Jonathan Herring
- Published in print:
- 2008
- Published Online:
- January 2009
- ISBN:
- 9780199545520
- eISBN:
- 9780191721113
- Item type:
- chapter
- Publisher:
- Oxford University Press
- DOI:
- 10.1093/oso:acprof/9780199545520.003.0021
- Subject:
- Law, Medical Law
This chapter focuses on the legal treatment of carers. It develops the claim that an individualized approach to caring relationships is inappropriate. It then considers in more detail two specific ...
More
This chapter focuses on the legal treatment of carers. It develops the claim that an individualized approach to caring relationships is inappropriate. It then considers in more detail two specific issues which demonstrate this issue. The first is the relevance of carers when issues of rationing health care resources. The second is the relevance of the interests of carers when decisions are made concerning people who lack capacity.Less
This chapter focuses on the legal treatment of carers. It develops the claim that an individualized approach to caring relationships is inappropriate. It then considers in more detail two specific issues which demonstrate this issue. The first is the relevance of carers when issues of rationing health care resources. The second is the relevance of the interests of carers when decisions are made concerning people who lack capacity.
David Barnard, Anna M. Towers, Patricia Boston, and Yanna Lambrinidou
- Published in print:
- 2000
- Published Online:
- November 2011
- ISBN:
- 9780195123432
- eISBN:
- 9780199999835
- Item type:
- book
- Publisher:
- Oxford University Press
- DOI:
- 10.1093/acprof:oso/9780195123432.001.0001
- Subject:
- Palliative Care, Patient Care and End-of-Life Decision Making, Palliative Medicine and Older People
This book provides a unique view of patients, families, and their caregivers striving together to maintain comfort and hope in the face of incurable illness. The narratives weave together emotions, ...
More
This book provides a unique view of patients, families, and their caregivers striving together to maintain comfort and hope in the face of incurable illness. The narratives weave together emotions, physical symptoms, spiritual concerns, and the stresses of family life, as well as the professional and personal challenges of providing hospice and palliative care. Based on a vast amount of participant observation and in-depth interviews, the book moves far beyond dry technical manuals for symptom control and tired clichés about death with dignity, to depict the sights, sounds, tastes, and smells of the daily in patients' homes and the palliative care unit. It captures the breathtaking diversity of people's aspirations and ideals as they face death, and the views of the professionals who care for them. Anger and fear, tenderness and reconciliation, jealousy and love, social support and falling through the cracks, unexpected courage and unshakable faith—all of these are part of facing death in late twentieth-century North America, and this book brings them to life in a portrait of the processes of giving and receiving palliative care.Less
This book provides a unique view of patients, families, and their caregivers striving together to maintain comfort and hope in the face of incurable illness. The narratives weave together emotions, physical symptoms, spiritual concerns, and the stresses of family life, as well as the professional and personal challenges of providing hospice and palliative care. Based on a vast amount of participant observation and in-depth interviews, the book moves far beyond dry technical manuals for symptom control and tired clichés about death with dignity, to depict the sights, sounds, tastes, and smells of the daily in patients' homes and the palliative care unit. It captures the breathtaking diversity of people's aspirations and ideals as they face death, and the views of the professionals who care for them. Anger and fear, tenderness and reconciliation, jealousy and love, social support and falling through the cracks, unexpected courage and unshakable faith—all of these are part of facing death in late twentieth-century North America, and this book brings them to life in a portrait of the processes of giving and receiving palliative care.
Sheila Payne and Caroline Ellis-Hill (eds)
- Published in print:
- 2001
- Published Online:
- November 2011
- ISBN:
- 9780192631671
- eISBN:
- 9780191730191
- Item type:
- book
- Publisher:
- Oxford University Press
- DOI:
- 10.1093/acprof:oso/9780192631671.001.0001
- Subject:
- Palliative Care, Patient Care and End-of-Life Decision Making, Pain Management and Palliative Pharmacology
Most chronically and terminally ill patients are cared for in their own homes by family and friends, rather than in hospitals or hospices. These carers are an invaluable free resource and there is an ...
More
Most chronically and terminally ill patients are cared for in their own homes by family and friends, rather than in hospitals or hospices. These carers are an invaluable free resource and there is an increasing amount of research into their role and the experiences of caring for the terminally ill, patients with cancer, and patients with other chronic diseases. This book provides a critique of the theoretical concept of caring, carers, and caregivers. The material is based on empirical evidence from recent studies of adults with acquired chronic illnesses, including terminal illness. The empirical data within the book has been gathered from the perspective of those providing personal, domestic, or emotional care to others already known to them by virtue of kinship, co-habitation, or friendship, rather than carers organised on a professional or voluntary basis. This new evidence is used to make suggestions about possible ways forward within health and social care practice.Less
Most chronically and terminally ill patients are cared for in their own homes by family and friends, rather than in hospitals or hospices. These carers are an invaluable free resource and there is an increasing amount of research into their role and the experiences of caring for the terminally ill, patients with cancer, and patients with other chronic diseases. This book provides a critique of the theoretical concept of caring, carers, and caregivers. The material is based on empirical evidence from recent studies of adults with acquired chronic illnesses, including terminal illness. The empirical data within the book has been gathered from the perspective of those providing personal, domestic, or emotional care to others already known to them by virtue of kinship, co-habitation, or friendship, rather than carers organised on a professional or voluntary basis. This new evidence is used to make suggestions about possible ways forward within health and social care practice.
Mary Briody Mahowald
- Published in print:
- 2006
- Published Online:
- September 2006
- ISBN:
- 9780195176179
- eISBN:
- 9780199786558
- Item type:
- chapter
- Publisher:
- Oxford University Press
- DOI:
- 10.1093/0195176170.003.0012
- Subject:
- Philosophy, Feminist Philosophy
Cases illustrating variables that arise in the health care of elderly women and their caregivers, and care of the dying are presented. These include questions about ageism, competence to perform ...
More
Cases illustrating variables that arise in the health care of elderly women and their caregivers, and care of the dying are presented. These include questions about ageism, competence to perform ordinary functions such as driving, possible loss of capacity for moral agency, advance directives, and decisions about forgoing or terminating life-support. For each topic, empirical and theoretical factors are discussed from an “egalitarian perspective” that imputes privileged status to the standpoint of women.Less
Cases illustrating variables that arise in the health care of elderly women and their caregivers, and care of the dying are presented. These include questions about ageism, competence to perform ordinary functions such as driving, possible loss of capacity for moral agency, advance directives, and decisions about forgoing or terminating life-support. For each topic, empirical and theoretical factors are discussed from an “egalitarian perspective” that imputes privileged status to the standpoint of women.
David E. Guinn
David E. Guinn (ed.)
- Published in print:
- 2006
- Published Online:
- September 2006
- ISBN:
- 9780195178739
- eISBN:
- 9780199784943
- Item type:
- chapter
- Publisher:
- Oxford University Press
- DOI:
- 10.1093/0195178734.003.0017
- Subject:
- Religion, Philosophy of Religion
Concerns about caregivers providing religious or spiritual care arise, in large part, out of a misunderstanding about religion and spirituality and what those terms really mean. Many people treat ...
More
Concerns about caregivers providing religious or spiritual care arise, in large part, out of a misunderstanding about religion and spirituality and what those terms really mean. Many people treat religion and spirituality as special and unique. This chapter argues that religion and spirituality are basic human facts as inseparable from what it means to be human in the same way as our sex, our age, our ethnicity or the other social and cultural factors that caregivers routinely address. The chapter begins by offering a functionalist definition of religion and spirituality. It then examines research on the needs of patients at the end of life and suggests how these express religious and spiritual concerns. Finally, it offers guidelines as to how the caregiver may meet those needs of a patient.Less
Concerns about caregivers providing religious or spiritual care arise, in large part, out of a misunderstanding about religion and spirituality and what those terms really mean. Many people treat religion and spirituality as special and unique. This chapter argues that religion and spirituality are basic human facts as inseparable from what it means to be human in the same way as our sex, our age, our ethnicity or the other social and cultural factors that caregivers routinely address. The chapter begins by offering a functionalist definition of religion and spirituality. It then examines research on the needs of patients at the end of life and suggests how these express religious and spiritual concerns. Finally, it offers guidelines as to how the caregiver may meet those needs of a patient.
Sofia Johnson Frankenberg
- Published in print:
- 2012
- Published Online:
- May 2012
- ISBN:
- 9780199652501
- eISBN:
- 9780191739217
- Item type:
- chapter
- Publisher:
- Oxford University Press
- DOI:
- 10.1093/acprof:oso/9780199652501.003.0030
- Subject:
- Law, Family Law, Human Rights and Immigration
Most caregivers regard it as their responsibility to teach children to behave appropriately. What is appropriate behaviour and how to make children behave as they should varies according to the local ...
More
Most caregivers regard it as their responsibility to teach children to behave appropriately. What is appropriate behaviour and how to make children behave as they should varies according to the local context. In Tanzania, although a signatory to the UN Convention on the Rights of the Child, corporal punishment is lawful in schools, in the penal system, in families, and in alternative care institutions. In a previous chapter, caregivers' conceptions of corporal punishment have been explored. This chapter takes point of departure in these findings and takes them a step further by investigating how they can be understood in the light of the caregiving relationship using the concepts zone of intimacy and ethics of care.Less
Most caregivers regard it as their responsibility to teach children to behave appropriately. What is appropriate behaviour and how to make children behave as they should varies according to the local context. In Tanzania, although a signatory to the UN Convention on the Rights of the Child, corporal punishment is lawful in schools, in the penal system, in families, and in alternative care institutions. In a previous chapter, caregivers' conceptions of corporal punishment have been explored. This chapter takes point of departure in these findings and takes them a step further by investigating how they can be understood in the light of the caregiving relationship using the concepts zone of intimacy and ethics of care.
Chloe Silverman
- Published in print:
- 2011
- Published Online:
- October 2017
- ISBN:
- 9780691150468
- eISBN:
- 9781400840397
- Item type:
- chapter
- Publisher:
- Princeton University Press
- DOI:
- 10.23943/princeton/9780691150468.003.0004
- Subject:
- Anthropology, Social and Cultural Anthropology
This chapter focuses on parents emerging from the experience of wide-ranging psychogenic theorizing about autism during the 1950s and 1960s, of which Bruno Bettelheim's work was but one well-known ...
More
This chapter focuses on parents emerging from the experience of wide-ranging psychogenic theorizing about autism during the 1950s and 1960s, of which Bruno Bettelheim's work was but one well-known example. Parents' accounts of their work during a period when the diagnostic category of autism was in flux highlight their unique authority as caregivers and “amateur” therapists. These accounts of parents' treatment activities make clear that expert knowledge and private life have continually intersected in the families of autistic children. The chapter examines how love, through parental efforts to help their children by training themselves in treatment practices, has functioned as a form of practice or technique in interventions to address the syndrome of autism. In both the case of the Orthogenic School's milieu therapy and parental work in behavior modification techniques, the affective involvement of “semiprofessionals” was key to what was experienced as the success of the interventions.Less
This chapter focuses on parents emerging from the experience of wide-ranging psychogenic theorizing about autism during the 1950s and 1960s, of which Bruno Bettelheim's work was but one well-known example. Parents' accounts of their work during a period when the diagnostic category of autism was in flux highlight their unique authority as caregivers and “amateur” therapists. These accounts of parents' treatment activities make clear that expert knowledge and private life have continually intersected in the families of autistic children. The chapter examines how love, through parental efforts to help their children by training themselves in treatment practices, has functioned as a form of practice or technique in interventions to address the syndrome of autism. In both the case of the Orthogenic School's milieu therapy and parental work in behavior modification techniques, the affective involvement of “semiprofessionals” was key to what was experienced as the success of the interventions.
Harriet P. Lefley
- Published in print:
- 2009
- Published Online:
- September 2009
- ISBN:
- 9780195340495
- eISBN:
- 9780199863792
- Item type:
- chapter
- Publisher:
- Oxford University Press
- DOI:
- 10.1093/acprof:oso/9780195340495.003.0007
- Subject:
- Social Work, Health and Mental Health, Children and Families
This chapter presents FPE models and research findings for various conditions, beginning with mental illness and substance abuse. Mueser and Fox's Family Intervention for Dual Disorders (FIDD) ...
More
This chapter presents FPE models and research findings for various conditions, beginning with mental illness and substance abuse. Mueser and Fox's Family Intervention for Dual Disorders (FIDD) includes both single and multi-family formats. Programs for obsessive-compulsive disorder, borderline personality disorder, easting disorders, and brain and spinal cord injury are presented. Family psychoeducation (FPE) for specialized groups or different family members include families of veterans, spouses, young parents with mental illness and their children, and elderly caregivers. Research findings on the concerns of older parents, and the role of siblings in subsequent caregiving, are presented and discussed.Less
This chapter presents FPE models and research findings for various conditions, beginning with mental illness and substance abuse. Mueser and Fox's Family Intervention for Dual Disorders (FIDD) includes both single and multi-family formats. Programs for obsessive-compulsive disorder, borderline personality disorder, easting disorders, and brain and spinal cord injury are presented. Family psychoeducation (FPE) for specialized groups or different family members include families of veterans, spouses, young parents with mental illness and their children, and elderly caregivers. Research findings on the concerns of older parents, and the role of siblings in subsequent caregiving, are presented and discussed.
Barbara J. Burns, Sarah A. Mustillo, Elizabeth M.Z. Farmer, David J. Kolko, Julie McCrae, Anne M. Libby, and Mary Bruce Webb
- Published in print:
- 2009
- Published Online:
- February 2010
- ISBN:
- 9780195398465
- eISBN:
- 9780199863426
- Item type:
- chapter
- Publisher:
- Oxford University Press
- DOI:
- 10.1093/acprof:oso/9780195398465.003.0012
- Subject:
- Social Work, Children and Families, Health and Mental Health
This chapter analyzes the mental health care needs and service use for caregivers involved with the child welfare system, who experience symptoms of depression warranting a psychiatric diagnosis. ...
More
This chapter analyzes the mental health care needs and service use for caregivers involved with the child welfare system, who experience symptoms of depression warranting a psychiatric diagnosis. Noteworthy findings include the high rate of caregiver depression, a 40% rate that greatly exceeds both the rate of depression in the general population and the rate for female welfare recipients; and the large gap between need for mental health care and reported use of such care for serious depression. An unusual feature of the chapter is the highly innovative use of NSCAW longitudinal data to group depressed caregivers into the categories early recovery, recovered and relapsed, and delayed recovery, in order that these caregivers' use of mental health services may be compared. It also reports a number of sobering consequences of caregivers' depressive illnesses for children and the role that mental health services may play in affecting those consequences. The chapter provides a model discussion of clinical and practice implications emerging from these empirical findings.Less
This chapter analyzes the mental health care needs and service use for caregivers involved with the child welfare system, who experience symptoms of depression warranting a psychiatric diagnosis. Noteworthy findings include the high rate of caregiver depression, a 40% rate that greatly exceeds both the rate of depression in the general population and the rate for female welfare recipients; and the large gap between need for mental health care and reported use of such care for serious depression. An unusual feature of the chapter is the highly innovative use of NSCAW longitudinal data to group depressed caregivers into the categories early recovery, recovered and relapsed, and delayed recovery, in order that these caregivers' use of mental health services may be compared. It also reports a number of sobering consequences of caregivers' depressive illnesses for children and the role that mental health services may play in affecting those consequences. The chapter provides a model discussion of clinical and practice implications emerging from these empirical findings.
Philip Mccallion
- Published in print:
- 2006
- Published Online:
- April 2010
- ISBN:
- 9780195173727
- eISBN:
- 9780199893218
- Item type:
- chapter
- Publisher:
- Oxford University Press
- DOI:
- 10.1093/acprof:oso/9780195173727.003.0030
- Subject:
- Social Work, Health and Mental Health
The success that the aging of persons with developmental disabilities (DD) represents also means challenges for families who must provide longer term and new forms of care. In addition, traditional ...
More
The success that the aging of persons with developmental disabilities (DD) represents also means challenges for families who must provide longer term and new forms of care. In addition, traditional views of family caregivers, particularly older parents as caregivers, must be expanded to include other relatives, such as siblings and grandparents. The aging of persons with DD and their caregivers requires all social workers to renew perspectives, tools, and approaches. The increasing complexity of life history and experiences, health needs, and life transitions also require that a holistic and multidisciplinary perspective be embraced. Drawing on the related research and practice literatures, this chapter outlines key demographic issues for adults with DD and their families, and describes changing family caregiving constellations. Suggestions are offered for the assessment and management of life transitions, and of grief and bereavement issues that are increasingly a feature of the older years of both caregivers and persons with DD.Less
The success that the aging of persons with developmental disabilities (DD) represents also means challenges for families who must provide longer term and new forms of care. In addition, traditional views of family caregivers, particularly older parents as caregivers, must be expanded to include other relatives, such as siblings and grandparents. The aging of persons with DD and their caregivers requires all social workers to renew perspectives, tools, and approaches. The increasing complexity of life history and experiences, health needs, and life transitions also require that a holistic and multidisciplinary perspective be embraced. Drawing on the related research and practice literatures, this chapter outlines key demographic issues for adults with DD and their families, and describes changing family caregiving constellations. Suggestions are offered for the assessment and management of life transitions, and of grief and bereavement issues that are increasingly a feature of the older years of both caregivers and persons with DD.
Kelli I. Stajduhar
- Published in print:
- 2011
- Published Online:
- January 2012
- ISBN:
- 9780199599295
- eISBN:
- 9780191731532
- Item type:
- chapter
- Publisher:
- Oxford University Press
- DOI:
- 10.1093/acprof:oso/9780199599295.003.0059
- Subject:
- Palliative Care, Patient Care and End-of-Life Decision Making
The rising number of people facing old age makes it likely that serious chronic and life-limiting illness will be a dominant challenge for health care delivery in the next half-century. Family carers ...
More
The rising number of people facing old age makes it likely that serious chronic and life-limiting illness will be a dominant challenge for health care delivery in the next half-century. Family carers will continue to play a major role in the provision of support and care. This chapter briefly summarizes what is known about family carers to lay the foundation to engage in discussions of difference. Specifically, it discusses ‘social differences’ that receive relatively little attention in the literature in relation to family care work: cultural and religious difference, and social class difference. The chapter uses examples to illustrate how these differences can challenge that which we have learned about carers and will suggest supportive interventions that take into account such difference.Less
The rising number of people facing old age makes it likely that serious chronic and life-limiting illness will be a dominant challenge for health care delivery in the next half-century. Family carers will continue to play a major role in the provision of support and care. This chapter briefly summarizes what is known about family carers to lay the foundation to engage in discussions of difference. Specifically, it discusses ‘social differences’ that receive relatively little attention in the literature in relation to family care work: cultural and religious difference, and social class difference. The chapter uses examples to illustrate how these differences can challenge that which we have learned about carers and will suggest supportive interventions that take into account such difference.
Alexandra Lee Crampton and Nancy P. Kropf
- Published in print:
- 2010
- Published Online:
- January 2011
- ISBN:
- 9780195394641
- eISBN:
- 9780199863365
- Item type:
- chapter
- Publisher:
- Oxford University Press
- DOI:
- 10.1093/acprof:oso/9780195394641.003.0012
- Subject:
- Social Work, Communities and Organizations
This chapter focuses on an important shared concern in gerontological social work and restorative justice: helping older adults who become frail, dependent, and vulnerable. It explores the benefits ...
More
This chapter focuses on an important shared concern in gerontological social work and restorative justice: helping older adults who become frail, dependent, and vulnerable. It explores the benefits and limitations of social work and restorative practice approaches when working with older adults. It explores a basic contrast between the two disciplines in that gerontological social work focuses on the care of individual older adults, while restorative justice focuses on harm caused to individuals, families, and the community. Social work outcomes focus on preserving or enhancing the older adult's autonomy and dignity, while restorative outcomes focus on healing injury and repairing relationships.Less
This chapter focuses on an important shared concern in gerontological social work and restorative justice: helping older adults who become frail, dependent, and vulnerable. It explores the benefits and limitations of social work and restorative practice approaches when working with older adults. It explores a basic contrast between the two disciplines in that gerontological social work focuses on the care of individual older adults, while restorative justice focuses on harm caused to individuals, families, and the community. Social work outcomes focus on preserving or enhancing the older adult's autonomy and dignity, while restorative outcomes focus on healing injury and repairing relationships.
Raymond H. Starr, Howard Dubowitz, Donna Harrington, and Susan Feigelman
- Published in print:
- 1999
- Published Online:
- January 2009
- ISBN:
- 9780195109405
- eISBN:
- 9780199865789
- Item type:
- chapter
- Publisher:
- Oxford University Press
- DOI:
- 10.1093/acprof:oso/9780195109405.003.0012
- Subject:
- Social Work, Children and Families
This chapter examines the nature of cross-informant reports of behavior programs of teens in kinship care. Specifically, it looks at the behavior problem rating differences between kinship care ...
More
This chapter examines the nature of cross-informant reports of behavior programs of teens in kinship care. Specifically, it looks at the behavior problem rating differences between kinship care providers and the youths who are in their care. Cross informants differ in their evaluation of externalizing problems. Caregivers of boys and boys themselves tend to report higher levels of problem behavior than caregivers of girls or girls themselves. The most significant finding is that more than a quarter of caregivers characterized the teenager in their care as having an Externalizing problem, while only nine percent of the youth reported a problem.Less
This chapter examines the nature of cross-informant reports of behavior programs of teens in kinship care. Specifically, it looks at the behavior problem rating differences between kinship care providers and the youths who are in their care. Cross informants differ in their evaluation of externalizing problems. Caregivers of boys and boys themselves tend to report higher levels of problem behavior than caregivers of girls or girls themselves. The most significant finding is that more than a quarter of caregivers characterized the teenager in their care as having an Externalizing problem, while only nine percent of the youth reported a problem.
Susan J. Zuravin, Mary Benedict, and Rebecca Stallings
- Published in print:
- 1999
- Published Online:
- January 2009
- ISBN:
- 9780195109405
- eISBN:
- 9780199865789
- Item type:
- chapter
- Publisher:
- Oxford University Press
- DOI:
- 10.1093/acprof:oso/9780195109405.003.0013
- Subject:
- Social Work, Children and Families
This chapter reviews findings from research that focused on describing and comparing the young adult functioning of former foster care children and a matched group of adults who had not spent time in ...
More
This chapter reviews findings from research that focused on describing and comparing the young adult functioning of former foster care children and a matched group of adults who had not spent time in foster care; and determining whether the functioning of former kinship foster children differs from that of their nonrelative care counterparts. The methodologies used by these studies are assessed in order to provide direction for future research. The main findings are that, in general, former foster children appear to be less self-sufficient than their nonfoster care counterparts; and that former kin foster care children appear to be more self-sufficient than their nonrelative foster care counterparts.Less
This chapter reviews findings from research that focused on describing and comparing the young adult functioning of former foster care children and a matched group of adults who had not spent time in foster care; and determining whether the functioning of former kinship foster children differs from that of their nonrelative care counterparts. The methodologies used by these studies are assessed in order to provide direction for future research. The main findings are that, in general, former foster children appear to be less self-sufficient than their nonfoster care counterparts; and that former kin foster care children appear to be more self-sufficient than their nonrelative foster care counterparts.
Sharon B. Berlin
- Published in print:
- 2002
- Published Online:
- January 2009
- ISBN:
- 9780195110371
- eISBN:
- 9780199865680
- Item type:
- chapter
- Publisher:
- Oxford University Press
- DOI:
- 10.1093/acprof:oso/9780195110371.003.0005
- Subject:
- Social Work, Health and Mental Health
In this chapter, the focus shifts from explaining the role of the memory system in creating meaning and meaning change to explaining the contributions of the physical and social environments to ...
More
In this chapter, the focus shifts from explaining the role of the memory system in creating meaning and meaning change to explaining the contributions of the physical and social environments to personal meanings. It considers the role of culture, social structures and institutions, and family life in shaping memories of the self, others, and the larger world. Current information from environmental sources may variously signal that things are just as they always have been or that things are now different from what one had thought or felt. The chapter also explores how chronic threats and deprivations narrow attention and interfere with optimal learning and problem solving. In addition, it considers the influence of early child-caregiver interactions on self-schema development and how lingering effects of problematic interactions might be buffered as a function of subsequent different experiences. Throughout the chapter, steps that practitioners might take to create and highlight environmental discrepancies (opportunities) are highlighted.Less
In this chapter, the focus shifts from explaining the role of the memory system in creating meaning and meaning change to explaining the contributions of the physical and social environments to personal meanings. It considers the role of culture, social structures and institutions, and family life in shaping memories of the self, others, and the larger world. Current information from environmental sources may variously signal that things are just as they always have been or that things are now different from what one had thought or felt. The chapter also explores how chronic threats and deprivations narrow attention and interfere with optimal learning and problem solving. In addition, it considers the influence of early child-caregiver interactions on self-schema development and how lingering effects of problematic interactions might be buffered as a function of subsequent different experiences. Throughout the chapter, steps that practitioners might take to create and highlight environmental discrepancies (opportunities) are highlighted.
Joseph Walsh
- Published in print:
- 2003
- Published Online:
- January 2009
- ISBN:
- 9780195149524
- eISBN:
- 9780199865154
- Item type:
- chapter
- Publisher:
- Oxford University Press
- DOI:
- 10.1093/acprof:oso/9780195149524.003.0010
- Subject:
- Social Work, Health and Mental Health, Children and Families
This chapter discusses multiple family psychoeducational group interventions and their rationale for use with the family members of persons who have schizophrenia. Psychoeducation offered in multiple ...
More
This chapter discusses multiple family psychoeducational group interventions and their rationale for use with the family members of persons who have schizophrenia. Psychoeducation offered in multiple family groups (MFGs) for schizophrenia can be helpful in decreasing stress to family caregivers of people with severe mental illness and preventing relapse and hospitalization. Common group topics include theories of schizophrenia, its course, the positive and adverse effects of medications, the relationship between stress and symptoms, available resources for persons with schizophrenia and their families, the nature of professional interventions, managing family emotional responses to the illness, and mobilizing strengths for improved family functioning. The group process, as exemplified through a case study, is intended to help families experience less burden and stress, reduce their sense of stigma, help them assist each other with parenting, and normalize their communications.Less
This chapter discusses multiple family psychoeducational group interventions and their rationale for use with the family members of persons who have schizophrenia. Psychoeducation offered in multiple family groups (MFGs) for schizophrenia can be helpful in decreasing stress to family caregivers of people with severe mental illness and preventing relapse and hospitalization. Common group topics include theories of schizophrenia, its course, the positive and adverse effects of medications, the relationship between stress and symptoms, available resources for persons with schizophrenia and their families, the nature of professional interventions, managing family emotional responses to the illness, and mobilizing strengths for improved family functioning. The group process, as exemplified through a case study, is intended to help families experience less burden and stress, reduce their sense of stigma, help them assist each other with parenting, and normalize their communications.
Nancy Berlinger, Bruce Jennings, and Susan M. Wolf
- Published in print:
- 2013
- Published Online:
- September 2013
- ISBN:
- 9780199974566
- eISBN:
- 9780199333332
- Item type:
- chapter
- Publisher:
- Oxford University Press
- DOI:
- 10.1093/acprof:oso/9780199974566.003.0003
- Subject:
- Palliative Care, Patient Care and End-of-Life Decision Making
This section presents nine practical, skills-based ethics competencies to support the use of these Guidelines among professionals who care for patients facing decisions about life-sustaining ...
More
This section presents nine practical, skills-based ethics competencies to support the use of these Guidelines among professionals who care for patients facing decisions about life-sustaining treatment or nearing the end of life. These patients rely on many different professionals, so responsibility for good care should be shared among professions, specialties, and care settings.Less
This section presents nine practical, skills-based ethics competencies to support the use of these Guidelines among professionals who care for patients facing decisions about life-sustaining treatment or nearing the end of life. These patients rely on many different professionals, so responsibility for good care should be shared among professions, specialties, and care settings.
Eric V. Edmonds
- Published in print:
- 2010
- Published Online:
- September 2010
- ISBN:
- 9780199558582
- eISBN:
- 9780191594397
- Item type:
- chapter
- Publisher:
- Oxford University Press
- DOI:
- 10.1093/acprof:oso/9780199558582.003.0004
- Subject:
- Public Health and Epidemiology, Public Health
Public health is important in the child labour discussion for more reasons than just the consequences of child labour. The morbidity and mortality of caregivers and earners may be central in ...
More
Public health is important in the child labour discussion for more reasons than just the consequences of child labour. The morbidity and mortality of caregivers and earners may be central in understanding how children end up in dangerous or exploitive conditions. This chapter outlines how public health issues enter into the economics of child labour. It examines both how public health influences child labour and how child labour influences child health. It begins by reviewing the state of economic research on why children work.Less
Public health is important in the child labour discussion for more reasons than just the consequences of child labour. The morbidity and mortality of caregivers and earners may be central in understanding how children end up in dangerous or exploitive conditions. This chapter outlines how public health issues enter into the economics of child labour. It examines both how public health influences child labour and how child labour influences child health. It begins by reviewing the state of economic research on why children work.
Christina M. Puchalski
- Published in print:
- 2006
- Published Online:
- November 2011
- ISBN:
- 9780195146820
- eISBN:
- 9780199999866
- Item type:
- chapter
- Publisher:
- Oxford University Press
- DOI:
- 10.1093/acprof:oso/9780195146820.003.0010
- Subject:
- Palliative Care, Patient Care and End-of-Life Decision Making, Palliative Medicine and Older People
This chapter provides an overview of Protestant approaches to end-of-life care. It presents stories of the dying and their caregivers which show how different people approach the impending dying ...
More
This chapter provides an overview of Protestant approaches to end-of-life care. It presents stories of the dying and their caregivers which show how different people approach the impending dying process and issues that attend death. The chapter describes the Protestant practice in attending to the dying and planning for pre-death and post-death, and also presents the text of prayers for a person near death, litany at the time of death, and a commendation at the time of death.Less
This chapter provides an overview of Protestant approaches to end-of-life care. It presents stories of the dying and their caregivers which show how different people approach the impending dying process and issues that attend death. The chapter describes the Protestant practice in attending to the dying and planning for pre-death and post-death, and also presents the text of prayers for a person near death, litany at the time of death, and a commendation at the time of death.
Christina M. Puchalski
- Published in print:
- 2006
- Published Online:
- November 2011
- ISBN:
- 9780195146820
- eISBN:
- 9780199999866
- Item type:
- chapter
- Publisher:
- Oxford University Press
- DOI:
- 10.1093/acprof:oso/9780195146820.003.0002
- Subject:
- Palliative Care, Patient Care and End-of-Life Decision Making, Palliative Medicine and Older People
This chapter examines the ethical aspects of spirituality in palliative care. It provides a roadmap for describing key spiritual interests in healthcare, the source of those interests, and the way ...
More
This chapter examines the ethical aspects of spirituality in palliative care. It provides a roadmap for describing key spiritual interests in healthcare, the source of those interests, and the way they find concrete expressions in the lives of patients, their caregivers, and families. The chapter also identifies and clarifies the moral warrants or the scope and grounds of the ethical obligation to address spirituality in the palliative care setting.Less
This chapter examines the ethical aspects of spirituality in palliative care. It provides a roadmap for describing key spiritual interests in healthcare, the source of those interests, and the way they find concrete expressions in the lives of patients, their caregivers, and families. The chapter also identifies and clarifies the moral warrants or the scope and grounds of the ethical obligation to address spirituality in the palliative care setting.
