{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,7]],"date-time":"2026-10-07T17:32:54Z","timestamp":1791394374594,"version":"4.3.3"},"reference-count":29,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2013,1,30]],"date-time":"2013-01-30T00:00:00Z","timestamp":1359504000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Child"],"published-print":{"date-parts":[[2013,11]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Background<\/jats:title><jats:p>Research suggests <jats:styled-content style=\"fixed-case\">T<\/jats:styled-content>ourette syndrome (<jats:styled-content style=\"fixed-case\">TS<\/jats:styled-content>) 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.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>Six 14\u2010 to 16\u2010year\u2010olds with <jats:styled-content style=\"fixed-case\">TS<\/jats:styled-content> took part in semi\u2010structured interviews to explore the perceived impact of this condition on self and on relationships with others. The transcripts were analysed using interpretative phenomenological analysis.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>The young people felt that <jats:styled-content style=\"fixed-case\">TS<\/jats:styled-content> 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.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>The adolescents described specific ways in which <jats:styled-content style=\"fixed-case\">TS<\/jats:styled-content> affects quality of life and social interactions, and the effort it can take to cope effectively with this condition.<\/jats:p><\/jats:sec>","DOI":"10.1111\/cch.12033","type":"journal-article","created":{"date-parts":[[2013,1,30]],"date-time":"2013-01-30T11:33:22Z","timestamp":1359545602000},"page":"880-886","source":"Crossref","is-referenced-by-count":39,"title":["\u2018Everybody just thinks I'm weird\u2019: a qualitative exploration of the psychosocial experiences of adolescents with <scp>T<\/scp>ourette syndrome"],"prefix":"10.1111","volume":"39","author":[{"given":"R.","family":"Wadman","sequence":"first","affiliation":[{"name":"Faculty of Medicine &amp; Health Sciences University of Nottingham  Nottingham UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"V.","family":"Tischler","sequence":"additional","affiliation":[{"name":"Faculty of Medicine &amp; Health Sciences University of Nottingham  Nottingham UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"G. 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