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Men as Caregivers
Despite the proliferation of books and articles on caregiving over the past three decades, the vast majority of research has centered on the experience of the female caregiver. This focus on women is neither unwarranted nor surprising given that women generally predominate in caregiving roles. Nonetheless, recent studies estimate that between 14 and 18 percent of men ranging in ages from nineteen to later middle age are providing care to a family member or friend with a serious illness or disability. And in men 75 or older, there are more husbands caring for wives than vice versa. Also among persons caring for AIDS sufferers in central cities, over 50 percent are men. In light of these subst...
Supporting the Caregiver in Dementia
Dementia is one of the greatest challenges facing seniors and their caregivers around the globe. Developed by experts in both research and practice, this guide for mental health clinicians explores the experience of caregiving in dementia, discussing the latest research developments and sharing clinical pearls of wisdom that can easily be translated to daily practice. The contributors explore the history of caregiving and then examine the current demographics of caregivers for persons with dementia. They discuss who provides care, the settings in which it is delivered, and the rewards and burdens of caregiving. They place special emphasis on understanding the psychological needs of both the ...
Care and Culture
Informal care provided by family members is central to current health and social care policy. Caregiving can be seen as a point where macro- and micro-level processes meet: it simultaneously concerns the organization of welfare states and the everyday lives of the millions of people giving and receiving informal care. This makes it important to understand how the carer role is conceptualized and performed by those occupying it. Care and Culture contributes to the sociology of caregiving by giving voice to mental health carers from a great variety of backgrounds and by placing personal experiences centre stage in its analysis. It addresses a number of questions: How do cultural notions of kin...
Helping Yourself Help Others
The chances are good that every one of us will become a caregiver at some point in our lives. We come to this challenge in the most personal way possible—we want to help someone we love, but we don't know how, and we're afraid of losing ourselves in this daunting task. If you have picked up this book, you are probably a caring person. You may prove that every day by helping someone who is elderly or developmentally disabled or who suffers from a physical or mental illness. It helps to know that Rosalynn Carter, former First Lady and a director of the Rosalynn Carter Institute for Human Development, which is committed to studying caregiving issues, knows firsthand the challenges of this lab...
Caregiving in the Illness Context
How does caregiving affect health and well-being and what resources help caregivers? This book provides a synthesis of psychological research on caregiver stress and brings attention to the personal, social and structural factors that affect caregivers' well-being and as well as recent behavioral interventions to enhance health.
Dementia Caregivers Share Their Stories
Replete with the powerful words of experienced caregivers, Dementia Caregivers Share Their Stories is an essential guidebook for anyone who must attend to the needs of a loved one suffering from Alzheimer's disease or another form of dementia. In these pages, members of caregivers' support groups - representing twenty-six families and a variety of professions and income levels - speak candidly about the challenges they have faced at every step in the caregiving process, from recognizing early symptoms of dementia to dealing with its advanced stages. Highlighting the ingenuity and resourcefulness of caregivers, the book brims with inspirational stories, practical advice, and creative approach...
The Reluctant Caregivers
Although Hendershott has spent many years teaching and writing about the sociological aspects of aging, she writes that none of this could have prepared me for the overwhelming challenge of caring for my own mother-in-law in my home. She introduces baby boomers as the unexpected caregivers of the coming decades. The process of family denial about symptoms, work-family conflict, and the unique problems of children of caregivers are explored in an effort to find solutions to the caregiving challenge. Social science research is made accessible and is coupled with anecdotal information gleaned from interactions with other caregivers and personal experience. Throughout the book, Hendershott shows family caregivers that by gaining insight into their motivations for caregiving and by drawing from family support and help from the community, they can move beyond maladaptive caregiving coping styles, to a rewarding reality-based caregiving experience.
Caring for the Family Caregiver
Caring for the Family Caregiver examines the high cost and poorly addressed exigencies of the family caregiver in chronic illness, including health literacy, palliative care, and health outcomes, through the prism of communication. This book uses an interdisciplinary approach to identify the impact of communication and its burdens on the caregiver and presents four caregiver profiles: the Manager, Carrier, Partner, and Lone caregiver, each emerging from a family system with different patterns of conversational sharing and expectations of conformity. By synthesizing current data assessing the experiences of caregivers, as well as integrating the narrative experiences of a range of caregivers ...
The Mental Health Effects of Informal Caregiving: Emerging Research and Opportunities
Because progressive advancements to healthcare practices are leading to longer lifespans, an increased number of aging individuals now require constant care from practiced caregivers. The financial costs of in-home care can be quite high; therefore, many families are opting to stand in as caregivers, and this can lead to various impacts on their own social and psychological wellbeing. The Mental Health Effects of Informal Caregiving: Emerging Research and Opportunities provides autobiographical accounts and statistical data associated with the caregiving experience, as well as the methods to discern the positive psychological forces that shape the subjective wellbeing of informal caregivers. Highlighting topics such as institutional vs. informal caregiving, special healthcare needs, and veteran care, this book is ideally designed for psychologists, therapists, researchers, medical institutions, academia, and students seeking current research on the subjective wellbeing of informal caregivers.
