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Duba, Jill D.; Magenta, Mary – Family Journal: Counseling and Therapy for Couples and Families, 2008
End-of-life care is continuously becoming an issue of paramount importance given an increase in medical advances, the aging of the population, and the movement toward contributing toward a quality of life among terminally ill patients. However, there is a dearth in literature related to this topic specifically in terms of preparing counselors to…
Descriptors: Quality of Life, Counselor Training, Patients, Counseling
Tait, Glendon R.; Hodges, Brian D. – Academic Psychiatry, 2009
Objective: The authors examined psychiatric residents' attitudes, perceived preparedness, experiences, and needs in end-of-life care education. They also examined how residents conceptualized good end-of-life care and dignity. Methods: The authors conducted an electronic survey of 116 psychiatric residents at the University of Toronto. The survey…
Descriptors: Curriculum Development, Death, Patients, Educational Experience
Niederriter, Joan E. – ProQuest LLC, 2009
Student nurses are involved in caring for patients who are actively dying or who have been told they have a terminal illness and are faced with the process of dying. Students encounter these patients in hospitals, nursing homes, at home or in hospice care settings. According to Robinson (2004), "nurses are the healthcare providers that are most…
Descriptors: Nursing Students, Hospices (Terminal Care), Nursing Education, Student Attitudes
Broughton, Katherine – Kairaranga, 2008
Few resources seem to be available to support school communities that have a child whose death is anticipated. The present article draws on the experiences of school staff and special education employees who have been involved in New Zealand school communities where a child was terminally ill and died. These experiences could help other school…
Descriptors: Foreign Countries, Death, Coping, Counseling Techniques
Stein, Gary L.; Sherman, Patricia A.; Bullock, Karen – Educational Gerontology, 2009
An educational program was developed to train practitioners to provide care for patients and families that are responsive to cultural concerns. The aim was to increase knowledge and improve attitudes toward providing culturally proficient and culturally sensitive care for patients and families facing life-threatening illnesses. The program…
Descriptors: Nursing Education, Patients, Program Effectiveness, Program Evaluation
Csikai, Ellen L.; Herrin, Charlotte; Tang, Maggie; Church, Wesley T., II – Child Welfare, 2008
A mailed survey of child welfare workers in one southern state assessed various aspects of encounters with end-of-life situations in practice. Findings revealed that child deaths, children with life-threatening or life-limiting illnesses, and parental deaths were most commonly encountered and that coworkers were relied on for support. Many had no…
Descriptors: Child Abuse, Child Welfare, Welfare Services, Caseworkers
Imagining the Alternatives to Life Prolonging Treatments: Elders' Beliefs about the Dying Experience
Winter, Laraine; Parker, Barbara; Schneider, Melissa – Death Studies, 2007
Deciding for or against a life-prolonging treatment represents a choice between prolonged life and death. When the death alternative is not described, individuals must supply their own assumptions. How do people imagine the experience of dying? The authors asked 40 elderly people open-ended questions about dying without 4 common life-prolonging…
Descriptors: Psychological Patterns, Patients, Terminal Illness, Death

Smith, Douglas C. – Omega: Journal of Death and Dying, 1993
Presents argument in favor of being supportive of terminally-ill person's choice to deny death's inevitability. Presents illustrative case study on choice of denial and draws upon supportive work of some of foremost experts in the field of death and dying. Addresses implications for dying person's counselor and consequences for dying person's…
Descriptors: Counselor Role, Death, Terminal Illness
Munn, Jean C.; Dobbs, Debra; Meier, Andrea; Williams, Christianna S.; Biola, Holly; Zimmerman, Sheryl – Gerontologist, 2008
Purpose: We designed this study to examine the end-of-life (EOL) experience in long-term care (LTC) based on input from key stakeholders. Design and Methods: The study consisted of 10 homogeneous focus groups drawn from a purposive sample of LTC residents (2 groups; total n = 11), family caregivers (2 groups; total n = 19), paraprofessional staff…
Descriptors: Grounded Theory, Proximity, Residential Care, Hospices (Terminal Care)
Keranen, Lisa – Quarterly Journal of Speech, 2007
"Code status" is a prominent feature of end-of-life discussions in U.S. hospitals. This essay analyzes how the rhetoric of code status articulates the terms of end-of-life decision-making in one hospital's "Patient" Preferences Worksheet. The Worksheet signifies the abandonment of the technological fix as the preferred…
Descriptors: Worksheets, Rhetoric, Patients, Personal Autonomy
Wilson, Donna M.; Birch, Stephen; Sheps, Sam; Thomas, Roger; Justice, Christopher; MacLeod, Rod – Canadian Journal on Aging, 2008
The vast majority of the 220,000 Canadians who die each year, principally of old age and progressive ill health, do not have access to specialized hospice or palliative care. Hospice and palliative care programs are unevenly distributed across Canada, with existing programs limited in capacity and services varying considerably across programs.…
Descriptors: Hospices (Terminal Care), Terminal Illness, Older Adults, Foreign Countries

Glazer, Hilda R.; Landreth, Garry L. – Journal of Humanistic Education and Development, 1993
Presents concept of dying as a developmental stage in the life of terminally ill children. Sees dying as a normal developmental process in which the child focuses on appreciating and prizing the moment rather than preparing for something yet to come. Discusses communication with the dying child and use of the language of play. (Author/NB)
Descriptors: Child Development, Children, Death, Terminal Illness
Hinds, Michael deCourcy – 1997
This paper questions how society should care for people who are suffering and near death? Underlying this issue are very difficult questions about the evolving rights of patients, medical standards, and societal norms--questions about the American way of death, which often involves needless pain and unwanted treatment. Three choices are presented…
Descriptors: Death, Decision Making, Suicide, Suicide

Baugher, Robert J.; And Others – Omega: Journal of Death and Dying, 1990
Examined responses of 1,110 terminally ill persons with cancer at varying time periods prior to death. Disengagement and Objective Self-Awareness theories, which suggest that people nearing death would increase desire to separate from others, were not supported. Found few differences in responses of persons further from, or closer to, death.…
Descriptors: Attitudes, Cancer, Death, Emotional Adjustment

Cochrane, Joyce B.; And Others – Omega: Journal of Death and Dying, 1991
Examined relationships among death anxiety, disclosure behaviors, and attitudes toward terminal care of 99 oncologists. Found death anxiety scores lower for oncologists than typically reported for physicians. Short-term repeated exposure to dying patients resulted in comfort with dying patients whereas long-term repeated exposure resulted in…
Descriptors: Anxiety, Cancer, Death, Disclosure