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2004, Group Analysis
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9 pages
1 file
It is no secret that there is a difficulty in accepting death and dying. The whole of our society shares this difficulty, tending to contemplate death as something which cannot and must not be discussed. This is reflected in the group which is the focus of this article, a group comprised of staff working with people close to death. The author documents his experience as conductor of this group, observing startling changes in personal and collective dynamics as, through group psychotherapy, members learn to discuss their own personal experiences of death.
World Futures, 2017
This article aims at summing up the reflections of a small group of psychologists who work in the domain of palliative treatment. The theory and methodology supporting it are borrowed by a group analysis approach; the group's purpose is a research based on the workers' experience elaboration, which aims at finding out both the specificities of the work apparatus with the people accompanied to the conclusion of their lives, and the main thematic areas of the relationship between healthcare team, patients, and families. The work we present aims at introducing the most meaningful themes that emerged during group meetings: first of all, some service criticalities examined in the area of terminal healthcare and the workers' possible saturation and psycho-social discomfort quotas, generating in some cases a common sense of professional precariousness.
Journal of Social Work Practice
The purpose of the present study was to gain insight into how death is a theme of communication and reflection among staff at a multicultural nursing home. Sixteen interviews with healthcare providers from five nursing homes in Norway were conducted and interpreted through a depth-hermeneutic approach. Our analysis across the dataset yielded an emergent finding related to a prominent lack of communication about death between the healthcare personnel and the patients, as well as among the staff community. We present a psychoanalytically informed interpretation of the absence of talk about death in the nursing homes. Our results indicate the operation of a social defence that helps health care providers maintain distance from anxiety associated with death. Reflection that foregrounds healthcare personnel's own experiences, feelings and thoughts related to death is needed to encourage staff to open up to, and digest, the various impressions death can generate.
British Journal of Community Nursing, 2020
2018
A thesis submitted to the University of Bedfordshire, in partial fulfilment of the requirements for the degree of Master of Science by Research.This thesis explores people’s attitudes towards death and dying. Humans have the ability to create meaning and attach these meanings to objects or events within their life, which then rouses some form of emotions. In respect of death emotions tend to be negative, but with meaning formation might provide the ability to develop positive emotions. Semi-structured interviews were utilised to explore the participants’ attitude towards death and dying. They comprised of seven women and two men with ages ranging from 21 to 81 years. Interpretive Phenomenological Analysis (IPA) was used, providing an explanation of an individual’s lived experience. Data revealed key factors influencing whether death was seen as normal part of life or an object of fear, included faith, meaning and communication, providing a more positive outlook to death and dying; d...
Mortality, 2023
Kenneth Doka's two seminal contributions to Death Studies and loss include the term Disenfranchised Grief, which initiated many studies on Transparent Bereavement, as well as raising extensive clinical attention to the phenomenon; and his book (with Terry Martin) 'Men Don't Cry, Women Do' on gender-based differences in the processing of loss, and specifically men's difficulty to express distress and be assisted by social networks during times of grief. By way of generalisation, I argue that Doka is a pioneer in what can be referred to as the study of 'Grief Regime'. Even more than that, and without him having meant to do so or maybe even been aware of it, he is also the leading contributor to the study of the 'Sociology of Grief'. Following his contributions hundreds of studies were initiated on topics involving the impact of social discourse on the ability to grieve. At the centre of Doka's new book, we find not the grievers, nor society or discourse, but the dying person. Here we see a clear transition from focusing on grief, to focusing on the 'phenomenology of the dying'. The dying person is the main character of the book, dictating its themes, its chapters and even its scientific concepts. Had Thomas Kuhn, the Sociologist of Science, who discussed how scientific paradigms are formed and how they closely and even violently protect their borders to prevent 'subversive' texts from penetrating scientific fields been alive today, he would undoubtedly have been intrigued to follow the book's reception in hegemonic scientific community, maybe even writing its preface. Each chapter of Doka's book 'captures' a delineated theme consistently recurring in the incredible life journey that Kenneth Doka has undergone. Into each theme he has deduced the most relevant moments, conversations and interactions that best correspond and illustrate it, showing how each theme exists in and characterises the dying person. Thus showing himself in a unique and exclusive matter (through conversations he held with those he accompanied, exceptional requests, memories that left their mark), while on the other hand, presenting themes that can be used to identify those who are in an 'End of life condition', having what can be identified as an 'End of life conversation'. This type of discourse is characterised by the persistent questions, passions, emotions and longings of this unique and emotional point in life. These themes, that have become the chapters of the book, were developed through unique interactions held by a unique researcher, who has dedicated his life to 'End of life interactions' with special people who have found in him the perfect partner to whom to expose their deepest emotions during this unique time. It should be said: as theoretical constructs, these chapters may have been perceived as quasi-legitimate in some academic circles, had they been included in a book on loss which is based on anything other than an ethnographic journey. But of course, Doka did not choose to include theoretical chapters in a deductive-scientific book about loss. The chapters were essentially dictated to him by his patients, following an inductive process. Those same chapters and themes are the organising and consistent categories which summarise the topics of conversation, the deliberations, thoughts and associations raised by his partners in dialogue, as they approached the end of their lives. They are an organisation of the empirics which the MORTALITY
EASA Medical Anthropology Network AAA Society for Medical Anthropology Universitat Rovira i Virgili, Tarragona, Catalunya Juny 12-14, 2013
During a year-long fieldwork that I realized in 2011 in a palliative care institution, I encountered cancer and death, but mainly the people who work within this liminal space and alongside liminal bodies, not fully alive, but on their way to something else. The ethnographic encounter that took place between me, the staff and the dying people and their families was mainly realized with, through and about emotions. The main norm regarding the embodied responses to death in this institutionnal setting was a complex control and release system of emotions, with a tendency of the staff to see death and dying as a « beautiful passage », even a « gift », while being able to cry sometimes and « let go ». Something that appeared quite loose in the first place – the right of everyone to approach death as (s)he feels – seemed in fact quite stiff, pointing directly to the presence of what Castra (2003) names a « ritual of pacification », a systematized evacuation of the violent pulsions related to death in palliative care environments. The main challenge of the encounter is to name this social fact and give back to the actors this ethnographic data in a constructive way, while understanding that good intentions and charismatic values, in Weber’s sense, are the basic motives for working with dying people. In fact, my fieldwork adresses directly the emotional dynamics and normativization of the professionalized accompaniment of the dying.
None to report OBJECTIVES • To acknowledge the context of dying/death in acute care settings • To identify challenges associated with dying/death in acute care settings • To recognize emotional and psychological issues in dying and death • To explore what HCPs can do to support patients, families, and themselves
Canadian Journal on Aging / La Revue canadienne du vieillissement, 2016
Death is the final democratic process we experience; it is one that fractures our remaining social ties. The dramatic changes in caregiving favored by the availability of drugs, hospital assistance, and increased life expectancy have deeply changed the screenplay of death. Today, dying has become the most difficult and conflicted experience people in the West face, but it has received little attention until recently. The scenario has changed further due to the availability of hospices and nursing homes, where sufferers, relatives, care givers, and health professionals meet to secure ''the good death.'' Do we really know what ''the good death'' is and how to achieve it? This book aims to dissect the most critical aspects of the end of life in institutional settings (nursing homes, hospices, hospitals). Nowadays, death often comes after a longlasting terminal phase of multiple coexisting diseases, sometimes spent in chronically critically ill conditions marked by multiple relapses, hospital admissions, and transient recoveries that rouse hope of healing. These circumstances are stressful for patients, care givers, and health professional relationships, which then impair even the best care and its perception. Much of a person's end of life is spent in hospices, nursing homes and palliative care units, where the relational dynamics between the patient, his or her relatives, family and professional care givers, and health professional are at stake.
Background Working within the landscape of death and dying, professionals in palliative and hospice care provide insight into the nature of mortality that may be of benefit to individuals facing the end of life. Much less is known about how these professionals incorporate these experiences into their personal lives and clinical practices. Methods This ethnographic inquiry used semi-structured interviews and participant observation to elicit an in-depth understanding of the impact of death and dying on the personal lives of national key leaders (n = 6) and frontline clinicians (n = 24) involved in end-of-life care in Canada. Analysis of findings occurred in the field through constant comparative method and member checking, with more formal levels of analysis occurring after the data-collection phase. Results Eleven specific themes, organized under three overarching categories (past, present and future), were discovered. Early life experiences with death were a common and prominent feature, serving as a major motivator in participants’ career path of end-of-life care. Clinical exposure to death and dying taught participants to live in the present, cultivate a spiritual life, reflect on their own mortality and reflect deeply on the continuity of life. Interpretation Participants reported that their work provided a unique opportunity for them to discover meaning in life through the lessons of their patients, and an opportunity to incorporate these teachings in their own lives. Although Western society has been described as a “death-denying” culture, the participants felt that their frequent exposure to death and dying was largely positive, fostering meaning in the present and curiosity about the continuity of life.
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