Families Caring for an Aging America
Families Caring for an Aging America

Author: National Academies of Sciences, Engineering, and Medicine

Publisher: National Academies Press

Published: 2016-12-08

Total Pages: 367

ISBN-13: 0309448069

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Family caregiving affects millions of Americans every day, in all walks of life. At least 17.7 million individuals in the United States are caregivers of an older adult with a health or functional limitation. The nation's family caregivers provide the lion's share of long-term care for our older adult population. They are also central to older adults' access to and receipt of health care and community-based social services. Yet the need to recognize and support caregivers is among the least appreciated challenges facing the aging U.S. population. Families Caring for an Aging America examines the prevalence and nature of family caregiving of older adults and the available evidence on the effectiveness of programs, supports, and other interventions designed to support family caregivers. This report also assesses and recommends policies to address the needs of family caregivers and to minimize the barriers that they encounter in trying to meet the needs of older adults.

Patient Safety and Quality
Patient Safety and Quality

Author: Ronda Hughes

Publisher: Department of Health and Human Services

Published: 2008

Total Pages: 592

ISBN-13:

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"Nurses play a vital role in improving the safety and quality of patient car -- not only in the hospital or ambulatory treatment facility, but also of community-based care and the care performed by family members. Nurses need know what proven techniques and interventions they can use to enhance patient outcomes. To address this need, the Agency for Healthcare Research and Quality (AHRQ), with additional funding from the Robert Wood Johnson Foundation, has prepared this comprehensive, 1,400-page, handbook for nurses on patient safety and quality -- Patient Safety and Quality: An Evidence-Based Handbook for Nurses. (AHRQ Publication No. 08-0043)." - online AHRQ blurb, http://www.ahrq.gov/qual/nurseshdbk/

A Journal for Family Caregivers
A Journal for Family Caregivers

Author: Harriet Hodgson

Publisher: BQB Publishing

Published: 2016-03-15

Total Pages: 210

ISBN-13: 1608081516

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This is Book three in The Family Caregiver’s Series. The books in this series are designed to support you, the family caregiver, which in turn will help you be supportive to your loved one. While caregiving is love in action, it is also a demanding job. One that requires a lot of self-care to keep us going. This journal is a place for thoughts and feelings, but also a place to jot down ideas and plans to make the job easier.

Dying at Home
Dying at Home

Author: Andrea Sankar

Publisher: JHU Press

Published: 2024-02-20

Total Pages: 485

ISBN-13: 1421447738

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"This will be the third edition of this title, heavily updated from the 1999 second edition"--

Taking Care of Our Own
Taking Care of Our Own

Author: Sherry N. Mong

Publisher: Cornell University Press

Published: 2020-10-15

Total Pages: 217

ISBN-13: 1501751468

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Mixing personal history, interviewee voices, and academic theory from the fields of care work, the sociology of work, medical sociology, and nursing, Taking Care of Our Own introduces us to the hidden world of family caregivers. Using a multidimensional approach, Sherry N. Mong seeks to understand and analyze the types of skilled work that family caregivers do, the processes through which they learn and negotiate new skills, and the meanings that both caregivers and nurses attach to their care work. Taking Care of Our Own is based on sixty-two in-depth interviews with family caregivers, home and community health care nurses, and other expert observers to provide a lens through which in-home care processes are analyzed, while also exploring how caregivers learn necessary procedures. Further, Mong examines the emotional labor of caregiving, as well as the identities of caregivers and nurses who are key players in the labor process, and gives attention to the ways in which the labor is transferred from medical professionals to family caregivers.

Caregivers' Journal
Caregivers' Journal

Author: Erin Lee

Publisher: Createspace Independent Publishing Platform

Published: 2012-05-14

Total Pages: 54

ISBN-13: 9781477454244

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This journal is for family and friends of people suffering from long term, chronic illnesses. Caregivers of such patients often experience their own illnesses as a result of giving all of themselves to their loved ones. Stress, physical exhaustion, depression, changes in mental and physical health, and many more things are often side effects that come with caregiving. This journal will help caregivers with having a safe place to express their challenges, fears, and hopes. It offers prompts that will encourage a caregiver to think about caring for themselves in the same way that they are caring for the people or person they love.

Family Caregiving in Mental Illness
Family Caregiving in Mental Illness

Author: Harriet P. Lefley

Publisher: SAGE Publications, Incorporated

Published: 1996-01-19

Total Pages: 280

ISBN-13:

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With the trend of deinstitutionalization, family members are finding themselves increasingly in the position of primary caregivers to mentally ill adults - a role for which they are often untrained and unprepared. This volume explores the experiences of these caregivers. The author: discusses the characteristics and conceptual models related to mental illness; surveys the experience of mental illness in the context of the family life cycle and developmental stages of the illness; appraises the burdens on the family including social stigma, refusal of treatment, stress and the relationship between the mentally ill and caregivers within the family; and reviews family responses including coping strategies and professional and

Family Caregiving
Family Caregiving

Author: Whitney A. Bailey

Publisher: Springer

Published: 2017-10-28

Total Pages: 154

ISBN-13: 3319647830

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This comprehensive resource offers a detailed framework for fostering resilience in families caring for their older members. Its aim is to improve the quality of life for both the caregivers themselves as much as for those they support. Robust interventions are presented to guide family members through chronic and acute challenges in areas such as emotional health, physical comfort, financial aspects of care, dealing with health systems, and adjusting to transition. Examples, models, interviews, and an extended case study identify core concerns of caregiving families and avenues for nurturing positive adaptation. Throughout, contributors provide practical applications for therapists and other service providers in diverse disciplines, and for advancing family resilience as a field. Included in the coverage: Therapeutic interventions for caregiving families. Facilitating older adults’ resilience through meeting nutritional needs. Improving ergonomics for the safety, comfort, and health of caregivers. Hope as a coping resource for caregiver resilience and well-being. Perspectives on navigating care transitions with individuals with dementia. Planning for and managing costs related to caregiving. Family Caregiving offers a new depth of knowledge and real-world utility to social workers, mental health professionals and practitioners, educators and researchers in the field of family resilience, as well as scholars in the intersecting disciplines of family studies, human development, psychology, sociology, social work, education, law, and medicine.

Family Caregiving in the New Normal
Family Caregiving in the New Normal

Author: Joseph E. Gaugler

Publisher: Academic Press

Published: 2015-05-08

Total Pages: 404

ISBN-13: 012417129X

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Family Caregiving in the New Normal discusses how the drastic economic changes that have occurred over the past few years have precipitated a new conversation on how family care for older adults will evolve in the future. This text summarizes the challenges and potential solutions scientists, policy makers, and clinical providers must address as they grapple with these changes, with a primary focus given to the elements that may impact how family caregiving is organized and addressed in subsequent decades, including sociodemographic trends like divorce, increased participation of women in the workforce, geographic mobility, fewer children in post-baby boom families, chronic illness trends, economic stressors, and the current policy environment. A section on the support of caregivers includes technology-based solutions that examine existing models, personal health records, and mobile applications, big data issues, decision-making support, person-centered approaches, crowd-sourced caregiving such as blogs and personal websites that have galvanized caregivers, and new methods to combine paid and unpaid forms of care. - Provides a concise "roadmap" of the demographic, economic, health trends, and policy challenges facing family caregivers - Presents potential solutions to caregiving so that scientists, policymakers, and clinical providers can best meet the needs of families and communities in the upcoming decades - Includes in-depth, diverse stories of caregivers of persons with different diseases who share perspectives - Covers person-centered care approaches to family caregiving that summarize effective community-based services of psychosocial intervention models - Examines how existing efficacious models can more effectively reach and serve individual families

CANCER AND THE FAMILY CAREGIVER
CANCER AND THE FAMILY CAREGIVER

Author: Ora Gilbar

Publisher: Charles C Thomas Publisher

Published: 2002-01-01

Total Pages: 338

ISBN-13: 0398083673

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This book is the product of the authors’ research and clinical practice in the field of psycho-oncology, stress, and coping for a period of over twenty years. It fills a gap that exists in the discussion of caregiver distress felt by both cancer researchers and psycho-oncologists in the vital area of predicting, acknowledging, and alleviating the distress of caregivers of cancer patients, and it focuses on the caregivers of cancer patients in various phases of the illness. The discussion of cancer-patient caregivers is divided into three aspects: theoretical (Part 1), research (Part 2), and practical (Part 3) issues. The analysis of these areas can be useful to clinicians, researchers, medical/psychological social workers, and nurses by familiarizing them with the spectrum of stresses experienced by cancer patients and their caregivers, and the coping methods that have proven most effective. Part One presents theoretical background on the structure and progression of the caregiver role and how caregivers cope with the illness as explored in recent literature. Part Two presents empirical research on caregiver psychological distress carried out by the authors during 1993-1999. Part Three examines two important issues. The first is intervention for reducing caregiver distress, and the second issue is the ethical question of caregiver involvement in the patient’s medical decisions. The book is timely, as it is felt that the issue at hand will have mounting importance and relevance to our society as it experiences growing longevity and concomitant challenges in cancer caregiving.