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• W4308364856 abstract "Research has demonstrated that Parkinson’s disease can have adverse psychological effects on caregivers. Very few studies have focused on the experiences of spouses who are not primary caregivers or who do not identify as primary caregivers. The aim of this study was to explore the experiences of spouses who are not primary caregivers or do not identify as primary caregivers. Twelve Israeli women, spouses of men with Parkinson’s disease, were interviewed using a semi-structured in-depth approach. Thematic analysis revealed five themes: before diagnosis, at diagnosis, after diagnosis, interpersonal ways of coping, and intrapersonal ways of coping. A dynamic of oscillation between confronting and avoiding losses was indicated. Non-death losses were mostly unacknowledged among spouses’ social circles. Results were interpreted in the context of grieving processes after diagnosis. Findings suggest a need for psychological interventions aimed at creating safe spaces for spouses to engage in a grieving process after diagnosis." @default.
• W4308364856 created "2022-11-11" @default.
• W4308364856 creator A5042211047 @default.
• W4308364856 creator A5049317576 @default.
• W4308364856 date "2022-11-07" @default.
• W4308364856 modified "2023-09-29" @default.
• W4308364856 title "Living with Parkinson’s disease: A qualitative study of spousal perspectives" @default.
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• W4308364856 doi "https://doi.org/10.1177/13591053221134740" @default.
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