Literature DB >> 23363392

'Everybody just thinks I'm weird': a qualitative exploration of the psychosocial experiences of adolescents with Tourette syndrome.

R Wadman1, V Tischler, G M Jackson.   

Abstract

BACKGROUND: Research suggests Tourette syndrome (TS) can have a negative impact on quality of life. To date, little research has examined the perspectives of young people with this condition in depth.
METHODS: Six 14- to 16-year-olds with TS took part in semi-structured interviews to explore the perceived impact of this condition on self and on relationships with others. The transcripts were analysed using interpretative phenomenological analysis.
RESULTS: The young people felt that TS was a constant presence in their lives, but one they have learnt to cope with well. Most had developed supportive friendships but encountered problems when interacting with the wider peer network. Specific concerns around meeting new people and future employment were voiced.
CONCLUSIONS: The adolescents described specific ways in which TS affects quality of life and social interactions, and the effort it can take to cope effectively with this condition.
© 2013 John Wiley & Sons Ltd.

Entities:  

Keywords:  Tourette syndrome; adolescence; psychosocial issues; qualitative methodology

Mesh:

Year:  2013        PMID: 23363392     DOI: 10.1111/cch.12033

Source DB:  PubMed          Journal:  Child Care Health Dev        ISSN: 0305-1862            Impact factor:   2.508


  7 in total

Review 1.  Stigma in youth with Tourette's syndrome: a systematic review and synthesis.

Authors:  Melina A Malli; Rachel Forrester-Jones; Glynis Murphy
Journal:  Eur Child Adolesc Psychiatry       Date:  2015-08-28       Impact factor: 4.785

2.  A Qualitative Exploration of the Experiences of Children and Adolescents with Tourette Syndrome.

Authors:  Kim R Edwards; Sandra Mendlowitz; Elana Jackson; Claire Champigny; Matt Specht; Paul Arnold; Daniel Gorman; Gina Dimitropoulos
Journal:  J Can Acad Child Adolesc Psychiatry       Date:  2017-03-01

Review 3.  Living with tics: Nursing care of pediatric tourette syndrome.

Authors:  Mei-Yin Lee
Journal:  Biomed J       Date:  2021-10-25       Impact factor: 7.892

4.  Comorbidities, Social Impact, and Quality of Life in Tourette Syndrome.

Authors:  Valsamma Eapen; Andrea E Cavanna; Mary M Robertson
Journal:  Front Psychiatry       Date:  2016-06-06       Impact factor: 4.157

Review 5.  The effects of Gilles de la Tourette syndrome and other chronic tic disorders on quality of life across the lifespan: a systematic review.

Authors:  Joel Evans; Stefano Seri; Andrea E Cavanna
Journal:  Eur Child Adolesc Psychiatry       Date:  2016-02-15       Impact factor: 4.785

6.  Face perception enhances insula and motor network reactivity in Tourette syndrome.

Authors:  Charlotte L Rae; Liliana Polyanska; Cassandra D Gould van Praag; Jim Parkinson; Samira Bouyagoub; Yoko Nagai; Anil K Seth; Neil A Harrison; Sarah N Garfinkel; Hugo D Critchley
Journal:  Brain       Date:  2018-11-01       Impact factor: 13.501

7.  Using Online Support Communities for Tourette Syndrome and Tic Disorders: Online Survey of Users' Experiences.

Authors:  Victoria Perkins; Neil S Coulson; E Bethan Davies
Journal:  J Med Internet Res       Date:  2020-11-03       Impact factor: 5.428

  7 in total

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