Myalgic encephalomyelitis (ME) and chronic fatigue syndrome (CFS) are serious, debilitating conditions that affect millions of people in the United States and around the world. ME/CFS can cause significant impairment and disability. Despite substantial efforts by researchers to better understand ME/CFS, there is no known cause or effective treatment. Diagnosing the disease remains a challenge, and patients often struggle with their illness for years before an identification is made. Some health care providers have been skeptical about the serious physiological - rather than psychological - nature of the illness. Once diagnosed, patients often complain of receiving hostility from their health care provider as well as being subjected to treatment strategies that exacerbate their symptoms. Beyond Myalgic Encephalomyelitis/Chronic Fatigue Syndrome proposes new diagnostic clinical criteria for ME/CFS and a new term for the illness - systemic exertion intolerance disease(SEID). According to this report, the term myalgic encephalomyelitis does not accurately describe this illness, and the term chronic fatigue syndrome can result in trivialization and stigmatization for patients afflicted with this illness. Beyond Myalgic Encephalomyelitis/Chronic Fatigue Syndrome stresses that SEID is a medical - not a psychiatric or psychological - illness. This report lists the major symptoms of SEID and recommends a diagnostic process.One of the report's most important conclusions is that a thorough history, physical examination, and targeted work-up are necessary and often sufficient for diagnosis. The new criteria will allow a large percentage of undiagnosed patients to receive an accurate diagnosis and appropriate care. Beyond Myalgic Encephalomyelitis/Chronic Fatigue Syndrome will be a valuable resource to promote the prompt diagnosis of patients with this complex, multisystem, and often devastating disorder; enhance public understanding; and provide a firm foundation for future improvements in diagnosis and treatment.

Complete Coverage of chronic fatigue syndrome The Handbook of Chronic Fatigue Syndrome provides authoritative coverage of Chronic Fatigue Syndrome (CFS). A leading group of international contributors present up-to-date information and guidance to improve the understanding, proper identification, and treatment of this debilitating disease. The handbook's comprehensive, multidisciplinary format draws on the medical, as well as mental health-related, aspects of CFS, including: History, diagnosis, and classification Phenomenology Symptomatology Assessment Treatment and intervention Pediatric and community issues Topics covered include complexity of diagnosis, social effects of chronic disorders, and a variety of treatment techniques, including phase-based therapy, cognitive-behavioral therapies, exercise therapy, and nutritional approaches. An insightful and unique resource, the Handbook of Chronic Fatigue Syndrome is an enlightening book for all mental health professionals, including psychologists, social workers, and counselors, as well as medical personnel, such as nurses, physicians, and physical-occupational therapists.

Written by the nation's most recognized CFIDS' authority, this book is the definitive, up-to-date guide to the history, symptoms, effects, theories, treatment, continuing research, and recent advances on CFIDS. Now anyone touched by this devastating illness can have the solid information they need to understand, treat, and live with CFIDS.

Chronic Fatigue Syndrome (CFS) is a complex, debilitating disorder, yet few current scientific biomedical books are available on the subject. The nonspecific symptoms, lack of diagnostic tests, and uncertainty as to the cause or causes of CFS make the disease that much more baffling. Chronic Fatigue Syndrome: A Biological Approach represents a monu

You’ve been repeatedly poked, prodded, tested and scanned, yet, despite how awful you feel, your doctor, like many of your friends, co-workers, and family members have begun dropping subtle (and some not-so-subtle) hints that they think it’s “all in your head.” Maybe you’re one of the lucky few CFS sufferers who’ve received an accurate diagnosis but nothing your health care provider does seems to help. Well, you’re not alone. According to recent estimates, of the approximately 800,000 Americans with CFS, more than 90% have been misdiagnosed, dismissed, or are not receiving proper treatment. Don’t despair, help has arrived. Written by a national expert who has successfully treated scores of CFS patients in her own practice, Chronic Fatigue Syndrome for Dummies gives you the knowledge and tools you need to beat CFS and get back to living a normal life. In plain English Doctor Susan Lisman fills you in on: What CFS is, how you get it, and how it effects your body Its major symptoms and warning signs Getting an accurate diagnosis Avoiding situations that might be making you sicker Teaming up with the right doctor and crafting a treatment plan The most effective drugs, therapies and alternative approaches Coping with CFS in your personal and professional lives Packed with checklists, self-tests, questionnaires, and other powerful tools, and featuring many inspiring real-life stories of patients who’ve licked CFS, Chronic Fatigue Syndrome for Dummies puts you on the road to recovery.

A guide for practitioners, scientists, and patients, Clinical Management of Chronic Fatigue Syndrome provides an insightful overview of current clinical management of CFS and guidelines for dealing with the disease and its compounding issues. It also provides, especially for patients, an objective framework in which they can approach the confusing psychological and physical ramifications of the disease so that they may sort through possibly misleading information on current treatments. CFS has been the focus of an increasing number of research investigators seeking to unravel the enigmatic interrelationship of immunologic, neurologic, endocrinologic, and psychologic abnormalities associated with this debilitating disorder. Because many practical issues have been underestimated by the medical community, and considerable misinformation exists regarding the appropriate evaluation and management of the CFS patient, the American Association for Chronic Fatigue Syndrome (AACFS) held its first clinical conference to address this problem, the results of which are presented in this book. Each chapter, based on material presented at the October 1994 conference has been completely updated and revised during a peer review process, making Clinical Management of Chronic Fatigue Syndrome a useful and up-to-date guide for practitioners and scientists, as well as patients. Despite the potential of nervous system functional assessments, the diagnosis of CFS continues to be a major problem because a consensus diagnostic tool is lacking, and the monitoring of the disorder is based primarily on patient report. Moreover, dealing with the financial aspects of CFS continues to be a major problem for patients, so professionals with experience dealing with insurance companies explored this issue, as well as ways in which CFS could be considered in a broader perspective of health care, particularly focusing on governmental involvement. The chapters provide an insightful overview of current clinical management of patients and guidelines for dealing with the disease and its complicating issues. General topics of relevance covered in the book's chapters include a review of advances in basic science neurocognitive dysfunction diagnostic issues use of alternative/complementary medicine cognitive behavioral and rehabilitative therapies financial issues advances in governmental role women's issues In this book, practitioners and scientists in the field and patients living with CFS have a thorough resource on current clinical and patient management of the disease.

Chronic Fatigue Syndrome is one of the most enigmatic medical disorders of our time, striking adults most often in their most productive years. With the controversial debate over cause and treatment of the illness in mind, the authors seek to unravel many of the questions surrounding the disorder and its features and characteristics. Integrating an overview of the latest research with patients' personal experiences, they look at CFS in relation to: * clinical features * personal and economic implications * biological and psychosocial factors * experiencing symptoms * coping with the illness. This book will provide hope for people with chronic fatigue syndrome and will assist health professionals in working with people with CFS to improve their quality of life.

Try cutting-edge treatments tested by international experts!Chronic Fatigue Syndrome: Critical Reviews and Clinical Advances presents the latest research and clinical findings of internationally recognized experts in chronic fatigue syndrome (CFS) and myalgic encephalomyelitis (ME). Edited by the organizer of the Second World Congress on Chronic Fatigue Syndrome and Related Disorders, this work focuses on the exciting research presented there. Starting with a thorough review of new literature, the volume continues with scientific reports of research on these mysterious, devastating illnesses. Chronic Fatigue Syndrome dispels some of the mystery and offers new avenues for research and treatment, as well as specific treatment regimes to combat the chlamydia and rickettsiae infections that sometimes underlie CFS/ME.Discover the latest theories on the etiology, physiology, and treatment of CFS/ME, including: links between CFS/ME and rheumatoid arthritis, Gulf War Illness, and fibromyalgia the disease's effects on neurologic function and the immune system the rhythms of fatigue and wellness caused by the disease human herpes virus 6 infection in patients with CFS/ME case reports on stress and hormones in CFS/ME patients role of rickettsiae and chlamydiae in the psychopathology of chronic fatigue The innovative research in Chronic Fatigue Syndrome: Critical Reviews and Clinical Advances will keep your knowledge of these disorders current and up-to-date and enable you to offer your CFS/ME patients the best possible care.