Literature DB >> 20650974

Children's experience of living with a craniofacial condition: perspectives of children and parents.

Rachel M Roberts1, Rosalyn Shute.   

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.

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Year:  2010        PMID: 20650974     DOI: 10.1177/1359104509355021

Source DB:  PubMed          Journal:  Clin Child Psychol Psychiatry        ISSN: 1359-1045            Impact factor:   2.544


  3 in total

1.  Health-related quality of life in children with hemifacial microsomia: parent and child perspectives.

Authors:  Mary A Khetani; Brent R Collett; Matthew L Speltz; Martha M Werler
Journal:  J Dev Behav Pediatr       Date:  2013 Nov-Dec       Impact factor: 2.225

2.  Examination of a theoretical model for oral health-related quality of life among youths with cleft.

Authors:  Hillary L Broder; Maureen Wilson-Genderson; Lacey Sischo
Journal:  Am J Public Health       Date:  2014-03-13       Impact factor: 9.308

3.  "Will You Still Feel Beautiful When You Find Out You Are Different?": Parents' Experiences, Reflections, and Appearance-Focused Conversations About Their Child's Visible Difference.

Authors:  Kristin J Billaud Feragen; Anita Myhre; Nicola Marie Stock
Journal:  Qual Health Res       Date:  2021-10-01
  3 in total

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