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Mom hasn’t been herself lately. She’s constantly misplacing her keys and she is more and more disoriented, even in her own home. Is this normal aging, or is it the start of dementia? FACT: one in three seniors in the United States is affected by dementia and Alzheimer’s disease. Whether it concerns a parent or perhaps a spouse, virtually everyone knows someone with the disease or knows a family touched by its effects. FACT: It is most beneficial to recognize the early symptoms of dementia and to respond to them, whether or not the disease is medically diagnosed. FACT: Dementia and Alzheimer’s disease are progressive and incurable. In UNLOCKING THE DOOR TO DEMENTIA BY LAUREN, families and caregivers will read how to understand and navigate their loved one’s new reality. They will learn: • What is normal behavior (ex., occasionally having difficulty finding the right word while speaking), vs. what is suspect (frequently struggling to find words or substituting words for others) • Practical suggestions concerning the behaviors of dementia, such as Wandering, Anxiety, and Financial Irresponsibility • Practical suggestions for handling difficult situations of dementia, such as moving a loved one to a new home or facility, reducing the risk of falling, and taking away the car keys From knowing the early signs of dementia, to managing daily activities, to handling palliative care and hospice, families and caregivers will gain the confidence and encouragement needed when their roles are reversed or changed, and they want to provide their loved ones with the best care possible.
Mom hasn't been herself lately. She's constantly misplacing her keys and she is more and more disoriented, even in her own home. Is this normal aging, or is it the start of dementia? FACT: one in three seniors in the United States is affected by dementia and Alzheimer's disease. Whether it concerns a parent or perhaps a spouse, virtually everyone knows someone with the disease or knows a family touched by its effects. FACT: It is most beneficial to recognize the early symptoms of dementia and to respond to them, whether or not the disease is medically diagnosed. FACT: Dementia and Alzheimer's disease are progressive and incurable. In UNLOCKING THE DOOR TO DEMENTIA BY LAUREN, families and caregivers will read how to understand and navigate their loved one's new reality. They will learn: -What is normal behavior (ex., occasionally having difficulty finding the right word while speaking), vs. what is suspect (frequently struggling to find words or substituting words for others) -Practical suggestions concerning the behaviors of dementia, such as Wandering, Anxiety, and Financial Irresponsibility -Practical suggestions for handling difficult situations of dementia, such as moving a loved one to a new home or facility, reducing the risk of falling, and taking away the car keys From knowing the early signs of dementia, to managing daily activities, to handling palliative care and hospice, families and caregivers will gain the confidence and encouragement needed when their roles are reversed or changed, and they want to provide their loved ones with the best care possible.
Dementia: The Basics provides the reader with a clear and compassionate introduction to dementia and an accessible guide to dealing with different parts of the dementia journey, from pre-diagnosis and diagnosis to post-diagnostic support, increasing care needs and end of life care. Co-authored by an academic, a person living with dementia and a family carer, the book endeavours to raise awareness of dementia, challenge stereotypical and negative ideas about what it means to have dementia and champion a society where people living with dementia can be active as they wish for as long as possible. The authors present an overview of current research at each step of the dementia journey as well as including knowledge from lived experience, enhancing understanding and challenging thinking about what it might be like to live with a diagnosis or to care for a loved one. As a whole, the book emphasises the importance of prioritising the person living with dementia, as well as considering the impact of what any initiative or action might mean for them, their families and their care supporters. Offering both an accessible introduction to dementia and practical tools, this book will be ideal for health and social care professionals, students of social care, health care and nursing, people with dementia, carers and anyone wanting to understand more about the condition.
Technogenarians investigates the older person?s experiences of health, illness, science, and technology. It presents a greater theoretical and empirical understanding of the biomedical aspects of aging bodies, minds, and emotions, and the rise of gerontechnology industries and professions. A unique scholarly investigation into elders as technology users Emphasizes the need to put aging, science, and technology in the center of analyses of health and illness Explores the rise of gerontechnology industries and professions Offers a critical study of the transformation of aging bodies, minds, and emotions into medical problems in need of medical solutions Combines two scholarly areas - Science and Technology Studies and the Sociology of Aging, Health, and Illness - to produce innovative scholarship
"Everyone is familiar with the terms "dementia" and "Alzheimer's disease," but not everyone knows exactly what they mean and how they are related. To begin our journey, we first need to develop a clear understanding of what dementia and Alzheimer's disease are"--
Cognitive disorders take a toll on everyone—the person living with the condition, their family, friends, caregivers, and the communities they live in. Most of the public's interest has been in the medical research area for this devastating disease, and advice is desperately needed from those who have created innovative solutions with their own first-hand experience. Voices in Dementia Care is based on a series of interviews with dementia care experts across Europe and the United States and with people living day-to-day with the condition. It provides an intimate look at the challenges of delivering high-quality dementia care with limited resources. The book provides readers a list of best practices that can be adapted and applied in the home and in institutional settings. Voices in Dementia Care is a must-read for anyone caring for loved ones with Alzheimer’s, dementia, or other cognitive disorders. From Voices in Dementia Care— In these pages, we include transcripts of our interviews with the elder care and long-term care providers we have interviewed about dementia care. The voices of these care professionals are important to hear in their entirety, as they describe the nuances of the challenges inherent in delivering innovative high quality dementia care with limited resources. Based on our analysis of these interviews, we have identified the critical best practices that we believe all elder and long-term care providers should consider when delivering care to people living with dementia. These best practices can be adapted and applied by the informal caregiver as well—the sister, brother, child, or other loved one who may be responsible for caring for a person living with dementia outside of a traditional care environment.
A hopeful and practical guide to taming the challenges of dementia with creative interventions inspired by real stories of sufferers and caregivers alike. If you've ever cared for someone with dementia, you might empathize with Alice, who tumbled down a rabbit hole and discovered herself in an unhappy world where time moved oddly, animals and plants spoke, but mostly to berate you. Familiar objects became terribly out of scale. If you're caring for someone with dementia now, you might feel like someone changed the rules of reality and that you need a guide, preferably someone kinder than the perennially late rabbit. This book supports the journey—taken by both the caregiver and the person with dementia—providing loved ones with practical recommendations and enriched with human empathy. This book helps ease the stress by offering interventions and non-pharmaceutical therapeutic suggestions. It helps decode dementia's visceral world and supports non-cognitive human experiences. It shares stories of real people struggling to survive the challenges presented by dementia paired with practical examples of interventions that target the miseries of dementia behaviors, triggers, and causalities induced by them. The book provides options in the art of caregiving alongside the power of place, furnishings, light, color, technology, nature, and the senses. Barbara Huelat explores options in human engagement, the experience of destinations, positive distractions, familiar settings, furnishings, light, color, technology, nature, and the emotion of the senses. She offers design interventions that support the family caregivers in functional and emotional outcomes. No cure exists for dementia, but the tips, tools, strategies and suggestions include here provide tools for caregivers and those with dementia to make the experience more comfortable and calm.
"When is it time to move a person living with dementia into a senior living community? How do you avoid an argument with someone who no longer knows what year it is? What do you do if the person you're caring for has trouble recognizing you? How can you lessen the guilt and anxiety that come with dementia caregiving? All of these questions-and more-are answered in this helpful guide through the difficulties of dementia care. Care partners to those living with dementia will find this book a helpful guide into an unfamiliar and challenging world, and professionals in the industry will come away with dementia knowledge they have not gotten anywhere else"--
The correlation between 'disengagement' and illness in people with dementia living in long-term care settings is becoming more widely recognised, and developing and adapting front-line staff responses to the changing needs of individuals is a crucial factor in addressing this problem. This book presents a complete practical framework for whole person assessment, care planning and review of persons with dementia or signs of dementia (including those with learning disabilities) who are in need of, or already receiving, health and/or social support. The book provides photocopiable assessment forms, guidelines for carrying out the assessment, and suggestions for tailored interventions based on the profile that emerges from the assessment process. The authors also include a clear explanation of the five theoretical components of dementia that are considered in the assessment: health, biography, personality, neurological impairment and social psychology. This good practice guide will provide a step up to the challenge of providing person centred care as a minimum standard rather than just an ideal. Care workers in residential settings and social workers assessing clients for their support requirements will find this an essential resource.
This book explores how dementia studies relates to dementia’s growing public profile and corresponding research economy. The book argues that a neuropsychiatric biopolitics of dementia positions dementia as a syndrome of cognitive decline, caused by discrete brain diseases, distinct from ageing, widely misunderstood by the public, that will one day be overcome through technoscience. This biopolitics generates dementia’s public profile and is implicated in several problems, including the failure of drug discovery, the spread of stigma, the perpetuation of social inequalities and the lack of support that is available to people affected by dementia. Through a failure to critically engage with neuropsychiatric biopolitics, much dementia studies is complicit in these problems. Drawing on insights from critical psychiatry and critical gerontology, this book explores these problems and the relations between them, revealing how they are facilitated by neuro-agnostic dementia studies work that lacks robust biopolitical critiques and sociopolitical alternatives. In response, the book makes the case for a more biopolitically engaged "neurocritical" dementia studies and shows how such a tradition might be realised through the promotion of a promissory sociopolitics of dementia.