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This book documents the experiences and opinions of a doctor in the management of chronic Lyme disease. It also contains eleven opinionated essays about this challenging disease.
Book Synopsis Treatment of Chronic Lyme Disease by : Waisbren Sr.
Download or read book Treatment of Chronic Lyme Disease written by Waisbren Sr. and published by Biomed Publishing Group. This book was released on 2011-10 with total page 192 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book documents the experiences and opinions of a doctor in the management of chronic Lyme disease. It also contains eleven opinionated essays about this challenging disease.
Lyme disease is the most common tick-borne illness in the United States, with more than 300,000 cases diagnosed each year. However, doctors are deeply divided on how to diagnose and treat it, giving rise to the controversy known as the “Lyme Wars.” Firmly entrenched camps have emerged, causing physicians, patient communities, and insurance providers to be pitted against one another in a struggle to define Lyme disease and its clinical challenges. Health care providers may not be aware of its diverse manifestations or the limitations of diagnostic tests. Meanwhile, patients have felt dismissed by their doctors and confused by the conflicting opinions and dubious self-help information found online. In this authoritative book, the Columbia University Medical Center physicians Brian A. Fallon and Jennifer Sotsky explain that, despite the vexing “Lyme Wars,” there is cause for both doctors and patients to be optimistic. The past decade’s advances in precision medicine and biotechnology are reshaping our understanding of Lyme disease and accelerating the discovery of new tools to diagnose and treat it, such that the great divide previously separating medical communities is now being bridged. Drawing on both extensive clinical experience and cutting-edge research, Fallon, Sotsky, and their colleagues present these paradigm-shifting breakthroughs in language accessible to both sides. They clearly explain the immunologic, infectious, and neurologic basis of chronic symptoms, the cognitive and psychological impact of the disease, as well as current and emerging diagnostic tests, treatments, and prevention strategies. Written for the educated patient and health care provider seeking to learn more, Conquering Lyme Disease gives an up-to-the-minute overview of the science that is transforming the way we address this complex illness. It argues forcefully that the expanding plague of Lyme and other tick-borne diseases can be confronted successfully and may soon even be reversed.
Book Synopsis Conquering Lyme Disease by : Brian A. Fallon
Download or read book Conquering Lyme Disease written by Brian A. Fallon and published by Columbia University Press. This book was released on 2017-12-12 with total page 608 pages. Available in PDF, EPUB and Kindle. Book excerpt: Lyme disease is the most common tick-borne illness in the United States, with more than 300,000 cases diagnosed each year. However, doctors are deeply divided on how to diagnose and treat it, giving rise to the controversy known as the “Lyme Wars.” Firmly entrenched camps have emerged, causing physicians, patient communities, and insurance providers to be pitted against one another in a struggle to define Lyme disease and its clinical challenges. Health care providers may not be aware of its diverse manifestations or the limitations of diagnostic tests. Meanwhile, patients have felt dismissed by their doctors and confused by the conflicting opinions and dubious self-help information found online. In this authoritative book, the Columbia University Medical Center physicians Brian A. Fallon and Jennifer Sotsky explain that, despite the vexing “Lyme Wars,” there is cause for both doctors and patients to be optimistic. The past decade’s advances in precision medicine and biotechnology are reshaping our understanding of Lyme disease and accelerating the discovery of new tools to diagnose and treat it, such that the great divide previously separating medical communities is now being bridged. Drawing on both extensive clinical experience and cutting-edge research, Fallon, Sotsky, and their colleagues present these paradigm-shifting breakthroughs in language accessible to both sides. They clearly explain the immunologic, infectious, and neurologic basis of chronic symptoms, the cognitive and psychological impact of the disease, as well as current and emerging diagnostic tests, treatments, and prevention strategies. Written for the educated patient and health care provider seeking to learn more, Conquering Lyme Disease gives an up-to-the-minute overview of the science that is transforming the way we address this complex illness. It argues forcefully that the expanding plague of Lyme and other tick-borne diseases can be confronted successfully and may soon even be reversed.
NEW YORK TIMES EDITORS’ CHOICE • In this vulnerable, insightful memoir, the New York Times columnist tells the story of his five-year struggle with a disease that officially doesn’t exist, exploring the limits of modern medicine, the stories that we unexpectedly fall into, and the secrets that only suffering reveals. “A powerful memoir about our fragile hopes in the face of chronic illness.”—Kate Bowler, bestselling author of Everything Happens for a Reason In the summer of 2015, Ross Douthat was moving his family, with two young daughters and a pregnant wife, from Washington, D.C., to a sprawling farmhouse in a picturesque Connecticut town when he acquired a mysterious and devastating sickness. It left him sleepless, crippled, wracked with pain--a shell of himself. After months of seeing doctors and descending deeper into a physical inferno, he discovered that he had a disease which according to CDC definitions does not actually exist: the chronic form of Lyme disease, a hotly contested condition that devastates the lives of tens of thousands of people but has no official recognition--and no medically approved cure. From a rural dream house that now felt like a prison, Douthat's search for help takes him off the map of official medicine, into territory where cranks and conspiracies abound and patients are forced to take control of their own treatment and experiment on themselves. Slowly, against his instincts and assumptions, he realizes that many of the cranks and weirdos are right, that many supposed "hypochondriacs" are victims of an indifferent medical establishment, and that all kinds of unexpected experiences and revelations lurk beneath the surface of normal existence, in the places underneath. The Deep Places is a story about what happens when you are terribly sick and realize that even the doctors who are willing to treat you can only do so much. Along the way, Douthat describes his struggle back toward health with wit and candor, portraying sickness as the most terrible of gifts. It teaches you to appreciate the grace of ordinary life by taking that life away from you. It reveals the deep strangeness of the world, the possibility that the reasonable people might be wrong, and the necessity of figuring out things for yourself. And it proves, day by dreadful day, that you are stronger than you ever imagined, and that even in the depths there is always hope.
Book Synopsis The Deep Places by : Ross Douthat
Download or read book The Deep Places written by Ross Douthat and published by Convergent Books. This book was released on 2021-10-26 with total page 225 pages. Available in PDF, EPUB and Kindle. Book excerpt: NEW YORK TIMES EDITORS’ CHOICE • In this vulnerable, insightful memoir, the New York Times columnist tells the story of his five-year struggle with a disease that officially doesn’t exist, exploring the limits of modern medicine, the stories that we unexpectedly fall into, and the secrets that only suffering reveals. “A powerful memoir about our fragile hopes in the face of chronic illness.”—Kate Bowler, bestselling author of Everything Happens for a Reason In the summer of 2015, Ross Douthat was moving his family, with two young daughters and a pregnant wife, from Washington, D.C., to a sprawling farmhouse in a picturesque Connecticut town when he acquired a mysterious and devastating sickness. It left him sleepless, crippled, wracked with pain--a shell of himself. After months of seeing doctors and descending deeper into a physical inferno, he discovered that he had a disease which according to CDC definitions does not actually exist: the chronic form of Lyme disease, a hotly contested condition that devastates the lives of tens of thousands of people but has no official recognition--and no medically approved cure. From a rural dream house that now felt like a prison, Douthat's search for help takes him off the map of official medicine, into territory where cranks and conspiracies abound and patients are forced to take control of their own treatment and experiment on themselves. Slowly, against his instincts and assumptions, he realizes that many of the cranks and weirdos are right, that many supposed "hypochondriacs" are victims of an indifferent medical establishment, and that all kinds of unexpected experiences and revelations lurk beneath the surface of normal existence, in the places underneath. The Deep Places is a story about what happens when you are terribly sick and realize that even the doctors who are willing to treat you can only do so much. Along the way, Douthat describes his struggle back toward health with wit and candor, portraying sickness as the most terrible of gifts. It teaches you to appreciate the grace of ordinary life by taking that life away from you. It reveals the deep strangeness of the world, the possibility that the reasonable people might be wrong, and the necessity of figuring out things for yourself. And it proves, day by dreadful day, that you are stronger than you ever imagined, and that even in the depths there is always hope.
Now completely revised and updated-the bible for the thousands who contract Lyme disease each year Lyme disease, transmitted through the bite of a tick, is one of our nation's fastest-growing epidemics. Since Coping with Lyme Disease was first published in 1993, the number of sufferers afflicted by this debilitating condition has grown alarmingly. Every chapter has been thoroughly revised and new information about the long-term neurological effects of Lyme disease and congential and chronic versions of the illness has been added. This comprehensive guide includes - basic prevention tips - a detailed catalog of the physical and psychological symptoms to look for - a complete look at the medical and home care options and insurance policies available to patients - a special discussion of Lyme's effects on women, children, and the elderly - an expanded resource guide, with listings of news publications, state-by-state support groups, and special family services This fully updated third edition informs readers of the latest medical findings in diagnosing and treating Lyme disease-providing crucial information about newly discovered Lyme-related illnesses, electromagnetic procedures, clinical and antibiotic therapies, and curative nutritional products now on the market. A longtime bestseller, this authoritative book is an essential tool for all Lyme disease sufferers.
Book Synopsis Coping with Lyme Disease, Third Edition by : Denise Lang
Download or read book Coping with Lyme Disease, Third Edition written by Denise Lang and published by Holt Paperbacks. This book was released on 2004-06-01 with total page 352 pages. Available in PDF, EPUB and Kindle. Book excerpt: Now completely revised and updated-the bible for the thousands who contract Lyme disease each year Lyme disease, transmitted through the bite of a tick, is one of our nation's fastest-growing epidemics. Since Coping with Lyme Disease was first published in 1993, the number of sufferers afflicted by this debilitating condition has grown alarmingly. Every chapter has been thoroughly revised and new information about the long-term neurological effects of Lyme disease and congential and chronic versions of the illness has been added. This comprehensive guide includes - basic prevention tips - a detailed catalog of the physical and psychological symptoms to look for - a complete look at the medical and home care options and insurance policies available to patients - a special discussion of Lyme's effects on women, children, and the elderly - an expanded resource guide, with listings of news publications, state-by-state support groups, and special family services This fully updated third edition informs readers of the latest medical findings in diagnosing and treating Lyme disease-providing crucial information about newly discovered Lyme-related illnesses, electromagnetic procedures, clinical and antibiotic therapies, and curative nutritional products now on the market. A longtime bestseller, this authoritative book is an essential tool for all Lyme disease sufferers.
A single tick bite can have debilitating consequences. Lyme disease is the most common disease carried by ticks in the United States, and the number of those afflicted is growing steadily. If left untreated, the diseases carried by ticks-known as tick-borne diseases-can cause severe pain, fatigue, neurological problems, and other serious health problems. The Institute of Medicine held a workshop October 11-12, 2010, to examine the state of the science in Lyme disease and other tick-borne diseases.
Book Synopsis Critical Needs and Gaps in Understanding Prevention, Amelioration, and Resolution of Lyme and Other Tick-Borne Diseases by : Institute of Medicine
Download or read book Critical Needs and Gaps in Understanding Prevention, Amelioration, and Resolution of Lyme and Other Tick-Borne Diseases written by Institute of Medicine and published by National Academies Press. This book was released on 2011-07-01 with total page 560 pages. Available in PDF, EPUB and Kindle. Book excerpt: A single tick bite can have debilitating consequences. Lyme disease is the most common disease carried by ticks in the United States, and the number of those afflicted is growing steadily. If left untreated, the diseases carried by ticks-known as tick-borne diseases-can cause severe pain, fatigue, neurological problems, and other serious health problems. The Institute of Medicine held a workshop October 11-12, 2010, to examine the state of the science in Lyme disease and other tick-borne diseases.
This User’s Guide is intended to support the design, implementation, analysis, interpretation, and quality evaluation of registries created to increase understanding of patient outcomes. For the purposes of this guide, a patient registry is an organized system that uses observational study methods to collect uniform data (clinical and other) to evaluate specified outcomes for a population defined by a particular disease, condition, or exposure, and that serves one or more predetermined scientific, clinical, or policy purposes. A registry database is a file (or files) derived from the registry. Although registries can serve many purposes, this guide focuses on registries created for one or more of the following purposes: to describe the natural history of disease, to determine clinical effectiveness or cost-effectiveness of health care products and services, to measure or monitor safety and harm, and/or to measure quality of care. Registries are classified according to how their populations are defined. For example, product registries include patients who have been exposed to biopharmaceutical products or medical devices. Health services registries consist of patients who have had a common procedure, clinical encounter, or hospitalization. Disease or condition registries are defined by patients having the same diagnosis, such as cystic fibrosis or heart failure. The User’s Guide was created by researchers affiliated with AHRQ’s Effective Health Care Program, particularly those who participated in AHRQ’s DEcIDE (Developing Evidence to Inform Decisions About Effectiveness) program. Chapters were subject to multiple internal and external independent reviews.
Book Synopsis Registries for Evaluating Patient Outcomes by : Agency for Healthcare Research and Quality/AHRQ
Download or read book Registries for Evaluating Patient Outcomes written by Agency for Healthcare Research and Quality/AHRQ and published by Government Printing Office. This book was released on 2014-04-01 with total page 396 pages. Available in PDF, EPUB and Kindle. Book excerpt: This User’s Guide is intended to support the design, implementation, analysis, interpretation, and quality evaluation of registries created to increase understanding of patient outcomes. For the purposes of this guide, a patient registry is an organized system that uses observational study methods to collect uniform data (clinical and other) to evaluate specified outcomes for a population defined by a particular disease, condition, or exposure, and that serves one or more predetermined scientific, clinical, or policy purposes. A registry database is a file (or files) derived from the registry. Although registries can serve many purposes, this guide focuses on registries created for one or more of the following purposes: to describe the natural history of disease, to determine clinical effectiveness or cost-effectiveness of health care products and services, to measure or monitor safety and harm, and/or to measure quality of care. Registries are classified according to how their populations are defined. For example, product registries include patients who have been exposed to biopharmaceutical products or medical devices. Health services registries consist of patients who have had a common procedure, clinical encounter, or hospitalization. Disease or condition registries are defined by patients having the same diagnosis, such as cystic fibrosis or heart failure. The User’s Guide was created by researchers affiliated with AHRQ’s Effective Health Care Program, particularly those who participated in AHRQ’s DEcIDE (Developing Evidence to Inform Decisions About Effectiveness) program. Chapters were subject to multiple internal and external independent reviews.
Following completion of his medical training and a one-year stint as attending physician on Howard Champion's Surgical Critical Care Service and MedStar Unit at Washington Hospital Center in the District of Columbia, Kenneth Liegner, M.D. returned to Westchester County, home of his Alma Mater, New York Medical College, to start a private practice. Unwittingly, he had 'plunked himself down' in the heart of a burgeoning epidemic of Lyme disease. His patients confronted him with puzzling syndromes that defied 'tidy' formulations of the illness and thrust him in to a Maelstrom of medical controversy. Lyme disease, a new poorly understood disease, emerged hand in hand with the rise 'managed care'. Physicians caring for persons with Lyme disease, loyal to the Hippocratic Oath and serving what they saw as patients' best medical interests, found themselves on a collision course with a new Corporate Medical Ethic dedicated to maximizing profit. One practitioner's work over 25 years is presented here along with correspondence with many principals in the field. Documentational in nature and not written as a narrative, the materials, nonetheless, convey the intensity of the struggle to characterize the nature of Lyme disease and the desperate fight for proper diagnosis and treatment upon the outcome of which patients' very lives depended. The volume includes protocols useful as reference materials for patients and practitioners alike, as well as photographic images of many persons important in the history of Lyme disease. Foreword by Pam Weintraub, Senior Editor of aeon digital magazine and author of award-winning book Cure Unknown: Inside the Lyme Epidemic. Preface by Paul W. Ewald, Professor of Evolutionary Biology at the University of Louisville and author of Plague Time.
Book Synopsis In the Crucible of Chronic Lyme Disease by : Kenneth B. Liegner
Download or read book In the Crucible of Chronic Lyme Disease written by Kenneth B. Liegner and published by . This book was released on 2015-10-08 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: Following completion of his medical training and a one-year stint as attending physician on Howard Champion's Surgical Critical Care Service and MedStar Unit at Washington Hospital Center in the District of Columbia, Kenneth Liegner, M.D. returned to Westchester County, home of his Alma Mater, New York Medical College, to start a private practice. Unwittingly, he had 'plunked himself down' in the heart of a burgeoning epidemic of Lyme disease. His patients confronted him with puzzling syndromes that defied 'tidy' formulations of the illness and thrust him in to a Maelstrom of medical controversy. Lyme disease, a new poorly understood disease, emerged hand in hand with the rise 'managed care'. Physicians caring for persons with Lyme disease, loyal to the Hippocratic Oath and serving what they saw as patients' best medical interests, found themselves on a collision course with a new Corporate Medical Ethic dedicated to maximizing profit. One practitioner's work over 25 years is presented here along with correspondence with many principals in the field. Documentational in nature and not written as a narrative, the materials, nonetheless, convey the intensity of the struggle to characterize the nature of Lyme disease and the desperate fight for proper diagnosis and treatment upon the outcome of which patients' very lives depended. The volume includes protocols useful as reference materials for patients and practitioners alike, as well as photographic images of many persons important in the history of Lyme disease. Foreword by Pam Weintraub, Senior Editor of aeon digital magazine and author of award-winning book Cure Unknown: Inside the Lyme Epidemic. Preface by Paul W. Ewald, Professor of Evolutionary Biology at the University of Louisville and author of Plague Time.
This landmark text is dedicated to the conversation had between a primary care physician and a dermatologist that is a true reflection of the way medicine works when these physicians collaborate on the same case. The book uses actual case studies from the authors' offices and provides an accurate and real portrayal of the types of skin conditions primary care physicians encounter. Answering questions such as when to treat, how to treat, when to refer, when to biopsy, and when to reassure, this book informs and educates primary care physicians with a dermatologist’s perspective. Top 50 Dermatology Case Studies for Primary Care gives the reader an entirely new vantage point from which to view dermatologic cases, and together with one of New York City's top dermatologists, the authors look at the same case, the same patient, and compare what each did or would have done. Written for family medicine and internal medicine physicians, residents and providers, Top 50 Dermatology Case Studies for Primary Care proves to be an invaluable resource in their day-to-day practices.
Book Synopsis Top 50 Dermatology Case Studies for Primary Care by : Danya Reich
Download or read book Top 50 Dermatology Case Studies for Primary Care written by Danya Reich and published by Springer. This book was released on 2016-12-08 with total page 356 pages. Available in PDF, EPUB and Kindle. Book excerpt: This landmark text is dedicated to the conversation had between a primary care physician and a dermatologist that is a true reflection of the way medicine works when these physicians collaborate on the same case. The book uses actual case studies from the authors' offices and provides an accurate and real portrayal of the types of skin conditions primary care physicians encounter. Answering questions such as when to treat, how to treat, when to refer, when to biopsy, and when to reassure, this book informs and educates primary care physicians with a dermatologist’s perspective. Top 50 Dermatology Case Studies for Primary Care gives the reader an entirely new vantage point from which to view dermatologic cases, and together with one of New York City's top dermatologists, the authors look at the same case, the same patient, and compare what each did or would have done. Written for family medicine and internal medicine physicians, residents and providers, Top 50 Dermatology Case Studies for Primary Care proves to be an invaluable resource in their day-to-day practices.
Health care journalist Connie Strasheim has conducted intensive interviews with thirteen of the world's most competent Lyme disease healers, asking them thoughtful, important questions, and then spent months compiling their information into organized, user-friendly chapters that contain the core principles upon which they base their medical treatment of chronic Lyme disease. --publisher.
Book Synopsis Insights Into Lyme Disease Treatment by : Connie Strasheim
Download or read book Insights Into Lyme Disease Treatment written by Connie Strasheim and published by BioMed Publishing Group. This book was released on 2009 with total page 446 pages. Available in PDF, EPUB and Kindle. Book excerpt: Health care journalist Connie Strasheim has conducted intensive interviews with thirteen of the world's most competent Lyme disease healers, asking them thoughtful, important questions, and then spent months compiling their information into organized, user-friendly chapters that contain the core principles upon which they base their medical treatment of chronic Lyme disease. --publisher.
Lyme disease is a global pandemic high on suffering with a low mortality. It is reminiscent of the global pandemic of Syphilis although Bb is not transmitted sexually. Most people are cured, once they are diagnosed and treated. Physicians should have and maintain a high index of suspicion for the diagnosis of Lyme disease. A few develop Long Lyme. Other causes of the exhaustion syndrome need to be excluded in these patients. No diagnosis of dementia should be accepted until Neurological Lyme has been excluded. Dogs bring ticks into the house.
Book Synopsis TRUE LYME by : John Froude MD FRCP
Download or read book TRUE LYME written by John Froude MD FRCP and published by AuthorHouse. This book was released on 2023-11-23 with total page 149 pages. Available in PDF, EPUB and Kindle. Book excerpt: Lyme disease is a global pandemic high on suffering with a low mortality. It is reminiscent of the global pandemic of Syphilis although Bb is not transmitted sexually. Most people are cured, once they are diagnosed and treated. Physicians should have and maintain a high index of suspicion for the diagnosis of Lyme disease. A few develop Long Lyme. Other causes of the exhaustion syndrome need to be excluded in these patients. No diagnosis of dementia should be accepted until Neurological Lyme has been excluded. Dogs bring ticks into the house.
