An Insight Into Dementia Care in India


Book Description

With the rapidly increasing population of the elderly in the country, dementia is increasingly becoming a cause for major concern. Apart from the patient, the disease also has a significant impact on caregivers and the patient’s family. This book outlines the existing research studies on dementia and explores the caregiving scenario in the country. Among other issues, the book explores the following areas: - Epidemiology, common types and causes of dementia - Caregiver activities and daily chores - Person-centred care and support - Assessment and management of dementia patients - Psychosocial interventions in the Indian context - Resources and services available in India Based on original research, this book will help bridge the gap between the dementia-related literature of the West and care-giving practices in India. This book will serve as a reference book for students and research scholars studying Psychology, Psychiatric Nursing, Social Work, and Rehabilitation. Professionals like Psychiatrists, Psychologists, Social Workers, Nurses, and paramedics and caregivers working with the elderly will also find the book to be valuable.







Dementia Care: International Perspectives


Book Description

Dementia is a challenge facing health and social care around the world. Due to factors such as growing elderly populations, improved recognition, and diagnosis, the number of people with the illness is set to double over the next two decades. As a result, improving the quality of life for dementia patients and carers is an international priority. Dementia Care: International Perspectives is a comprehensive resource offering a global view of the clinical management and resources offered to carers and patients. Featuring 47 country profiles across 5 continents, this resource offers invaluable insights into dementia care across borders and different cultures. Each country profile features a helpful summary of key points, and contains an up-to-date, concise discussion on the clinical management of dementia within the country. This unique compendium has been written in collaboration with the International Dementia Alliance (IDEAL) to develop understandings of clinical practice and services available around the world, hoping to unify ideas and ultimately improve quality of care. Written and edited by the world's leading experts, Dementia Care: International Perspectives is a useful tool for researchers, clinicians, policy makers, academics, and international commentators wishing to expand their knowledge of the subject.




Unforgotten


Book Description

As life expectancy increases in India, the number of people living with dementia will also rise. Yet little is known about how people in India cope with dementia, how relationships and identities change through illness and loss. In addressing this question, this book offers a rich ethnographic account of how middle-class families in urban India care for their relatives with dementia. From the husband who wakes up at 3 am to feed his wife ice-cream to the daughters who gave up employment for seven years to care for their mother with dementia, this book illuminates the local idioms on dementia and aging, the personal experience of care-giving, the functioning of stigma in daily life, and the social and cultural barriers in accessing support.










Insights into the Caregiver Perspective: Involvement, Well-being, and Interventions


Book Description

The range, duration, and intensity of informal caregiving across different illnesses and disabilities have increased in the 21st century due to an increase in longevity and de-institutionalization in most countries. Caregiving is demanding and hence can be stressful in terms of time, effort, and financial requirements, depending on the nature of the illness or disability, the relationships between the person in need of support and the caregiver, and the role played by available health and social care services. However, research evidence has demonstrated that it can be also rewarding, and enables a different type of bonding than was the case before caregiving became a necessity.




Global status report on the public health response to dementia


Book Description

Dementia is a leading cause of disability and dependency globally. It is a syndrome, usually of a chronic or progressive nature, that leads to deterioration in cognitive function (i.e. ability to process thought) beyond what would be expected from normal ageing. Dementia can be overwhelming not only for the person who has it, but also for carers, families and society as a whole. Globally, a lack of awareness and understanding of dementia continues to lead to widespread stigmatization and discrimination, which may prevent people from accessing diagnosis and care. The World Health Organization (WHO) has long recognized the importance of addressing dementia and the need for increased investments in health and social care systems. The First Ministerial Conference on Global Action Against Dementia was held in March 2015, convening health ministers and delegations from 89 countries around the world to discuss comprehensive actions to address dementia. Two years later, WHO Member States unanimously approved the Global action plan on the public health response to dementia 2017–2025. Further, WHO’s Global Dementia Observatory (GDO) was established to monitor global progress on key targets and indicators within these action areas.




Dementia Care


Book Description

This book discusses the contemporary medico-social, psychological, legal, and therapeutic concerns related to people affected by dementia as a patient or as a caregiver. It provides global emerging responses to dementia. It highlights different dimensions of dementia in terms of issues, concerns, policies, and strategies all around the globe. The contributing authors present issues from cross-cultural education visible in dementia studies and discuss the power of music, art therapy, artistic collaborations, and many innovative practices in dealing with dementia. Written by international specialists from various disciplines, the chapters include challenges and emerging issues related to the role of family caregivers, the concern with vulnerability to elder abuse and neglect, and the role of technology in dementia care. The book provides a diverse perspective to dementia care not covered in such a broad way by any other books on the topic. This book is intended for academics from a wide range of fields such as sociology, geriatrics, community medicine, public health, clinical psychology, social work all of which, collectively, bear on the problem and the solutions for better dementia care.




Reducing the Impact of Dementia in America


Book Description

As the largest generation in U.S. history - the population born in the two decades immediately following World War II - enters the age of risk for cognitive impairment, growing numbers of people will experience dementia (including Alzheimer's disease and related dementias). By one estimate, nearly 14 million people in the United States will be living with dementia by 2060. Like other hardships, the experience of living with dementia can bring unexpected moments of intimacy, growth, and compassion, but these diseases also affect people's capacity to work and carry out other activities and alter their relationships with loved ones, friends, and coworkers. Those who live with and care for individuals experiencing these diseases face challenges that include physical and emotional stress, difficult changes and losses in their relationships with life partners, loss of income, and interrupted connections to other activities and friends. From a societal perspective, these diseases place substantial demands on communities and on the institutions and government entities that support people living with dementia and their families, including the health care system, the providers of direct care, and others. Nevertheless, research in the social and behavioral sciences points to possibilities for preventing or slowing the development of dementia and for substantially reducing its social and economic impacts. At the request of the National Institute on Aging of the U.S. Department of Health and Human Services, Reducing the Impact of Dementia in America assesses the contributions of research in the social and behavioral sciences and identifies a research agenda for the coming decade. This report offers a blueprint for the next decade of behavioral and social science research to reduce the negative impact of dementia for America's diverse population. Reducing the Impact of Dementia in America calls for research that addresses the causes and solutions for disparities in both developing dementia and receiving adequate treatment and support. It calls for research that sets goals meaningful not just for scientists but for people living with dementia and those who support them as well. By 2030, an estimated 8.5 million Americans will have Alzheimer's disease and many more will have other forms of dementia. Through identifying priorities social and behavioral science research and recommending ways in which they can be pursued in a coordinated fashion, Reducing the Impact of Dementia in America will help produce research that improves the lives of all those affected by dementia.