'The cold reality of my gender was dawning on me. It was motherhood that forced me to understand the timeless horror of our position. The reason women had not written novels or commanded armies or banked or doctored or explored or painted at the same rate as men. The cause was not, as I had been led to believe, that women had been prevented from working. Quite the opposite: We had been doing all of the work, around the clock, for centuries.'

After her first book was published to acclaim, journalist Megan K. Stack got pregnant and quit her job to write. She pictured herself pen in hand while the baby napped, but instead found herself traumatised by a difficult birth and shell-shocked by the start of motherhood.

Living abroad provided her with access to affordable domestic labour, and, sure enough, hiring a nanny gave her back the ability to work. At first, Megan thought she had little in common with the women she hired. They were important to her because they made her free. She wanted them to be happy, but she didn't want to know the details of their lives. That didn't work for long.

When Poonam, an Indian nanny who had been absorbed into the family, disappeared one night with no explanation, Megan was forced to confront the truth: these women were not replaceable, and her life had become inextricably intertwined with theirs. She set off on a journey to find out where they really come from and to understand the global and personal implications of wages paid, services received, and emotional boundaries drawn in the home. As she writes herself: 'Somebody should investigate. Somebody should write about all of this. But this is my life. If I investigate, I must stand for examination. If I interrogate, I'll be the one who has to answer.'

Breastfeeding rarely conforms to the idealized Madonna-and-baby image seen in old artwork, now re-cast in celebrity breastfeeding photo spreads and pro-breastfeeding ad campaigns. The personal accounts in Others' Milk illustrate just how messy and challenging and unpredictable it can be-an uncomfortable reality in the contemporary context of high-stakes motherhood in which "successful" breastfeeding proves one's maternal mettle. Exceptional breastfeeders find creative ways to feed and care for their children-such as by inducing lactation, sharing milk, or exclusively pumping. They want to adhere to the societal ideal of giving them "the best" but sometimes have to face off with dogmatic authorities in order to do so. Kristin J. Wilson argues that while breastfeeding is never going to be the feasible choice for everyone, it should be accessible to anyone.

Breastfeeding rarely conforms to the idealized Madonna-and-baby image seen in old artwork, now re-cast in celebrity breastfeeding photo spreads and pro-breastfeeding ad campaigns. The personal accounts in Others' Milk illustrate just how messy and challenging and unpredictable it can be-an uncomfortable reality in the contemporary context of high-stakes motherhood in which "successful" breastfeeding proves one's maternal mettle. Exceptional breastfeeders find creative ways to feed and care for their children-such as by inducing lactation, sharing milk, or exclusively pumping. They want to adhere to the societal ideal of giving them "the best" but sometimes have to face off with dogmatic authorities in order to do so. Kristin J. Wilson argues that while breastfeeding is never going to be the feasible choice for everyone, it should be accessible to anyone.

This indispensable guide aims to be a one-stop-shop for the huge percentage of the population who, now or later, find themselves in a caring role, whether that involves shopping for a housebound neighbour, or giving up work to care full-time for a disabled child or confused parent. This book will also help carers care for themselves. It looks at the difficult feelings that go hand in hand with caring, including how relationships are affected. There's guidance on what to do when a carer stops coping, and how to prepare emotionally and practically for the time when caring comes to an end.

Reducing the use of psychotropic drugs in the symptomatic treatment of dementia is key to successfully implementing compassionate, person-centered practices in your organization-and this book shows clearly why and how it can be done. The revised second edition of this award-winning resource introduces new research, language, and examples to reinforce the core message that antipsychotic medications are not the solution to ease the distress experienced by individuals living with dementia. Outlined here is the information and inspiration you need to provide alternative solutions for individualized support and care. IN THIS BOOK YOU'LL FIND: enlightened models to reduce the use of harmful medications by understanding and addressing underlying causes of distress a pathway to accomplish drug-reduction goals established by the U.S. Centers for Medicare and Medicaid Services (CMS) discussions of new drug studies and government reports on the dangers and ineffectiveness of antipsychotic medications in the treatment of people with dementia recognized best practices in dementia care and their transformational results case studies, stories, and other educational tools illustrating positive outcomes for people living with dementia ways to respond to anxiety and distress in people with dementia . An essential read for all professionals in long-term care, including administrators, medical directors, nursing staff, psychologists and counselors, social workers, and policy makers, the ideas presented here call for a revolution in dementia care-one that always puts the person first.

As the average lifespan increases, so does the number of living generations, a recipe for some potentially complex family issues. This book offers therapeutic strategies to navigate the unique dynamics and experiences of today's aging families, from the "sandwich generation" and caregiver burdens to divorce, bereavement, and much more.

Ann Burack-Weiss explores a rich variety of published memoirs by authors who cared for ill or disabled family members. Contrary to the common belief that caregiving is nothing more than a stressful situation to be endured, memoirs describe a life transforming experience-self-discovery, a reordering of one's priorities, and a changed view of the world. "The Caregiver's Tale" offers insight and comfort to individuals caring for a loved one and is a valuable resource for all health care professionals.

Identifying common themes, Burack-Weiss describes how the illness career and social meaning of cancer, dementia, HIV/AIDS, mental illness, and chemical dependence affect the caregiving experience. She applies the same method to an examination of family roles: parents caring for ailing children, couples and siblings caring for one another, and adult children caring for aging parents.

Jamaica Kincaid, Sue Miller, Paul Monette, Kenzaburo O?, and Philip Roth are among the many authors who share their caregiving stories. Burack-Weiss provides an annotated bibliography of the more than one hundred memoirs and an accompanying chart to help readers locate those of greatest interest to them.

The current imperative to make healthcare and long-term care services more person centered is hampered by leaders and providers who are stuck in old management paradigms. Transformational leader Nancy Fox takes you through real-life experiences and succinct, powerful lessons in human, social, and organizational behavior to help teach the skills needed for creating and sustaining high-performing caring communities populated with engaged and committed staff. Valuable features include: Key principles illustrated with compelling stories Assessment and change-guiding tools Grounding in the modern sciences of human behavior Hopeful, encouraging, and inspirational message 2018 National Mature Media Award (Merit Award Winner)

Whether You Are A Friend Or Relative Of Someone Suffering From Cancer, This Book Offers Help. The Only Book Available To Provide Both The Professional Healthcare Giver's And Patient's Views, 100 Questions & Answers About Caring For Family Or Friends With Cancer, Second Edition Gives You Authoritative, Practical Answers To Your Questions About Treatment Options, Home Care, Insurance, Quality Of Life And More. This Book, Completely Revised And Updated For This New Edition, Is An Invaluable Resource For Family And Friends Who Are Coping With The Physical And Emotional Turmoil Of Cancer.

Few experiences stir the emotions and throw a person into crisis as illness does. If affects not only the body but also the spirit and soul. Illness is about life and death, fear and hope, love and conflict, spirit and body. And yet, the healthcare system is not structured around these considerations--our doctors and other medical professionals are not trained to deal with the whole person. Care of the Soul In Medicine is Moore's manifesto about the future of healthcare. In this new vision of care, Moore speaks to the importance of healing a person rather than simply treating a body. He gives advice to both healthcare providers and patients for maintaining dignity and humanity. He provides spiritual guidance for dealing with feelings of mortality and threat, encouraging patients to not only take an active part in healing but also to view illness as a positive passage to new awareness. While we don't fully understand the extent to which healing depends on attitude; it has been shown that healing needs to focus on more than the body. The future of medicine is not only in new technical developments and research discoveries; it is also in appreciating the state of soul and spirit in illness.

Gentle Dying is a wonderful tool to help anyone with a terminal illness or those caring for someone who is dying. A modern death often means being cared for by strangers in an unfamiliar place, away from home where the emphasis is on preventing death rather than embracing it in a compassionate way. Gentle Dying is about switching the focus from cure to human touch and emotional support. This title is full of practical advice and simple techniques to support the dying process for carers and those that are dying. "Gentle Dying" will show you that death isn't something to be feared but a rite of passage, a time of gentle reflection, optimism and a preparation for the next life.

These first-person accounts portray, with thoughtfulness and clarity, a wide range of caregiver experiences: the possibility of deepening relationships; the opportunity for forgiveness; the ability to reach out and to look within to find strength; the sorrow of watching a parent grow old; and the chance to say goodbye.

Sensory Stories contain just a few lines of text, and are brought to life through a selection of meaningful sensory experiences. They have been found to be highly effective in helping care for people with dementia, and can enable them to engage with their memories, life history and more, in a way that would otherwise not be possible. Despite these benefits, there is very little guidance on how to incorporate this approach in everyday care. This book looks at how sensory engagement can help someone with dementia feel safe and secure, minimise their anxieties, support their cognitive abilities, as well as other benefits. Full of practical advice, this book provides everything you need to put Sensory Stories into practice. Written at a level suitable for both family members and practitioners, this innovative book will be invaluable for anyone supporting a person with dementia.

With contributions from an esteemed otolaryngologist, talented photographer, and multidisciplinary specialists, Mastering Medical Photography of the Head and Neck demystifies the process of medical photography. The succinct text and high quality images serve as a practical primer for physicians without any prior photographic background to learn techniques specific to photography for facial surgery and otolaryngology. Understanding the basic techniques of photography for medical documentation is useful-for speaking at medical conferences, publishing in journals, and settling insurance claims. These situations typically require inclusion of well-defined anatomical images. Furthermore, head and neck photography is an educational tool to explain specific procedures to patients prior to undergoing surgery. Key Highlights Comprehensive coverage of standard external anatomy, with smaller sections on endoscopic photography and intraoperative photography Ancillary online content including more than 150 high quality photographs and 8 instructional videos supplement the text Sample comparative photographs illustrate the potential to create stellar results using several different camera systems Each photograph extensively annotated with relevant camera and lighting settings Recommendations provided for image archiving, organization, and processing Visually rich and practical, this step-by-step guide of medical photographic techniques is an essential tool for all physicians who treat diseases and disorders of the ear, nose, throat, and related head and neck structures.

First published in 1980, "Disabled" examines the practical difficulties faced by people with a range of disabilities, and offers a range of practical solutions.
From the psychological challenges faced by those with disabilities, to special needs for housing, communications, travel, to diet and nutrition, health care, sport, legal aid and educational opportunities, Lewis Forbes' offers an invaluable primer of disabled experience.
"Disabled" remains a useful practical guide and reference to a host of long-term and everyday challenges.