Hughes Syndrome: The Antiphospholipid Syndrome, A Guide for Students provides an in-depth analysis into the main effects of Hughes Syndrome. In 1983, Dr Graham Hughes, and his team in London, described a syndrome and subsequently developed simple blood tests to diagnose the condition. This syndrome is characterised by thrombosis (both in limbs and internal organs), headaches, memory loss, strokes and, in pregnant women, placental clotting and recurrent miscarriage. The syndrome, now known worldwide as Hughes Syndrome, or the Antiphospholipid Syndrome, is common - being responsible for example, for up to 1 in 5 cases of young stroke and more importantly, it is treatable. Hughes Syndrome: The Antiphospholipid Syndrome, A Guide for Students details the effects of Hughes Syndrome on the major organs, making it a valuable reference tool for students in training.

G Serratrice Les organisateurs de ce symposium en ont choisi le titre: " Syndrome de fatigue chronique ", titre dont chacun des termes doit etre defini avec precision, ce qui, paradoxalement, n'est pas aise. Syndrome: ensemble de symptomes ou de signes s'observant dans des etats pathologiques differents mais ne determinant pas a eux seuls la cause de la maladie. Fatigue: symptome plus ou moins exprime, moteur, intellectuel, sensoriel, sexuel selon les cas. Mais aussi signe traduit par l'incapacite a maintenir une force initiale pendant un effort continu. Ceci separe la fatigue de la faiblesse, qui est l'incapacite a produire une force. Stricto sensu, l'asthenie et la fai- blesse sont equivalentes. Mais l'usage, tout au moins en France, fait souvent confondre asthenie et fatigue. Chronique enfin. C'est sans doute sur cet adjectif que s'accumulent les plus grandes ambiguites. La simple lecture du programme d'aujour- d'hui indique la difficulte de se situer entre une definition stricte - chronique signi- fiant " permanent ", " qui dure " - et l'usage, surtout dans l'acception anglo-ameri- caine, qui reserve l'appellation de chronique a une forme particuliere de fatigue, parfois dite post-virale. En fait, il convient, pour une claire comprehension, de sepa- rer ce que l'on pourrait nommer les etats de fatigue chronique " determines " dans leur mecanisme et ceux qui restent " indetermines ". A l'evidence, les etats dont le mecanisme est determine sont tres diversifies.

Hepatologie konkret - komplett - kompakt Erfahrene Kliniker fuhren ubersichtlich, zusammenfassend und gewichtet durch das Gebiet der Leber- und Gallenwegserkrankungen. Komplexe Inhalte werden anschaulich, klar und gut verstandlich dargestellt. Differenzierte Diagnostik und Therapie: Was - Wann - Warum Neueste diagnostische und therapeutische Konzepte Rasche, prazise Information Konzentration auf krankheitsbezogene klinische Informationen Therapie individuell abgestimmt auf Ihre Patienten Standards Therapie fur multimorbide Patienten Loesungen fur typische und atypische Therapieprobleme Zur sofortigen sicheren Anwendung Entsprechend der neuesten Studien und Leitlinien aller wichtigen deutschen, europaischen und amerikanischen Fachgesellschaften

Whether in movies, cartoons, commercials, or even fast food marketing, psychology and mental illness remain pervasive in popular culture. In this collection of essays, domestic and international scholars from a range of fields explore representations of mental illness across various mediums of popular culture. Contributors address how forms of psychiatric disorder have been addressed in film, on stage, and in literature, examine how genres of popular culture are utilized to communicate our often confusing and conflicted relationship with the mentally ill, and investigate popular culture's reflection of mental illness around the world. Analyses of sources as disparate as the Batman films, Broadway musicals and Nigerian home movies reveal how definitions of mental illness, mental health, and of psychology itself intersect with discourses on race, gender, law, capitalism, and globalization.

Why do racial and ethnic controversies become attached, as they often do, to discussions of modern genetics? How do theories about genetic difference become entangled with political debates about cultural and group differences in America? Such issues are a conspicuous part of the histories of three hereditary diseases: Tay-Sachs, commonly identified with Jewish Americans; cystic fibrosis, often labeled a "Caucasian" disease; and sickle cell disease, widely associated with African Americans.

In this captivating account, historians Keith Wailoo and Stephen Pemberton reveal how these diseases -- fraught with ethnic and racial meanings for many Americans -- became objects of biological fascination and crucibles of social debate. Peering behind the headlines of breakthrough treatments and coming cures, they tell a complex story: about different kinds of suffering and faith, about unequal access to the promises and perils of modern medicine, and about how Americans consume innovation and how they come to believe in, or resist, the notion of imminent medical breakthroughs.

With Tay-Sachs, cystic fibrosis, and sickle cell disease as a powerful backdrop, the authors provide a glimpse into a diverse America where racial ideologies, cultural politics, and conflicting beliefs about the power of genetics shape disparate health care expectations and experiences.

Eight out of ten blind people live in the developing world, and the vast majority of this blindness is preventable. These facts constitute A Journey in Sight, a project by photographer Jarret Schecter who was astounded by the conditions he witnessed in Burkina Faso, one of the world's poorest countries. Here Schecter illuminates the link between poverty and blindness--40 million people suffer from preventable blindness that arises from Vitamin A deficiency, unsanitary conditions, minimal health care, and other issues. Presented are touching and heartfelt images of these persons in their habitats. But this isn't merely a journey into the world's less fortunate regions--a percentage of each sale of A Journey in Sight will be donated to Orbis, an organization that provides free or inexpensive eye treatment to people who needlessly suffer from preventable blindness.

Severe pain, debilitating fatigue, sleep disruption, severe gastrointestinal distress these hallmarks of chronic illness complicate treatment as surely as they disrupt patients lives, in no small part because of the overlap between biological pathology and resulting psychological distress. Cognitive Behavioral Therapy for Chronic Illness and Disability cuts across formal diagnostic categories to apply proven therapeutic techniques to potentially devastating conditions, from first assessment to end of treatment.

Four extended clinical case examples of patients with chronic fatigue, rheumatoid arthritis, inoperable cancer, and Crohn s disease are used throughout the book to demonstrate how cognitive-behavioral interventions can be used to effectively address ongoing medical stressors and their attendant depression, anxiety, and quality-of-life concerns. At the same time, they highlight specific patient and therapist challenges commonly associated with chronic conditions.

From implementing core CBT strategies to ensuring medication compliance, Renee Taylor offers professionals insights for synthesizing therapeutic knowledge with practical understanding of chronic disease. Her nuanced client portraits also show how individual patients can vary even within themselves.

This book offers clinicians invaluable help with

- Conceptualizing patient problems

- Developing the therapeutic relationship

- Pacing of therapy

- Cognitive restructuring

- Behavioral modification

- Problem solving

- Fostering coping and adapting skills

Taylor s coverage is both clean and hands-on, with helpful assessments and therapy worksheets for quick reference. Cognitive Behavioral Therapy for Chronic Illness and Disability gives practitioners of CBT new insights into this population and provides newer practitioners with vital tools and tactics. All therapists will benefit as their clients can gain new confidence and regain control of their lives."

Global impairment of the central nervous system, whether stable or progressive, is often called severe neurological impairment (SNI). A child who has SNI will be cared for both by specialist clinicians and by parents at home. A parent is a child's best expert and advocate, and many parents become highly skilled in managing their child's care. This guide provides information to help parents increase their knowledge and improve their caregiving skills.

In "Caring for Children Who Have Severe Neurological Impairment, " Dr. Julie M. Hauer advocates shared decision making between family caregivers and healthcare providers. She details aspects of medical care such as pain, sleep, feeding, and respiratory problems that will be particularly useful to parents. Tables and key points summarize discussions for clear, quick reference, while case studies and stories illustrate how different families approach decision making, communication, care plans, and informed consent.

Parents and other caregivers will find this book to be indispensable--as will bioethicists and clinicians in pediatrics, neurology, physical and rehabilitative medicine, palliative care, and others who care for children with neurological and neuromuscular disorders. Dr. Hauer offers hope and practical coping strategies in equal measure.

'Billy Connolly says he's no idea who Parkinson was and just wishes he'd kept his disease to himself. He should read this book.' Jeremy Paxman Parkinson's disease is one of the most common forms of dementia, with 10,000 new cases each year in the UK alone, and yet few know anything about the man the disease is named after. In 1817 - exactly 200 years ago - James Parkinson (1755-1824) defined the disease so precisely that we still diagnose it today by recognising the symptoms he identified. The story of this remarkable man's contributions to the Age of the Enlightenment is told through his three passions - medicine, politics and fossils. As a political radical Parkinson was interrogated over a plot to kill King George III and revealed as the author of anti-government pamphlets, a crime for which many were transported to Australia; while helping Edward Jenner set up smallpox vaccination stations across London, he wrote the first scientific study of fossils in English, which led to fossil-hunting becoming the nation's latest craze - just a glimpse of his many achievements. Cherry Lewis restores this neglected pioneer to his rightful place in history, while creating a vivid and pungent portrait of life as an 'apothecary surgeon' in Georgian London.