This book addresses the concerns of patients and families living with amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease. Writing in plain language, contributors from around the country explain what ALS is and what is known about its causes, then describe methods for diagnosis and treatment of symptoms, and examine medical and rehabilitative management areas such as physical therapy, wheelchair selection, respiratory management, and alternative therapies. A section on living with ALS discusses support groups, financial realities, and home care agencies. There is also material on end of life issues such as palliative care and hospice care. A final section describes the work of major organizations and gives contacts for organizations, resources, and vendors. This third edition is updated to reflect the latest research and treatment options, with new information on noninvasive ventilators, the use of riluzole (Rilutek), and new patient guidelines developed by the American Academy of Neurology. B&w photos of medical equipment are included. Mitsumoto is director of the Eleanor and Lou Gehrig MDA/ALS Research Center and professor of neurology at Columbia University. Annotation ©2009 Book News, Inc., Portland, OR (booknews.com)