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Making Sense of Fibromyalgia: New and Updated

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A comprehensive, must-read guide for fibromyalgia patients, their loved ones, and those who care for them Six million people in the United States meet the criteria for fibromyalgia, which is a disorder characterized by a combination of pain, fatigue, and related symptoms. On average, these patients see about four doctors before they are correctly diagnosed, and many are convinced they have a life-threatening illness such as an advanced stage of cancer. About $600 billion is spent annually in the United States to diagnose or manage chronic pain, including litigation fees, and it is estimated that fibromyalgia patients run up $20 billion in medical expenses annually. Despite these alarming numbers, there is a lack of understanding and a dearth of reliable information about fibromyalgia for patients. This fully updated edition of Making Sense of Fibromyalgia distills complex concepts and symptoms into an easily understandable narrative. Daniel J. Wallace, a leading rheumatologist at Cedars- Sinai Medical Center, and Janice Brock Wallace, an expert medical writer, have updated the original classic resource, which has sold over 100,000 copies since 1999. Making Sense of Fibromyalgia provides clear answers to common questions, explains findings from the latest research, and discusses treatment options for complex symptoms. Detailed information is provided about topics such as who gets fibromyalgia and why; how stress, hormones, and your immune system interact and relate to fibromyalgia; what conditions are associated with it; why and how you might be misdiagnosed; how to overcome fibromyalgia; and how to understand your prognosis. The authors share all there is to know about the syndrome as well as how our understanding of it has changed over time. This comprehensive companion covers the entire spectrum of issues for those suffering from fibromyalgia, as well as their families, friends, caretakers, primary care physicians, and other health p

272 pages, Paperback

First published January 14, 1999

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About the author

Daniel J. Wallace

27 books9 followers
Daniel Jeffrey Wallace is an American rheumatologist, clinical professor, author, and fellow. Wallace has published 400 peer reviewed publications, 8 textbooks, and 25 book chapters on topics such as lupus, Sjögren syndrome, osteoarthritis, and fibromyalgia. He has the largest cohort of lupus patients in the United States (2000).

A full professor of medicine (Cedars-Sinai Medical Center, David Geffen School of Medicine at UCLA), he is associate director of the Rheumatology Fellowship Program at Cedars-Sinai. His seminal contributions to research include being an author of the first paper to demonstrate vitamin D dysfunction and the importance of interleukin 6 in lupus, conducting the first large studies of apheresis in rheumatoid arthritis and lupus, and insights into the mechanisms of action of antimalarials.

Wallace's research accomplishments also include conducting many clinical rheumatic disease trials, examining the role of microvascular angina and accelerated atherogenesis in lupus, and work on anti-telomere antibodies which have garnered him 5 papers in The New England Journal of Medicine. Wallace's monograph, The Lupus Book, has sold over 100,000 copies since 1995.

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1,155 reviews28 followers
February 25, 2019
This book had a lot of good information, but I only understood about half of it - it seems like this book is geared more towards medical providers than patients.
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