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Meanings of fatigue for women with Parkinson’s disease
Luleå University of Technology, Department of Health Sciences, Nursing Care.
Division of Medicine, Sunderby Hospital.
Luleå University of Technology, Department of Health Sciences, Nursing Care.
2013 (English)In: Qualitative Health Research, ISSN 1049-7323, E-ISSN 1552-7557, Vol. 23, no 6, p. 741-748Article in journal (Refereed) Published
Abstract [en]

The existing knowledge of women’s experiences of living with Parkinson’s disease and fatigue is limited. To gain first-hand knowledge, we interviewed 11 women using a phenomenological hermeneutic interpretation. The results indicate that the familiar daily routines of women with Parkinson’s disease had changed in the sense that their bodily attachment to the world had been altered. The body no longer provided smooth access to the surrounding world; rather, the body served as a barrier to daily living. In practice, understanding this barrier can be significant in recognizing how to create positive conditions that support the women’s experiences and how to formulate their care in congruence with their needs.

Place, publisher, year, edition, pages
2013. Vol. 23, no 6, p. 741-748
National Category
Nursing
Research subject
Nursing
Identifiers
URN: urn:nbn:se:ltu:diva-4279DOI: 10.1177/1049732313482398ISI: 000336257700003PubMedID: 23515300Scopus ID: 2-s2.0-84876797725Local ID: 233cfc4d-a321-4384-8ea7-17cfd97239e9OAI: oai:DiVA.org:ltu-4279DiVA, id: diva2:977143
Note
Validerad; 2013; 20121004 (andbra)Available from: 2016-09-29 Created: 2016-09-29 Last updated: 2018-07-10Bibliographically approved

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Olsson, MalinSöderberg, Siv

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