検索キーワード： 高齢者介護・医療

Any of us could receive a diagnosis - a curable sickness, chronic disease, serious condition, or a terminal illness. Today, dying is usually an elongated process. So, how can we live well while suffering, and avoid being bullied by the obsessive inner voices of anxiety that leave us disconnected from the very life we hope to save? Instead, we can learn to embrace mystery, to understand that all of life’s suffering can be transformative, leaving behind a legacy of pure, powerful, and eternal love.

Should doctors be allowed to help terminally ill people kill themselves? How should a humane society respond to those who are suffering terribly at the end of life? What laws are being proposed, and what will be the consequences for dying people, for health-care services, and for society as a whole? John Wyatt has worked as a frontline doctor in the UK National Health Service for more than 30 years and brings his clinical, ethical, and personal experience to this crucial debate. Assisted Dying is a concise, audible, and authoritative guide to a vital question of our times.

In The Busy Caregiver's Guide to Advanced Alzheimer Disease, Dr. Jennifer Stelter, a psychologist working in memory care, shares a new model designed to help caregivers understand, cope with, and handle some of the most challenging behaviors associated with the disease while encouraging and reinforcing independence and quality of life for their loved ones.

Expertly combining practical advice with Dr. Scharmaine Lawson, NP’s personal experience as a leading figure in the world of house calls, this complete handbook provides expert insights and essential strategies to help healthcare workers and nurse practitioners navigate the demands of in-home care and set up a flourishing house-call practice. With more and more people requiring in-home care, there has never been a better time to kick-start your house-call practice and familiarize yourself with house call procedures and culture.

Becoming a caregiver for a terminally ill family member is an enormous challenge. This guide is a gift to my late husband, who not only taught me how to live well, but how to die well. I hope it will carry on his legacy of always teaching and sharing, even as he faced the end of his life. A compact guide that you can easily reference along your personal journey, it is filled with practical suggestions to help you, as the caregiver, honor the way your family member would like to create his or her final journey toward paradise.

Caregiver Important Information is all about sharing information to caregivers and those who are now placed in that position to help those in need. This information is from the point of a family member, who had to step in and learn about medications, therapies, and making sure people were doing their jobs. Your family member is precious and should be treated as such.

Dementia caregivers frequently suffer from emotional stress, financial hardship, and fractured families. Discover successful care techniques and useful resources that decrease these stresses from day one. Caregiver Overwhelmed is written by a registered nurse with over 20 years of hands-on experience in elderly care and dementia. As a memory care director and home care clinical manager, she focuses on providing education to both professional and family caregivers. Her expertise is now available for home caregivers in this resource-rich, how-to guide.

Diabetes is a growing health concern worldwide, and in the US alone, about 1.5 million new cases are diagnosed each year. Of those cases, almost 95 percent are diagnosed with Type 2 diabetes. While the prevalence of Type 2 diabetes is a concern, there is some good news: both Type 2 diabetes and prediabetes - an early warning sign that Type 2 diabetes could be round the corner - are possible to reverse.

The sea change of convenience and immediacy that has overtaken our lives has also led to a tremendous gap between what professionals and patients believe to be quality care. This has propagated the tragic environment where almost everyone hates going to the dentist. In The Patient First Manifesto, Dr. Bryan Laskin explains the counterintuitive reasons why patients still complain in our offices everyday, and why patients drive doctors crazy (or at least drive them to drink too often).

Today's caregivers are under extraordinary stress. Right now, we are all looking at the challenges of dealing with a huge aging population (every eight seconds a baby boomer turns 65). This leads to an increasing amount of care being rendered by people who aren’t health care professionals. This wonderful program speaks to all types of caregivers. It consists of a heart-to-heart talk, a reminder of the true source of healing, how the relationship with a caregiver can support this healing, and how important it is to recognize caregiver stress and prevent caregiver burnout.

Nancy C. Caralla, Founding President, Executive Director of the C Diff Foundation, and the C Diff Foundation’s Chairperson of Nutrition Wellness, Karen F. Factor, MS, RD, LDN, share their knowledge and experience with patients who have been diagnosed, treated for, and recovering from a C. difficile infection (CD), with family members, caregivers, and individuals sharing a common interest.

In this lecture, Thomas Moore — internationally known theologian and author of New York Times best sellers Care of The Soul, Soul Mates, and A Life At Work, among other titles — talks about his views on extending the scope of medicine beyond the scientific to include spirituality and deep matters of soul. While a purely scientific approach to medicine can work well in and of itself, Moore also considers the importance of emotions, fantasies, dreams, the physical healing environment, and the relationship of caregiver and patient.

We live in uncertain times when a crisis like critical illness in the family does not come as a staccato. Traversing through any such crisis requires personal rituals that leverage our full entelechy. Nothing transforms until you move. Don’t let caregiver burnout beat you. When Things Change helps you devise those positive constructs in any such crisis that empower you to sculpt the best version of yourself and fight the adversity with mindfulness widening your impact radius.

On May 3, 2006, Ted Giovanis emailed a US government official, seeking clarity on an arcane issue: the calculation used by Medicare to determine reimbursement rates for certain kinds of hospitals. Though he expected a routine exchange, what unfolded was anything but.

Be empowered for a healthier, happier you with a personal physician at your side. Living with a chronic illness can feel like a constant battle. This audiobook is designed to equip you with the tools you need to overcome the symptoms of pain, fatigue, shortness of breath, anxiety, and stress while effectively managing and reversing the diseases that cause them. By encouraging you to create personal healthy living goals and then providing valuable tools to help you achieve them, this guide will give you the confidence you need to take control of your health.

Do you want to be slim, healthy and fit? Are you over 40 and confused about what your exercise plan should look like? Are you discouraged and ready to give up? If so, Strength Training for Life is the perfect book for you! This book will teach you everything you need to know about weight lifting and muscle building for achieving your body's natural potential. It will show you exactly how often and at what pace to exercise and help you design a personalized fitness plan that will show real, visible results!

We all have a story. As each of us walks this journey in life, there are defining moments that shape us and make us who we are. Our stories are unique. No one has the same story to tell. Your story defines the individual you are. This book is for those who are caregivers to someone with dementia.

In this anthology, we see from the point of view of patients, caregivers, and family members. Physician and writer Sarah Sasson has curated a collection that is international and unforgettable. This is not a book about death and dying. This is a book about life and how we live it. These stories reveal what is truly valued in this world and speak to the ferocity with which we love.

It’s true that strength declines with age, and your abilities are changing with each passing year. That doesn’t have to mean you give up and let your body rot away. Your muscles can still be exercised and strengthened, and your balance and coordination can improve greatly. You just need to find different exercises that work for you -ones designed specifically for people your age.

If you are a baby boomer like me, you may be having to take care of your parents, spouse, or partner at home; either by yourself or have a hired caregiver to help. My book is filled with my 40 years of nursing caregiving experience on how you can do this.

Grab-and-go inspirations are here in bite-sized pieces. There are my rules and gifts to you for growing a good life - even in the confusing soils of caregiving. Inside-out survival that is both practical and doable. Caregiving is love’s race. And that is the miracle of taking care. This book is about those more balanced choices.

Caring for a parent, spouse, or relative who cannot care for themselves due to age, infirmity, or illness is one of the noblest human activities. It’s also one of the most stressful, posing challenges that can be painful, confusing, frustrating, and deeply rewarding - sometimes all at once. When Caregiving Calls is an invitation to a deep conversation about caregiving and its meaning for you.

Elderly Parent Caregiver Guide is the ultimate guide for adult children who are or will become their parents’ caregivers. Filled with valuable information and ideas, this book offers hope, support, and plenty of practical advice for anyone caring for their elderly parents. As the author guides you through the maze of caregiving, she shares her knowledge as a nurse and examples from her own journey of caregiving for her elderly parents.

Approximately 90 percent of caregiving situations at home occur with little or no warning. This book outlines, from the author's experience over a six-year caregiving period, those things that you should consider to ease the stress of caregiving; these include financial planning to afford the cost of in-home private care, estate planning to ensure your heirs receive the maximum value of your estate, the benefits of long-term healthcare insurance, outfitting your home to minimize accidents, and obtaining household support so you can focus your time and efforts on the patient.

From a probability of death or life in a vegetative state after a severe traumatic brain injury, Nicole used a negative prognosis as a powerful motivator to build a successful career as a rehabilitation counsellor. She is a living testament to how the strategies outlined in this book can work for you. Has a brain injury thrown your life into a cycle of chaos and frustration? Are you worried about the future for yourself or someone you care about because of the impact of a brain injury?

In June of 2012, I suddenly found myself in a caregiving role with my dad overnight. Due to an accident my mother had, I stepped into a caregiving role that was unfamiliar and unexpected. I realized that you can know someone all your life but have no clue how to care for them physically, emotionally, and mentally. I also realized that caregiving stretches you in ways that you can't prepare for a head of time.

Surviving Myotonic Dystrophy is about Ann S. Woodbury’s struggle to care for her family who have a rare disease - myotonic dystrophy (DM). Ann’s four children and her husband have DM. In 1998, at the time of the diagnosis, even the doctors didn’t know all of the effects of DM or that it was a brain disorder. Listening to this book will take you on a journey of understanding this disease and its effects on Ann’s family members.

This heart-wrenching and triumphant love story is a tale of advocacy and caregiving. Donna's husband, David, stumbled into their bedroom, his hand covering a blood-filled eye from a brain hemorrhage. Donna called 911. David slipped into a coma. At that moment, Donna was thrust onto the path of caregiver for her best friend and the love of her life. In her debut memoir, Donna shares how a neurosurgeon said that David would make a "great organ donor".

After a life marbled with exploration, academia, and domesticity, the writer Valerie Lester retired to a residential hospice and set about enjoying the final act of her life. Yes. Enjoying. She knew just where she wanted to be, with whom, doing what, and she communicated this to her family and friends with clarity and consistency. She died nine weeks later, having engaged in dying with equanimity, curiosity, and even amusement.

Are you troubled by inexplicable pain for years? Have you made it a habit of taking painkillers? Are doctors helpless on your condition? Do you want to get rid of your pain right now? Are you looking for a treatment that is simple, affordable, and can be practiced on your own? In this practical and action-oriented book, patients share their experience and feedback on a variety of pains by trying a therapy that has a proven record of 2,500+ years, and is still serving billions of people all over the world.