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Cure Unknown: Inside the Lyme Epidemic Hardcover – June 10, 2008

ISBN-13: 978-0312378127 ISBN-10: 0312378122 Edition: First Edition

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Product Details

  • Hardcover: 432 pages
  • Publisher: St. Martin's Press; First Edition edition (June 10, 2008)
  • Language: English
  • ISBN-10: 0312378122
  • ISBN-13: 978-0312378127
  • Product Dimensions: 6.8 x 1.4 x 9.1 inches
  • Shipping Weight: 3.2 pounds (View shipping rates and policies)
  • Average Customer Review: 4.9 out of 5 stars  See all reviews (126 customer reviews)
  • Amazon Best Sellers Rank: #505,045 in Books (See Top 100 in Books)

Editorial Reviews

From Booklist

*Starred Review* When journalist Weintraub and her family moved from their cramped, treeless home in New York City to a spacious, tree-shaded manse in suburban Chappaqua, they believed it was all good. Or at least the big yard with deer cavorting in nearby woods would be better, healthier, than their city digs. Within a short time, first one son, then the other, became sick with a series of increasingly debilitating disorders. Soon Weintraub and her husband presented a laundry list of similar complaints, many serious enough to threaten to sidetrack their careers. The family turned to local physicians for answers. Lyme disease, an infection communicated by the bite of a tick carried by those cavorting deer, was mentioned but discounted for a variety of reasons. Weintraub turned to the most prestigious medical centers New York had to offer and got similar responses. Hearing one implausible diagnosis after another and, worse, seeing no improvement in their individual conditions, the credentialed science writer began independent research and turned up what amounts to a controversy as contentious as creationism versus evolution. Weintraub turns a tragic (her children are still unwell) yet eye-opening experience into a shocking exposure of what can happen when egos, greed, and peer pressure supercede objective evidence, allowing patients to suffer chronic, disabling illness. --Donna Chavez


“Pamela Weintraub's book is compelling, clear and troubling.”
–Patti Adcroft, editorial director of Discover magazine


“In Cure, Unknown, Pamela Weintraub has produced both the definitive book about Lyme disease and associated disorders and a survivor’s account of a grueling medical odyssey. Weintraub is a masterful science writer and storyteller, and she tackles the quarrels and quagmires surrounding this baffling illness with intelligence and pathos. This is an important and unforgettable book, destined to make a lasting contribution to the field of investigative health journalism.”
–Kaja Perina, editor in chief of Psychology Today


"A thoroughly researched and well-written account of the disease's controversial history."
--Jane Brody, New York Times
"Pam Weintraub, veteran science writer, weaves personal narrative with hard-hitting investigative journalism to bring the underground epidemic of Lyme and other tick-borne diseases up from under the
-Rebecca Wells, author of Ya-Yas in Bloom and Divine Secrets of the Ya-Ya Sisterhood.
"I sometimes wonder if the only investigative writers who will possess the necessary temerity to remove the white gloves and tackle these putative experts to the ground will be those, like Weintraub and the
late Randy Shilts, whose personal experience demands that they follow the rocky trail that leads to the truth."
-Hillary Johnson, author of Osler's Web: Inside the Labyrinth of the Chronic Fatigue Syndrome
"Millions suffering from symptoms of a mysterious disease need suffer confusion and loss no longer. If you want to know the real story behind Lyme disease and how to find your way back to health, read this book."
-Mark Hyman, MD, author of the New York Times bestseller, UltraMetabolism.
"Science journalism at its best."
--Amiram Katz, MD, Clinical Faculty, Neurology Department, Yale School of Medicine
"Weintraub turns a tragic yet eye-opening experience into a shocking exposure of what can happen when egos, greed, and peer pressure supercede objective evidence, allowing patients to suffer chronic,
disabling illness."
–Donna Chavez, Booklist
"Exhaustively researched and highly recommended."
–Tina Neville, Library Journal
"A tale of biological complexities, scientific turf battles, political intrigue, human egos and money – lots of it."
–Dorothy Kupcha Leland, Sacramento Bee
"Living with Lyme gave Weintraub both the insight and the dogged ambition to find out some truths ...  rather than remaining stuck at the pro-Lyme, anti-Lyme debate, Weintraub spent many hours
interviewing researchers who are experts in the ticks that spread Lyme, and the bacterial spirochete, Borrelia burgdorferi, that causes it. What she found is that these researchers -- at places like the
State University of New York at Stony Brook on Long Island, and the University of California at Davis -- are slowly figuring out how complex the bacteria and the disease are. And Weintraub said, these
researchers, by and large, confirm what many Lyme patients have learned through bitter experience -- the bacteria can cause a persistent infection that may not be treated easily by a couple of
weeks of antibiotics."
--Robert Miller, Danbury News-Times
"The view from inside the tick tornado: Sober but scary ...A science and health journalist, Weintraub writes clearly and passionately about a mysterious illness that has confounded physicians, patients and
scientists for more than three decades, while she tries to balance personal narrative and objective journalism... a comprehensive and compassionate guide to a dreaded illness named after a bucolic,
tick-infested town on Long Island Sound."
--Bill Williams, Hartford Courant
"In the war of information on Lyme disease, patient activist groups have started from a marked disadvantage to the medical establishment in terms of visibility and credibility. That may be changing, and science journalist Pamela Weintraub's new book, "Cure Unknown: Inside the Lyme Epidemic" (St. Martin's Press), could be one reason. Weintraub, a senior editor at Discover magazine, uses her family's protracted Lyme odyssey as the jumping off point for an exploration into the history, politics and, predominantly, the patient experience of the tick-borne disease."
--- Susan Morse, Washington Post

Customer Reviews

This book is excellent & very informative.
I wish every doctor who said 'you can't have Lyme disease' would read Pamela Weintraub's book.
I was very sad when the book ended--- I just wanted to keep reading!
T. Park

Most Helpful Customer Reviews

197 of 206 people found the following review helpful By Dr Tedde M. Rinker on June 11, 2008
Format: Hardcover
As a California physician, I have found myself diagnosing Lyme disease in an increasing number of patients who come to me with vague, multi-system complaints, but certain consistent patterns: living, working or playing in outdoor brush or field areas (gardening, golf, hiking, camping)is the first, but many have only a little outdoor exposure. Second, complaints of the slow onset of stiff, aching joints that get better and worse, sore muscles, that spasm, tingle and turn numb off and on, headaches and fatigue, problems with sleep, an up and down course that slowly gets worse. Pamela Weintraub, a professional writer and editor, tells her story of her family's move to a rural New York community as healthy active people, only to have all four family members contract Lyme disease in the early 90's, and face not only the disability of this infection but also the confusing double talk of a medical community in denial. She tells not only her story but those of others, and in the telling reveals the difficulties in getting an accurate diagnosis, in finding a doctor to believe and treat the patient, and in being able emotionally and financially to continue the treatment until the disease is resolved. If you are a patient with Lyme disease, perhaps you will learn some things you didn't know before. If you are someone who has believed that perhaps Lyme disease is a myth, or that the people who have it are exaggerating, this is the book for you. If you are a physician, and have quoted the Infectious Disease Society of America's treatment guidelines to a suffering patient to explain why you will not treat them, or will only treat them for three weeks- this is the book for you.Read more ›
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68 of 72 people found the following review helpful By sharilee on June 18, 2008
Format: Hardcover
I'm not a doctor, nor a medical researcher. But I am a parent who's been fighting for the life of my teenage daughter who has now been diagnosed with Lyme Disease + 2 co-infections. I have a biology degree and have been through a lot of illnesses myself, but I've never seen anything like the story of Lyme. This book is a must-read for all parents. It is a fact-based narrative that tells it like it is, from the political in-fighting in the medical community to the important research that's not getting the attention it should. And the stories it tells about those infected with Lyme are mesmerizing. We fight for a diagnosis, then we fight for treatment. If my family wasn't living this story ourselves, I'd think this was a Stephen King novel.
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48 of 51 people found the following review helpful By Skydog on June 12, 2008
Format: Hardcover Verified Purchase
Superb book that reads like a scientific who-done-it. Rarely has Lyme Disease been as accurately presented in the variety of symptoms, treatments and policies. But most of all it describes a heartless medical bureaucracy that sacrificed thousands of families into bankruptcy, permanent illness and even death to satisfy insurance company lobbyists. Lyme is the Tuskegee experiment of this century.
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27 of 28 people found the following review helpful By Kimberly Kooyers on March 23, 2009
Format: Hardcover
I just finished Pamela Weintraub's Cure Unknown, required reading for anyone with Lyme disease. But really, EVERYONE should read this. To protect yourself, your family, and your friends, not just from this rising epidemic, but also from our broken medical system where misdiagnosis of Lyme is the norm--not the exception--and the powers that be seem to have their own interest at heart.

Weintraub, as a science journalist, herself and her family afflicted with Lyme, opens your eyes to the limitations of mainstream doctors and uncovers disturbing efforts by the CDC and IDSA to under-treat and even deny the existence of a debilitating disease affecting millions.

Referring to the authors of the IDSA guidelines on the treatment of Lyme, Weintraub writes: "They consulted for big pharma and owned Lyme related patents; they received fees as expert witnesses in medical malpractice, civil, and criminal cases related to Lyme disease; and they were paid by insurance companies to field--and help reject--Lyme related claims. Of the fourteen authors, nine received money from vaccine manufacturers and four were funded to create test kits, products that would be more likely to reap profit if the definition of Lyme disease remained essentially unchanged."

The stories in this book will make you angry--babies, children, teenagers, moms, dads, doctors themselves--suffering from chronic, debilitating Lyme, being told that it's all in their head, or to be misdiagnosed with developmental disabilities, chronic fatigue, fibromyalgia, multiple sclerosis, arthritis, bipolar disorder, Parkinson's or even ALS.

Sadly, I concur with someone who said to me, "this book is more disturbing than hopeful." But, information is power. And now I know what I'm reckoning with.
Read more ›
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36 of 39 people found the following review helpful By free thinker on March 26, 2010
Format: Paperback Verified Purchase
Ms. Weintraub, editor of the science magazine Discover, provides a detailed and well-researched account of her family's struggle with Lyme disease and the devastation it can cause. Also included are other gripping case-studies, a very interesting and useful history of the discovery of this tick-born illness, and a summary of current research and findings regarding Borrelia burgdorferi (the bacteria that causes Lyme). The account of current standard medical policy as dictated by the IDSA (Infectious Disease Society of America) and the CDC (Centers for Disease Control) offer a disturbing, and often tragic, portrait of how basic science research and evidence-based clinical practice can be ignored in favor of poor and unreliable "standard diagnostic tests" and guidelines that ignore vast bodies of evidence and research, yet form today's mainstream approach to medicine. Indeed, the most disturbing part of the Lyme disease epidemic is not the disease itself (which, if detected early, can usually be successfully treated with antibiotics), but the distortion of the peer-reviewed research by a few, so-called "medical experts" that have set current medical diagnostic guidelines. The result of this is the under-diagnosis of Lyme disease by several orders of magnitude. Under-diagnosis and poor detection by the majority of doctors leads to dissemination of the bacteria n the body, which burrow into almost every tissue type, most notably the central and peripheral nervous system, heart, and joints. Once disseminated, the disease becomes more serious and can cause long-lasting and permanent damage. In late-stage, or disseminated Lyme disease, treatment becomes more difficult, as antibiotics often take months..if not years..to reach bacteria in the brain and nervous system.Read more ›
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