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“I’ve Never Not Had it So I Don’t Really Know What it’s Like Not to”: Nondifference and Biographical Disruption Among Children and Young People With Cystic Fibrosis

Williams, Brian; Corlett, Joanne; Dowell, Jon S.; Coyle, Joanne; Mukhopadhyay, Somnath

Authors

Brian Williams

Joanne Corlett

Jon S. Dowell

Joanne Coyle

Somnath Mukhopadhyay



Abstract

The relevance of biographical disruption and loss of self for children and young people is unclear, particularly in cases of congenital illness such as cystic fibrosis, where no prior period of wellness, stability, or perceived normality might exist. We explored the meaning, importance, and forms of maintenance of ideas of normality among 32 children and young people with cystic fibrosis. We examine the ways in which normalcy is produced, maintained, and threatened, and discuss the implications for the applicability and relevance of these traditional sociological concepts. Analysis of children's and young people's accounts resulted in a conceptualization of four forms of normalcy based on personal and social definitions and audiences. Biographical disruption appeared relevant but in a more nuanced form than its usual conceptualization when applied to adult populations. Maintaining normality within the family resulted in continual biographical revision in anticipation of future illness trajectory and life course.

Citation

Williams, B., Corlett, J., Dowell, J. S., Coyle, J., & Mukhopadhyay, S. (2009). “I’ve Never Not Had it So I Don’t Really Know What it’s Like Not to”: Nondifference and Biographical Disruption Among Children and Young People With Cystic Fibrosis. Qualitative Health Research, 19(10), 1443-1455. https://doi.org/10.1177/1049732309348363

Journal Article Type Article
Online Publication Date Oct 5, 2009
Publication Date Oct 1, 2009
Deposit Date Sep 13, 2016
Journal Qualitative Health Research
Print ISSN 1049-7323
Electronic ISSN 1552-7557
Publisher SAGE Publications
Peer Reviewed Peer Reviewed
Volume 19
Issue 10
Pages 1443-1455
DOI https://doi.org/10.1177/1049732309348363
Keywords Chronic illness; Cystic fibrosis; Children; Adolescents; Sociology
Public URL http://researchrepository.napier.ac.uk/Output/379406