Lupus, a disease of the immune system, can be quite deadly, claiming the lives of thousands of patients yearly. Dr. Daniel J. Wallace is one of the world's leading authorities on this disorder, an eminent clinician who has treated over 2000 lupus patients, the largest such practice in America. His The Lupus Book , originally published in 1995, immediately established itself as the most readable and helpful book on the disease. Now Dr. Wallace has once again completely revised The Lupus Book , incorporating a wealth of new information. This Third Edition discusses the newest breakthroughs in drug treatments and alternative therapies as well as updated information on the immune system--all laid out in user-friendly language that any patient could understand. Readers will discover new blood tests and new drugs introduced since the last edition, an extensive table of herbs that can be used for the disorder, and a large section on cognitive therapy and biofeedback. And as in past editions, the book provides absolutely lucid answers to such questions What causes lupus? How and where is the body affected? Can a woman with lupus have a baby? And how can one manage this disease? There is also a glossary of terms and an appendix of lupus resource materials compiled by the Lupus Foundation of America. Over a million Americans have lupus and some tens of thousands of patients die every year from the disease. The Third Edition of The Lupus Book offers these patients and their families a wealth of reliable, up-to-date information that will help them manage the disease and live a happier life. · Endorsed by the Lupus Foundation of America · A portion of the proceeds goes to Lupus research
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.
great for those who may have an autoimmune disorder. You'll gain a wealth of inside information that most Doctors so not discuss with you. It will validate what you have been going through and most importantly...why
I run a support group online at http://www.LupusMCTD.com for fellow patients. I hope you check us out. Live chats, "library" charts, resources and muchmore.
Obviously this is a book with a limited audience, but if you have lupus, have a loved one with lupus, or for whatever reason have a particular interest in the disease, this is an incredibly informative text. For many this is the gold standard of lupus books (for the layperson, at least), and I can see why: Wallace goes into a lot of detail, and I learned tons of stuff that my internet searches hadn't revealed. Of course it's not a fun or light read, but 5 stars for being an excellent reference.
Very easy read for understanding lupus. I refer back to it regulalry. Even booked a medical appt. with the author who practices in Los Angeles a few years back. Still a patient of his on a consult-basis and I consult with him and his nurses from time to time.
This is my bible in terms of dealing with SLE Lupus--it has answered all my questions in a sinmple, non-alarmist way. Clear, concise user-friendly information. An added bonus is a thorough discussion of the medications typically used to treat Lupus and their side effects.
Well-written book about lupus. Written by a rheumatologist, this book simplifies medical jargon and answers many questions about the disease. This is not a boring book either. The doctor has a sense of humor and injects the chapters with experiences from people with the disease.
A must read for anyone with lupus and any friend or relative of a Lupie! It is an excellent book, easy to understand, well written and very informative. Absolutely essential to regaining control and understanding lupus. The only reason I did not give it 5 stars is that it takes a conventional, biomedical approach. I believe this approach in combination with alternative treatments are most effective in treating Lupus. I encourage you to read this book first and as a priority, but then explore treatments not mentioned in the books (preferably that pertain to healing the gut in a permanent way). The latter is useful is you have moved passed the life threatening stage of the illness and looking to reach optimal health (I.e reduce or eliminate the more mild symptoms of pain, fatigue, mental fog, low grade fevers...). The book is essential knowledge for any lupus diagnosis right from the start and is especially relevant to a more active state of the illness.
This is not a fun read; it actually falls in the horror genre in places. However, it is well-written, and anecdotes are interspersed with the technical medical discussion. This is by far the top lay resource on lupus. It has been almost 10 years since my diagnosis, but I still learned a lot from the book.
I'd just like to chime in to agree that this must be the definitive reference for lupus patients. Wallace explains the auto-immune response in understandable terms, and discusses how each physical system is involved in lupus, making this an accessible & indispensable guide particularly for the newly diagnosed or those wanting a deeper understanding of this disease.
This book is really geared towards medical people. I regularly read this type of information because there isn't much out there for lay people when it comes to Lupus. There is a lot of information that was also in the previous edition.
Very informative and thorough guide of a very complicated disease. In some places it is seems very medical-jargon-y, but is very helpful overall. It gave me an excellent overview, helped me review the areas I currently have issues with and allowed me to prepare questions for my doctor team.
This is a tough read. The first 9 chapters are very technical and full of medical jargon. Once you get past that it starts to become a little easier to understand. There is a ton of information in this book. At times I felt a bit overwhelmed and had to step back from it. If you or someone you know has Lupus and have little to no knowledge of it and you want to get that information quickly, this is the book for you.
Well, I now see where the Dr. House joke of “It’s not Lupus” comes from – any part of the human body can be affected by Lupus - from the top of the head (alopecia) to the tip of the toes (Raynaud's phenomenon) and every single part in between. Wallace carefully makes his way through the human body and lays out in clear language and easy to understand diagrams and charts just how each part of the body can be affected.
And this disease affects women at a much higher percentage than men, so Wallace, bless him, spends a chunk of time assuring Lupus patients they aren’t crazy or imagining symptoms, even though, sadly, medical “professionals” are statistically likely to dismiss a woman with Lupus as just exaggerating or imagining her symptoms and pain and quickly misdiagnose her with something minor, so fight for your patient rights, ask questions, ask for help, and look for real support networks.
Easily accessible for the lay person with no medical background to read and digest. A well done introduction to the disease, laying out all parts of it in a calm and reassuring manner, addressing both physical and mental issues this disease brings with it, and, most importantly, letting people who have just gotten this diagnosis know that it is OK to rant and rave and be angry and that you shouldn’t blame yourself. As logical as that sounds, sometimes it’s what we really need to hear from someone else.
Very thorough. Written in laymen's terms but with in-depth explanations to give the reader a more comprehensive knowledge of the disease without getting too bogged down with technical terms. It still satisfied my need to gobble up any and all medical info I can find, so the technical terms that were there by necessity didn't bother me.
good information but very technical even for a nurse. Was looking more for coping strategies, more than technical read on lupus pathophysiology. Good reference book to keep on your shelf to review during disease exacerbation.
Could be helpful from an overall medical perspective, but not particularly helpful for "patients and their families." I did not find it helpful in guiding at all. It spouted many statistics, protocols, theories, and overall medical ideologies, but very few things that would be important to the patient. Good thing I didn't have a problem with all the medical jargon...but I honestly don't think most people would make it through this book 🙄 and once they did, what would they have gained? I made it through and feel like I learned nothing more than what quick Google searching has revealed.
Never thought I’d need to read a book like this, but here we are. I was disappointed by the depth and clarity of information online concerning Lupus. One quick library search later and I found this book. The information presented can be overwhelming in its medical terminology but you are informed beforehand which chapters might be challenging to follow (6th edition btw) and encouraged to skip around as needed. This book helped me understand so much more than any I resource I found online and strongly suggest reading if you think you may have, do have, or love someone who has Lupus.
I’ve been wanting to learn more in depth about lupus due to the possibility of me having it and this book was helpful to me ( I have MCTD and we’re not sure which autoimmune diseases yet but this is suspected). It explains a lot and does have a few tips that are helpful. Definitely recommend if you are suspected of lupus or have it.
Appreciated the information clearly written in this book. Wish I had met this doctor thirty years ago when my condition was dismissed as being depression. A very thorough, a must read.
Feels a little outdated in its presentation, despite being a 2008 edition. Learned some new lupus and autoimmune disorder details, as well as undifferentiated connective tissue disease (UCTD). Understand differences between lupus and fibromyalgia more clearly now.
I didn't read this for fun, but because I was diagnosed with crossover lupus scleroderma and raynaud's phenomenon. It gave me lots of info that I didn't even get from my doctor and gave me lots to ask him and gave me new knowledge about what is wrong with me.
Read this book for work -- seeking resources & literature for patients and their families. Although it is still very medical/technical, this can serve as a great reference book particularly when needing general information about labs, medications, and lupus symptoms.