Dementia Caregiver Guide


Book Description

This simple, easy to read, 100 page guidebook helps family members, friends, and caregivers to better understand the changes that come with advancing dementia or other impairments in thinking, reasoning or processing information. It also reinforces the impact of Teepa Snow's guidance and person-centered care interventions including the GEMS and Positive Approach to Care techniques. The goal is to provide better support and care practices when someone is living with an ever-changing condition. By appreciating what has changed but leveraging what is still possible, care partners can choose interactions that are more positive, communication that is more productive, and care that is more effective and less challenging for all involved.




Supporting the Caregiver in Dementia


Book Description

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 person with dementia and the caregiver, as well as interpersonal bonds, spiritual dimensions, and reactions to grief and loss. Using a multidisciplinary approach to treatment for caregivers, this book addresses the role of pharmacotherapy, individual and family interventions, and social supports. Finally, the authors reflect on societal issues such as health care policies, ethnic elders, and ethics. This volume offers health professionals insights into the daily lives of caregivers, along with tools to provide their patients with the support they need.




Families Caring for an Aging America


Book Description

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.




Dementia & Alzheimers Caregiver Journal: A Journal for Those Taking Care of a Loved One with Memory Loss


Book Description

In home caregivers need daily reflection and encouragement. Especially if it is their own loved one they are caring for. This 35 day journal helps caregivers get in touch with their emotions, needs, discouragements and the reason why they sacrifice so much to take care of the ones they love. Each day is a different thought provoking prompt to help the caregiver find closure on each day. With prompts like; What new challenges have you encountered in the past week? What happened in your day to make you smile? And, What has been the hardest task for you in the past day or two? This journal is sure to help the caregiver's emotions flow from day to day with a little more clarity and organization of their thoughts and feelings. Although this journal was written from the perspective of a caregiver for memory loss disease such as dementia and Alzheimer, the prompts are rather general and can be used for other caregiver situations. It is very therapeutic to write about our feelings and the prompts in this journal offer an easy way for the caregiver to release thoughts and feelings they may not otherwise put a voice to. Whether you are the caregiver or you know someone who could benefit from this journal, it is a valuable tool.




Begins the Night Music


Book Description

BEGINS THE NIGHT MUSIC: A Dementia Caregiver's Journal "I forgot how to use the microwave," said Emma one evening in 2005. Emma was beautiful, petite and feminine, loved travel, entertaining and humor. Multi-talented, she played the piano and electronic organ and was an accomplished watercolorist. She raised toy poodles, one of them becoming a champion. She loved hosting dinner parties and long weekends for family and friends at her beachfront home in Southern New Jersey. Her friends raved about these events until their dying days. Then Emma was diagnosed with dementia. She was 90. She needed help. There was no one but me. I felt the floor of my chest open and my heart plunge into my stomach. My lifestyle and the self I knew ceased to exist thenceforth. Thus began my mother's and my decade-long trek through dark tunnels and along half-lit paths. I stumbled often. Emma simply fell: I ran and got neighbors to help pick her up. I, the unpaid sole caregiver, often found no response of help from state and healthcare agencies. There were days when I told healthcare aides to leave and never come back, days when the aides left Emma alone for hours without telling me. Only near the end did we find the extraordinary support team we needed. For me the experience was spiritually life changing. This is the story of our long journey, Volume One. Frustration, tears and laughter combine with recipes, humorous essays, magazine stories, and photos. -Samantha Mozart A Salmon Salad and Mozart Book, Volume I




Dementia Diary


Book Description

PAPERBACK & DOWNLOAD EDITIONS---For 15 years, Robert Tell was his widowed Mom's caregiver as her mind and personality disappeared into the fog of dementia. He tells the tale with compassion and humor in this full length, fast moving memoir. His lesson: Caregiver burnout can be helped. If you are watching your loved one vanish into the sinkhole of Alzheimer's Disease (or another dementia), "Dementia Diary" will lift your spirits.




Caregiving for Alzheimer’s Disease and Related Disorders


Book Description

Assisting someone with Alzheimer’s disease or another illness that causes dementia is incredibly demanding and stressful for the family. Like many disabling conditions, Alzheimer’s disease leads to difficulty or inability to carry out common activities of daily life, and so family members take over a variety of tasks ranging from managing the person’s finances to helping with intimate activities such as bathing and dressing. Key coverage in Caregiving for Alzheimer’s Disease and Related Disorders includes: Early diagnosis and family dynamics Emotional needs of caregivers Developmentally appropriate long-term care for people with Alzheimer’s Family caregivers as members of the Alzheimer’s treatment Team Legal and ethical issues for caregivers Faith and spirituality The economics of caring for individuals with Alzheimer’s disease Cultural, racial, ethnic, and socioeconomic issues of minority caregivers Advances in Alzheimer’s disease research Caregiving for Alzheimer’s Disease and Related Disorders offers a wealth of insights and ideas for researchers, practitioners, and graduate students across the caregiving fields, including psychology, social work, public health, geriatrics and gerontology, and medicine as well as public and education policy makers.




Supporting the Caregiver in Dementia


Book Description

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 person with dementia and the caregiver, as well as interpersonal bonds, spiritual dimensions, and reactions to grief and loss. Using a multidisciplinary approach to treatment for caregivers, this book addresses the role of pharmacotherapy, individual and family interventions, and social supports. Finally, the authors reflect on societal issues such as health care policies, ethnic elders, and ethics. This volume offers health professionals insights into the daily lives of caregivers, along with tools to provide their patients with the support they need.




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.




Ageing, Dementia and the Social Mind


Book Description

A groundbreaking exploration of the sociology of dementia — with contributions from distinguished international scholars and practitioners. Organised around the four themes of personhood, care, social representations and social differentiation Provides a critical look at dementia and demonstrates how sociology and other disciplines can help us understand its social context as well as the challenges it poses Contributing authors explore the social terrain, responding in part, to Paul Higgs’ and Chris Gilleard’s highly influential work on ageing Breaks new ground in giving specific attention to the social and cultural dimensions of responses to dementia