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Author: Diane Waller Publisher: Routledge ISBN: 1134601263 Category : Psychology Languages : en Pages : 232
Book Description
This book has a multidisciplinary appeal, covering a range of therapies No existing text on this topic for arts therapies This book further expands the arts therapies, something Diane Waller has done in her previous books
Author: Diane Waller Publisher: Routledge ISBN: 1134601263 Category : Psychology Languages : en Pages : 232
Book Description
This book has a multidisciplinary appeal, covering a range of therapies No existing text on this topic for arts therapies This book further expands the arts therapies, something Diane Waller has done in her previous books
Author: Terra Diane Ziporyn Publisher: ISBN: 9780813518008 Category : Medical Languages : en Pages : 234
Book Description
You know you are sick, but no one can put a name to your illness. You go from doctor to doctor, seeking a diagnosis. You have lost track of the tests that have been done on you and failed to give an answer. People tell you, "It's all in your head." Your medical insurance refuses to pay the bills. You feel all the worse because no one believes that something is really wrong. Sound familiar? Countless people suffer enormous physical, psychological, and financial distress from nameless diseases--any disease that hasn't been diagnosed yet, or whose very existence is a matter of medical controversy: AIDS, in the early 1980s, for example, as well as chronic fatigue syndrome, postpartum depression, premenstrual syndrome, and dyslexia. Terra Ziporyn, a medical journalist, explains why it can be so hard to find out what's wrong, why it matters so much, and what to do about it. As her examples vividly show, people with nameless diseases often feel that the pain of not knowing is worse than the disease. Anxious to help their patients, doctors sometimes find themselves forced to put a name on a condition they can't identify. Yet, a disease that hasn't been diagnosed correctly cannot be treated effectively. Nameless Diseases draws on the first-hand accounts of real patients, case studies, medical literature, and the history of medicine (which is littered with the names of discarded diseases) to explore all these issues. Nameless Diseases is compelling reading for anyone who has ever suffered from a medical mystery or seeks to understand the limitations of medical progress. The book includes a list of organizations devoted to education the public about commonly overlooked, unrecognized, rare, or misdiagnosed diseases.
Author: B. Jain Publisher: B. Jain Publishers ISBN: 9788170217138 Category : Chronic diseases Languages : en Pages : 166
Book Description
The speciality of the book is its easy grasping language. It is so simple if anyone with a little knowledge of English goes through it, this will inspire him to read it continuously and he will go on reading it to the end.
Author: Sana Loue Publisher: Springer Science & Business Media ISBN: 144195659X Category : Medical Languages : en Pages : 1553
Book Description
There is increasing interest in the scientific literature on immigrant health and its impact on disease transmission, disease prevention, health promotion, well-being on an individual and population level, health policy, and the cost of managing all these issues on an individual, institutional, national, and global level. The need for accurate and up-to-date information is particularly acute due to the increasing numbers of immigrants and refugees worldwide as the result of natural disasters, political turmoil, the growing numbers of immigrants to magnet countries, and the increasing costs of associated health care that are being felt by governments around the world. Format and Scope: The first portion of the encyclopedia contains chapters that are approximately 25 to 40 manuscript pages in length. Each overview chapter includes a list of references and suggested readings for cross referencing within the encyclopedia. The opening chapters are: Immigration in the Global Context, Immigration Processes and Health in the U.S.: A Brief History, Alternative and Complementary Medicine, Culture-Specific Diagnoses, Health Determinants, Occupational and Environmental Health, Methodological Issues in Immigrant Health Research, Ethical Issues in Research with Immigrants and Refugees, Ethical Issues in the Clinical Context. The second portion of the book consists of alphabetical entries that relate to the health of immigrants. Entries are interdisciplinary and are drawn from the following fields of study: anthropology, demographics, history, law, linguistics, medicine, population studies, psychology, religion, and sociology. Each entry is followed by a listing of suggested readings and suggested resources, and also links to related terms within the whole book. Outstanding Features The book adopts a biopsychosocial-historical approach to the topics covered in the chapters and the entries. Each entry includes suggested readings and suggested resources. The chapters and entries are written graduate level that is accessible to all academics, researchers, and professionals from diverse backgrounds. We consider the audience for the entries to be well educated, but a non expert in this area. The primary focus of the book is on the immigrant populations in and immigration to magnet countries. References are made to worldwide trends and issues arising globally. In addition to the comprehensive subject coverage the text also offers diverse perspectives. The editors themselves reflect the multidisciplinary nature of the topics, with expertise in psychiatry, law, epidemiology, anthropology, and social work. Authors similarly reflect diverse disciplines.
Author: Chloe Atkins Publisher: Cornell University Press ISBN: 0801459656 Category : Medical Languages : en Pages : 247
Book Description
How Patients Think At age twenty-one, Chloë Atkins began suffering from a mysterious illness, the symptoms of which rapidly worsened. Paralyzed for months at a time, she frequently required intubation and life support. She eventually became quadriplegic, dependent both on a wheelchair and on health professionals who refused to believe there was anything physically wrong with her. When test after test returned inconclusive results, Atkins's doctors pronounced her symptoms psychosomatic. Atkins was told not only that she was going to die but also that this was her own fault; they concluded she was so emotionally deranged that she was willing her own death. My Imaginary Illness is the compelling story of Atkins's decades-long battle with a disease deemed imaginary, her frustration with a succession of doctors and diagnoses, her immersion in the world of psychotherapy, and her excruciating physical and emotional journey back to wellness. As both a political theorist and patient, Atkins provides a narrative critique of contemporary medicine and its problematic handling of uncertainty and of symptoms that are not easily diagnosed or known. She convincingly illustrates that medicine's belief in evidence-based practice does not mean that individual doctors are capable of objectivity, nor that the presence of biomedical ethics invokes ethical practices in hospitals and clinics. A foreword by Bonnie Blair O'Connor, who teaches medical students how to listen to patients, and a clinical commentary by Dr. Brian David Hodges, a professor of psychiatry, enrich the book's narrative with practical guidance for medical practitioners and patients alike.
Author: Diane Waller
Author: Diane Waller
Author: Samuel Hahnemann
Author: Samuel Hahnemann
Author: Terra Diane Ziporyn
Author: B. Jain
Author: Eduard von Grauvogl
Author: 
Author: J. Henry Allen
Author: Sana Loue
Author: Chloe Atkins