A revealing account of how families adapt to living with a chronically ill child What is it like to live with a child who has a chronic, life-threatening disease? What impact does the illness have on well siblings in the family? Myra Bluebond-Langner suggests that understanding the impact of the illness lies not in identifying deficiencies in the lives of those affected, but in appreciating how family members carry on with their lives in the face of the disease's intrusion. The Private Worlds of Dying Children, Bluebond-Langner's previous book, now considered a classic in the field, explored the world of terminally ill children. In her new book, she turns her attention to the lives of those who live in the shadow of chronic illness: the parents and well siblings of children who have cystic fibrosis. Through a series of narrative portraits, she draws us into the daily lives of nine families of children at different points in the natural history of the illness—from diagnosis through the terminal phase. In these portraits, as family members talk about their experiences in their own words, we see how parents, well siblings, and the ill children themselves struggle, in different ways, to contain the intrusion of the disease into their lives. Bluebond-Langner looks at how parents adjust their priorities and their idea of what constitutes a normal life, how they try to balance the needs of other family members while caring for the ill child, and how they see the future. This context helps us understand how well siblings view the illness and how they relate to their ill sibling and parents. Since the issues raised are not unique to cystic fibrosis but are common to other chronic and life-threatening illnesses, this book will be of interest to all who study, care for, or live with the seriously ill.

The practice of medicine has advanced dramatically in recent years, but the language used to discuss illness – by medical practitioners, patients and carers – has not kept pace. As a result, clinicians and, just as importantly, patients and their relatives and carers, are not able to communicate clearly in relation to illness. The upshot is misunderstanding and confusion on all sides. In this ground-breaking book, Dr Fergus Shanahan, an eminent gastroenterologist who has practised in Ireland, the United States and Canada, and published widely around the world, looks at memoirs of illness, and outlines the lessons we can learn from a better understanding of the words we use to describe illness. He looks at the ways in which language can act as a barrier with regard to illness, and proposes practical ways in which we can dismantle these barriers. The book is written for the general reader: as Dr Shanahan puts it himself, he is "enough of an expert to be wary of experts". The Language of Illness, part manifesto, part memoir, and part instruction manual, is an appeal for the use of clearer, more holistic language, by all those involved with, and affected by, illness. Like the great American poet-doctor William Carlos Williams, he aims to help us develop a new language by means of which we can develop a new way of living with illness – which is an integral part of the human condition. Put simply, it is a book for all those who care about caring.

A monthly magazine of political science and industrial progress.

This most current Tibetan-English dictionary surpasses existing dictionaries in both scope and comprehensiveness.

Tiredness, exhaustion, muscular pain, listlessness, shortness of breath with exertion, profuse sweating, morning stiffness, joint pains, concentration disorder, forgetfulness, depressive moods, aggressive behaviour, anxieties, visual disturbance, dizziness, sleeping disorder Toxoplasma gondii is a tiny parasite which infects 30 - 50% of the world's population. The symptoms listed above can result if it becomes chronically active - an alarming disease which affects far more people than has been historically assumed. In Germany about 800.000 patients could be affected, and it can be assumed that there are many more worldwide. Toxoplasma gondii is equipped with outstanding camouflage abilities, and often cannot be detected by our standard lab tests, and therefore the prevalence of Toxoplasma related diseases is vastly underestimated by medicine. The result is that many patients who suffer from this disease do not have a chronic active toxoplasmosis considered by their physician. Often these patients receive treatment for a supposed psychosomatic disorder, fibromyalgia, chronic fatigue, seronegative rheumatoid arthritis and many more rather than the treatment they need for their very real problem. This book shows, based on basic research and in a comprehensible and comprehensive way, how chronic active toxoplasmosis can be diagnosed and how health can readily be restored by the appropriate therapy. Many patients could have a significant benefit from this, if only medicine could free itself from the incorrect and outdated idea that Toxoplasma were harmless and that its activity could be diagnosed easily and securely by standard lab procedures.

Includes Abstracts section, previously issued separately.