scholarly journals Body Boundaries and Discursive Practices in Life Threatening Illness: Narratives of the Self

2021 ◽  
Author(s):  
◽  
Patricia McClunie-Trust

<p>This thesis tells a story from within and between the boundaries of my professional work as a nurse and my private life as the wife of a patient with life threatening illness. The events related in the thesis are told using a technique I have called writing back to myself, where my own journals and stories of the experience of living with life threatening illness provide data for analysis. The reader is invited to participate in these representations and to consider the potential for the skilful practice of nursing which may be read in the stories, and the analysis I have developed from them. I have developed the theoretical and methodological positionings for the thesis from the work of Foucault (1975,1979,1982,1988), Deleuze (1988), Ellis (1995), Richardson (1998) and other writers who utilise genealogical or narrative approaches. The analysis of my own stories in the thesis explores the philosophical and contextual positionings of the nurse as a knowledge worker through genealogies of practice and the specific intellectual work of the nurse. Local and contextual epistemologies are considered as ways of theorising nursing practice through personal knowledge, which is surfaced through the critical analysis of contextual positionings and the process of writing as inquiry. The idea of harmonising nursing practice in the patient's local world through contingent and thinking responses, and the recognition of one's own agency as the nurse, are considered in terms of what might constitute ethical practice. The thinking nurse is a specific intellectual, who critically engages with the context of her/his own practice to form new discourses derived from local and contextual 'truths' about illness, suffering and dying. The capacities for vision that are developed through the stories in the thesis, are explored as having the potential to present new possibilities for the practice of professional nursing. Notions of what constitutes ethical practice are negotiated and contested through local conversations, which privilege the capacities of the patient and the nurse in taking up new discursive positionings as alternatives to those prescribed through the sovereignty of expert power. In the local and contextual world of the patient, visions for practice may be negotiated moment by moment through careful exploration of discursive tensions and the critical appraisal of the utility of alternative possibilities. This development of local knowledge relies on the ability of the nurse to explore and trust her/his own judgement and nursing responses in situations where visions for practice may not be clear. The 'un-picking' and 're-sewing' of stories related in the analysis of the discursive production of the cancer patient and the 'private nurse' present new possibilities for the ethical substance of nursing. This ethical substance creates the potential for new conceptualisations of practice, where nurses and other health professionals take responsibility for the effects of their activities with patients. In this 'un-picking' of the stories in the thesis, I am concerned with the discursive positionings that are taken up by the patient and the health professional in the story. I identify the means through which subjects become visible in discursive statements and the effects of these subject positionings on specific moments of practice with the patient. The 're-sewing' of events involves the telling of alternative stories, negotiated between the actors in the events, to produce a more ethically desirable outcome in the specific contexts of nursing practice.</p>

2021 ◽  
Author(s):  
◽  
Patricia McClunie-Trust

<p>This thesis tells a story from within and between the boundaries of my professional work as a nurse and my private life as the wife of a patient with life threatening illness. The events related in the thesis are told using a technique I have called writing back to myself, where my own journals and stories of the experience of living with life threatening illness provide data for analysis. The reader is invited to participate in these representations and to consider the potential for the skilful practice of nursing which may be read in the stories, and the analysis I have developed from them. I have developed the theoretical and methodological positionings for the thesis from the work of Foucault (1975,1979,1982,1988), Deleuze (1988), Ellis (1995), Richardson (1998) and other writers who utilise genealogical or narrative approaches. The analysis of my own stories in the thesis explores the philosophical and contextual positionings of the nurse as a knowledge worker through genealogies of practice and the specific intellectual work of the nurse. Local and contextual epistemologies are considered as ways of theorising nursing practice through personal knowledge, which is surfaced through the critical analysis of contextual positionings and the process of writing as inquiry. The idea of harmonising nursing practice in the patient's local world through contingent and thinking responses, and the recognition of one's own agency as the nurse, are considered in terms of what might constitute ethical practice. The thinking nurse is a specific intellectual, who critically engages with the context of her/his own practice to form new discourses derived from local and contextual 'truths' about illness, suffering and dying. The capacities for vision that are developed through the stories in the thesis, are explored as having the potential to present new possibilities for the practice of professional nursing. Notions of what constitutes ethical practice are negotiated and contested through local conversations, which privilege the capacities of the patient and the nurse in taking up new discursive positionings as alternatives to those prescribed through the sovereignty of expert power. In the local and contextual world of the patient, visions for practice may be negotiated moment by moment through careful exploration of discursive tensions and the critical appraisal of the utility of alternative possibilities. This development of local knowledge relies on the ability of the nurse to explore and trust her/his own judgement and nursing responses in situations where visions for practice may not be clear. The 'un-picking' and 're-sewing' of stories related in the analysis of the discursive production of the cancer patient and the 'private nurse' present new possibilities for the ethical substance of nursing. This ethical substance creates the potential for new conceptualisations of practice, where nurses and other health professionals take responsibility for the effects of their activities with patients. In this 'un-picking' of the stories in the thesis, I am concerned with the discursive positionings that are taken up by the patient and the health professional in the story. I identify the means through which subjects become visible in discursive statements and the effects of these subject positionings on specific moments of practice with the patient. The 're-sewing' of events involves the telling of alternative stories, negotiated between the actors in the events, to produce a more ethically desirable outcome in the specific contexts of nursing practice.</p>


2010 ◽  
Vol 8 (3) ◽  
pp. 353-358 ◽  
Author(s):  
Karimah Alidina ◽  
Ildico Tettero

AbstractHope is a multi-dimensional concept that is integral to a dying person's needs. It is an essential resource that assists individuals with a life-threatening illness to cope during times of intense physical and psychological distress. The objective of this article is to explore and analyze the therapeutic value of hope. The phenomenon of hope will be explored through the analysis and application of Dufault and Martocchio's Multidimensional Model of Hope (MMH) to a clinical scenario. Factors determining hope in cancer patients as well as interventions that can foster hope in dying patients will be identified. Discussion includes examination of literature gaps, relevance to nursing practice, and practical strategies to engender hope and thereby enhance quality of life (QOL) in advanced cancer patients.


2008 ◽  
Vol 12 (1) ◽  
pp. 50-54 ◽  
Author(s):  
Sandra J. Tanis, ◽  
Pamela P. DiNapoli,

Hope is a phenomenon that, although difficult to define, is experienced in various ways and to different degrees by individuals when confronted with a life-threatening illness. Often a paradox of hope exists in the same moment of time or along a continuum for a patient receiving palliative care. The purpose of this manuscript is to conceptually define the paradox of hope, to operationalize the concept, and to apply the concept to nursing practice. By providing a link between the paradox of hope and the practice of nursing, nurses have the potential to relieve patient suffering by fostering and supporting a patient’s concept of hope in receiving palliative care.


1987 ◽  
Vol 32 (10) ◽  
pp. 906-906
Author(s):  
No authorship indicated

2013 ◽  
Author(s):  
Lawrence G. Calhoun ◽  
◽  
Jay Azarow ◽  
Tzipi Weiss ◽  
Joel Millam

2008 ◽  
Vol 5 (1) ◽  
pp. 81-88
Author(s):  
Philip Berry

When life-threatening illness robs a patient of the ability to express their desires, medical personnel must work through the issues of management and prognosis with relatives. Management decisions are guided by medical judgement and the relatives’ account of the patient’s wishes, but difficulties occur when distance grows between these two factors. In these circumstances the counselling process may turn into a doctor-led justification of the medical decision. This article presents two strands of dialogue, in which a doctor, counselling for and against continuation of supportive treatment in two patients with liver failure, demonstrates selectivity and inconsistency in constructing an argument. The specific issues of loss of consciousness (with obscuration of personal identity), statistical ‘futility’ and removal of autonomy are explored and used to bolster diametrically opposed medical decisions. By examining the doctor’s ability to interpret these issues according to circumstance, the author demonstrates how it is possible to shade medical facts depending on the desired outcome.


2019 ◽  
Vol 18 (1) ◽  
Author(s):  
S. Robin Cohen ◽  
Lara B. Russell ◽  
Anne Leis ◽  
Javad Shahidi ◽  
Pat Porterfield ◽  
...  

Abstract Background Domains other than those commonly measured (physical, psychological, social, and sometimes existential/spiritual) are important to the quality of life of people with life-threatening illness. The McGill Quality of Life Questionnaire (MQOL) – Revised measures the four common domains. The aim of this study was to create a psychometrically sound instrument, MQOL – Expanded, to comprehensively measure quality of life by adding to MQOL-Revised the domains of cognition, healthcare, environment, (feeling like a) burden, and possibly, finance. Methods Confirmatory factor analyses were conducted on three datasets to ascertain whether seven new items belonged with existing MQOL-Revised domains, whether good model fit was obtained with their addition as five separate domains to MQOL-Revised, and whether a second-order factor representing overall quality of life was present. People with life-threatening illnesses (mainly cancer) or aged > 80 were recruited from 15 healthcare sites in seven Canadian provinces. Settings included: palliative home care and inpatient units; acute care units; oncology outpatient clinics. Results Good model fit was obtained when adding each of the five domains separately to MQOL-Revised and for the nine correlated domains. Fit was acceptable for a second-order factor model. The financial domain was removed because of low importance. The resulting MQOL-Expanded is a 21-item instrument with eight domains (fit of eight correlated domains: Comparative Fit Index = .96; Root Mean Square Error of Approximation = .033). Conclusions MQOL-Expanded builds on MQOL-Revised to more comprehensively measure the quality of life of people with life-threatening illness. Our analyses provide validity evidence for the MQOL-Expanded domain and summary scores; the need for further validation research is discussed. Use of MQOL-Expanded will enable a more holistic understanding of the quality of life of people with a life-threatening illness and the impact of treatments and interventions upon it. It will allow for a better understanding of less commonly assessed but important life domains (cognition, healthcare, environment, feeling like a burden) and their relationship to the more commonly assessed domains (physical, psychological, social, existential/spiritual).


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