Children’s experience of living with a craniofacial condition: Perspectives of children and parents

Author:

Roberts Rachel M.1,Shute Rosalyn2

Affiliation:

1. University of Adelaide, Australia,

2. Flinders University and University of Ballarat, Australia

Abstract

This is the first study to examine the range of experiences of children living with a wide range of craniofacial anomalies (CFAs), from the perspectives of children and parents. We interviewed 26 young people and 28 parents about both stressors and positive aspects for young people of living with a CFA. Thematic analysis revealed four major stress-related themes (self-acceptance, responses of others, disabilities and impairments, and treatment). Positive themes included personal qualities and support. Psychological theories often applied to those with CFAs relate to attractiveness, stigma and teasing, but the present findings suggest that these are not as useful as the conceptualization of CFAs as chronic conditions which influence adaptive tasks. Implications for clinical practice are discussed.

Publisher

SAGE Publications

Subject

Psychiatry and Mental health,Clinical Psychology,General Medicine,Pediatrics, Perinatology and Child Health

Reference34 articles.

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2. Adolescents’ Perspectives on Living and Growing up with Treacher Collins Syndrome: A Qualitative Study

3. Psychologic and Social Consequences of Craniofacial Disfigurement in Children

4. Psychotherapy for Persons with Craniofacial Deformities: Can We Treat without Theory?

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