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Showing 61 to 75 of 148 results Save | Export
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Carr, Deborah; Khodyakov, Dmitry – Journal of Health and Social Behavior, 2007
Dying persons are encouraged to name as durable power of attorney for health care (DPAHC) someone who will thus be empowered to make end-of-life treatment decisions for them in the event that they become incapacitated. We use data from the Wisconsin Longitudinal Study to investigate whether and whom older adults designate as their DPAHC. DPAHC…
Descriptors: Terminal Illness, Decision Making, Empowerment, Death
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Martin, Robert W.; Wylie, Norma – Academic Medicine, 1989
A successful seven-day course offered to third-year medical students is an integrated program for teaching them how to deal with terminal illness. The course uses lectures, audiovisual aids, and group and individual sessions to enhance self-awareness and practical application of the material in a clinical setting. (Author/MSE)
Descriptors: Death, Diseases, Higher Education, Medical Education
Lidstone, Sheila S. – Principal, 1992
Describes a Texas elementary school's efforts to cope with the special needs of Kenneth, a fourth grader slowly dying of kidney cancer. Besides learning their subjects like other students, Kenneth's classmates learned how to care. Every student volunteered to be Kenneth's assistant and was enriched by the boy's positive attitude and determination…
Descriptors: Coping, Death, Elementary Education, Grade 4
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Farrugia, David – Counseling and Values, 1993
Explores issues related to "right to die." Makes case for counselors to assist clients and families with concerns related to refusal or withdrawal of medical treatment in cases of terminal illness or in cases where quality of life is severely impaired such as permanent comatose state. Presents historical, ethical, and legal perspectives.…
Descriptors: Counselor Role, Death, Ethics, Euthanasia
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Smith, Douglas C. – Journal for Specialists in Group Work, 1994
Suggests and describes a six-session group for people with AIDS. Each session is related to a theoretical base and includes a related activity. Sessions are intended to meet psychological needs of the dying. In evaluations, participants recommend the format to others with AIDS. Includes 25 references. (Author/CRR)
Descriptors: Acquired Immune Deficiency Syndrome, Counseling Techniques, Death, Group Counseling
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Smith, Douglas C.; Maher, Michael F. – Journal for Specialists in Group Work, 1991
In an effort to address the stressors accompanying work with the dying, a special "Phoenix" group for caregivers is introduced. Planning considerations, group format, and accompanying structured activities are presented. Describes individual sessions which focus on mourning, transition from mourning to disengaging, disengaging, transition from…
Descriptors: Caregivers, Death, Family Caregivers, Social Support Groups
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Levy, Joseph J.; Nouss, Alexis – Omega: Journal of Death and Dying, 1993
Reviews novels dealing with the Acquired Immune Deficiency Syndrome (AIDS) epidemic, noting that their perspectives on death can be extracted through content analysis. Concludes that, overall, these novels present weak symbolization about death with rituals that are not highly elaborated and that complex images of the afterlife are not offered.…
Descriptors: Acquired Immune Deficiency Syndrome, Death, Foreign Countries, Homosexuality
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Kelner, Merrijoy J.; And Others – Death Studies, 1994
Examined perceptions of 20 physicians and 20 nurses of need for, feasibility of, and value of regulations and legislation to govern dying process. Found little unanimity in their attitudes. Some believed such regulations were needed, but others believed they would seriously compromise good patient care. Also found disagreement on who should…
Descriptors: Attitudes, Death, Decision Making, Foreign Countries
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O'Halloran, Colleen M.; Altmaier, Elizabeth M. – Journal of Counseling & Development, 1996
A review of studies on death awareness among children who are healthy, chronically ill, and terminally ill reveals that children with life-threatening diseases demonstrate increased understanding of death. In contrast, healthy and chronically ill children appear to require certain age, cognitive development level, or intelligence thresholds to…
Descriptors: Age, Children, Chronic Illness, Cognitive Development
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Ferrell, Betty R.; Virani, Rose; Grant, Marcia – Nursing Outlook, 1999
As the members of the health care team who spend the most time with patients who are facing death, nurses are aware of the need for improved end-of-life (EOL) care and have identified resources to achieve that goal by improving education. A survey of 725 nursing faculty and state boards indicates an awareness of the need for improved EOL care and…
Descriptors: Curriculum Development, Death, Educational Change, Higher Education
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Manis, Amie A.; Bodenhorn, Nancy – Counseling and Values, 2006
This article presents a review of the literature on counseling adults with terminal illness, particularly the literature on the nature of preparation that counselors and other professionals who attend to the needs of adults with a terminal illness require. The authors review information and findings from philosophical, psychological, practical,…
Descriptors: Terminal Illness, Adults, Counseling Techniques, Literature Reviews
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Foytack, Jane; West, Daniel J. – Omega: Journal of Death and Dying, 1994
Discusses, in context of physician-patient relationship, workable model on advance directives for physicians to use with patients along with appropriate guidelines. Examines variables involved in establishment of guidelines for use by physician in office and inpatient settings. Identifies key management and clinical factors for initiating and…
Descriptors: Death, Guidelines, Medical Services, Physician Patient Relationship
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Wear, Delese – Omega: Journal of Death and Dying, 1991
Presents cubism as metaphor to think about medical humanities curriculum in medical school curriculum. Uses Kafka's "The Metamorphosis," Tolstoy's "The Death of Ivan Ilych," and Olsen's "Tell Me a Riddle" to illustrate how literary inquiry might enable medical students and other health care providers to think about…
Descriptors: Curriculum Enrichment, Death, Humanities, Medical Education
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Hayslip, Bert, Jr.; And Others – Omega: Journal of Death and Dying, 1991
Analyzed response bias among 34 recipients of care in hospice. Found nonrespondents to have better bereavement prognoses and tended to care for patients who were younger, male, and in program for shorter time. Nonrespondents were in contact with staff less than were respondents. Data are consistent with earlier research showing significant…
Descriptors: Caregivers, Death, Hospices (Terminal Care), Participant Characteristics
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deMontigny, Johanne – Omega: Journal of Death and Dying, 1993
Notes that role of psychologist on palliative care unit is to be there for terminally ill, their friends, and their families, both during the dying and the bereavement and for the caregiver team. Focuses on work of decoding ordinary words which for many patients hide painful past. Stresses necessity to remain open to unexpected. (Author/NB)
Descriptors: Cancer, Counselor Role, Death, Foreign Countries
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