Hemvård
1 320 produkter
1 320 produkter
Häftad, Engelska, 2024
115 kr
Skickas
**** PRE-ORDER KC'S NEXT BOOK: WHO DESERVES YOUR LOVE ****Simple tools to make home care easy when life is hard. When you are neurodivergent, have undiagnosed ADHD or are struggling with your mental or physical health, keeping on top of the laundry pile and tackling dishes in the sink can feel like climbing a mountain. But it doesn’t have to be that way.Licensed therapist KC Davis has been there. Having relearnt the basics of self-care after an adult diagnosis of ADHD, she is here to revolutionise the way you look after your home and your mind. This gentle guide to staying afloat when life is tough shares practical strategies to create a functional home, make your space work for you rather than against you, and treat yourself with more compassion and kindness.KC’s philosophy: good enough is perfect. With her help, your home will feel like a sanctuary again.‘A kind and understanding book to help us all feel a little better about ourselves and how we live’ Helen Russell, bestselling author of The Year of Living Danishly
Häftad, Svenska, 2022
189 kr
Skickas inom 5-8 vardagar
Vi möttes i mitt samtalsrum. Hon beskrev hur hon tog hand om sin demenssjuke man dag efter dag. Hur hon hjälpte honom att klä på sig på morgonen, hjälpte honom att klara dagens alla bekymmer och hjälpte honom i säng på kvällen. Sedan suckade hon och sa med eftertryck:
- Jag orkar inte en dag till! Hur ska det gå med allt? Hur ska det gå?
Jag svarade inte, och hon fortsatte:
- Men jag måste, jag bara måste klara det, det finns ju ingen annan som kan göra det.
Lars Björklund mötte i sitt arbete som sjukhuspräst inte bara sjuka människor -- alla de som finns runt den som är sjuk, eller bara gammal, är också i en utsatt situation. Under de senaste åren har han träffat ännu fler av dem vid föreläsningsdagar för anhörigvårdare.
Hur ska jag orka? är en bok skriven för alla anhörigvårdare men också för dem som möter familjer och ensamma människor i vård och omsorg. Vad gör man när ansvar för, beroende av och kärlek till en annan människa blir en alldeles för tung börda?
Ensamma klarar vi inte så mycket. Vi behöver varandra, och vi behöver hitta praktiska lösningar som kan hjälpa oss med det som blivit vårt ansvar. Men vi behöver också hitta ord och tankar för det svåra.
ur bokens förord
Ung, frisk och lycklig - då är det ingen match att lova att älska varandra i nöd och lust. Men hur orkar man den dag den andre är sjuk och hjälplös, behöver passning dygnet runt och ens egen frihet obefintlig?
Lars Bjöklund intervjuas i Svenska Dagbladet
Lars Björklund har skrivit en varm och inkännande bok om vad det är att vara anhörig och var gränserna till det möjliga går.
Corren
Ett stort antal konkreta exempel och en välskriven text förmedlar en stark närvaro från författarens sida som gör att boken berör läsaren på ett bra och närgående sätt.
Björn Nilsson Bibliotekstjänst
Häftad, Engelska, 2023
128 kr
Skickas inom 7-10 vardagar
***A Waterstones Best Books of 2022 pick***'David Haslam is uniquely placed to reflect on how healthcare has lost its way, what needs to be done to fix it and why all of us are responsible for doing so... The importance and timeliness of his messages shines through.' Dr Phil Hammond'A fascinating and important book.' Dr Amanda BrownWith a single drug in the UK currently costing £340,000 per patient per year, or a gene therapy in the USA being costed at $1.2million, who should get such treatments, and how can we begin to afford them? Should we all be entitled to timely mental health therapy? How should we care for our old? As we grapple with the world's worst pandemic for a century, our minds are on our health more than ever. But what should we rightfully expect of doctors? In this original and thought-provoking book, Sir David Haslam explores what good healthcare should achieve and asks how we pay for it. Informed by patient stories and data from across the world - from US big pharma to Britain's NHS - this is an urgent and often moving examination of our most important asset: our health.
Häftad, Engelska, 2025
127 kr
Skickas
A Silent Tsunami is a unique combination of memoir and medicine – Rowan forensically examines the development of her mother’s illness and explores dementia in a frank but illuminating, lyrical and moving way.Anthea Rowan writes about her mother’s struggles of living with Dementia, while interpreting the science that surrounds this devestating illness. Grounded in personal observation, she casts an unflinching eye on the realities of living with a mother who has forgotten her daughter and a determination that her children will not face the same. There is hope here, too.As a portrayal of the relationships we share with our mothers, an examinaion of their influences on us, as well as asking questions about how illness impacts lives, A Silent Tsunami is a powerful story of family, life, love and loss.
Inbunden, Engelska, 2025
266 kr
Skickas
“This book is a game changer for caregivers of loved ones with dementia. This book will help millions of families, like hers, like yours, like mine, like everyone’s. It’s a book for our time.” – Maria Shriver From Emma Heming Willis, wife of Bruce Willis, a deeply personal and richly compassionate supportive guide that helps caregivers care for themselves while they navigate a loved one's dementia. By sharing her personal journey as a care partner and the latest research and insights from the world’s top dementia, caregiving, and integrative experts Emma offers the guidance and wisdom caregivers everywhere so desperately need to hear, including: A diagnosis isn’t just a label, it’s a starting point. It helps you better understand your person’s behavior and respond with more clarity and compassion.Taking care of yourself is not optional; it's mandatory. It will make you a better care partner. It’s not selfish, it’s self-preserving.You don’t have a choice about being on the dementia caregiving journey. But you do have a choice in terms of how you approach it and reframe it.Caregivers are human so you aren’t always going to be patient and selfless. You have challenges and struggle with conflicting emotions and that’s okay.The day Emma Heming Willis’ husband, Bruce Willis, was diagnosed with frontotemporal dementia (FTD), all they were given was a pamphlet and told to check back in a few months.With no hope or direction, Emma walked out of that doctor’s appointment frozen with fear, confusion and a sense that her world had just fallen apart.In fact, it had. Bruce and Emma had their story written, their future mapped out. Yet all those dreams crumbled with that diagnosis, and Emma felt alone and more isolated than ever. How would she care for her husband while parenting their young daughters? With The Unexpected Journey, Emma has written the book she wishes she’d been handed on the day of Bruce’s diagnosis: a supportive guide to navigating the complicated, heartbreaking, and transformative experience that is caregiving for your loved one.Ultimately, The Unexpected Journey shows you how to care for yourself while doing one of the hardest, most heartbreaking jobs in the world. Because if you don’t take care of yourself, you are not going to be able to look after anyone else—especially your loved one with dementia. 'I know that no two caregiving journeys are the same, but we are connected by the same unchosen thread. It’s not an easy path for you, your loved one or your family. But I’m here to let you know that you are not alone, and, in time, you will find your footing, and a way forward.'
Häftad, Engelska, 2025
212 kr
Skickas
“This book is a game changer for caregivers of loved ones with dementia. This book will help millions of families, like hers, like yours, like mine, like everyone’s. It’s a book for our time.” – Maria Shriver From Emma Heming Willis, wife of Bruce Willis, a deeply personal and richly compassionate supportive guide that helps caregivers care for themselves while they navigate a loved one's dementia. By sharing her personal journey as a care partner and the latest research and insights from the world’s top dementia, caregiving, and integrative experts Emma offers the guidance and wisdom caregivers everywhere so desperately need to hear, including: A diagnosis isn’t just a label, it’s a starting point. It helps you better understand your person’s behavior and respond with more clarity and compassion.Taking care of yourself is not optional; it's mandatory. It will make you a better care partner. It’s not selfish, it’s self-preserving.You don’t have a choice about being on the dementia caregiving journey. But you do have a choice in terms of how you approach it and reframe it.Caregivers are human so you aren’t always going to be patient and selfless. You have challenges and struggle with conflicting emotions and that’s okay.The day Emma Heming Willis’ husband, Bruce Willis, was diagnosed with frontotemporal dementia (FTD), all they were given was a pamphlet and told to check back in a few months.With no hope or direction, Emma walked out of that doctor’s appointment frozen with fear, confusion and a sense that her world had just fallen apart.In fact, it had. Bruce and Emma had their story written, their future mapped out. Yet all those dreams crumbled with that diagnosis, and Emma felt alone and more isolated than ever. How would she care for her husband while parenting their young daughters? With The Unexpected Journey, Emma has written the book she wishes she’d been handed on the day of Bruce’s diagnosis: a supportive guide to navigating the complicated, heartbreaking, and transformative experience that is caregiving for your loved one.Ultimately, The Unexpected Journey shows you how to care for yourself while doing one of the hardest, most heartbreaking jobs in the world. Because if you don’t take care of yourself, you are not going to be able to look after anyone else—especially your loved one with dementia. 'I know that no two caregiving journeys are the same, but we are connected by the same unchosen thread. It’s not an easy path for you, your loved one or your family. But I’m here to let you know that you are not alone, and, in time, you will find your footing, and a way forward.'
E-bok
Engelska, 2025151 kr
Läs direkt efter köp
“This book is a game changer for caregivers of loved ones with dementia. This book will help millions of families, like hers, like yours, like mine, like everyone’s. It’s a book for our time.” – Maria Shriver From Emma Heming Willis, wife of Bruce Willis, a deeply personal and richly compassionate supportive guide that helps caregivers care for themselves while they navigate a loved one's dementia. By sharing her personal journey as a care partner and the latest research and insights from the world’s top dementia, caregiving, and integrative experts Emma offers the guidance and wisdom caregivers everywhere so desperately need to hear, including: A diagnosis isn’t just a label, it’s a starting point. It helps you better understand your person’s behavior and respond with more clarity and compassion.Taking care of yourself is not optional; it's mandatory. It will make you a better care partner. It’s not selfish, it’s self-preserving.You don’t have a choice about being on the dementia caregiving journey. But you do have a choice in terms of how you approach it and reframe it.Caregivers are human so you aren’t always going to be patient and selfless. You have challenges and struggle with conflicting emotions and that’s okay.The day Emma Heming Willis’ husband, Bruce Willis, was diagnosed with frontotemporal dementia (FTD), all they were given was a pamphlet and told to check back in a few months.With no hope or direction, Emma walked out of that doctor’s appointment frozen with fear, confusion and a sense that her world had just fallen apart.In fact, it had. Bruce and Emma had their story written, their future mapped out. Yet all those dreams crumbled with that diagnosis, and Emma felt alone and more isolated than ever. How would she care for her husband while parenting their young daughters? With The Unexpected Journey, Emma has written the book she wishes she’d been handed on the day of Bruce’s diagnosis: a supportive guide to navigating the complicated, heartbreaking, and transformative experience that is caregiving for your loved one.Ultimately, The Unexpected Journey shows you how to care for yourself while doing one of the hardest, most heartbreaking jobs in the world. Because if you don’t take care of yourself, you are not going to be able to look after anyone else—especially your loved one with dementia. 'I know that no two caregiving journeys are the same, but we are connected by the same unchosen thread. It’s not an easy path for you, your loved one or your family. But I’m here to let you know that you are not alone, and, in time, you will find your footing, and a way forward.'
Inbunden, Engelska, 2025
243 kr
Skickas
The story of a national treasure we won't soon forget – by the woman who knew him best. I mention you’ve been smoking. ‘He mustn’t!’ she says, alarmed. ‘There’s so much oxygen in your house he’d explode.’ There is a funny side to this — a cartoonish end: Johnnie Walker DJ Explodes! Just try not to take the house with you. In Johnnie Walker – Both Sides Now, his devoted wife Tiggy shares the final chapter of their life together: the slow, painful goodbye to the man she adored. She reflects on the soaring highs of Johnnie’s legendary Radio 2 career, as they navigate the heartbreak, frustration, and strange intimacy of anticipatory grief.This is an honest, deeply personal portrait of love and loss — a raw, life-affirming tribute to a remarkable life well-lived. With wit and unflinching clarity, Tiggy lays bare the emotional toll of caring for someone at the end of life, and the impossible task of letting go while still holding on.Not just for those who loved Johnnie Walker — this is for anyone who’s known the tangled, messy grace of caring, grieving and loving, all the way to the final breath.
E-bok
Engelska, 202586 kr
Läs direkt efter köp
The story of a national treasure we won't soon forget – by the woman who knew him best. I mention you’ve been smoking. ‘He mustn’t!’ she says, alarmed. ‘There’s so much oxygen in your house he’d explode.’ There is a funny side to this — a cartoonish end: Johnnie Walker DJ Explodes! Just try not to take the house with you. In Johnnie Walker – Both Sides Now, his devoted wife Tiggy shares the final chapter of their life together: the slow, painful goodbye to the man she adored. She reflects on the soaring highs of Johnnie’s legendary Radio 2 career, as they navigate the heartbreak, frustration, and strange intimacy of anticipatory grief.This is an honest, deeply personal portrait of love and loss — a raw, life-affirming tribute to a remarkable life well-lived. With wit and unflinching clarity, Tiggy lays bare the emotional toll of caring for someone at the end of life, and the impossible task of letting go while still holding on.Not just for those who loved Johnnie Walker — this is for anyone who’s known the tangled, messy grace of caring, grieving and loving, all the way to the final breath.
Ljudbok
Engelska, 2025201 kr
Lyssna direkt efter köp
The story of a national treasure we won't soon forget - by the woman who knew him best. I mention you've been smoking. 'He mustn't!' she says, alarmed. 'There's so much oxygen in your house he'd explode.' There is a funny side to this - a cartoonish end: Johnnie Walker DJ Explodes! Just try not to take the house with you.In Johnnie Walker - Both Sides Now, his devoted wife Tiggy shares the final chapter of their life together: the slow, painful goodbye to the man she adored. She reflects on the soaring highs of Johnnie's legendary Radio 2 career, as they navigate the heartbreak, frustration, and strange intimacy of anticipatory grief.This is an honest, deeply personal portrait of love and loss - a raw, life-affirming tribute to a remarkable life well-lived. With wit and unflinching clarity, Tiggy lays bare the emotional toll of caring for someone at the end of life, and the impossible task of letting go while still holding on.Not just for those who loved Johnnie Walker - this is for anyone who's known the tangled, messy grace of caring, grieving and loving, all the way to the final breath.
- Nyhet
Häftad, Engelska, 2026
137 kr
Skickas
The story of a national treasure we won't soon forget – by the woman who knew him best. I mention you’ve been smoking. ‘He mustn’t!’ she says, alarmed. ‘There’s so much oxygen in your house he’d explode.’ There is a funny side to this — a cartoonish end: Johnnie Walker DJ Explodes! Just try not to take the house with you. In Johnnie Walker – Both Sides Now, his devoted wife Tiggy shares the final chapter of their life together: the slow, painful goodbye to the man she adored. She reflects on the soaring highs of Johnnie’s legendary Radio 2 career, as they navigate the heartbreak, frustration, and strange intimacy of anticipatory grief.This is an honest, deeply personal portrait of love and loss — a raw, life-affirming tribute to a remarkable life well-lived. With wit and unflinching clarity, Tiggy lays bare the emotional toll of caring for someone at the end of life, and the impossible task of letting go while still holding on.Not just for those who loved Johnnie Walker — this is for anyone who’s known the tangled, messy grace of caring, grieving and loving, all the way to the final breath.
Häftad, Engelska, 2011
244 kr
Skickas inom 3-6 vardagar
E-bok
PDF, Engelska, 2001209 kr
Läs direkt efter köp
An essential resource for all caregivers
A must-read reference for those of you who are caregivers to either a member of your family or a friend, this heartwarming, supportive book explains to you the intricacies of the caregiving experience. The Caregiver''s Sourcebook features separate sections on caregiving for specific disorders including AIDS/HIV, Alzheimer''s disease, Parkinson''s disease, heart disease, old age, and much more.
Häftad, Engelska, 2009
193 kr
Skickas
The compassionate and practical guide to managing dementia and Alzheimer's, from a clinical psychologist and Sunday Times bestselling author.Dementia is a little understood illness but, while there is currently no cure, much can be done to support wellbeing and maintain quality of life for people living with this condition.In Contented Dementia, clinical psychologist and bestselling author, Oliver James, outlines a groundbreaking and practical method for managing dementia that will allow both sufferer and carer to maintain the highest possible quality of life, throughout every stage of the illness.The SPECAL method (Specialised Early Care for Alzheimer’s) was developed to help carers, families and professionals respond to memory loss and behavioural changes with understanding, confidence, and a personalised approach.The method is based on a simple but powerful principle: although recent memory fades, emotional memory and long-term memories often remain strong. By working with, rather than against, the reality experienced by the person with dementia, SPECAL helps reduce distress, improve communication and create a calmer, more contented daily life.Drawing on real-life examples and user-friendly tried-and-tested methods, Contented Dementia provides essential information and guidance for families, caregivers and healthcare professionals seeking a more positive approach to dementia care.Praise for Contented Dementia:‘A revolutionary new way of treating dementia [that] brings amazing benefits for patients and carers alike’ Guardian‘An indispensable handbook for anyone coping with the effects of dementia and who wants to keep a sufferer as happy as is humanly possible’ Daily Express‘Explains a revolutionary way to care for dementia patients . . . tender techniques that can ease absent minds’ Telegraph‘Anyone who wants help in caring for the condition will find this excellent work a revelation’ Mail on Sunday‘Shows how to minimize distress and manage dementia…I expected this book to be depressing; it is exactly the opposite.’ The Independent
Häftad, Engelska, 1997
182 kr
Skickas
HEAVEN'S COAST is an anatomy of loss: tender, heartbreaking, consoling and, ultimately, incredibly moving. Beginning with the first onset of AIDS and its lengthening shadow over a blissful relationship, the book follows the shifting patterns between two loves as the illness takes hold - the change in them and the change in the way they perceive the world, through the lens of grief. Doty examines the nature of AIDS as opposed to other illnesses, the responses of society, the frustration of medical care and the exhausting - and occasionally uplifting - burden of caring for the dying at home.
Häftad, Engelska, 2015
692 kr
Skickas inom 10-15 vardagar
Family Caregiving in the New Normal discusses how the drastic economic changes that have occurred over the past few years have precipitated a new conversation on how family care for older adults will evolve in the future.
This text summarizes the challenges and potential solutions scientists, policy makers, and clinical providers must address as they grapple with these changes, with a primary focus given to the elements that may impact how family caregiving is organized and addressed in subsequent decades, including sociodemographic trends like divorce, increased participation of women in the workforce, geographic mobility, fewer children in post-baby boom families, chronic illness trends, economic stressors, and the current policy environment.
A section on the support of caregivers includes technology-based solutions that examine existing models, personal health records, and mobile applications, big data issues, decision-making support, person-centered approaches, crowd-sourced caregiving such as blogs and personal websites that have galvanized caregivers, and new methods to combine paid and unpaid forms of care.
Provides a concise "roadmap" of the demographic, economic, health trends, and policy challenges facing family caregivers Presents potential solutions to caregiving so that scientists, policymakers, and clinical providers can best meet the needs of families and communities in the upcoming decades Includes in-depth, diverse stories of caregivers of persons with different diseases who share perspectives Covers person-centered care approaches to family caregiving that summarize effective community-based services of psychosocial intervention models Examines how existing efficacious models can more effectively reach and serve individual families
E-bok
Engelska, 20031 079 kr
Läs direkt efter köp
Geriatric Palliative Care covers a broad spectrum of issues characterizing care near the end of life for older adults. Beginning with the social and cultural context of old age and frailty, this volume details specific aspects of palliative care relevant to particular disorders (e.g. cancer, strokes, dementia, etc.) as well as individual symptoms (e.g., pain, fatigue, anxiety, etc.). Communication between care-givers and patients, in a variety of settings, is also discussed. The theme of this book is that palliative care is the best approach to the care of chronically ill and frail elderly because of its focus on: quality of life; support for functional independence; and the centrality of the patient''s values and experiences in determining the goals of medical care. Indeed, Geriatric Palliative Care provides a comprehensive medical reference for all clinicians who care for older adults.
Häftad, Engelska, 2021
437 kr
Skickas inom 5-8 vardagar
Language exercises a powerful impact on medical care as the words that physicians use with patients have the power to heal or harm. The practice of medicine is shaped by the potent metaphors that are prevalent in clinical care, especially military metaphors and the words of war that bring with them unfortunate consequences for patients and physicians alike. Physicians who fight disease turn the patient into a passive battlefield. Patients are encouraged to remain stoic, blamed for "failing" chemotherapy and sadly remembered in heroic obituaries of lost battles. The search for disease as enemy shifts the doctor's gaze to the computer and imaging technologies that render the patient transparent, unseen and unheard. Modern treatments save lives but patients can be the victims of collateral damage and friendly fire. In The Language of Medicine, Abraham Fuks, physician, medical educator, and former Dean of Medicine at McGill University, shows us how words are potent drugs that must be tailored to the individual patient and applied in carefully chosen and measured doses to offer benefits and avoid toxicity. The book shines a light on our culture that deprecates the skill of listening that is, paradoxically, the attribute that patients most desire of their doctors. Societal metronomes beat rapidly and compress clinic visits into stroboscopic encounters that leave patients puzzled, fearful and uncertain.Building on research about physicians in practice, the experiences of patients, stories of medical students as well as the history of medicine, Dr. Fuks promotes an ideal of clinical practice that is achieved by humble physicians who provide time and space for listening, select words with care, and choose metaphors that engender healing.
E-bok
PDF, Engelska, 2021312 kr
Läs direkt efter köp
Language exercises a powerful impact on medical care as the words that physicians use with patients have the power to heal or harm. The practice of medicine is shaped by the potent metaphors that are prevalent in clinical care, especially military metaphors and the words of war that bring with them unfortunate consequences for patients and physicians alike. Physicians who fight disease turn the patient into a passive battlefield. Patients are encouraged to remain stoic, blamed for "failing" chemotherapy and sadly remembered in heroic obituaries of lost battles. The search for disease as enemy shifts the doctor''s gaze to the computer and imaging technologies that render the patient transparent, unseen and unheard. Modern treatments save lives but patients can be the victims of collateral damage and friendly fire.In The Language of Medicine, Abraham Fuks, physician, medical educator, and former Dean of Medicine at McGill University, shows us how words are potent drugs that must be tailored to the individual patient and applied in carefully chosen and measured doses to offer benefits and avoid toxicity. The book shines a light on our culture that deprecates the skill of listening that is, paradoxically, the attribute that patients most desire of their doctors. Societal metronomes beat rapidly and compress clinic visits into stroboscopic encounters that leave patients puzzled, fearful and uncertain.Building on research about physicians in practice, the experiences of patients, stories of medical students as well as the history of medicine, Dr. Fuks promotes an ideal of clinical practice that is achieved by humble physicians who provide time and space for listening, select words with care, and choose metaphors that engender healing.
E-bok
Engelska, 2021312 kr
Läs direkt efter köp
Language exercises a powerful impact on medical care as the words that physicians use with patients have the power to heal or harm. The practice of medicine is shaped by the potent metaphors that are prevalent in clinical care, especially military metaphors and the words of war that bring with them unfortunate consequences for patients and physicians alike. Physicians who fight disease turn the patient into a passive battlefield. Patients are encouraged to remain stoic, blamed for "failing" chemotherapy and sadly remembered in heroic obituaries of lost battles. The search for disease as enemy shifts the doctor''s gaze to the computer and imaging technologies that render the patient transparent, unseen and unheard. Modern treatments save lives but patients can be the victims of collateral damage and friendly fire.In The Language of Medicine, Abraham Fuks, physician, medical educator, and former Dean of Medicine at McGill University, shows us how words are potent drugs that must be tailored to the individual patient and applied in carefully chosen and measured doses to offer benefits and avoid toxicity. The book shines a light on our culture that deprecates the skill of listening that is, paradoxically, the attribute that patients most desire of their doctors. Societal metronomes beat rapidly and compress clinic visits into stroboscopic encounters that leave patients puzzled, fearful and uncertain.Building on research about physicians in practice, the experiences of patients, stories of medical students as well as the history of medicine, Dr. Fuks promotes an ideal of clinical practice that is achieved by humble physicians who provide time and space for listening, select words with care, and choose metaphors that engender healing.
Inbunden, Engelska, 2010
437 kr
Skickas inom 5-8 vardagar
Approximately 2.5 million people in the United States--one percent of the population--have an intellectual disability (previously referred to as mental retardation). These conditions range from genetic disorders such as Down syndrome to disabilities caused by infectious diseases and brain injury. Intellectual Disability: A Guide for Families and Professionals, by one of the country's foremost authorities on intellectual disability, is a comprehensive resource that will be of importance to anyone with a personal connection to a child or adult with a neurodevelopmental disorder. Emphasizing the humanity of persons with intellectual and related developmental disabilities, psychiatrist and pediatrician James Harris provides essential information on assessment and diagnosis of intellectual disability, treatments for specific disorders, and ways to take advantage of the wide array of services available today. The focus throughout is on the development of the person, the positive supports necessary for self-determination, and, to the extent possible, independent decision making. Harris also surveys historical attitudes toward intellectual disability, the medical community's current understanding of its causes and frequency, and the associated physical, behavioral, and psychiatric conditions (such as seizure disorder, depression, and autism) that often accompany particular types of intellectual disability. The book addresses legal, medical, mental health, and research-related issues as well as matters of spirituality, highlighting the ways in which individuals with intellectual disability can meaningfully participate in the spiritual lives of their families and their communities. Each chapter ends with a series of key points to remember, and the book concludes with a list of additional resources of further interest.Intellectual Disability is a must-read for parents and families of those with neurodevelopmental disorders, providing guidance and essential information to help their family members effectively, and to make a significant, positive difference in their lives now and in the future.
Inbunden, Engelska, 2007
702 kr
Skickas inom 5-8 vardagar
In Dialysis Without Fear, psychiatrist and dialysis patient Dr. Daniel Offer joins with his wife, Marjorie Kaiz Offer, and daughter, Susan Offer Szafir, to reveal how life can be lived, and lived well, on dialysis. Drawing on his long medical career and more than seven years of personal experience with dialysis, Dr. Offer dispels many misconceptions surrounding this treatment, explaining how you can adapt to the new diet, travel, work and continue to partake in life's joys and celebrations. But the fears and hardships can be quite real, and Dr. Offer brings his years as a psychiatrist to bear as he provides practical advice on how patients can overcome them. Walking through each step of dialysis, he explains different types of treatment, examines the pros and cons of a transplant, and discusses side effects. Since dialysis affects the entire family, Dr. Offer and his co-authors also provide realistic insights into how relatives can cope and thrive together, sharing the humour, courage, and triumphs of real families who have successfully faced the challenges of dialysis. The result is an inspiring, practical guide that will help patients and their families learn to overcome the difficulties of dialysis, live without fear, and enjoy every day.
Häftad, Engelska, 2007
431 kr
Skickas inom 5-8 vardagar
In Dialysis Without Fear, psychiatrist and dialysis patient Dr. Daniel Offer joins with his wife, Marjorie Kaiz Offer, and daughter, Susan Offer Szafir, to reveal how life can be lived, and lived well, on dialysis. Drawing on his long medical career and more than seven years of personal experience with dialysis, Dr. Offer dispels many misconceptions surrounding this treatment, explaining how you can adapt to the new diet, travel, work and continue to partake in life's joys and celebrations. But the fears and hardships can be quite real, and Dr. Offer brings his years as a psychiatrist to bear as he provides practical advice on how patients can overcome them. Walking through each step of dialysis, he explains different types of treatment, examines the pros and cons of a transplant, and discusses side effects. Since dialysis affects the entire family, Dr. Offer and his co-authors also provide realistic insights into how relatives can cope and thrive together, sharing the humour, courage, and triumphs of real families who have successfully faced the challenges of dialysis. The result is an inspiring, practical guide that will help patients and their families learn to overcome the difficulties of dialysis, live without fear, and enjoy every day.
Häftad, Engelska, 2022
610 kr
Skickas inom 5-8 vardagar
Loss and Grief: Personal Stories of Doctors and Other Healthcare Professionals is a unique collection of personal narratives that chronicle the journeys of doctors and other healthcare professionals who have been personally impacted by life-altering losses. Edited by internationally recognized practitioners of supportive care medicine and grief counseling, these are unflinching, first-person narratives of authors walking in their own shoes. The narratives reveal losses of cherished loved ones, integrity, dreams, naïve views of colleagues, and the lack of institutional support for these inevitable experiences. Although the narrators are well-established leaders in their fields, serious loss brought each back to the exposed core of their most basic selves. They learned that the professional veneer was too thin to be instructive or protective. Readers might resonate with their own painful experiences and memories, and others might wonder how they will imagine their own future when these inevitable aspects of being human-loss and grief-strike them, too. In Loss and Grief, it is our hope that such openly shared feelings of isolation and suffering will humanize the loss experience, ignite prospective discussions, and illuminate opportunities for education, research and interventions to prepare us for multiple loss experiences endemic to life.
E-bok
PDF, Engelska, 2022367 kr
Läs direkt efter köp
Loss and Grief: Personal Stories of Doctors and Other Healthcare Professionals is a unique collection of personal narratives that chronicle the journeys of doctors and other healthcare professionals who have been personally impacted by life-altering losses. Edited by internationally recognized practitioners of supportive care medicine and grief counseling, these are unflinching, first-person narratives of authors walking in their own shoes. The narratives reveal losses of cherished loved ones, integrity, dreams, naïve views of colleagues, and the lack of institutional support for these inevitable experiences. Although the narrators are well-established leaders in their fields, serious loss brought each back to the exposed core of their most basic selves. They learned that the professional veneer was too thin to be instructive or protective. Readers might resonate with their own painful experiences and memories, and others might wonder how they will imagine their own future when these inevitable aspects of being human-loss and grief-strike them, too.In Loss and Grief, it is our hope that such openly shared feelings of isolation and suffering will humanize the loss experience, ignite prospective discussions, and illuminate opportunities for education, research and interventions to prepare us for multiple loss experiences endemic to life.
E-bok
Engelska, 2022367 kr
Läs direkt efter köp
Loss and Grief: Personal Stories of Doctors and Other Healthcare Professionals is a unique collection of personal narratives that chronicle the journeys of doctors and other healthcare professionals who have been personally impacted by life-altering losses. Edited by internationally recognized practitioners of supportive care medicine and grief counseling, these are unflinching, first-person narratives of authors walking in their own shoes. The narratives reveal losses of cherished loved ones, integrity, dreams, naïve views of colleagues, and the lack of institutional support for these inevitable experiences. Although the narrators are well-established leaders in their fields, serious loss brought each back to the exposed core of their most basic selves. They learned that the professional veneer was too thin to be instructive or protective. Readers might resonate with their own painful experiences and memories, and others might wonder how they will imagine their own future when these inevitable aspects of being human-loss and grief-strike them, too.In Loss and Grief, it is our hope that such openly shared feelings of isolation and suffering will humanize the loss experience, ignite prospective discussions, and illuminate opportunities for education, research and interventions to prepare us for multiple loss experiences endemic to life.
Häftad, Engelska, 2023
931 kr
Skickas inom 5-8 vardagar
Crossing Over provides a unique view of patients, families, and their caregivers in the face of incurable illness. Twenty richly-detailed narratives bring vividly to life the experiences of dying and bereavement, weaving together emotions, physical symptoms, spiritual concerns, and the stresses of family life, as well as the professional and personal challenges of providing hospice and palliative care. Drawing on a variety of qualitative research methods, including participant-observation, interviews, and journal keeping, the narratives depict the sights, sounds, tastes, and smells of daily life in patients' homes and in the palliative care unit. Crossing Over moves far beyond conventional case reports in medicine, which typically concentrate narrowly on symptoms and treatments, and beyond clichés about "dying with dignity." It provides intimate views of the anger and fear, tenderness and reconciliation, jealousy and love, unexpected courage and unshakable faith, social support and "falling through the cracks," which are all part of facing death in North American society. It provides an extraordinary portrait of the processes of giving and receiving hospice and palliative care in the real world, as opposed to idealized versions in many textbooks. This edition of Crossing Over has been thoroughly revised and updated to reflect changes in hospice and palliative care and in North American society since the first edition in 2000. Chief among these are the expansion of hospice and palliative care as a field, the ravages of the COVID-19 pandemic, the wider availability of medical aid in dying, and a heightened awareness of how structural racism, classism, and other forms of discrimination shape individuals' and families' experiences right up to the close of life.
E-bok
PDF, Engelska, 2022550 kr
Läs direkt efter köp
Crossing Over provides a unique view of patients, families, and their caregivers in the face of incurable illness. Twenty richly-detailed narratives bring vividly to life the experiences of dying and bereavement, weaving together emotions, physical symptoms, spiritual concerns, and the stresses of family life, as well as the professional and personal challenges of providing hospice and palliative care. Drawing on a variety of qualitative research methods, including participant-observation, interviews, and journal keeping, the narratives depict the sights, sounds, tastes, and smells of daily life in patients'' homes and in the palliative care unit. Crossing Over moves far beyond conventional case reports in medicine, which typically concentrate narrowly on symptoms and treatments, and beyond clich?s about "dying with dignity." It provides intimate views of the anger and fear, tenderness and reconciliation, jealousy and love, unexpected courage and unshakable faith, social support and "falling through the cracks," which are all part of facing death in North American society. It provides an extraordinary portrait of the processes of giving and receiving hospice and palliative care in the real world, as opposed to idealized versions in many textbooks. This edition of Crossing Over has been thoroughly revised and updated to reflect changes in hospice and palliative care and in North American society since the first edition in 2000. Chief among these are the expansion of hospice and palliative care as a field, the ravages of the COVID-19 pandemic, the wider availability of medical aid in dying, and a heightened awareness of how structural racism, classism, and other forms of discrimination shape individuals'' and families'' experiences right up to the close of life.
E-bok
Engelska, 2022550 kr
Läs direkt efter köp
Crossing Over provides a unique view of patients, families, and their caregivers in the face of incurable illness. Twenty richly-detailed narratives bring vividly to life the experiences of dying and bereavement, weaving together emotions, physical symptoms, spiritual concerns, and the stresses of family life, as well as the professional and personal challenges of providing hospice and palliative care. Drawing on a variety of qualitative research methods, including participant-observation, interviews, and journal keeping, the narratives depict the sights, sounds, tastes, and smells of daily life in patients'' homes and in the palliative care unit. Crossing Over moves far beyond conventional case reports in medicine, which typically concentrate narrowly on symptoms and treatments, and beyond clich?s about "dying with dignity." It provides intimate views of the anger and fear, tenderness and reconciliation, jealousy and love, unexpected courage and unshakable faith, social support and "falling through the cracks," which are all part of facing death in North American society. It provides an extraordinary portrait of the processes of giving and receiving hospice and palliative care in the real world, as opposed to idealized versions in many textbooks. This edition of Crossing Over has been thoroughly revised and updated to reflect changes in hospice and palliative care and in North American society since the first edition in 2000. Chief among these are the expansion of hospice and palliative care as a field, the ravages of the COVID-19 pandemic, the wider availability of medical aid in dying, and a heightened awareness of how structural racism, classism, and other forms of discrimination shape individuals'' and families'' experiences right up to the close of life.
Inbunden, Engelska, 2023
351 kr
Skickas inom 5-8 vardagar
FDA's approval of aducanumab has radically changed the world of Alzheimer's disease and you're going to need guidance regarding whether they should take it or not. This book conveys all the insight.As you age, you may find yourself worrying about your memory. Where did I put those car keys? What time was my appointment? What was her name again? With more than 41 million Americans over the age of 65 in the United States, the question becomes how much (or, perhaps, what type) of memory loss is to be expected as one gets older and what should trigger a visit to the doctor.Seven Steps to Managing Your Aging Memory addresses these key concerns and more, such as:· What are the signs that suggest your memory problems are more than just part of normal aging?· Is it normal to have concerns about your memory?· What are the markers of mild cognitive impairment, dementia, Alzheimer's, and other brain diseases?· How should you talk about your memory concerns to your doctor?· What should your doctor do to evaluate your memory?· Which healthcare professional(s) should you see?· What medicines, alternative therapies, diets, and exercises actually work to improve your memory?· Can crossword puzzles, computer brain-training games, memory aids, and strategies help strengthen your memory?· What other resources are available when dealing with memory loss?Seven Steps to Managing Your Aging Memory is written in an easy-to-read yet comprehensive style, featuring clinical vignettes and character-based stories that provide real-life examples of how to successfully manage memory loss.