検索キーワード： 高齢者介護・医療

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.

Mixing personal history, interviewee voices, and academic theory from the fields of care work, the sociology of work, medical sociology, and nursing, Taking Care of Our Own introduces us to the hidden world of family caregivers. By taking a multidimensional approach, Sherry N. Mong seeks to understand and analyze the types of skilled work that family caregivers do, the processes through which they learn and negotiate these new skills, and the meanings that both caregivers and nurses attach to their care work.

While the nightmare of Alzheimer’s is progressing at an alarming rate, society will never solve it if it continues on the same path. Dr. Zielonka’s simple seven-step solution to prevent the nightmare of Alzheimer’s is the logical, science-based solution to end the nightmare. Discover the real causes of Alzheimer's, learn about true brain detoxification, autophagy, type 3 diabetes, cellular health, and so much more.

Caring for someone who has Alzheimer’s or other forms of dementia is a daunting task that can leave most caregivers drained, strained, and depressed. Many find comfort in knowing they are not alone and in being able to share their experiences with someone who understands what they are going through. Caregivers need all the support and tools they can garner to help them survive this experience. Such was the reason for writing I Love You Always, which is an honest account of one family’s experiences from diagnosis and beyond.

Die An- und Zugehörigen sind die wichtigsten BegleiterInnen und engsten Vertrauten schwerkranker und sterbender PatientInnen. Im Bewusstsein, dass die gemeinsame Zeit begrenzt ist, wollen Angehörige einen Beitrag leisten und die PatientInnen in der oft leidvollen letzten Lebensphase begleiten. Dann liegt es an den Pflegenden und dem professionellen Betreuungssystem, sie in Achtung ihrer individuellen Bewältigungsstrategien dabei zu unterstützen.

Dr. Stefanie Green has been forging new paths in the field of medical assistance in dying since 2016. In her landmark memoir, Dr. Green reveals the reasons a patient might seek an assisted death, how the process works, what the event itself can look like, the reactions of those involved, and what it feels like to oversee proceedings and administer medications that hasten death. Deeply authentic and emotional, This Is Assisted Dying contextualizes the myriad personal, professional, and practical issues surrounding assisted dying by bringing listeners into the room with Dr. Green.

This is the story of 25-year-old Rochelle as she nurses her mum through a terminal brain tumour having already lost her dad to pancreatic cancer, aged 14. Based on the author's popular blog, this accessible guide provides a unique in-depth look at the reality of being a young carer.

A deeply moving story of what it means to care for those we love by best-selling author Kate Mosse, a celebration of older people and ageing, and of finding joy in the smallest acts of everyday caregiving. As our population ages, more and more of us find ourselves caring for parents and loved ones - some 8.8 million people in the UK. An invisible army of carers holding families together.

Caregiving for those who suffer from Parkinson's disease comes with many challenges, from how to deal with guilt and loneliness to avoiding burnout and figuring out what to expect from an unpredictable disease. When giving care, too often caregivers neglect their own well-being. Everything You Need to Know About Caregiving for Parkinson's Disease is not just about caring for your loved one, but also about taking care of yourself.

A diagnosis of Parkinson's disease is as disorienting as it is devastating. The Complete Guide for People with Parkinson's Disease and Their Loved Ones helps make sense of what comes next and what can be done, not just for those suffering from the disease, but for their family and friends as well.

Medicare for All is the leading proposal to achieve to universal health coverage in America. But what is it exactly? How would it work? More importantly, is it practical or practicable? This book goes beyond partisan talking points to offer a serious examination of how Medicare for All would transform the way we give, receive, and pay for healthcare in America.

In this book, board-certified neuropsychologist Dr. Michelle Braun inspires listeners to make lasting improvements by understanding the truth about brain health and provides expert guidance through the maze of conflicting media advice on supplements, brain games, nutrition, and exercise. She interviews eight leading brain-health experts, combining their insights with cutting-edge research to offer proven strategies to implement the five steps of the High-Octane Brain. Interactive exercises guide listeners to develop a personalized program for optimal brain health.

Press Ganey's chief nursing officer Christina Dempsey has worked everywhere in healthcare, from the ward floor to the hospital boardroom. She has also experienced the system as a patient and as a family member of a critically ill patient. In The Antidote to Suffering, this 30-year healthcare veteran and patient-experience thought leader argues that the key to improving healthcare is to reduce the suffering - physical, psychological, and emotional - of patients and caregivers alike through Compassionate Connected CareTM.

Despite being the wealthiest nation on earth, the United States spends much of its health-care money and resources pursuing the wrong goal: curing people after they get sick. In this provocative book, Nicholas J. Webb charts a bold new path that puts the focus not on reactionary treatment, but on anticipation and prevention.

End-of-life doula Anna Lyons and funeral director Louise Winter have joined forces to share a collection of the heartbreaking, surprising and uplifting stories of the ordinary and extraordinary lives they encounter every single day. From working with the living, the dying, the dead and the grieving, Anna and Louise reveal the lessons they’ve learned about life, death, love and loss. Together they’ve created a profound but practical guide to rethinking the one thing that’s guaranteed to happen to us all.