. https://doi.org/10.7912/C2KQ0Z.

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Indiana University-Purdue University Indianapolis (IUPUI)<br>This research explores the illness experiences of women and men who received a Celiac Disease Diagnosis as an adult in addition to the impact it had on their social interactions and every-day lives. Investigation of illness experiences were conducted through the use of semi-structured interviews which explored diagnosis experiences, gendered experiences, and life style impact. Significant findings of this research indicated that there are gendered diagnosis experiences among women and men who are diagnosed with this disease. More spe
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Books on the topic "Contested illness"

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Rachel, Morello-Frosch, Zavestoski Stephen, and Contested Illnesses Research Group, eds. Contested illnesses: Citizens, science, and health social movements. University of California Press, 2012.

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Toxic exposures: Contested illnesses and the environmental health movement. Columbia University Press, 2007.

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Brown, Phil. Toxic exposures: Contested illnesses and the environmental health movement. Columbia University Press, 2007.

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1947-, Kroll-Smith J. Stephen, Brown Phil, and Gunter Valerie J. 1961-, eds. Illness and the environment: A reader in contested medicine. New York University Press, 2000.

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(Editor), Steve Kroll-Smith, Phil Brown (Editor), and Valerie J. Gunter (Editor), eds. Illness and the Environment: A Reader in Contested Medicine. New York University Press, 2000.

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(Editor), Steve Kroll-Smith, Phil Brown (Editor), and Valerie J. Gunter (Editor), eds. Illness and the Environment: A Reader in Contested Medicine. New York University Press, 2000.

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Madness Contested: Power and Practice. PCCS Books, 2013.

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Divided Bodies: Lyme Disease, Contested Illness, and Evidence-Based Medicine. Duke University Press, 2020.

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Dumes, Abigail A. Divided Bodies: Lyme Disease, Contested Illness, and Evidence-Based Medicine. Duke University Press, 2020.

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Phillips, Tarryn. Law, Environmental Illness and Medical Uncertainty: The Contested Governance of Health. Taylor & Francis Group, 2016.

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Book chapters on the topic "Contested illness"

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Trundle, Catherine. "Translating Proof: Contested Illness, Radiation Exposure, and the Health Claims of Nuclear Test Veterans." In Personhood in the Age of Biolegality. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-27848-9_5.

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Dew, Kevin, Anne Scott, and Allison Kirkman. "Medicalization and Contested Illnesses." In Social, Political and Cultural Dimensions of Health. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-31508-9_8.

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Schone, Harry Quinn. "Contested illnesses." In Contested Illness in Context. Routledge, 2019. http://dx.doi.org/10.4324/9780429398551-2.

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Schone, Harry Quinn. "Introduction." In Contested Illness in Context. Routledge, 2019. http://dx.doi.org/10.4324/9780429398551-1.

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Schone, Harry Quinn. "Work and welfare." In Contested Illness in Context. Routledge, 2019. http://dx.doi.org/10.4324/9780429398551-10.

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Schone, Harry Quinn. "Care." In Contested Illness in Context. Routledge, 2019. http://dx.doi.org/10.4324/9780429398551-11.

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Schone, Harry Quinn. "Conclusion." In Contested Illness in Context. Routledge, 2019. http://dx.doi.org/10.4324/9780429398551-12.

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Schone, Harry Quinn. "Main concepts." In Contested Illness in Context. Routledge, 2019. http://dx.doi.org/10.4324/9780429398551-3.

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Schone, Harry Quinn. "Definitions of disease." In Contested Illness in Context. Routledge, 2019. http://dx.doi.org/10.4324/9780429398551-4.

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Schone, Harry Quinn. "Shorter, Showalter, Hacking." In Contested Illness in Context. Routledge, 2019. http://dx.doi.org/10.4324/9780429398551-5.

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Conference papers on the topic "Contested illness"

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Rittossa, Dalida. "THE INSTITUTE OF VULNERABILITY IN THE TIME OF COVID-19 PANDEMIC: ALL SHADES OF THE HUMAN RIGHTS SPECTRUM." In EU 2021 – The future of the EU in and after the pandemic. Faculty of Law, Josip Juraj Strossmayer University of Osijek, 2021. http://dx.doi.org/10.25234/eclic/18354.

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The vulnerability thesis is one of the most important legal concepts in contemporary legal theory. Apart from being studied by legal scholars, the notion of vulnerability has been embodied in concrete legal rules and transferred to national case law allowing courts to set its boundaries by the power of judicial interpretation. Even though it would be hard to contest Schroeder and Gefenas’s statement that it is not necessary for an academic to say what vulnerability is because common sense dictates the existence of it, recent scholarly analysis clearly shows that the concept itself has become i
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