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Lundi : 8h-18h30
Mardi : 8h-17h30
Mercredi 9h-16h30
Jeudi : 8h30-18h30
Vendredi : 8h30-12h30 et 13h-14h30
Votre centre de documentation sera exceptionnellement fermé de 12h30 à 13h ce lundi 18 novembre.
Egalement, il sera fermé de 12h30 à 13h30 ce mercredi 20 novembre.
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Détail de l'auteur
Auteur Jeffrey D. Holmes |
Documents disponibles écrits par cet auteur
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Understanding Parkinson’s through visual narratives: “I’m not Mrs. Parkinson’s” / Sarah G. Lutz in The British Journal of Occupational Therapy, Vol.81 Issue 2 (February 2018)
[article]
Titre : Understanding Parkinson’s through visual narratives: “I’m not Mrs. Parkinson’s” Type de document : texte imprimé Auteurs : Sarah G. Lutz ; Jeffrey D. Holmes ; Debbie Laliberte Rudman ; [et al...] Année de publication : 2018 Article en page(s) : p. 90-100 Langues : Anglais (eng) Mots-clés : ergothérapie maladie de Parkinson identité représentation Résumé : Introduction
Although it is accepted that individuals with Parkinson’s disease must navigate challenges such as receiving their diagnosis and changing daily occupations, little is known about how they navigate. The purpose of this study is to deepen the current understanding of the experience of living with Parkinson’s disease and its implications for occupation through a narrative visual methodology (photo-elicitation).
Method
Six individuals with Parkinson’s disease were asked to take photographs and share verbal narrative accounts to illustrate their experience of living with Parkinson’s disease.
Findings
Results highlight the interrelationship between occupation and identity, as many of the participants’ stories were interpreted as foregrounding the negotiation of occupation, and how such negotiation shaped their sense of identity. Overall, three major themes were identified: (1) Framing the meaning of Parkinson’s disease (accepting the disease as part of who they were); (2) Negotiating engagement in occupation (ongoing deliberation over whether to continue engaging in certain aspects of life as Parkinson’s disease progressed); and (3) Being ready to accept changes that impact personal or social identity (readiness to accept help and to identify as someone with Parkinson’s disease).
Conclusion
Attending to insights regarding the lived experience of Parkinson’s disease will enhance quality of care through informing an enriched client-centered, occupation-based approach.Permalink : ./index.php?lvl=notice_display&id=57837
in The British Journal of Occupational Therapy > Vol.81 Issue 2 (February 2018) . - p. 90-100[article] Understanding Parkinson’s through visual narratives: “I’m not Mrs. Parkinson’s” [texte imprimé] / Sarah G. Lutz ; Jeffrey D. Holmes ; Debbie Laliberte Rudman ; [et al...] . - 2018 . - p. 90-100.
Langues : Anglais (eng)
in The British Journal of Occupational Therapy > Vol.81 Issue 2 (February 2018) . - p. 90-100
Mots-clés : ergothérapie maladie de Parkinson identité représentation Résumé : Introduction
Although it is accepted that individuals with Parkinson’s disease must navigate challenges such as receiving their diagnosis and changing daily occupations, little is known about how they navigate. The purpose of this study is to deepen the current understanding of the experience of living with Parkinson’s disease and its implications for occupation through a narrative visual methodology (photo-elicitation).
Method
Six individuals with Parkinson’s disease were asked to take photographs and share verbal narrative accounts to illustrate their experience of living with Parkinson’s disease.
Findings
Results highlight the interrelationship between occupation and identity, as many of the participants’ stories were interpreted as foregrounding the negotiation of occupation, and how such negotiation shaped their sense of identity. Overall, three major themes were identified: (1) Framing the meaning of Parkinson’s disease (accepting the disease as part of who they were); (2) Negotiating engagement in occupation (ongoing deliberation over whether to continue engaging in certain aspects of life as Parkinson’s disease progressed); and (3) Being ready to accept changes that impact personal or social identity (readiness to accept help and to identify as someone with Parkinson’s disease).
Conclusion
Attending to insights regarding the lived experience of Parkinson’s disease will enhance quality of care through informing an enriched client-centered, occupation-based approach.Permalink : ./index.php?lvl=notice_display&id=57837 Exemplaires (1)
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