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Parkinson's Disease: A Complete Guide for Patients and Families (A Johns Hopkins Press Health Book)

by William J. Weiner, Lisa M. Shulman, and Anthony E. Lang

As a result of actor Michael J. Fox's disclosure that he has Parkinson's disease, public discussion about both the symptoms and treatment of this illness has heightened. This attention is important, according to these authors, all specialists in the treatment of Parkinson's and other neurological disorders, because it is a progressive, chronic disease whose symptoms including trembling, uneasy gait and loss of dexterity mimic those of other diseases, which can often lead to misdiagnosis. One of the most frustrating aspects of Parkinson's is that it manifests itself differently in each of its victims, which makes coping with this disease particularly challenging. Nonetheless, what is most important, aver the authors, is that both Parkinson's patients and their families have access to the most up-to-date treatment including new drugs, surgery and other therapies (diet, speech therapy, acupuncture), and with compassionate, clear writing, they provide an excellent overview. Leaving no stone unturned, Weiner, Shulman and Lang also advise patients about less clinical but equally important matters such as dealing with health insurance companies and informing employers. Particularly useful for readers are the Q&A section and a comprehensive resource directory. Obtaining an accurate diagnosis is the first step, after which patients and their loved ones will find this practical guide the perfect complement to a physician's care.

What Your Doctor May Not Tell You About Parkinson's Disease: A Holistic Program for Optimal Wellness

by Jill Marjama-Lyons and Mary J. Shomon

This guide explains the mechanisms behind Parkinson's and provides detailed information about common - and lesser-known - symptoms. It summarizes the primary means of diagnosis and covers all the conventional treatments along with their pros and cons. However, a large part of the book is devoted to alternative treatments for Parkinson's, including Dr Perlmutter's glutathione therapy - a programme designed around an over-the-counter natural supplement. Other alternative therapies are also covered. A special section of the book focuses on ways that patients can deal with symptoms such as sleep problems, freeze attacks, anxiety, depression and muscle spasms, and attention is also given to carers, friends and families of sufferers.

Parkinson's Disease: An Essential Guide for the Newly Diagnosed

Parkinson's disease—a chronic disorder that causes a progressive loss of nerve cell function in the part of the brain that controls muscle movement—is an incurable neurological condition with debilitating symptoms. Over 1.5 million Americans are affected, and the numbers continue to grow. From the first moment of her Parkinson's diagnosis, author Jackie Christensen took charge and educated herself on every aspect of her condition. Now, as a "patient-expert," she guides those newly diagnosed step by step through their first year with Parkinson's. She provides crucial information about the nature of the disease, treatment options, diet, exercise, charts and tables, social concerns, emotional issues, networking with others, and much more. The First Year—Parkinson's Disease will be an invaluable guide for all those who want to be an informed, active participant in the management of their condition.

Parkinson's Disease: 300 Tips for Making Life Easier

Being diagnosed with Parkinson's disease can be distressing, and adjusting to the effects of the disease is often difficult. This indispensable resource for patients, family, friends, and caregivers helps patients rise above PD’s challenges by working smarter, maintaining a positive outlook, and conserving time and energy. Organized by subject, the book covers a wide range of topics, including making the home more accessible; dressing aids and simple clothing adaptations; using technology to improve communication; eating and drinking tips for people with difficulty swallowing; mobility and exercise; managing home health care; cars and driving; leisure and recreational activities; travel; and much more. A resource section at the end of each chapter contains contact information for the agencies, organizations, and products mentioned. Completely revised and updated to include over 65 new tips and 40 additional resources, the book enables readers to become more independent and lead remarkably unlimited lives.

HOPE: Four Keys to a Better Quality of Life for Parkinson's People

This book is a book of hope for both the newly diagnosed Parkinson's Person as well as a helpful reminder to a better quality of life for those who have had the disease for many years. The writing is succinct and easy to read. Hal outlines the four basics of hope as 1) Help; 2) Optimism; 3) Physician; and 4) Exercise. His personal stories on these four points are candid and powerful. He has experienced some changes in his life as a result of Parkinson's but he remains positive, upbeat and full of vitality. He shares some personal guidelines he now lives by and offers some tips on how to on how to face the challenges that may lie ahead. This is not a lecture on what you should do but merely an insight into what is working for a fellow person with Parkinson's. This is an essential tool to improve one's quality of life for those living with Parkinson's.

The A to Z of Parkinson's Disease (Library of Health and Living)

by Anthony D. Mosley and Deborah S. Romaine

About half a million Americans are diagnosed with Parkinson's disease every year. Parkinson's is a chronic neurological disorder with symptoms most commonly present in people ages 50 and older, though recent trends have shown an increase in the number of people ages 40 and younger who have developed the disease. Public awareness of and interest in Parkinson's disease have never been greater due to the number of public figures such as Muhammad Ali, Michael J. Fox, and Janet Reno who are living with the disease. It is also at the center of the controversy surrounding stem cell research. The A to Z of Parkinson's Disease presents the most current information pertaining to the complex issues and news-making topics relating to this disease, including etiology, symptoms, treatments, medications, surgeries, research, medical terms, coping and caregiving, living with Parkinson's disease, and much more. More than 600 accessible entries cover aspects of the medical, scientific, social, and lifestyle implications of Parkinson's disease. Appendixes include an extensive bibliography, a directory of key support groups and organizations, a glossary, and other valuable resources.

Stop Parkin' And Start Livin': Reversing the Symptoms of Parkinson's Disease

by John C. Coleman

Stop Parkin'and Start Livin': Reversing the Symptoms of Parkinson's Disease is an invaluable resource for those diagnosed with Parkinson's Disease. It provides a plan of action and significant information which the reader can use to return to good health and as an adjunct to working with supportive therapists.

100 Questions & Answers About Parkinson Disease

by Abraham Lieberman

Whether you're newly diagnosed with Parkinson Disease, a long-term PD patient, or a friend or relative of either, this book offers help. The only text to provide the doctor and patient's view, 100 Questions & Answers About Parkinson Disease gives authoritative, practical answers to questions about treatment options, quality of life, and sources of support. Dr. Lieberman explains the disease, its progression, and its treatment, making this book an invauluable resource for anyone coping with this disease.

Parkinson's Disease and the Family: A New Guide (The Harvard University Press Family Health Guides)

by Nutan, M.D. Sharma and Elaine, Ph.D. Richman

Parkinson's disease is a movement disorder characterized by tremor, stiffness, and slow gait. It affects 500,000 people in the United States, with approximately 50,000 new cases diagnosed annually. But its impact is much wider. Family members with little understanding of the disease often find themselves struggling to help their loved one navigate the complexities of the health care system. Patients wonder, Which treatments are best for me? Will I be able to live on my own? Should I join a drug trial? In this straightforward, compassionate guide, Nutan Sharma and Elaine Richman address these concerns and more. They provide a thorough review of the etiology, diagnosis, and current treatment of Parkinson's, with special consideration given to the effect on family dynamics and routines--including the often neglected topics of long-term care and sexual function. The authors also review the pros and cons of various alternative therapies, including nutritional supplements, massage therapy, and traditional Chinese medicine.
Too often, with Parkinson's disease, a loved one serves as medical interpreter, patient advocate, and caregiver. In Parkinson's Disease and the Family, Nutan Sharma and Elaine Richman draw on the latest research and clinical practice techniques to offer valuable suggestions for managing patient care and, perhaps more important, for healing the family unit.

Parkinson's Disease: A Guide for Patient and Family

by Roger C Duvoisin and Jacob Sage

Univ. of Medicine and Dentistry of New Jersey, New Brunswick. Offers basic knowledge of the features of Parkinson's disease and provides a sound knowledge base for patients. Includes an increased focus on genetics and molecular biology and a new chapter on Levodopa showing how this agent affects disease progression. Previous edition: c1996. Softcover.

The Comfort of Home for Parkinson Disease: A Guide for Caregivers

by Maria M. Meyer, Paula Derr, and Susan C. Imke

This comprehensive guide to the day-to-day issues confronted by Parkinson disease patients and their caregivers covers every caregiving stage.It's all here in an illustrated, easy-to-read format, including the decision to provide home care, preparing the home, assisting with daily activities, financial management, and strategies for avoiding caregiver burnout. This guide also includes information on the specific issues that PD patients and caregivers face, as well as tips on purchasing equipment, travel, therapies, loss of motor skills, and communicating effectively with physicians.

Making the Connection Between Brain and Behavior: Coping with Parkinson's Disease

by Joseph H. Friedman

While patients and families are aware of the physical challenges that accompany Parkinson’s disease, few are prepared for the common behavioral issues that impact their quality of life, including depression, anxiety, dementia, paranoid delusions, and sleep disorders. This book, the only one of its kind, focuses entirely on an area that most doctors overlook. Written in layman’s terms, it helps readers understand and cope with a wide variety of Parkinson’s-related behavioral issues and offers guidance on communicating with the healthcare team.

A Life Shaken: My Encounter with Parkinson's Disease

by Joel Havemann and Stephen G. Reic

In 1990, Los Angeles Times senior editor Havemann was diagnosed with Parkinson's disease at the early age of 45. Here he movingly chronicles the physical and emotional effects the disease has had on his life since the diagnosis. He briefly discusses Parkinson's history, possible causes, medical and surgical treatments, and research progress, but the strength of this book is the account of his personal struggle with the disease. Initially denying that the diagnosis would adversely affect his personal and professional life, he accepted a posting to Brussels and dealt with the resulting frustrations of seeing physicians who did not speak English. The disease's progressive effects on his body are vividly detailed. Havemann's realistic acceptance of and resistance to limitations, as well as his appreciation of life in spite of disability, is inspiring. While Abraham Lieberman's Shaking Up Parkinson Disease: Fighting Like a Tiger, Thinking Like a Fox provides more medical information, Havemann offers a wonderful personal view for patients and families. Recommended for consumer health collections. Janet M. Schneider, James A. Haley Veterans' Hosp., Tampa, FL

Motor Neuron Disease (The Facts)

by Kevin Talbot and Rachael Marsden

Motor neuron disease (MND) is a common but devastating disability that has a profound impact on people's lives. This book provides an easily-accessible guide to the disease for patients with motor neuron disease and their carers. The authors have organised it around a series of the commonest questions asked in their clinic, emphasising the variation in the course of MND and the individual nature of the patient journey through the disease. After an initial description of the symptoms for MND and how neurologists make the diagnosis the authors describe what is known about the causes and how scientists are trying to understand the disease. The book also looks at how a team of specialists can provide support and symptom control for the patient.

Palliative Care in Amyotrophic Lateral Sclerosis (Motor Neuron Disease)

by David Oliver, Gian Domenico Borasio, and Declan Walsh

Review
"This book is reasonably priced and will prove valuable to medical and paramedical staff caring for MND patients. It provides comprehensive, evidence based information clearly written and accessible to a multidisciplinary readership. The advice is practical, compassionate and based on extensive clinical experience."Brain

"Throughout the book, a positive tone emerges reflecting the view that, despite the devastating effects of MND, much can be done to alleviate symptoms, improve the quality of life of the afflicted person and to assist patients and their families to cope throughout the various phases of the disease."Palliative Medicine

"Palliative Care in Amyotrophic Lateral Sclerosis comprehensively and successfully fills what was previously a noticable gap in palliative care literature and should be regarded as the essential reference text for any unit or individual professional involved in any way with the care of patients with ALS."Progress in Palliative Care

"This volume crystallises current perspectives on the palliative management of ALS with consummate skill. Although not a long volume it covers the many important and complex in a very balanced manner. All health professionals involved in the care of ALS sufferers will benefit from reading it."..."It should be available to all departments providing care for ALS patients and carers and is an outstanding contribution to the ALS literature."Jnl of Neurology

"This book is reasonably priced and will prove valuable to medical and paramedical staff caring for MND patients. It provides comprehensive, evidence based information clearly written and accessible to a multidisciplinary readership. The advice is practical, compassionate and based on extensive clinical experience." Brain

"Throughout the book, a positive tone emerges reflecting the view that, despite the devastating effects of MND, much can be done to alleviate symptoms, improve the quality of life of the afflicted person and to assist patients and their families to cope throughout the various phases of the disease." Palliative Medicine

"Palliative Care in Amyotrophic Lateral Sclerosis comprehensively and successfully fills what was previously a noticeable gap in palliative care literature and should be regarded as the essential reference text for any unit or individual professional involved in any way with the care of patients with ALS." Progress in Palliative Care

"This volume crystallises current perspectives on the palliative management of ALS with consummate skill. Although not a long volume it covers the many important and complex in a very balanced manner. All health professionals involved in the care of ALS sufferers will benefit from reading it."..."It should be available to all departments providing care for ALS patients and carers and is an outstanding contribution to the ALS literature." Journal of Neurology

`This book is reasonably priced and will prove valuable to medical and paramedical staff caring for MND patients. It provides comprehensive, evidence based information clearly written and accessible to a multidisciplinary readership. The advice is practical, compassionate and based on extensive clinical experience.' Brain

`Throughout the book, a positive tone emerges reflecting the view that, despite the devastating effects of MND, much can be done to alleviate symptoms, improve the quality of life of the afflicted person and to assist patients and their families to cope throughout the various phases of the disease.' Palliative Medicine

Motor Neurone Disease: The 'At Your Fingertips' Guide

by Stuart Neilson and Frank Rose

Motor Neurone Disease (MND) is a progressive disorder of the nervous system. Its effects on the body can be so severe that it eventually changes the lives of those affected and hence those of their families, friends and work colleagues. Motor Neurone Disease (MND) – the ‘at your fingertips’ guide is packed full of sensible advice. The expert authors address the physical and emotional upheaval that MND brings on, discussing its impact on the whole family, offering positive help and advice. The book provides up-to-date and medically accurate information on a whole range of topics from diagnosis and treatment to adapting to life with MND including mobility, feelings, sexual relationships and much more.

Motor Neurone Disease: A Family Affair (New Revised Edition) (Overcoming Common Problems)

by David Oliver

Associated with known sufferers such as David Niven and Jill Tweedie, Motor Neurone Disease is a serious illness which affects around 6000 people in the UK and causes more deaths than MS. This book - endorsed by the Motor Neurone Disease - offers practical advice and support to sufferers and their families. It explains the facts about MND and describes diagnosis and treatments, and advises who can help. The emotional issues are addressed, including coming to terms with dying. A list of contact addresses is included.

Motor Neurone Disease

by Maggie Hunter

Motor Neurone Disease, also known as Lou Gehrig's disease, is one of the most difficult conditions to manage medically and socially. A disease which leads to the loss of control of most muscle systems of the body, it has no known cause and no cure. For this reason, clinicians have traditionally been reluctant to reveal the diagnosis to sufferers or their families and the condition has become known as one of the best kept secrets of medical practice. However in recent years a number of organizations have set up to support sufferers and their families and consequently, the public profile of the condition has changed dramatically. Motor Neurone Disease provides an extremely helpful guide to the medical facts relating to the condition and considers the psycho-social effects on sufferers and those who care for them.

Motor Neurone Disease (Therapy in Practice)

by S. Beresford

Managing the Symptoms of Multiple Sclerosis

by Randall T. Schapiro

In clear language and using helpful illustrations, this comprehensive guide deals with both the symptoms of multiple sclerosis and the most effective, clinically tested ways to help patients manage the disease. All symptoms are discussed, from spasticity, tremor, and fatigue to bladder, bowel, and sexual difficulties. In addition, newer ways to manage complex and routine symptoms are explored. The book, now in its fifth edition, covers the most recent advances in drug therapies and other treatments, including new discoveries, recently developed medications, and medical breakthroughs. Also included are an overview of the disease, a glossary of common medical terms, a list of helpful exercises, and information on transfer and mobility resources. Organized to reflect the three areas of MS management — management of the disease, management of its symptoms, and management of lifestyle and general wellness issues — the book is an invaluable reference for MS patients, families, and providers.

Multiple Sclerosis: Understanding the Cognitive Challenges

by Nicholas LaRocca and Rosalind C. Kalb

The National Multiple Sclerosis Society estimates that more than half of all people with MS suffer some form of cognitive difficulty. Although symptoms and severity can vary, the emotional and social impact can be devastating. This invaluable resource, written for patients and their families, offers an in-depth discussion of cognitive difficulties, including changes that can occur; helpful strategies for dealing with their impact in daily life; and a detailed overview of treatment options.

Multiple Sclerosis: New Hope and Practical Advice for People with MS and Their Families

by Louis Rosner and Shelley Ross

"MS is one of the most misunderstood diseases," maintains Rosner, associate clinical professor of neurology at UCLA, and Ross, a freelance writer, in this clear, comprehensible guide intended for those afflicted with the disorder of the central nervous system, as well as for their family and friends. In addition to dispensing practical advice (clarifying signs and symptoms and the complex diagnostic process), they debunk misconceptions, asserting that "75 percent of people with MS will never need a wheelchair, and 40 percent will experience no interference with activity"; and "each and every symptom can remit completely." Emotional coping on the part of patients and their loved ones is likewise addressed. Case histories, a thorough explanation of various treatments, including diets and nutritional supplements, an evaluation of recent medical diagnostic findings (including magnetic resonance imaging, a scanning device) and a discussion of breakthroughs in cures will enlighten and encourage.
Copyright 1987 Reed Business Information, Inc.

Multiple Sclerosis: The Facts (Oxford Medical Publications)

by Bryan Matthews and Margaret Rice-Oxley

For someone recently diagnosed with MS, or who lives with someone affected by MS, there are enormous new demands placed upon them, both physical and psychological. What has caused the illness? How will it affect their life? What can be done to alleviate the symptons? Though much information on MS is available, there is a dearth of reliable advice the is based on proper medical research. For the sufferer, the conflicting and unrelaible advice available can be a source of great confusion and frustration.

Multiple Sclerosis: The Questions You Have - The Answers You Need

by Rosalind C. Kalb

This book, developed under the auspices of the Consortium of Multiple Sclerosis Centers and made possible by an educational grant to the consortium by Bertex Laboratories, the manufacturer of Betaseron, the first drug approved by the FDA for treatment of multiple sclerosis, represents an interdisciplinary approach to the disease. Its goal is to help those with MS and their families formulate questions to ask their healthcare providers so they can manage life with MS. Written by experts, chapters cover topics ranging from neurology and treatment to emotional, sexual, and employment issues. Introductory material is followed by a series of questions most often asked of the authors in their work with MS, as well as questions received by the Information Center at the National Multiple Sclerosis Society. Chapters conclude with a list of recommended readings and other available resources. Appendixes include information sheets about drugs commonly used to treat and manage MS, as well as a comprehensive glossary of terms. This work is more inclusive and comprehensive than most single-authored, consumer-oriented publications, and the authors recommend it not necessarily be read cover to cover but treated as a reference source to be referred to according to individual need. Recommended to supplement other, more traditional sources such as Louis Rosner Jr. and Shelley Ross's Multiple Sclerosis (S. & S., 1992) in consumer health collections.?Sue Hollander, Univ. of Illinois Lib. of the Health Sciences at Rockford

The MS Workbook: Living Fully With Multiple Sclerosis

by George H., M.D. Kraft, Dawn M., Ph.D. Ehde, Kurt L., Ph.D. Johnson, and Robert T. Fraser

Multiple sclerosis (MS) can be a terrifying diagnosis for anyone to face. But, as with many other potentially devastating problems, MS can be best controlled and best lived with when sufferers balance prudent lifestyle changes with effective treatment—and these sorts of choices require sound and current information. This workbook, written by a team of doctors and psychologists from the renowned Western MS Center at the University of Washington School of Medicine, is the first available for people with MS. It covers a wide variety of problems, everything from symptom management to sexual function to career opportunities to spirituality.
"The MS Workbook is the most in-depth guide to living well with MS that I have seen yet. The pages are filled with practical, reader-friendly information on everything from cognitive challenges and fatigue, to relapse triggers and unconventional therapies. But it is the checklists, worksheets, and quizzes that will actively engage readers and empower them to fully incorporate these life-changing strategies." - Editor, MSFocus, national magazine of the Multiple Sclerosis Foundation

The Multiple Sclerosis Diet Book

by Roy Laver Swank and Barbara Brewer Dugan

Hundreds of new recipes for dishes that taste terrific but stick to the diet rules so important for controlling M.S.--now completely revised to conform to the latest medical research.

Facing the Cognitive Challenges of Multiple Sclerosis

by Jeffrey N. Gingold

About the Author
Jeffrey N. Gingold is an outspoken advocate regarding cognitive disability and has been a federal and state lobbyist. He helped procure funding for an MS early diagnosis program for indigent women in Wisconsin. He was the recipient of the NMSS Wisconsin Chapters 2003 Outstanding Volunteer Award.

The MS Recovery Diet

by Ann Sawyer and Judith Bachrach

More than half a million people live with multiple sclerosis, yet conventional medicine still has little to offer patients. There is no known cure-and even recent breakthroughs in drug therapy do not work to control many of the symptoms or promise any degree of recovery.
But there is an alternative to drugs that can stop and reverse the ravaging symptoms of MS-the MS Recovery Diet. As this book explains, there are five common food triggers that can set off the symptoms of MS-dairy, grains containing glutens, legumes, eggs, and yeast. Yet because MS is such a complex disease, other foods play a role, as culprits or aides. The MS Recovery Diet explains the background, science, and development of this treatment in one source for the first time, and shows readers how to pinpoint their specific problem foods and sensitivities. It also offers more than one hundred simple recipes, as well as strategies to improve digestion, balance the immune system, and repair the body's myelin-crucial steps toward healing the body.
Both of the authors, Ann D. Sawyer and Judith E. Bachrach, who had been diagnosed and disabled by multiple sclerosis, have experienced incredible recovery on the diet. Within the first three months on this program, Sawyer was able to stop the disease progression and begin to walk short distances with an even gait. Bachrach, whose health has been declining because of MS for thirty-eight years, regained feeling in her toes in one week and after one year on the diet, has stopped taking all medication. This book shares the treatment plan that has dramatically changed their lives, and the lives of others who have discovered it. With inspiring personal stories throughout, it offers real help-and hope-for sufferers of MS.

Speech and Language Disorders in Multiple Sclerosis

by Bruce Murdoch

A comprehensive examination of the communication impairments that occur in association with multiple sclerosis. It covers the more widely recognized motor speech disorders seen in association with this condition, and the more recently identified language disorders reported to occur in persons with diseases of the cerebral white matter. A full description of the neuropathophysiology, epidemiology, aetiology, clinical manifestations and medical treatment of multiple sclerosis is also included. The findings of studies relating to the effects of multiple sclerosis on the physical functioning of the articulatory, velopharyngeal, laryngeal and respiratory systems are also included. In addition, contemporary methods for treating speech and language disorders in multiple sclerosis are described and discussed and recommendations are made.

Multiple Sclerosis: The Guide to Treatment and Management

by Chris H. Polman, Alan J. Thompson, T. Jock Murray, and Allen C. Bowling

This completely revised edition of the best-selling "Multiple Sclerosis: The Guide to Treatment and Management is a comprehensive, accessible guide to the present therapeutic options and their efficacy. Special features include expert opinion statements for each MS therapy; a unique guide to the wide diversity of therapeutic options available; a thorough discussion of the usefulness, effectiveness, and side effects of individual treatments; a new chapter on unconventional therapies; and a detailed guide to further reading.
This compendium of the most frequently used treatments for multiple sclerosis is an authoritative reference for all physicians and a factual guide for patients who need information about therapies. For reader accessibility, the book is organized into sections dealing with the treatment of acute exacerbations, disease-modifying therapies, symptom management, and alternative therapies. Each chapter in the new edition concludes with references, especially useful for readers who want more information about the therapies discussed.

The First Year: Multiple Sclerosis: An Essential Guide for the Newly Diagnosed (The First Year)

by Margaret Blackstone and Saud A. Sadiq

- Completely revised and updated: From the first moment of her diagnosis, Margaret Blackstone educated herself on every aspect of MS. As a regular contributor to Inside MS magazine and with regular contact with Dr. Sadiq, director of The Multiple Sclerosis Research and Treatment Center at St. Luke's Hospital, Blackstone has continued to follow the latest research and developments.
- The most recent, up-to-date information on MS: MS has been in the news due to controversy over Tysabri. There have also been many reports on the shifting demographics of the illness. Blackstone includes new information on who gets MS, treatments, medications, and trends in research.
- MS affects approximately 2.5 million people worldwide: Multiple sclerosis is as much a mystery as it is a disease; this chronic and often-disabling condition of the central nervous system affects an estimated 400,000 nationwide.

The 36-Hour Day: A Family Guide to Caring for People with Alzheimer Disease, Other Dementias, and Memory Loss in Later Life 4th Edition (A Johns Hopkins Press Health Book)

The bestselling family guide to caring for people with Alzheimer's and other dementias is updated with new information on medical research and the delivery of care. Includes resources for families and adult children who care for people with dementia, the latest information on nursing homes and other communal living arrangements, and more.

From The Publisher: This best-selling book is the "bible" for families caring for people with Alzheimer disease, offering comfort and support to millions worldwide. In addition to the practical and compassionate guidance that have made The 36-Hour Day invaluable to caregivers, the fourth edition includes new information on medical research and the delivery of care.

The new edition includes:    new information on diagnostic evaluation-resources for families and adult children who care for people with dementia-updated legal and financial information-the latest information on nursing homes and other communal living arrangements-new information on research, medications, and the biological causes and effects of dementia.

When Your Loved One Has Dementia: A Simple Guide for Caregivers

by Joy A. Glenner, Jean M. Stehman, Judith Davagnino, and Margaret J. Galante

Eighty percent of persons with dementia live at home, and the family members caring for them are often overwhelmed by the enormous responsibility and the complexities of care. This book is designed to support the caregivers and help them understand the needs and feelings of the person for whom they are caring. A central focus is the goal of sustaining a loving family relationship between the caregiver and the patient.

Developed from a training program for professionals and family caregivers, this book teaches the basics of dementia care while emphasizing communication, understanding and acceptance, and personal growth through the caregiving experience. The result is a guide that integrates the practicalities of caregiving with the human emotions that accompany it.

Alzheimer Disease and Other Dementias: A Practical Guide (Practical Guides in Psychiatry)

by Marc E Agronin

Learning to Speak Alzheimer's: A Groundbreaking Approach for Everyone Dealing with the Disease by Joanne Koenig Coste and Robert Butler

Now in its Second Edition, this practical guide focuses on assessment, diagnosis, and management of the complex array of dementia disorders seen in older patients. Using the conversational style and clinical vignettes found in all Practical Guides in Psychiatry titles, Dr. Agronin addresses all the subtypes of dementia and associated psychiatric conditions such as agitation, psychosis, and depression. This edition features a new chapter on mild cognitive impairment and expanded coverage of Alzheimer disease and risk factors.

Chapters offer advice on caregiver support and legal and ethical concerns. Handy pocket-card appendices include tests used in the dementia workup and treatment guides for agitation, psychosis, and depression.

Alzheimer's from the Inside Out

by Richard Taylor

This collection of more than 80 short essays offers readers a rare exploration of the often incomprehensible world of individuals with Alzheimer's disease. Written by a retired psychologist diagnosed with Alzheimer's disease at age 58, topics covered include loss of independence, communication difficulties with caregivers, unwanted personality shifts, and never-ending uncertainty about the future. This is a captivating read for anyone affected personally or professionally by Alzheimer's disease, especially individuals with early-stage Alzheimer's disease, family caregivers, and professional caregivers, such as nurses, social workers, and counselors.

A Caregiver's Guide to Alzheimer's Disease: 300 Tips for Making Life Easier

by Patricia Callone, Barbara Vasiloff, Roger Brumback, and Janaan Manternach

An estimated 5 million Americans have Alzheimer's disease. That number continues to grow — by 2050 the number of individuals with Alzheimer's could range from 11.3 million to 16 million. Alzheimer's disease is not a normal part of aging. It is a devastating disorder of the brain's nerve cells that impairs memory, thinking, and behavior. Winner of the 2006 American Journal of Nursing Book of Year Award, A Caregiver's Guide to Alzheimer's DiseaseA Caregiver's Guide to Alzheimer's Disease is essential for all readers who want to focus on the capabilities that remain instead of those that have been lost. This book will help readers understand what is physically happening to the brain so they can empower their own special skills and talents throughout the disease process. Chapters cover legal and financial issues, family forums in the caregiving process, the role of medication at various stages of the disease, helping children understand what is happening to a loved one, handling the holidays and celebrations, and making the living environment more stimulating and enjoyable. With an abundance of pointers and guidelines for affected individuals, their families, friends and caregivers.

Supporting the Caregiver in Dementia: A Guide for Health Care Professionals

by Sheila M. LoboPrabhu, Victor A. Molinari, and James W. Lomax

Dementia is one of the greatest challenges facing seniors and their caregivers around the globe. Developed by experts in both research and practice, this guide for mental health clinicians explores the experience of caregiving in dementia, discussing the latest research developments and sharing clinical pearls of wisdom that can easily be translated to daily practice.
The contributors explore the history of caregiving and then examine the current demographics of caregivers for persons with dementia. They discuss who provides care, the settings in which it is delivered, and the rewards and burdens of caregiving. They place special emphasis on understanding the psychological needs of both the person with dementia and the caregiver, as well as interpersonal bonds, spiritual dimensions, and reactions to grief and loss. Using a multidisciplinary approach to treatment for caregivers, this book addresses the role of pharmacotherapy, individual and family interventions, and social supports. Finally, the authors reflect on societal issues such as health care policies, ethnic elders, and ethics.
This volume offers health professionals insights into the daily lives of caregivers, along with tools to provide their patients with the support they need.

Handbook Of Dementia

by Peter A. Lichtenberg, Daniel L. Murman, and Alan M. Mellow

Broad, interdisciplinary guide to understanding diagnosing, and treating dementia and its related illnesses and conditions. Provides specialized knowledge about the psychological, neurological, and psychiatric aspects of dementia, including etiology and diagnosis, assessment tools, treatments, and comorbidities. Also addresses multicultural issues. DNLM: Dementia.

Voices Of Alzheimer's: Courage, Humor, Hope, And Love In The Face Of Dementia

by Betsy Peterson

Betsy Peterson spent fourteen years caring for her husband who was suffering from dementia, an experience that put her in touch with others inside the struggle to have or to care for someone with the disease. A combination of contributions from patients, their families, friends, and caregivers, Voices of Alzheimer's gathers the poignant stories, funny quotes, and priceless encouragement that Peterson heard and that helped her along the way. Capturing the many dimensions of the Alzheimer experience-the challenges, the struggles, the humor, and even the rewards-aVoices presents a varied, and realistic, look at what it's like to be affected by the disease. With compassion, humor, and grace, it offers the simple advice, wisdom, and understanding of others who have traveled the same uncertain path.

Understanding Dementia

by Alan Jacques and Graham A. Jackson

Royal Edinburgh Hospital, UK. Provides a practical approach to the problems of dementia. The difficulties associated with the condition are discussed but are combined with a positive attitude to ways of facing up to and coping with those problems. For nurses of dementia patients.

Creating Moments of Joy for the Person with Alzheimer's or Dementia, 3rd. Ed.

by Jolene Brackey

Jolene Brackey has a vision. A vision that will soon look beyond the challenges of Alzheimer's disease and focus more of our energy on creating moments of joy. When a person has short-term memory loss, his life is made up of moments. But if you think about it, our memory is made up of moments, too. We are not able to create a perfectly wonderful day with someone who has dementia, but it is absolutely attainable to create a perfectly wonderful moment; a moment that puts a smile on their face, a twinkle in their eye, or triggers a memory. Five minutes later, they won't remember what you did or said, but the feeling you left them with will linger.

Caregiving Tips A-Z: Alzheimer's & Other Dementias

by Starr Calo-oy and Bob Calo-oy

About the Authors
Starr & Bob Calo-oy were both born and raised in San Antonio and have been joyfully married for twenty-eight years. From 1989 to 2006, they owned and operated a personal care home specializing in the care of terminally ill patients and people with Alzheimer s disease and other forms of dementia in their San Antonio home.
They also cared for the well-minded elderly who could no longer care for themselves at home. In addition to caring for the elderly in their home, they give in-service training for doctors, nurses, and the staffs of hospices and home health agencies, sharing tips and unique ideas for caring for people with dementia.
Starr & Bob host a one-hour radio talk show in San Antonio (KKYX-680 AM) called Caregiving 101. They have guests on the live show and take questions from callers. Those who want to access their past shows can do so by visiting their website, caregiversadvice.net.
They also do a segment by the same title on television every Sunday morning, which can be viewed on their website.
Starr gives private consultations to individuals on how to start and operate a successful personal care home, as well as helping family caregivers set up their home for care. She is a columnist for SAWorship.com as well as an occasional freelance writer for the San Antonio Express-News.

ABC's of Activities for Alzheimers

by Amira Choukair Tame

My unique activities are designed to stimulate memory function, enhance social skills and improve the quality of life for individuals at any stage of dementia.

Living With An Impostor: A Confluence of Art, Depression and Dementia

by Lawrence Lee

Insights into Lawrence W. Lee's 40-year battle with severe depression, his wife's slow descent into dementia, and his life and work as an artist are combined into a cautionary tale that will ring true to anyone over 50. You will laugh. You will cry. You will ask yourself some of the hard questions most people forget to ask while there is still time. The author uses excerpts from personal journals and other writings to weave together the three related stories of art, dementia, and depression into a book that reveals something of the disjointed nature of human experience and points again and again to the role small, seemingly trivial decisions can have in all our lives: how chance can become a most powerful conspirator, leading us down paths un-chosen and changing our lives forever.

As the author attempts to find personal meaning in the course his life has taken, the reader is swept along in their own personal journey, wondering about their own past and future, and about those decisions both grand and small that have brought them to their particular place on their unique road into the future. Some will find solace. Others will find heartbreak. All will come away looking at themselves and their lives differently, for better or for worse.

Communication Disability in the Dementias

by Karen Bryan and Jane Maxim

This book focuses on language and communication issues with older people with mental health problems. Radically revised and updated from the authors’ earlier book, “Communication Disability and the Psychiatry of Old Age”, this book recognizes that language and communication is not just the business of speech and language therapy but is relevant to all staff involved with people who have mental health difficulties. 
This book focuses on what older people with mental health difficulties require to maintain their independence and to minimize the effects of degenerative disease processes for as long as possible from a speech and language perspective.
•    Relevant to all members of the multidisciplinary team involved within older people’s mental health services
•    Each chapter is evidence-based and factual
•    Reflects the substantial advances in the diagnosis and treatment of dementias

Feeding and Swallowing Disorders in Dementia

by Jacqueline Kindell

Neurological Differential Diagnosis

by John P. Patten

This unique text, which fills the gap between shorter texts containing little explanatory material and the advanced compendia for those with a good working knowledge of neurological disorders, is intended for the novice and those physicians who require an update on the diagnosis of neurological disorders. To understand the symptoms and signs requires a good knowledge of the gross anatomy of the central nervous system and supporting tissues. This is achieved by the liberal use of the author's own detailed diagrams backed up with concise and practical guidance on diagnosis and treatment as well as appropriate case studies. This long awaited second edition of a highly popular guide reflects recent advances in the subject such as computed tomography and MRI which have replaced more invasive examination techniques. The tutorial approach will present readers with an authoritative view of the fundamentals of neurology in practice.

The Fearless Caregiver: How to Get the Best Care for Your Loved One and Still Have a Life of Your Own (Capital Cares)

by Gary Barg

While they are giving care, the nation's 25 million family caregivers rarely get a rest. Gone are the days when you could rely on others to do the work of caring for a loved one in your family. America's healthcare system throws many of the vital decisions, costs and burdens back on the family.
This book clearly defines your vital role in developing your loved one's care plan. It teaches you to deal successfully with managed care organizations, home health services, and especially your loved one; and arms you with the knowledge and skills you need for deciding if your loved one's care is appropriate, if your doctor is the right one, if something more is needed. From wills and powers-of-attorney, to practical tips for dealing with disabilities, to long term care options, to battling stress and depression -- the shared wisdom in this book comes not only from the experienced editors of "Today's Caregiver Magazine", but also from the inspiring personal stories of readers of the magazine who have learned to "stand up to the system when the system no longer stands up for your loved one."

Dysarthria: A Physiological Approach to Assessment and Treatment

by Bruce Murdoch

A study of research and theory in the classification, assessment and treatment of dysarthria, including instrumental methods. It discusses the neurological/neuropathological bases of dysarthria and studies the physiological basis of speech for each type of dysarthria.

Table of Contents: The neuroanatomical framework of dysarthia; perceptual analysis of dysarthia speech; instrumental assessment of the speech mechanism; acoustic analysis of dysarthia speech; treatment of dysarthia; flaccid dysarthia; spastic dysarthia; ataxic dysarthia; hypokinetic dysarthia; hyperkinetic dysarthia; mixed dysarthia; acquired and developmental dysarthia in childhood.

From the Brain to the Mouth: Acquired Dysarthria and Dysfluency in Adults (Neuropsychology and Cognition)

by Y. Lebrun

The book offers new insights into acquired dysarthria in adults as well as a detailed discussion of the problems raised by the nature, assessment and therapy of acquired dysfluency in adults. It highlights the relationships that obtain between the two conditions and proposes a neurobiological interpretation of stuttering. The book is designed for neuropsychologists, neurolinguists, neurologists, neuropsychiatrists, speech therapists and speech scientists.

Dysarthria Sourcebook

by Barbara Tanner, Fay Young, and Sandra J. Robertson

Motor Speech Disorders: Substrates, Differential Diagnosis, and Management

by Joseph R. Duffy and Mayo Clinic

With expanded and updated information including current techniques, approaches, and case studies, the 2nd edition of this bestselling book continues its reputation as a dependable and outstanding evidence-based source on acquired motor speech disorders in adults. It covers the substrates of motor speech and its disorders, the disorders and their diagnoses, and management -- focusing on integrating what is known about the bases of motor speech disorders with the realities of clinical practice to ensure readers have the key content they need to be effective practitioners.
•    Evidence-based practice focus with relevant research evidence and data from the Mayo Clinic speech pathology practice
•    Includes the clinical characteristics of the primary motor speech disorders as well as general guidelines for differential diagnosis
•    Offers authoritative guidance on the diagnosis and management of motor speech disorders by a highly respected expert in the field of motor speech disorders
•    73 case studies demonstrate concepts as they apply to real-world practice
•    Over 100 table and boxes highlight important information
•    Chapters include new research and theories, new techniques, current trends, and updated and new information sources
•    22 new illustrations showcase the latest technology in the field
•    Fresh, new book design highlights case studies, boxed text, and tables - making it easier to find key information
•    Nine new case studies reflect the realities of clinical practice today

Motor Speech Disorders

Textbook on the neurology of communication. Covers the causes, symptoms, diagnosis, and management of the most common neurologic communication disorders.

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FDA-2: Frenchay Dysarthria Assessment (Complete Kit)

by Pamela Enderby and Rebecca Palmer

Ages: 12 years to adult Testing Time: 20 minutes Administration: Individual The second edition of Frenchay Dysarthria Assessment (FDA-2) includes new powerful knowledge about motor speech disorders and their contribution to neurological DIAGNOSIS. This updated edition remains a well-established test for the measurement, differential description, and DIAGNOSIS of dysarthria. It can be used in international research, as well as all clinical settings. Norms are provided for ages 12 to 97. FDA-2 is quick and simple to administer, accurate, reliable, and cost-efficient. The client is rated on a number of simple performance tasks related to speech function.
It is divided into eight sections:
1. Reflexes   Ratings for cough, swallow, and dribble/drool
2. Respiration   Ratings at rest and in speech
3. Lips   Ratings for at rest, spread, seal, alternate, and in speech
4. Palate   Ratings for fluids, maintenance, and in speech
5. Laryngeal   Ratings for time, pitch, volume, and in speech
6. Tongue   Ratings for at rest, protrusion, elevation, lateral, alternate, an in speech
7. Intelligibility   Ratings for words, sentences, and conversation
8. Influencing Factors   Includes hearing, sight, teeth, language, mood, posture, rate (words per minute), and sensation The test results can be recorded on the FDA-2 Rating Form, indicating both the client s strengths and weaknesses. The Rating Form also allows the clinician to compare the patient s performance across all the items. Normative data are reported for adults without dysarthria as well as patients with specific dysarthria associated with confirmed medical diagnoses. Separate tables enable speech therapists to compare individual results with those of known dysarthric groups. The results are easily communicated to other professionals via the three-part carbonized record form.

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The Handbook of Adult Language Disorders

by Argye Hillis

This handbook provides clinicians and researchers with a comprehensive reference resource on the study of acquired language disorders - or aphasia. The focus is on how the study of acquired language disorders has contributed to our understanding of normal language and its neural substrates, and to the clinical management of language disorders. The handbook is unique in reviewing studies from all of the major disciplines in which aphasia research is conducted - cognitive neuropsychology, linguistics, neurology, neuroimaging, and speech-language pathology - as they apply to each topic of language. For each language domain, e.g. reading, spelling, naming, there is a chapter devoted to recent neuroimaging studies and a chapter devoted to clinical diagnosis and treatment of impairments in that domain. Featuring contributions from leading experts in the field, The Handbook of Adult Language Disorders is a truly integrated and authoritative reference work on aphasia research that will prove invaluable to anyone working in the field.

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Neurogenic Disorders Of Language

by Laura Murray and Heather M Clark

Brain damage due to stroke, traumatic brain injury (TBI), progressive neurological disease, and other etiologies is extremely common worldwide. Neurogenic language disorders that result from the illnesses, accidents, or progressive diseases that cause brain damage can negatively impact an individualas communicative and cognitive well-being. This thoughtful text provides speech-language pathologists and related health care professionals with a comprehensive examination of the concepts and procedures surrounding the management of adult neurogenic disorders. Information is provided on the major disorders including aphasia, traumatic brain injury, right hemisphere disorders, and dementia and assessment procedures and treatment approaches are discussed. In addition, clinical issues--both theoretical and applied--are highlighted throughout the book, making this an excellent choice for anyone working with neurogenic language disorders.

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Language Intervention Strategies in Aphasia and Related Neurogenic Communication Disorders

by Roberta Chapey (Editor)

This thoroughly revised and updated Fifth Edition is the most comprehensive resource on aphasia and related neurogenic communication disorders from the most distinguished authorities of our time. This classic text has been used by graduate speech language pathology students for over 25 years, and continues to be the definitive resource across the speech sciences for aphasia.

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Aphasia and Related Neurogenic Language Disorders

by Leonard LaPointe

Now thoroughly updated, this important new book builds on the classic first edition to provide complete coverage of aphasia and related neurogenic language disorders. For the first time, the larger psychological aspects of neurogenic language conditions are examined, including adaptation to chronicity, treatment of accompanying mood disorders, and the role of both the family and clinician in improving patient care. A Brandon-Hill selection.
Highlights of this important work: - Systematic discussion of the pathophysiology, differentiating features, evaluation, and treatment of each neurogenic disorder - Special chapters on right hemisphere syndrome, traumatic brain injury, and dementia - New research on dyslexia and dysgraphia - Comprehensive, up-to-date references and suggestions for additional reading

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Dysphagia: Diagnosis and Management

by Michael E. Groher

Veterans Administration Hospital, Tampa, FL. Third edition of a multidisciplinary text on swallowing disorders, for physicians, nurses, speech/language pathologists, dieticians, and physical therapists. Halftone illustrations. 14 contributors, 13 U.S.

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Evaluation and Treatment of Swallowing Disorders

by Jeri A. Logemann

Review:
The first few chapters explain typical anatomical structures, such as the muscles involved in swallow, cranial nerve function, the sequence of muscular action that bring about a swallow, and the events following introduction of various types/textures of food in the mouth. Dr. Logemann distinguishes clearly between an oral phase and a pharyngeal phase of swallow. (Some researchers, question this distinction and consider the swallow process more along a continuum, rather than as two distinct phases). Typical changes in swallow with age are explained.

• Chapter 3 explains various instrumental evaluation techniques briefly.

• Chapter 4 deals with disorders of swallow. (I find the table on page 73 comparing patient description to actual symptoms during a bedside screen and radiographic study particularly useful. It helped me a lot to watch videotaped radiographic studies of swallows as I read this chapter.)

• Chapter 5 describes screening and evaluation procedures. (I like the quick screen checklist on page 137. I use a modified version of this form.) This chapter also describes assessment of patients dependent on tracheostomy tube, and contrasts it with patients who are intubated. As in many other texts, assessment procedures discussed in this chapter assume that the patient is able to interact/participate in the evaluation process, at least moderately. I would like to see more information on swallow assessment of patients with various levels of dementia in a future edition of this book. Refer Lou Eaves' course - check the nss-nrs website mentioned earlier.)

• Chapter 6 looks at treatment planning and the important determination of whether the patient will benefit from therapy considering case history and other factors. Also included is a general guideline to decide on oral vs. non-oral feeding. The use of compensatory strategies such as postural changes, and diet modification guidelines with rationale for their use are provided. Various types/examples of direct (ex. - swallow of saliva), and indirect (ex. - oromotor exercise) therapy are provided for oral and pharyngeal stage swallow.

• Chapter 7 and 8 describe various surgical procedures for oral and pharyngeal stage cancer, associated reconstruction techniques, neurological conditions such as Guillan-Barre and Poliomyelitis, resulting swallowing disorders and rehab strategies for these populations.

• Chapter 10 addresses parkinson's disease, ALS, MS, Myasthenia Gravis and other degenerative diseases and suggests rehab strategies.

• Chapter 11 explains medical procedures for various pharyngeal stage swallow dysfunction, such as cricopharyngeal myotomy to permanently open the upper esophageal sphincter, followed by an explanation of when such procedure is used.

• Chapter 12 follows a question and answer format. Some frequently asked questions on clinical decision making are discussed, such as - When should a patient receive an in-depth diagnostic assessment? The last chapter discusses the role of the many members in an interdisciplinary dysphagia management team.

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The Dysphagia Cookbook: Great Tasting and Nutritious Recipes for People With Swallowing Difficulties

by Elayne Achille

Product Description
The Dysphagia Cookbook is a specialty cookbook filled with nutritious, great-tasting recipes for those whose eating options are limited by chewing and swallowing difficulties. All of the recipes focus on enhancing flavor, presentation, texture, aroma, and color, for there are many other products that supply nutritious calories or liquids but give little attention to these quality-of-life concerns.
Some of the unique aspects of The Dysphagia Cookbook make it particularly useful and practical. These include:
• A classification of S, G, or P indicates consistency levels of soft, ground, or puréed.
• Flexible instructions provide suggestions for adapting recipes to accommodate increasing levels of chewing and swallowing difficulties.
• There are many recipes with an international flavor that do not use difficult-to-find ingredients.
• Ready-made products that have been tested for thickness, flavor, ease of chewing, and ease of purchase and preparation are listed.
• A section on must-have kitchen supplies helps cooks deal with the new ways of preparing food for people with swallowing difficulties.
• The approach is practical rather than clinical.
The ritual of eating gives shape and meaning to our lives. Many meals are consumed in a pleasant atmosphere with the company of loved ones and friends in lively conversation. The Dysphagia Cookbook is an attempt to restore this joy and dignity to those whose pleasure in this area has been limited to one degree or another.

Easy-to-Swallow, Easy-to-Chew Cookbook: Over 150 Tasty and Nutritious Recipes for People Who Have Difficulty Swallowing

by Donna L. Weihofen, JoAnne Robbins, and Paula A. Sullivan

Delicious and nourishing recipes that are easy to eat and swallow
The simple act of eating is a challenge for millions of people whose ability to chew and swallow has been compromised by the debilitating effects of age or disease. The Easy-to-Swallow, Easy-to-Chew Cookbook presents a collection of more than 150 nutritious recipes that make eating enjoyable and satisfying for anyone who has difficulty chewing or swallowing. It also shares helpful tips and techniques to make eating easier for the elderly and those with such diseases as Parkinsons, AIDS, or head and neck cancers.
Donna L. Weihofen, RD, MS (Verona, WI), is a nutritionist and the author of The Cancer Survival Cookbook and Magic Spices. JoAnne Robbins, PhD, is founder of the University of Wisconsins clinical Swallowing Service. Paula A. Sullivan, is a speech pathologist who specializes in swallowing rehabilitation.

Augmentative & Alternative Communication: Supporting Children & Adults With Complex Communication Needs

by David R. Beukelman and Pat Mirenda

Approaching severe communication disorders from an intervention perspective, this trusted resource thoroughly prepares students and practicing professionals to serve individuals with augmentative and alternative communication needs. In this revised third edition, professionals working or preparing to work with children and adults who use AAC will get new and expanded content on adults with degenerative language or cognitive disorders, adults with acquired disabilities, students who use AAC in general education classrooms, use of capability assessment to determine needs and identify AAC options, and the most recent AAC devices and interventions. Readers will still have everything that made the earlier editions of this text so useful: extensive coverage of AAC assessment, intervention planning, and the many different types of congenital and acquired communication disorders (see sidebar), plus a step-by-step guide to clinical application. A comprehensive textbook for students in introductory courses and a valuable reference for in-service educators and therapists, this book will help professionals guide children and adults as they increase their communicative competence and participate more fully in all aspects of life.

AAC from A to Z (Augmentative and Alternative Communications Perspectives)

Augmentative and Alternative Communication: Developmental Issues

by Stephen von Tetzchner and Nicola Grove

This text describes the development of augmentative and alternative communication. The focus is not on disabilities, although the atypical developmental paths to language described in this book are caused by a variety of disabilities, but on the developmental achievements of children using augmentative and alternative communication systems.

This book is a first attempt to look at the achievements of children using alternative language forms from a broad developmental perspective and discuss how their semantic, grammatical and pragmatic development is promoted through social interactions, both planned and incidental in nature, that take place in particular sociocultural circumstances. The authors use small group data and dialogues to show how the children use grammatical structures and strategies to convey meaning and solve communicative challenges.

The overall aim of the book is to inspire a shift towards a developmental understanding of augmentative and alternative communication in both research and clinical practice, leading to new knowledge and a better basis for intervention practices, and thereby to improved social and societal participation for children using augmentative and alternative communication.

The Efficacy of Augmentative and Alternative Communication: Toward Evidence-Based Practice

by Ralf W. Schlosser, Helen H. Arvidson, and Lyle L. Lloyd

This book provides readers with essential tools for appraising evidence and outlining steps for planning and implementing better efficacy research. It aims to help researchers and practitioners develop the necessary skills for moving the augmentative and alternative communication field toward evidence-based practice. The Efficacy of Augmentative and Alternative Communication: Toward Evidence Based Practice is a crucial addition to anyone's bookshelf who is involved in the AAC enterprise, including speech-language pathologists, special educators, physical therapists, occupational therapists, students in professional programs, individuals using AAC, their families, and applied researchers.

• Provides solutions to avoid common pitfalls of prominent research designs for evaluating efficacy

• Discusses how to formulate research questions and deal with issues of participant selection

• Suggests how to plan and evaluate the integrity and social validity of interventions

Assistive Technology: Principles and Applications for Communication Disorders and Special Education

by Raymond W. Quist, Lyle L. Lloyd, and Helen H. Arvidson

This book explains the role and range of applications of technology in augmentative and alternative communication (AAC). It also demonstrates principles for the selection of technology and explains the basic operations of and procedures for computers and peripheral devices used by AAC professionals It attempts to understand the effects of technology on the development and use of communication. A variety of technologies are covered for speech, hearing, and vision impairments.

Will appeal to students and professionals directly involved in service delivery (speech-language pathologists, special educators, occupational therapists, physical therapists)

Will serve as a professional resource for practicing clinicians/educators, a primary text for special emphasis/focus AAC courses, seminars, and in-service programs, and a supplemental text for broad-based AAC courses.

Communicating without Speech: Practical Augmentative and Alternative Communication for Children (Clinics in Developmental Medicine )

by Helen Cockerill and Lesley Carroll-Few

Purchase fromThis volume presents current research and accepted good practice in the field of augmentative and alternative communication (AAC) systems. The authors give detailed information on the neurology of speech and language, and offer guidelines for the assessment of non-speaking children. The chapters discuss such topics as issues of prognosis for speech, timing of intervention, and the importance of working within a multidisciplinary framework. The central role of families and schools in the successful introduction and support of AAC for social communication and curriculum access is recognized, and a range of AAC systems and resources are described, as are the views of AAC users and their families.

Augmentative and Alternative Communication and Severe Disabilities: Beyond Poverty

by Erna Alant and Lyle Lloyd

Communities and countries who are not affluent or economically and socially disadvantaged present their own set of intervention circumstances that need to be taken into account when planning intervention for people with disabilities particularly those with AAC need. These contexts provide not only professionals, but all partners involved in the intervention process with unique challenges that require a reevaluation of AAC intervention programmes. This book presents a different perspective on AAC intervention by focusing on the application of various AAC related issues within a poverty context. It is intended for advanced students and professionals across disciplines that are interested in extending their knowledge and critical thinking to advance issues surrounding AAC intervention within a poverty context.

Handbook Of Augmentative And Alternative Communication

by Sharon L. Glennen and Denise C. DeCoste

Augmentative and alternative communication (AAC) is a field which crosses many disciplinary boundaries. It is a rapidly changing field that uses the latest innovations and technologies to aid the language-disabled, and requires fluency not only in the hands-on technological aspect, but the service-delivery side as well. This well-written handbook addresses that need and is filled with practical information and extensive referencing. A valuable text for graduate students studying communication disorders and special education, the book would be a useful addition to the professional library of anyone working with AAC users, most especially for those working with children.

Augmentative and Alternative Communication: A Handbook of Principles and Practices

by Lyle L. Lloyd, Donald R. Fuller, and Helen H. Arvidson

This is a valuable source of information and reference for the field of augmentative and alternative communication (AAC) in speech-language pathology. This handbook outlines the history and growth of the field from its beginnings a few decades ago to its current status as an integral element in the clinical and educational programs of individuals with severe communication disabilities. Legislation and funding opportunities which influence the provision of AAC services are presented and discussed along with current legal and ethical issues and future research needs. Speech pathologists, language and communication specialists and therapists.

Augmentative and Alternative Communication for Adults with Acquired Neurologic Disorders

by David R. Beukelman, Kathryn M. Yorkston, and Joe, Ph.D. Reichle

Now that Medicare and an increasing number of insurance companies are funding AAC devices for adults, you'll find it's more important than ever to have this research-based resource on hand. Practical and accessible, it addresses social, medical, and technical changes and how they affect adults with communication disorders. Part 1 discusses the everyday issues adults transitioning from speaking to using AAC struggle with--such as establishing new communication roles and integrating their natural speech with AAC--while Part 2 covers the six leading neurological disorders in adults: amyotrophic lateral sclerosis, Huntington disease and Parkinson's disease, traumatic brain injury, aphasia, and dementia. You'll learn new ways to design individualized AAC systems that will help rebuild users' communicative confidence and encourage acceptance of their lives.

Building Communicative Competence With Individuals Who Use Augmentative and Alternative Communication

by Janice C., Ph.D. Light and Cathy Binger

This book is an introductory book for Speech-Language Pathology students and SLPs beginning to work with individuals who use augmentative and alternative communication. The book outlines in each chapter how to obtain communication goals with the person using AAC. The chapters become a bit repetitive in their teaching tactics, but this does help the reader remember the strategies used. It does focus on individuals with cognitive skills who are able to make choices regarding their communication systems. The material, however, can be applied to individuals who are in the severe to profound range of mental retardation.

Introduction to Augmentative and Alternative Communication

by Von Tetzchner, Stephen Von Tetzchner, and Harald Martinsen

An introduction to augmentative and alternative communication. The authors discuss factors that are important when choosing communication systems, assessment strategies, environmental adaptation, and the principles for teaching comprehension and use of such communication systems to individuals with different disabilities, including motor impairments, learning disabilities and autism. The text has its basis in modern developmental theories of language and communication. It has a practical approach with many examples and focuses on every-day situations.

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