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Ryan, Karen; Guerin, Suzanne; Dodd, Philip; McEvoy, John – Journal of Applied Research in Intellectual Disabilities, 2011
Background: Little is known of paid carers' perspectives when caring for people with intellectual disabilities at the end-of-life. Materials and methods: Sixty four individuals from intellectual disability services took part in 12 focus groups. Interviews were analysed using framework analysis. Results: Participants wanted to provide palliative…
Descriptors: Caring, Mental Retardation, Focus Groups, Caregiver Attitudes
Kurt, Layla J.; Piazza, Nick J. – ADULTSPAN Journal, 2012
In 2005, the American Counseling Association (ACA) introduced a new ethical standard for counselors working with clients with terminal illness who are considering hastened death options. The authors' purpose is to inform counselors of the Death With Dignity Act and explore relevant ethical guidelines in the "ACA Code of Ethics" (ACA, 2005).
Descriptors: Professional Associations, Counseling, Ethics, Standard Setting
Sodowsky, Karen – Qualitative Report, 2012
This article is taken from a larger longitudinal study that used caregiver interviews, caregiver surveys, and caregiver statistical information of one community. The interviews were conducted with six spousal caregivers to examine the narratives produced by spouses actively caring for their partners with dementia. The spousal caregivers were…
Descriptors: Dementia, Caregivers, Spouses, Caring
Tremethick, Mary Jane; Johnson, Maureen K.; Carter, Mary R. – International Electronic Journal of Health Education, 2011
Quality end-of-life care is subjective and based on individual values and beliefs. An advance directive provides a legal means of communicating these values and beliefs, as well as preferences in regards to end-of-life care when an individual is no longer able to make his or her desires known. In many nations, advance directives are underused…
Descriptors: Terminal Illness, Health Services, Death, Values
Heyman, Janna C.; Sealy, Yvette M. – Educational Gerontology, 2011
This study examined physicians' attitude, involvement, and perceived barriers with the health care proxy. A cross sectional, correlational design was used to survey practicing physicians (N = 70). Physicians had positive attitudes toward the health care proxy and indicated that the most significant barriers to health care proxy completion were…
Descriptors: Physicians, Terminal Illness, Health Services, Decision Making
Patrizi, Patricia A. – New Directions for Evaluation, 2010
The author discusses an assessment of the Robert Wood Johnson Foundation's work over a 20-year period to improve end-of-life care in America. The case illustrates the evolution of the strategy from one focused on a multiyear randomized control trial of a series of hospital-based interventions that produced findings of "no effects" into several…
Descriptors: Terminal Illness, Health Services, Hospices (Terminal Care), Patients
Rayburn, Carole A. – ADULTSPAN Journal, 2008
How might counseling professionals interact with clients facing their own or a loved one's serious illness or death and help prepare them for this severe stress and loss? Counseling professionals are encouraged to do no harm, be sensitive to beliefs and traditions, use life stories, and help resolve unfinished business.
Descriptors: Counseling Techniques, Counseling Services, Caseworker Approach, Death
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
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