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  1. Care as a mutual endeavour: Experiences of a multiple sclerosis patient and her healthcare professionals. [REVIEW]Barth Oeseburg & Tineke A. Abma - 2006 - Medicine, Health Care and Philosophy 9 (3):349-357.
    In Dutch healthcare policy patients are seen as informed, autonomous experts and active decision makers with control over their illness and care. Healthcare professionals are expected to operate as providers of information. The purpose of this article is to argue that the consumerist approach of the patient–professional relationship is not a productive way to envision the patient–professional relationship. We argue that an interpretive/deliberative model is a more productive way to envision this relationship, especially in the care for people with a (...)
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  • Balancing Risk Prevention and Health Promotion: Towards a Harmonizing Approach in Care for Older People in the Community. [REVIEW]Bienke M. Janssen, Tine Regenmortel & Tineke A. Abma - 2012 - Health Care Analysis (1):1-21.
    Many older people in western countries express a desire to live independently and stay in control of their lives for as long as possible in spite of the afflictions that may accompany old age. Consequently, older people require care at home and additional support. In some care situations, tension and ambiguity may arise between professionals and clients whose views on risk prevention or health promotion may differ. Following Antonovsky’s salutogenic framework, different perspectives between professionals and clients on the pathways that (...)
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  • Moral Learning in an Integrated Social and Healthcare Service Network.Merel Visse, Guy A. M. Widdershoven & Tineke A. Abma - 2012 - Health Care Analysis 20 (3):281-296.
    The traditional organizational boundaries between healthcare, social work, police and other non-profit organizations are fading and being replaced by new relational patterns among a variety of disciplines. Professionals work from their own history, role, values and relationships. It is often unclear who is responsible for what because this new network structure requires rules and procedures to be re-interpreted and re-negotiated. A new moral climate needs to be developed, particularly in the early stages of integrated services. Who should do what, with (...)
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  • To care or not to care a narrative on experiencing caring responsibilities.Karin van der Heijden, Merel Visse, Gerty Lensvelt-Mulders & Guy Widdershoven - 2016 - Ethics and Social Welfare 10 (1):53-68.
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  • Balancing Risk Prevention and Health Promotion: Towards a Harmonizing Approach in Care for Older People in the Community.Bienke M. Janssen, Tine Van Regenmortel & Tineke A. Abma - 2014 - Health Care Analysis 22 (1):82-102.
    Many older people in western countries express a desire to live independently and stay in control of their lives for as long as possible in spite of the afflictions that may accompany old age. Consequently, older people require care at home and additional support. In some care situations, tension and ambiguity may arise between professionals and clients whose views on risk prevention or health promotion may differ. Following Antonovsky’s salutogenic framework, different perspectives between professionals and clients on the pathways that (...)
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  • Citizenship and autonomy in acquired brain injury.Karen Schipper, Guy A. M. Widdershoven & Tineke A. Abma - 2011 - Nursing Ethics 18 (4):526-536.
    In ethical theory, different concepts of autonomy can be distinguished. In this article we explore how these concepts of autonomy are combined in theory in the citizenship paradigm, and how this turns out in the practice of care for people with acquired brain injury. The stories of a professional caregiver and a client with acquired brain injury show that the combination of various concepts of autonomy in practice leads to tensions between caregivers and clients. These dynamics are discussed from a (...)
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  • Living with end-stage renal disease: Moral responsibilities of patients.Karen Schipper, Elleke Landeweer & Tineke A. Abma - 2018 - Nursing Ethics 25 (8):1017-1029.
    Background: Living with a renal disease often reduces quality of life because of the stress it entails. No attention has been paid to the moral challenges of living with renal disease. Objectives: To explore the moral challenges of living with a renal disease. Research design: A case study based on qualitative research. We used Walker’s ethical framework combined with narrative ethics to analyse how negotiating care responsibilities lead to a new perspective on moral issues. Participants and research context: One case (...)
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  • An interpretative phenomenological analysis of dignity in people with multiple sclerosis.Katarína Žiaková, Juraj Čáp, Michaela Miertová, Elena Gurková & Radka Kurucová - 2020 - Nursing Ethics 27 (3):686-700.
    Background:Dignity is a fundamental concept in healthcare. The symptoms of multiple sclerosis have a negative effect on dignity. Understanding of lived experience of dignity in people with multiple...
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  • Dialogue for Air, Air for Dialogue: Towards Shared Responsibilities in COPD Practice.Merel A. Visse, Truus Teunissen, Albert Peters, Guy A. M. Widdershoven & Tineke A. Abma - 2010 - Health Care Analysis 18 (4):358-373.
    For the past several years patients have been expected to play a key role in their recovery. Self management and disease management have reached a hype status. Considering these recent trends what does this mean for the division of responsibilities between doctors and patients? What kind of role should healthcare providers play? With findings based on a qualitative research project of an innovative practice for people with Chronic Obstructive Pulmonary Disease (COPD) we reflect on these questions. In-depth interviews conducted with (...)
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