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.

Depression affects many people at some point in their lives. Fortunately, we now know that by changing certain thoughts and behaviour patterns you can greatly improve how you feel. Overcoming Depression and Low Mood: A Five Areas Approach explains how low mood can affect your life. It helps you understand why you sometimes feel low, anxious, angry, or guilty. It also teaches proven practical skills to help you change how you feel. By using the clearly described practical tools inside, you can make helpful changes to your life. Ultimately, the hope is that this book will help you to regain a sense of control over how you feel. The book is based on a cognitive behavioural therapy approach. The developers of this approach found many effective ways of tackling common symptoms and problems people face when feeling low. The course can make a big difference if you can commit to using it. Having someone else to encourage you is also important. Interactive questions and worksheets, which are a key feature of the series, are plentiful in this new edition. An award-winning companion website, www.livinglifetothefull.com, includes additional support materials and information.

A cutting-edge account of the latest science of autism, from the best-selling author and advocate When Temple Grandin was born in 1947, autism had only just been named. Today it is more prevalent than ever, with one in 88 children diagnosed on the spectrum. And our thinking about it has undergone a transformation in her lifetime: Autism studies have moved from the realm of psychology to neurology and genetics, and there is far more hope today than ever before thanks to groundbreaking new research into causes and treatments. Now Temple Grandin reports from the forefront of autism science, bringing her singular perspective to a thrilling journey into the heart of the autism revolution. Weaving her own experience with remarkable new discoveries, Grandin introduces the neuroimaging advances and genetic research that link brain science to behavior, even sharing her own brain scan to show us which anomalies might explain common symptoms. We meet the scientists and self-advocates who are exploring innovative theories of what causes autism and how we can diagnose and best treat it. Grandin also highlights long-ignored sensory problems and the transformative effects we can have by treating autism symptom by symptom, rather than with an umbrella diagnosis. Most exciting, she argues that raising and educating kids on the spectrum isn't just a matter of focusing on their weaknesses; in the science that reveals their long-overlooked strengths she shows us new ways to foster their unique contributions. From the "aspies" in Silicon Valley to the five-year-old without language, Grandin understands the true meaning of the word spectrum. The Autistic Brain is essential reading from the most respected and beloved voices in the field.

After progressive multiple sclerosis landed Dr Wahls in a tilt/recline wheelchair, she exhaustively researched autoimmune disease and brain biology, and embraced the concepts of functional medicine. Determined to overcome her initial dismal diagnosis,, she made a choice to rely on food as her medicine and begun using paleo concepts as guidelines for her unique, nutrient rich plan. As her broken biochemistry began to fix itself, Dr Wahls soon retained full mobility and left her wheel chair behind for good. Dr Wahls transformation was nothing short of miraculous, and she knew these treatments could be life-changing for anyone struggling with an autoimmune condition. Now, Dr Wahls shares her pioneering research along with three levels of nutrient-rich diets that can help you reverse the debilitating symptoms of your disease. The Wahls Protocol gave Dr Wahls her life back. Give it the chance to restore yours.

Using his now familiar image of a garden and a personal, plain English style, renowned breast cancer specialist Professor John Boyages MD, PhD, walks you slowly through the stress and confusion of diagnosis, treatment, and life after DCIS of the breast. Your whole life stops after a diagnosis of DCIS. The condition is extremely confusing. Treatment advice varies and there is a danger of both undertreatment and overtreatment. One doctor recommends a lumpectomy and radiation and another recommends a mastectomy. One tells you it's a cancer and the other tells you it's not cancer. In"DCIS of the Breast: Taking Control," John Boyages provides you with all the information you, your family, and your friends need to take control, understand what DCIS is, and how to best treat this condition. Learn how to identify the twenty control points, and about the important decisions you must make to navigate the medical maze and take control if DCIS or cancer returns.

For nearly 70 years, this resource has been the standard for diabetes education and meal planning. Based on input from current users, this new edition has been streamlined and redesigned and enhanced with more food images. It also features updated carbohydrate, protein, and fat information for a wide variety of food and beverages that reflect the diverse populations living with diabetes. This edition includes action-oriented eating plan tips throughout, a new section on Snacks and Extras, dedicated pages for notes, and a customizable eating plan.

Join Sheila Walsh on her journey from despair to joy Beautiful and talented, Sheila Walsh was at the pinnacle of her career, appearing daily on television as cohost of The 700 Club. One day she found herself walking away from it all and checking in to a psychiatric hospital, where she stayed for a month. From the outside everything seemed fine, but on the inside Sheila was in trouble. In her journal she wrote, "Lord, please hold me. I'm falling into a dark well. I feel as if I am disappearing a little more every day. I am so angry inside that I am afraid of myself. I feel so alone." How did this happen? What brought her to her knees? Loved Back to Life takes readers on Sheila's journey of the soul from hopelessness to joy as she finds that although the road was scary, at every turn God beckoned her to follow and trust Him. And He did not let her down.

Multiple Sclerosis affects hopes and expectations, restructures relationships, modifies careers and changes lives. It is a disease of variable onset, problematic diagnosis, unpredicatable prognosis and no effective treatment. Using unique autobiographical accounts of people with the disease, Ian Robinson sensitively portrays the difficulties and frustrations of the struggle to make sense of the clinical diagnosis and management of an illness which is effectively a way of life.

Depression doesn't happen all at once. It starts gradually and builds momentum over time. If you go through a difficult experience, you may stop taking care of yourself. You may stop exercising and eating healthy, which will end up making you feel even worse as time goes on. You are caught in a downward spiral, but you may feel too tired, too overwhelmed, and too scared to try and pull yourself back up. The good news is that just one small step can be a step in the right direction. In The Upward Spiral, neuroscientist Alex Korb demystifies the neurological processes in the brain that cause depression and offers effective ways to get better-one little step at a time. In the book, you'll discover that there isn't "one big solution" that will solve your depression. Instead, there are dozens of small, practical things you can do to alleviate your symptoms and start healing. Some are as simple as relaxing certain muscles to reduce feelings of anxiety, while others involve making small efforts toward more positive social interactions. Small steps in the right direction can have profound effects-giving you the power to literally "reshape" your brain. Like most people, you probably didn't wake up one day and find yourself completely depressed. Instead, it probably happened over time, as a series of reactions to difficult situations and negative thinking. But if you are ready to reverse the trajectory of your depression and find lasting happiness, this book will show you how.

A workbook to help children deal with feelings about serious illness. An excellent resource for helping children learn the basic concepts of illness and various age-appropriate ways of coping with someone else's illness.

Winner of the 2015 Samuel Johnson Prize for Non-Fiction Shortlisted for the Wellcome Book Prize A Sunday Times and New York Times bestseller Foreword by Oliver Sacks What is autism: a devastating developmental condition, a lifelong disability, or a naturally occurring form of cognitive difference akin to certain forms of genius? In truth, it is all of these things and more - and the future of our society depends on our understanding it. Following on from his groundbreaking article 'The Geek Syndrome', Wired reporter Steve Silberman unearths the secret history of autism, long suppressed by the same clinicians who became famous for discovering it, and finds surprising answers to the crucial question of why the number of diagnoses has soared in recent years. Going back to the earliest autism research and chronicling the brave and lonely journey of autistic people and their families through the decades, Silberman provides long-sought solutions to the autism puzzle while casting light on the growing movement of 'neurodiversity' and mapping out a path towards a more humane world for people with learning differences.

A unique worship resource that includes practical suggestions for visiting and offering spiritual support to those with dementia

Often dementia hides the person from us, but never from God. "We have accounts of people with dementia coming to faith on hearing the gospel," says Louise. "God never gives up, and neither should we. Visiting and supporting, ministering and caring is not about what it does for us, but what it means to the person with dementia."

This practical book explains why Christians are called to care spiritually for people who may not be able to show their response. It assures us that once we commit our lives to Christ, His Holy Spirit comes to live in us, and He has promised never to leave us. This is true hope for weary caregivers and good news for sufferers.

The large selection of Scripture verses, prayers, and devotional entries along with practical advice from an author with considerable experience working with dementia sufferers make this a one-stop worship resource for caregivers, sufferers, families, pastors, church groups, and medical professionals.

Covering everything from recognising symptoms and obtaining initial diagnosis to living with the condition on a daily basis, this complete guide to living with and managing Ehlers-Danlos Syndrome (Hypermobility Type - formerly known as Type III) has been revised and fully-updated in this accessible new edition. The author, who has the condition, looks at how it affects children and adolescents and explores pain management, pregnancy, physical and psychological aspects, and how it widely affects dancers and other performance artists. New material includes: changes in terminology information on how osteopathy and nutrition can help psychological approaches beyond CBT how to deal with professionals what to expect from support groups and rehabilitation programmes This new edition will be a must for anybody who suffers, or suspects they might be suffering from, Ehlers-Danlos Syndrome (Hypermobility Type) and provides everything needed to enjoy a fulfilling life with this complex condition. It will also be of interest to their families and friends, and professionals working with Hypermobility Type EDS.

Robert Ariss - activist and academic - had a unique vision of HIV/AIDS. As an HIV seropositive individual for many years before his death on May 9, 1994, he was a full participant in, and critic of, the development of the gay community's response to the HIV epidemic both in Australia and internationally. Though Ariss' life is a definite presence in this study, Against Death: The Practice of Living with AIDS is not an autobiography. Instead, it is a unique and critical account of a public health crisis, a community's response, and the politics of sexuality. It was in Sydney, Australia, world-famous for its Gay and Lesbian Mardi Gras, that Robert Ariss lived and worked. It is his vision of that community - of its members infected with and affected by HIV - which is documented in this remarkable anthropological study. Yet the study's implications reach beyond Sydney to all communities living with HIV and AIDS.

Though medically minor and very common, herpes simplex is a condition which is capable of causing considerable distress, for psychological and social as much as physical reasons. Herpes Simplex contrasts the image of the condition presented in the media with the medical and epidemiological evidence, and discusses ways in which the distress associated with the condition can be alleviated.
The first part of the book examines the impact of diagnosis and then explains the roles of accurate information and empathic support, medical treatment and support groups in learning to live with recurrent symptoms. Other chapters use the experiences of people with the condition in different parts of their bodies to illustrate how the meaning of herpes simplex and response to the symptoms alters in association with life changes. The final chapters review psychosocial research, discuss the importance of the Herpes Viruses Association in acquiring a store of knowledge about people's experiences, and highlight the significance of herpes simplex as a public health problem.
Herpes Simplex demonstrates the importance of a biopsychosocial approach. It will be invaluable to doctors, nurses and other health professionals, as well as to people troubled by the condition.

eBook available with sample pages: 0203137132

If you or someone you love is walking through a season of loss, disappointment, pain, or other difficulties, The Art of Overcoming will teach you how to grieve what has died within you and celebrate the new life set before you by the God who brings good from evil, light from dark, and life from death. Pastor Tim Timberlake uses the imagery of a traditional funeral ceremony as a framework to look at the "death experiences" we face regularly in this crazy journey called life. These experiences include all the grief, disappointment, tragedy, loss, pain, suffering, abuse, or sorrow that comes our way. Death is not the end, although it often feels like it is in the moment. Instead, it is a season to reflect, to honor, and to grow. It is the end of one chapter but the beginning of a new one. The new doesn't diminish the old and looking toward the future doesn't mean we forget the past. Instead, we must learn to hold loss and hope at the same time. The chapters are divided into four sections that represent specific stages of dealing with our death experiences. Living with Death explores five foundational perspectives about grief and loss The Processional encourages us to face head-on the reality of our experiences The Eulogy helps us memorialize and honor what has been lost and how to process grief in a healthy way The Recessional is about closure as we discover life after death and move forward No matter what you've gone through or are in the middle of right now, better days are ahead. But don't hurry to get there. Instead, let Jesus heal your heart in His timing, take time to grieve what needs to be grieved, and then celebrate the new life God lays out before you.

"Adelman and Frey take advantage of every opportunity to leave their audience with a splendid reading experience that will prompt one to think about community and communication in new and exciting ways. And as it should be, the reader also will not soon forget the echoes of the voices of the ordinary, but remarkable, men and women who inspired the work -- the residents who live and have lived in the fragile community at BH". -- Journal of Health Communication

This book examines the concept of "community", focusing on how communication practices help manage the tensions of creating and sustaining everyday communal life amidst the crisis of human loss. While acknowledging how the contradictory and inconsistent nature of human relationships inevitably affects community, this intimate and compelling text shows how community is created and sustained in concrete communication practices.

The authors explore these ideas at Bonaventure House, an award-winning residential facility for people with AIDS, where the web of social relationships and the demands of a life-threatening illness intersect in complex ways. Facing a life-threatening illness can defy meaningful social connections, but it can also inspire such ties, sometimes in ways that elude us in the course of daily life. By understanding how collective communication practices help residents forge a sense of community out of the fragility and chaos f living together with AIDS, we are able to better understand how communication is inexorably intertwined with the formation of community in other environments.

Based on seven years of ethnographic research including participant-observation, in-depth interviews, and questionnaires, thisbook weaves together narratives and visual images with conceptual analysis to uncover the ongoing oppositional forces of community life, and to show how both mundane and profound communication processes ameliorate these tensions, and thereby sustain this fragile community. Because the average length of stay for a resident is seven months -- in which time he or she moves from being a newcomer to a community member to someone the community remembers -- the text reflects this short, but crystallized life, starting with the day a new resident opens the door to the day he or she passes away.

The writing is very rich -- intimate, engaging, personal, compelling, and vivid. The stories told discuss such deeply personal topics as the dilemmas of romantic relationships in a context fraught with many perils; issues of power, authority, and control that enable and constrain social life; and communicative practices that help residents cope with bereavement over the loss of others as well as their own impending deaths. The text concludes by examining the lessons learned from Bonaventure House about creating and sustaining a health community, and serves as an inspiration for strengthening interpersonal relationships and communities in other environments.

David Lovelace, along his brother and both his parents, is bipolar. This is his extraordinary and vivid memoir of life within his memorable, maddening, loving and unique family. Full Blown is Lovelace's poignant, humorous, and vivid account of growing up and coming to terms with the highs and lows of manic depression. David's father was a Princeton-trained theology professor deemed too eccentric for the ministry and his mother battled depression all her life. Manic episodes were part of family life - they called them the 'whim-whams'. David was a teenager when his first serious depression hit, and at college when he first became manic. He ran to escape it - to Mexico, South America and then New York, to drugs and alcohol - before he realised the futility of running. A father himself, a son and a brother, David's matter-of-fact approach to growing up surrounded by the unique creativity often sparked by manic depression is compelling. In the vein of Stuart, A Life Backwards and Augusten Burroughs' Running with Scissors , David's poetic ability to detail the unique highs and harrowing lows makes a remarkable and gripping read.

From the bestselling authors of Keto Diet For Dummies Keto Desserts for Dummies debunks the rumor that you need to give up your favorite sweet treats when you go keto. Rami and Vicky Abrams provide in-depth details on how to maintain the popular low-carb, low-sugar diet while still enjoying delicious desserts and treats. Created by the founders of the wildly popular Tasteaholics.com, along with the Total Keto Diet App, Keto Desserts For Dummies explains how to swap out standard baking ingredients, including sugar, flour, and milk, for keto-friendly ones. You'll maintain the flavor of your favorite desserts while making them compatible with the keto diet. This handy guide shows you how to: Make delicious desserts while sticking to the keto regimen Choose keto-friendly versions of your favorite desserts so you don't ruin your daily macros Incorporate keto-approved desserts into your overall keto meal plans Keto Desserts For Dummies includes more than 150 easy-to-follow and tasty recipes sure to make your taste buds light up. All the recipes are designed to be simple and easy to follow, ensuring that anyone can make them, even people new to the keto program.

In the U.S. approximately one percent of the population (2.6 million) have a bipolar disorder - also called manic-depressive illness - characterized by mood cycles of depression and mania (excessive elation, activity, talkativeness, etc.). In this book, the "pieces" that compose the "bipolar puzzle" come together in a unique question-and-answer format. Written by a bipolar sufferer, coauthor Bryan L. Court, typical questions heard in bipolar support groups are provided and each is followed by an in-depth answer. Each topical section also includes an extensive "Psychiatrist's Response" by coauthor Gerald E. Nelson, M.D., who has been working with bipolar disordered individuals for over 20 years. Answering questions about bipolar illness and how to live with it, this book addresses 187 recovery-related questions over the broad range of interest to the patient, family, and friend, and utilizes the same question-and-answer format heard in bipolar support groups. Subjects cover a wide spectrum, including: understanding the illness; treatment methods; medications; attitudes; acceptance; faith; living with the disorder; relationships with friends, family, and psychiatrists; support groups; disability; hospitalization; and employment difficulties. The answers were obtained from a psychiatrist, a labor law attorney, and a hospital worker. A psychiatrist (Nelson) reviewed the answers to the questions and provided a response to each section of the book.

An essential resource for anyone who has a close relationship with a person who is bipolar

This book provides a much-needed resource for family and friends of the more than 5 million American adults suffering from bipolar disorder. From psychotic behavior that requires medication to milder mood swings with disturbing ups and down, this book offers a warm and often humorous user-friend guide for coping with bipolar loved ones, colleagues, and friends. The book includes Guidance for identifying bipolar disorder symptoms and how to get the diagnosis confirmedStrategies for dealing with rants, attacks, blame, depression, mania and other behaviorsCrucial information on medication and its effectiveness and potential side-effectsTechniques for dealing with attempts to self-medicate with drugs and alcoholHow many people with bipolar disorders can care for themselves, get help, feel supported and go on with their own lives

This important book contains real-life illustrative examples and a wealth of helpful strategies and coping mechanisms that can be put into action immediately.

First symptoms of depression often occur during teenage years, and it can be a disturbing and confusing time for families as well as the teenager themselves. How can you tell whether it is just typical teenage ups and downs that will pass, or something more serious? How can we reliably identify and support teenagers with depression? In this book experienced clinician and researcher Gordon Parker explains how to systematically identify different mood disorders and contributing factors. He and co-author Kerrie Eyers explain when clinical treatment is required and outline treatment options. They also discuss the particular challenges faced by adolescents and approaches to effective management. Drawing on insightful personal accounts from teenagers and young adults about their experiences, and based on extensive clinical research, this is essential reading for every parent, carer or professional looking after a young person with depression.

In many countries there has been an alarming increase in rates of suicide and self-harm, yet the stigma attached to these difficulties often leads to sub-optimal care. Life After Self-Harm: A Guide to the Future is written for individuals who have deliberately harmed themselves. Developed through a major research project the contents of the manual have been informed and shaped by many users and expert professionals. Illustrated with multiple case-histories, it teaches users important skills: for understanding and evaluating self-harm for keeping safe in crisis for dealing with seemingly insolvable problems for developing coping strategies for re-connecting with life. Health workers who regularly come into contact with individuals who have self-harmed will find the wealth of practical advice in this book extremely valuable for recommendation to patients either as a self-help book, or in the context of brief therapy.