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  1. Disability, bioethics, and rejected knowledge.Christopher Newell - 2006 - Journal of Medicine and Philosophy 31 (3):269 – 283.
    In this article I explore disability as far more than individual private tragedy, suggesting it has a social location and reproduction. Within this context we look at the power relations associated with bioethics and its largely uncritical use of the biomedical model. Within that context the topics of genetics, euthanasia, and biotechnology are explored. In examining these topics a social account of disability is proposed as rejected knowledge. Accordingly we explore the political nature of bioethics as a project.
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  • The Foundations of Social Research: Meaning and Perspective in the Research Process.Michael Crotty - 1998 - SAGE Publications.
    Choosing a research method can be bewildering. How can you be sure which methodology is appropriate, or whether your chosen combination of methods is consistent with the theoretical perspective you want to take? The Foundation of Social Research links methodology and theory with great clarity and precision, showing students and researchers how to navigate the maze of conflicting terminology. The major epistemological stances and theoretical perspectives that colour and shape current social research are detailed: positivism, constructionism, interpretivism, critical inquiry, feminism (...)
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  • The Goals of Medicine. Towards a Unified Theory.Bengt Brülde - 2001 - Health Care Analysis 9 (1):1-13.
    The purpose of this article is to present a normative theory of the goals of medicine (a theory that tells us in what respects medicine should benefit the patient) that is both comprehensive and unified. A review of the relevant literature suggests that there are at least seven plausible goals that are irreducible to each other, namely to promote functioning, to maintain or restore normal structure and function, to promote quality of life, to save and prolong life, to help the (...)
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  • If We Think It’s Futile, Can’t We Just Say No?Susan B. Rubin - 2007 - HEC Forum 19 (1):45-65.
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  • Quality of life: The contested rhetoric of resource allocation and end-of-life decision making.David Nantais & Mark Kuczewski - 2004 - Journal of Medicine and Philosophy 29 (6):651 – 664.
    The term "quality of life" has a long history in the bioethics literature. It is usually used in one of two contexts: in resource allocation discussions in the hope of arriving at an objective measure of the worth of an intervention; and in end-of-life discussions as a concept that can justify the forgoing of life-sustaining treatment. In both contexts, the term has valid uses as it is meant to measure the efficacy of a treatment. However, the term has the unfortunate (...)
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  • Disability or end-of-life? Competing narratives in bioethics.Joseph Kaufert & Thomas Koch - 2003 - Theoretical Medicine and Bioethics 24 (6):459-469.
    Bioethics, and indeed much ethicalwriting generally, makes its point throughnarratives. The religious parable no less thanthe medical teaching case uses a simple storyto describe appropriate action or theapplication of a critical principle. Whilepowerful, the telling story has limits. In thispaper the authors describe a simple teachingcase on ``end-of-life'' decision making that wasill received by its audience. The authors ill-receivedexample, involving the disconnection ofventilation in a patient with ALS (Lou Gherig'sDisease) was critiqued by audience members withlong-term experience as ventilation users. Inthis (...)
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