Only a few studies explore the lifeworld of the spouses of persons affected by early-onset Alzheimer disease (AD). The aim of this study is to explore the lifeworld of spouses when their partners are diagnosed with AD, focusing on spouses' lived experience. The study employs an interpretative phenomenological framework. Ten in-depth interviews are performed. The results show that spouses' lifeworld changes with the diagnosis. They experience an imprisoned existence in which added obligations, fear, and worry keep them trapped at home, both physically and mentally. In their longing for freedom, new strategies and attitudes helps the spouses to create an extended "lived space" with their partner. The findings stress the importance of paying attention to the lifeworld of spouses and making clinical recommendations on this basis. Most importantly, the lifeworld perspective has implications for how we understand what care is. We hope to challenge all different healthcare professionals and invite them to discuss the deep meaning of care and the definition of being professional in encounters with vulnerable others from a lifeworld perspective.
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http://dx.doi.org/10.1007/s11019-016-9696-3 | DOI Listing |
Gerontologist
May 2019
Department of Psychology, Trinity Western University, Langley, British Columbia, Canada.
Background And Objectives: We explored the meaning of the experience of involuntary separation, as defined formally by the Canadian government and informally by our participants, in formerly caregiving spouses whose partners had been admitted to long-term care. Our goal was to explore their lifeworld experience of separation, including factors influencing well-being as spouses shifted from at-home caregiving to involuntary separation.
Research Design And Methods: Guided, semi-scripted personal interviews were conducted with 10 individuals who had become involuntarily separated up to 4 years prior to the interview.
Med Health Care Philos
March 2017
School of Life and Health Sciences, Aston University, Birmingham, B4 7ET, UK.
We investigated family members' lived experience of Parkinson's disease (PD) aiming to investigate opportunities for well-being. A lifeworld-led approach to healthcare was adopted. Interpretative phenomenological analysis was used to explore in-depth interviews with people living with PD and their partners.
View Article and Find Full Text PDFInt J Qual Stud Health Well-being
April 2017
Faculty of Health Sciences, Oslo and Akershus University College of Applied Sciences, Oslo, Norway.
Objective: Intimate partner violence (IPV) is a large public health problem with far-reaching consequences for those involved. The aim of this study was to explore fathers' experiences of change during pregnancy and early parenthood in the context of IPV.
Methods: The methodological approach in this interview study was hermeneutics, based on a lifeworld perspective.
Med Health Care Philos
September 2016
Department of Technology & Welfare, The Red Cross University College, Box 55676, 102 15, Stockholm, Sweden.
Only a few studies explore the lifeworld of the spouses of persons affected by early-onset Alzheimer disease (AD). The aim of this study is to explore the lifeworld of spouses when their partners are diagnosed with AD, focusing on spouses' lived experience. The study employs an interpretative phenomenological framework.
View Article and Find Full Text PDFBr J Community Nurs
January 2016
Associate Professor, Department of Nursing, Health and Culture, University West, Trollhättan, Sweden.
Introduction: Caring for people affected by dementia is a collective effort that involves public health, primary care, and informal care. The third mainly comprises the efforts of spouses.
Aim: This study aimed to describe spouses' experiences of living with a partner affected with dementia.
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