This book is intended to provide to the eye movement desensitization and reprocessing (EMDR) clinician advanced tools to treat children with complex trauma, attachment wounds, and dissociative tendencies. It covers key elements to develop case conceptualization skills and treatment plans based on the adaptive information processing (AIP) model. A broader perspective is presented by integrating concepts from attachment theory, affect regulation theory, affective neuroscience, and interpersonal neurobiology. These concepts and theories not only support the AIP model, but they expand clinicians’ understanding and effectiveness when working with dissociative, insecurely attached, and dysregulated children. The book presents aspects of our current understanding of how our biological apparatus is orchestrated, how its appropriate development is thwarted when early, chronic, and pervasive trauma and adversity are present in our lives, and how healing can be promoted through the use of EMDR therapy. In addition, it provides a practical guide to the use of EMDR within a systemic framework. It illustrates how EMDR therapy can be used to help caregivers develop psychobiological attunement and synchrony as well as to enhance their mentalizing capacities. Another important goal of the book is to bring strategies from other therapeutic approaches, such as play therapy, sand tray therapy, Sensorimotor Psychotherapy, Theraplay, and Internal Family Systems (IFS) into a comprehensive EMDR treatment, while maintaining appropriate adherence to the AIP model and EMDR methodology. This is done with the goal of enriching the work that often times is necessary with complexly traumatized children and their families.
Your search for all content returned 56 results
This book delivers analyses of 30 core concepts that define nursing theory, research, education, and professional practice. Grounded in the concept analysis framework developed by Walker and Avant, the book clearly demonstrates how concepts are used to build theory, support research, and improve education and professional practice. Expert authors from clinical and research disciplines focus on the core of nursing-- the nurse-patient relationship--grouping concepts into the categories of patient/client-focused concepts, career-focused concepts, and organizational/systems-focused concepts. The concept analyses follow a specific method, with defining attributes, antecedents, and consequences given. It talks about the personal characteristics of patients/clients experiencing health/illness. These concepts include hardiness, hope, motivation and self-motivation. The book then explains the caregiver-focused concepts such as anxiety, caregiver burden, clinical autonomy, compassion fatigue, cultural competence, decision making, emotional intelligence, empathy and so on. It also presents analysis of concepts pertinent to nurse workaround, commitment, teamwork, transformational leadership, work engagement, and nurse manager accountability. Nurse workarounds are described as nurses devising an alternative work procedure to address a block in the workforce, even though these alternatives are deviations from policies, procedures, and work processes. The book also includes diagrams of characteristics across concepts for comparison. It helps nurse scholars to develop a sophisticated analytic ability and provide graduate nursing students with a foundation for developing a DNP capstone or PhD research project.
The primary objective of this book is to describe how a relationship-building approach can be used in the delivery of child welfare services to kinship caregivers and the children who reside with them. To accomplish this objective, the book entails a review and evaluation of the three major child welfare goals: protection, permanency, and well-being. Specifically, it explores how these three goals can be better achieved when informed by a relationship-building approach. The book assists child welfare practitioners in framing how they view kinship caregivers and acquiring knowledge and skills about the use of relationship-building models (emanating from social work practice perspectives) and is designed to increase positive outcomes for maltreated children. The multifaceted issue of relative caregiving is in dire need of attention from virtually every social work service domain level. Specifically, micro-level practice interventions are needed, as well as mezzo-level programming for particular groups and macro-level policy redesigns that support services to relative caregivers are also warranted. The book integrates practice, policy, and research, and includes study tools and resources (a glossary, discussion questions, and activities for ongoing learning) and thus can be easily incorporated into such courses as child welfare, family practice, social work and the law, social work practice, cultural diversity, policy, child welfare integrative seminars, and special topic electives.
The concept of trauma-informed care in the neonatal intensive care unit (NICU) aligns with the mission of transdisciplinary neonatal colleagues around the world. This book provides the steps to adopt and implement a trauma-informed paradigm in their NICU. Part I of the book reviews trauma and trauma-informed care and evidence-based updates to the core measures for age-appropriate care. Core measures for age-appropriate care in the NICU define measurable, evidence-based best practices in developmentally supportive, whole-person care. Integrating the concept of trauma-informed care operationalized by the core measures for age-appropriate care in the NICU meets the developmentally sensitive and critical needs of the hospitalized infant, and aims to restore health through healing relationships and integrative care. Part II discusses each core measure set, providing updated evidence-based research to substantiate the practice recommendations, and includes practical implementation strategies and resources to support success. This part presents guidelines for the healing environment; guidelines for the family as well as for pain and stress prevention, assessment and management; guidelines for protected sleep including discussions on safe sleep environment and sudden infant death syndrome (SIDS); guidelines for the activities of infants’ daily living; and guidelines for family collaborative care while explaining the correlation between acute stress disorder (ASD) symptoms in NICU parents and posttraumatic stress disorder (PTSD) and depression. Part III addresses the topic of trauma and the neonatal clinician’s experience with guidelines and recommendations to support and promote self-care for the clinicians.
This book is intended as an approachable reference guide for one of the most common neurological conditions, Parkinson’s disease and the spectrum of Parkinson-like syndromes. Parkinson’s disease is a slowly progressing neurodegenerative disease that primarily affects older adults. The book outlines the new advances in the management and treatment of the Parkinson patient, comparing risks and benefits as well as efficacy of new and older anti-Parkinson’s disease drugs. The task of diagnosing Parkinson’s disease and providing comprehensive guided treatment requires a multidisciplinary approach. Those involved in the diagnosis and care of the patient include neurologists; nurse practitioners; nurses; physical, occupational, and speech therapists; sleep medicine specialists; neuropsychologists; psychiatrists; radiologists; nutritionists; and social workers. The book is divided into seventeen chapters spread across four sections. The first section, Parkinson’s Disease, describes the following: neurobiology of Parkinson’s disease, patient exam, idiopathic Parkinson’s disease, imaging and advanced studies, neuropsychological analysis, and additional evaluations. The second section, Parkinsonisms, discusses Parkinson-plus syndromes and other Parkinsonisms. The third section, Treatment of Motor and Non-Motor Symptoms in Parkinson’s Disease, describes treatment of motor symptoms and non-motor symptoms such as autonomic dysfunction, sleep disturbances, disturbances of thought, and neuropsychiatric symptoms. The final section, Alternative Therapies and Other Considerations, talks about exercise, complementary and alternative therapies, nutrition, and caregiver burden. The book provides additional details such as Hoehn and Yahr Scoring scale, drugs that should be avoided in patients with Parkinson’s disease, patient-prepared information, standardized intake questions for evaluating a Parkinson’s patient, standardized questions for evaluating the patient in a follow-up visit, and resources in the appendices.
This book provides innovative ways to incorporate aging content into courses, trainings, and workshops for students or professionals. It presents activities which offer hands-on approaches to engage students of all backgrounds–from social workers to family caregivers, medical students to demographers, nurses to community planners, personal care attendants to students in introduction to gerontology courses. These faculty-tested, peer-reviewed educational activities cover topics ranging from physical aging, media, and demographic portrayals of older adults to disaster planning, public policy, and diversity among older adults. The book includes 32 unique and interesting activities. Each activity comes with detailed instructions, basic back-ground information, a materials list, and an explanation of how the specific content aligns with one or more of the Association for Gerontology in Higher Education (AGHE) competencies for undergraduate and graduate education in gerontology. The book is divide into eleven chapters. The first chapter explores teaching courses on aging, and the potential of experiential learning activities to engage students. The second chapter discusses ageism and aging in the media. The next four chapters talk about dementia, demography, health care, and housing for older adults. The seventh chapter describes physical aging. Chapter 8 analyzes public policy and aging. Chapter 9 describes positive interactions with older adults. Chapter 10 explains research projects and papers, and the final chapter discusses spirituality.
As incredible it is to us to consider how far the ketogenic diet has come in 100 years, it is equally amazing to realize that this Ketogenic Diets book is now in its seventh edition, 25 years after its first publication by Demos Health. This edition continues the recent tradition of updating us every five years on what’s new and noteworthy in the use of ketogenic diets, and the authors appreciate many comments from parents and patients that this book has become a “gold standard” guide. The author’s intention is to continue to make this book helpful for everyone on the ketogenic journey: parents, patients, caregivers for sure, but also physicians, dietitians, scientists, nurses, and social workers. They consider it a success if it helped make ketogenic diet therapies more approachable and effective for you, your family, and/or your ketogenic diet center. Now, with over 10 years of experience, this seventh edition includes all-new material and guidance for adults starting dietary therapies, including information from a recent international expert guideline publication. For children, the 2009 pediatric ketogenic diet consensus statement was recently revised in 2018; details and changes from this important paper will be seen throughout this book. New chapters include exogenous ketones, a fifth ketogenic diet entitled the “modified ketogenic diet”, intermittent fasting, the influence of ketogenic diets on the gut microbiome, and expanded use for infants. Much of the final editing of this edition occurred during the COVID-19 pandemic, and the authors included information learned about how to manage ketogenic diet therapies in a crisis/pandemic situation. Finally, as ketogenic diets continue to be used by more countries every year, this book highlights some of the international recipes, cultures, and even scientific initiatives of this worldwide expansion.
This book provides education, tools, and support for caregivers who care for high-risk maternal and neonatal patients so that they too can learn how to effectively and successfully provide high quality care coordination and family-centered care to patients and families in their daily care practice. It looks at the high-risk antepartum patient stay, the high-risk delivery, the NICU admission, the NICU journey, discharge home, special situations in the NICU, palliative and bereavement in the perinatal and neonatal period, and caring for the caregiver. Each chapter focuses on one of these areas and provides real examples of care situations, positive care coordination efforts, and exceptional psychosocial support that were provided to patients and families. One may even come across a few examples of where care coordination and psychosocial support did not go as well as it could have. Eighteen families have shared their very personal stories and experiences to increase the depth of the book and their words have not been altered. The book is intended primarily for the nursing and nurse practitioner audience. It is organized into six parts comprising 16 chapters. The first part presents an overview of nursing history, care coordination, and family-centered care. The second part discusses supporting patients in high-risk pregnancy and delivery. The third part deals with supporting patients and families in the NICU. The fourth part provides description on supporting patients with special challenges in the NICU. The fifth part talks about bereavement and palliative care support. The final part discusses therapeutic strategies for caregivers and patients.
Despite the increasing awareness of delirium as a cause of altered mental status, many of these patients will not be diagnosed as such. This book has evolved out of more than four decades of the author's gerontological nursing experiences caring for people with dementia in a wide range of clinical settings, including acute care, long-term care, and home and community settings. The basic premise is that although the short-term nature of the care setting focuses on nursing interventions for immediate medical problems, nurses have numerous opportunities to incorporate dementia-specific interventions in care plans. The second edition includes two new chapters on the Emotional Needs of People with Dementia and Self-Neglect and Elder Abuse. The book has eighteen chapters organized into six parts. Part I discuss types of dementia and other commonly occurring conditions that have similar manifestations; the chapters focus on nursing responsibilities for assessment and management of patients whose mental status is altered by underlying conditions such as dementia or delirium. Part II describes how nurses can apply a person-centered approach to address dementia-related issues. Part III discusses nursing care issues at various stages of dementia, and Part IV provides information about addressing emotional and behavioral issues. Part V describes considerations related to specific care settings and provides information about nursing strategies for daily care, safety, and pain. Chapters in Part VI are a guide to broader aspects of care for people with dementia, including self-neglect and elder abuse and ethical and legal issues. The last chapter discusses nursing strategies to address the needs of caregivers of people with dementia. A major emphasis throughout the text is on relatively simple interventions that nurses can incorporate in their discharge plans to teach families and care partners about sources of information and support to address the needs of people with dementia.
This book deals with a number of issues and strategies for counseling people with disabilities. It allows counselors and other related health professionals to learn from the writings of 16 people with disabilities across North America. The book provides information on how other professional disciplines perceive and are trained to view disability. It discusses the medical and psychosocial aspects of caregiving in the country and highlights some of the most difficult decisions individuals and families may have to make in this process. The book is organized into four parts containing sixteen chapters. Part I explores disability from a sociological perspective. The topics covered are: the history of how people with disabilities have been viewed and treated in society; attitude formation, societal attitudes, and myths about disabilities; culturally different issues and attitudes toward disability; and attitudes toward disability by specific special interest and occupational groups. Part II focuses on the psychology of disability surrounding the individual and his or her family. The topics address: theories of adjustment to disability by the individual; family adaptation across cultures toward a loved one who is disabled; sexuality and disability; and the psychosocial world of the injured worker. Part III addresses pertinent topics concerning psychosocial issues of disability. The topics include: disability and quality of life over the life span; implications of social support and caregiving of loved ones with a disability; and thriving versus succumbing to disability: psychosocial factors and positive psychology. Part IV addresses counseling strategies and insights for working with persons with disabilities. The topics discuss: which counseling theories and techniques work best with different disability populations and why; social justice, oppression, and disability; counseling families in the community; ethical responsibilities in working with persons with disabilities and our duty to educate; and basic dos and don’ts in counseling persons with disabilities.