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The first book to provide a comprehensive look at what it's like to have dementia and the subjective experience of living with progressive memory loss. Few families are untouched by Alzheimer's disease or a related dementia. Moving accounts of what it is like to care for someone with this disease have already been published, as well as how-to books that offer caregivers advice and information on coping. But this book is the first to provide a comprehensive report of what it is like to have dementia oneself—the subjective experience of living with progressive memory loss. Each chapter discusses a different aspect of having dementia, from the initial assessment and diagnosis through placemen...
This volume seeks to instigate a discussion about dementia in theatre. The discussions in this book borrow from the literature on dementia’s representation in other artforms, while reflecting on theatre’s unique capacity to incorporate multiple artforms in a live context (hypermediacy). The author examines constructions of diegesis and the use of various performance tools, including physical theatre, puppetry, and postdramatic performance. She discusses stage representations of interior experiences of dementia; selfhood in dementia; the demarcation of those with dementia from those without; endings, erasure, and the pursuit of catharsis; placelessness and disruptions of traditional dramatic constructions of time; and ultimately, performances creatively led by people with dementia. The book traces patterns of narrativisation on the stage—including common dramaturgical forms, settings, and character relationships—as well as examples that transcend mainstream representation. This book is important reading for theatre and performance students, scholars, and practitioners, as well as cultural studies writers engaged in research about narratives of dementia.
The book is divided into two major parts, the first on husbands and the second on sons, with Chapter 1 providing background for both parts. Chapter 1 gives a brief description of previous research on husbands and sons as caregivers. It also describes the method used to gather information for this study from the 60 men interviewed and outlines the four research questions that guided the study: (1) What is it like for a man to take on a major caregiving role? (2) How does he adapt to and cope with his new functions? (3) What are his motivations for taking on this role? And (4) What, if any, meaning does he derive from this caregiving experience? First published in 1997. Routledge is an imprint of Taylor & Francis, an informa company.
Your Name Is Hughes Hannibal Shanks is Lela Knox Shanks’s personal account of caring for her husband, Hughes, in their home after he was stricken with Alzheimer’s disease. Lela describes her initial denial, her discovery of coping skills, her eventual acceptance of his illness, and her ultimate recognition that the key to successful caregiving lies in never losing sight of the patient’s humanness. The book outlines twenty coping and survival strategies to guide caregivers to untapped inner resources and shows caregiving’s intangible rewards of increased self-respect and self-knowledge.
Suitable for students and practitioners, this title introduces social work students to a range of clients and offers an overview of many social work services in the health arena. It also includes 29 casebook chapters.
As the most comprehensive text of its kind, Social Work in Health Settings introduces social work students to a range of clients and provides an overview of many social work settings and services in the health arena. If you're a practitioner, you'll find the book useful for examining and evaluating your practice. This second edition features 18 new chapters and chapter subjects and rewritten and updated versions of the 14 chapters which were part of the first edition.
Drawing on a selection of carefully curated autobiographical and fictional portrayals of the dementia experience, this book gives voice to some of the most pressing ethical issues that commonly arise in the context of a dementing disorder, and calls attention to various forms of narrative resistance in contemporary American literature on early-onset Alzheimer’s disease (AD). Based on the premise that the current public discourse on AD is largely dominated by an anxiety and fear-promoting conception of the illness, this multilayered inquiry strives to look beyond the widespread horrors of forgetting and loss in AD, and, in doing so, attempts to give a better, more accurate, and more balanced impression of what it means to be living with such a diagnosis.
What happens when older men become widowers? Popular books, movies, and television present widowers as lost and unable to cope or care for themselves. These stereotypes do not encapsulate the experiences of real widowers, how their daily lives change, and what being a widower means to individuals in both sociological and practical ways. By Himself is based on in-depth interviews with twenty-six widowers over the age of sixty living in the United States and Canada. Using these interviews, Deborah K. van den Hoonaard explores masculine identity and traces the stories that widowers tell about their wives' illnesses and deaths. She also focuses on the widowers' changed relationships with their children and friends, as well as with women, and details the men's encounters with tasks such as housework and cooking. An eminently readable and accessible book, By Himself sheds new light on the social meaning of being a widower.
Have Japan's relative economic decline and China's rapid ascent altered the dynamics of Asian regionalism? Peter Katzenstein and Takashi Shiraishi, the editors of Network Power, one of the most comprehensive volumes on East Asian regionalism in the 1990s, present here an impressive new collection that brings the reader up to date. This book argues that East Asia's regional dynamics are no longer the result of a simple extension of any one national model. While Japanese institutional structures and political practices remain critically important, the new East Asia now under construction is more than, and different from, the sum of its various national parts. At the outset of a new century, the interplay of Japanese factors with Chinese, American, and other national influences is producing a distinctively new East Asian region.
Dementia presents a significant social issue in a hyper-cognitive culture where stigma, relational neglect, and isolation still accompany forgetfulness. This raises serious theological, ecclesiological, and pastoral questions calling for a Christian response. To fight against a malignant social positioning of anyone as an "an empty shell" is crucial; nonetheless, there is another pressing reality, the reality of ongoing loss. Often the focus is on one or the other side: affirming personhood or acknowledging loss and grief. Spiritual caregiving and Christian pastoral caregiving are uniquely placed to offer both sustaining relationship and grief support to both caregivers and persons with deme...