Brian Williams
“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
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 |
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