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Réouverture dès ce lundi 19 août.
Lundi : 8h-18h30
Mardi : 8h-18h30
Mercredi 9h-16h30
Jeudi : 8h-18h30
Vendredi : 8h-16h30
Votre centre de documentation fermera de 12h30 à 13h ce vendredi 28 juin et fermera à 14h30.
Dès ce lundi 1er juillet jusqu'au mercredi 10 juillet l'horaire du centre de documentation sera adapté :
Lundi 1er juillet : de 8h à 12h et de 12h30 à 16h
Mardi 2 juillet : de 8h à 12h15
Mercredi 3 juillet : de 9h à 12h et de 12h30 à 15h15
Jeudi 4 juillet : de 8h à 12h30 et de 13h à 18h30
Lundi 8 juillet : de 8h à 12h et de 12h30 à 16h
Mardi 9 juillet : de 8h à 12h15
Réouverture dès ce lundi 19 août.
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Détail de l'auteur
Auteur Karen Sheridan |
Documents disponibles écrits par cet auteur
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Experiences of university students disclosing epilepsy to peers: ‘It's a shared thing now’ / Karen Sheridan in The British Journal of Occupational Therapy, Vol.79 N°8 (August 2016)
[article]
Titre : Experiences of university students disclosing epilepsy to peers: ‘It's a shared thing now’ Type de document : texte imprimé Auteurs : Karen Sheridan ; Nancy Salomon ; Nicole O'Connell Année de publication : 2016 Article en page(s) : p. 484-491 Langues : Anglais (eng) Mots-clés : épilepse jeune adulte ergothérapie Résumé : Introduction While disclosure of concealable conditions like epilepsy can create social support, it may cause relationships to disintegrate. Friendship in young adulthood is pivotal in the transition to emotional autonomy, yet little is known about peer disclosure by university students with epilepsy. This qualitative study aimed to map key features in the process of epilepsy disclosure.
Method Semi-structured interviews were completed with eight young adults (aged 18–25 years) with epilepsy enrolled in or recently graduated from Irish universities.
Findings Thematic analysis yielded four main themes: (1) Assessing the disclosure recipient; (2) Managing the presentation of epilepsy; (3) Forging alliances; and (4) Feeling more positive. The process of disclosure centred on enlisting the support of allies deemed trustworthy by participants. Disclosure messages presented epilepsy neutrally to bolster allies' commitment to the role. Although participants viewed disclosure as beneficial to wellbeing, concern was expressed about acquiring a stigmatised social identity.
Conclusion Occupational therapists are well placed to support young adults through the process of disclosure. Promoting a positive collective identity through peer mentorship promises to disrupt stigma. More broadly, partnerships between occupational therapists and epilepsy organisations or disability support services in third level education could establish an academic culture where supports are readily available to people with concealable illnesses.Permalink : ./index.php?lvl=notice_display&id=45788
in The British Journal of Occupational Therapy > Vol.79 N°8 (August 2016) . - p. 484-491[article] Experiences of university students disclosing epilepsy to peers: ‘It's a shared thing now’ [texte imprimé] / Karen Sheridan ; Nancy Salomon ; Nicole O'Connell . - 2016 . - p. 484-491.
Langues : Anglais (eng)
in The British Journal of Occupational Therapy > Vol.79 N°8 (August 2016) . - p. 484-491
Mots-clés : épilepse jeune adulte ergothérapie Résumé : Introduction While disclosure of concealable conditions like epilepsy can create social support, it may cause relationships to disintegrate. Friendship in young adulthood is pivotal in the transition to emotional autonomy, yet little is known about peer disclosure by university students with epilepsy. This qualitative study aimed to map key features in the process of epilepsy disclosure.
Method Semi-structured interviews were completed with eight young adults (aged 18–25 years) with epilepsy enrolled in or recently graduated from Irish universities.
Findings Thematic analysis yielded four main themes: (1) Assessing the disclosure recipient; (2) Managing the presentation of epilepsy; (3) Forging alliances; and (4) Feeling more positive. The process of disclosure centred on enlisting the support of allies deemed trustworthy by participants. Disclosure messages presented epilepsy neutrally to bolster allies' commitment to the role. Although participants viewed disclosure as beneficial to wellbeing, concern was expressed about acquiring a stigmatised social identity.
Conclusion Occupational therapists are well placed to support young adults through the process of disclosure. Promoting a positive collective identity through peer mentorship promises to disrupt stigma. More broadly, partnerships between occupational therapists and epilepsy organisations or disability support services in third level education could establish an academic culture where supports are readily available to people with concealable illnesses.Permalink : ./index.php?lvl=notice_display&id=45788 Exemplaires (1)
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