Literature DB >> 12927469

The radicalized self: the impact on the self of the contested nature of the diagnosis of chronic fatigue syndrome.

Juanne N Clarke1, Susan James.   

Abstract

Chronic fatigue syndrome (CFS) is a relatively new disease that is difficult to diagnose. It is also a contested disease immersed in dispute about whether it is a physical or psychiatric reality. Sufferers often claim to experience not only the physical challenges of the disease, and these can be extensive, but also, initially, the anomie of suffering from a condition whose very reality is debated both in the medical and in the wider communities. Theories of self in illness emphasize how people who are diagnosed as chronically ill work hard as they seek to maintain previous, or to develop supernormal, selves. Such goals are cast in a critical light by Foucault's notion of the technologies of self in the context of circulating neo-liberal discourses. As people with CFS, lacking an uncontested medical diagnosis, search for meaningful self-identities, they resist previously available discourses to take up an alternative discourse, one that we call radicalized selves. This paper raises questions about the constraints and liberties, power and powerlessness associated with a clear and undisputed medical diagnosis. It suggests a model of the self in chronic illness that considers not only changes in body and biography but also the availability of an uncontested diagnosis.

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Year:  2003        PMID: 12927469     DOI: 10.1016/s0277-9536(02)00515-4

Source DB:  PubMed          Journal:  Soc Sci Med        ISSN: 0277-9536            Impact factor:   4.634


  19 in total

1.  Dying cancer patients' experiences of powerlessness and helplessness.

Authors:  Lisa Sand; Peter Strang; Anna Milberg
Journal:  Support Care Cancer       Date:  2007-11-20       Impact factor: 3.603

2.  Self-referent constructs and medical sociology: in search of an integrative framework.

Authors:  Howard B Kaplan
Journal:  J Health Soc Behav       Date:  2007-06

3.  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

4.  Bad news and first impressions: patient and family caregiver accounts of learning the cancer diagnosis.

Authors:  Karen Sue Schaepe
Journal:  Soc Sci Med       Date:  2011-07-23       Impact factor: 4.634

Review 5.  A review and meta-synthesis of qualitative studies on myalgic encephalomyelitis/chronic fatigue syndrome.

Authors:  Valerie R Anderson; Leonard A Jason; Laura E Hlavaty; Nicole Porter; Jacqueline Cudia
Journal:  Patient Educ Couns       Date:  2011-05-14

6.  Emplotting Hikikomori: Japanese Parents' Narratives of Social Withdrawal.

Authors:  Ellen Rubinstein
Journal:  Cult Med Psychiatry       Date:  2016-12

7.  The PRIME project: developing a patient evidence-base.

Authors:  Sophie Staniszewska; Sally Crowe; Douglas Badenoch; Carol Edwards; Jan Savage; Will Norman
Journal:  Health Expect       Date:  2010-06-23       Impact factor: 3.377

8.  Next of kin's experience of powerlessness and helplessness in palliative home care.

Authors:  Anna Milberg; Peter Strang; Maria Jakobsson
Journal:  Support Care Cancer       Date:  2003-12-18       Impact factor: 3.603

9.  A qualitative natural history study of ME/CFS in the community.

Authors:  Valerie R Anderson; Leonard A Jason; Laura E Hlavaty
Journal:  Health Care Women Int       Date:  2013-02-27

Review 10.  The expressed needs of people with chronic fatigue syndrome/myalgic encephalomyelitis: a systematic review.

Authors:  Maria de Lourdes Drachler; Jose Carlos de Carvalho Leite; Lee Hooper; Chia Swee Hong; Derek Pheby; Luis Nacul; Eliana Lacerda; Peter Campion; Anne Killett; Maggie McArthur; Fiona Poland
Journal:  BMC Public Health       Date:  2009-12-11       Impact factor: 3.295

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