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| leprosy book: Colonizing Leprosy Michelle T. Moran, 2012-09-01 By comparing institutions in Hawai'i and Louisiana designed to incarcerate individuals with a highly stigmatized disease, Colonizing Leprosy provides an innovative study of the complex relationship between U.S. imperialism and public health policy in the late nineteenth and early twentieth centuries. Focusing on the Kalaupapa Settlement in Moloka'i and the U.S. National Leprosarium in Carville, Michelle Moran shows not only how public health policy emerged as a tool of empire in America's colonies, but also how imperial ideologies and racial attitudes shaped practices at home. Although medical personnel at both sites considered leprosy a colonial disease requiring strict isolation, Moran demonstrates that they adapted regulations developed at one site for use at the other by changing rules to conform to ideas of how natives and Americans should be treated. By analyzing administrators' decisions, physicians' treatments, and patients' protests, Moran examines the roles that gender, race, ethnicity, and sexuality played in shaping both public opinion and health policy. Colonizing Leprosy makes an important contribution to an understanding of how imperial imperatives, public health practices, and patient activism informed debates over the constitution and health of American bodies. |
| leprosy book: Moloka'i Alan Brennert, 2010-04-01 Young Rachel Kalama, growing up in idyllic Honolulu in the 1890s, is part of a big, loving Hawaiian family, and dreams of seeing the far-off lands that her father, a merchant seaman, often visits. But at the age of seven, Rachel and her dreams are shattered by the discovery that she has leprosy. Forcibly removed from her family, she is sent to Kalaupapa, the isolated leper colony on the island of Moloka'i. In her exile she finds a family of friends to replace the family she's lost: a native healer, Haleola, who becomes her adopted auntie and makes Rachel aware of the rich culture and mythology of her people; Sister Mary Catherine Voorhies, one of the Franciscan sisters who care for young girls at Kalaupapa; and the beautiful, worldly Leilani, who harbors a surprising secret. At Kalaupapa she also meets the man she will one day marry. True to historical accounts, Moloka'i is the story of an extraordinary human drama, the full scope and pathos of which has never been told before in fiction. But Rachel's life, though shadowed by disease, isolation, and tragedy, is also one of joy, courage, and dignity. This is a story about life, not death; hope, not despair. It is not about the failings of flesh, but the strength of the human spirit. |
| leprosy book: Leprosy Charlotte A. Roberts, Clark Spencer Larsen, 2020 The Biology of Leprosy Bacteria and How They Are Transmitted to Humans -- How Leprosy Affects the Human Body -- Past and Present Diagnosis, Treatment, and Prognosis -- The Bioarchaeology of Leprosy -- The Bioarchaeological Evidence of Leprosy -- Reconstructing the Origin, Evolution, and History of Leprosy -- Conclusions: A Future for Leprosy; Clinical and Bioarchaeological Perspectives. |
| leprosy book: Carville's Cure Pam Fessler, 2020-07-14 The unknown story of the only leprosy colony in the continental United States, and the thousands of Americans who were exiled—hidden away with their “shameful” disease. The Mississippi River between Baton Rouge and New Orleans curls around an old sugar plantation that long housed one of America’s most painful secrets. Locals knew it as Carville, the site of the only leprosy colony in the continental United States, where generations of afflicted Americans were isolated—often against their will and until their deaths. Following the trail of an unexpected family connection, acclaimed journalist Pam Fessler has unearthed the lost world of the patients, nurses, doctors, and researchers at Carville who struggled for over a century to eradicate Hansen’s disease, the modern name for leprosy. Amid widespread public anxiety about foreign contamination and contagion, patients were deprived of basic rights—denied the right to vote, restricted from leaving Carville, and often forbidden from contact with their own parents or children. Neighbors fretted over their presence and newspapers warned of their dangerous condition, which was seen as a biblical “curse” rather than a medical diagnosis. Though shunned by their fellow Americans, patients surprisingly made Carville more a refuge than a prison. Many carved out meaningful lives, building a vibrant community and finding solace, brotherhood, and even love behind the barbed-wire fence that surrounded them. Among the memorable figures we meet in Fessler’s masterful narrative are John Early, a pioneering crusader for patients’ rights, and the unlucky Landry siblings—all five of whom eventually called Carville home—as well as a butcher from New York, a 19-year-old debutante from New Orleans, and a pharmacist from Texas who became the voice of Carville around the world. Though Jim Crow reigned in the South and racial animus prevailed elsewhere, Carville took in people of all faiths, colors, and backgrounds. Aided by their heroic caretakers, patients rallied to find a cure for Hansen’s disease and to fight the insidious stigma that surrounded it. Weaving together a wealth of archival material with original interviews as well as firsthand accounts from her own family, Fessler has created an enthralling account of a lost American history. In our new age of infectious disease, Carville’s Cure demonstrates the necessity of combating misinformation and stigma if we hope to control the spread of illness without demonizing victims and needlessly destroying lives. |
| leprosy book: Leprosy in China Angela Ki Che Leung, 2009-01-01 Angela Ki Che Leung's meticulous study begins with the classical annals of the imperial era, which contain the first descriptions of a feared and stigmatized disorder modern researchers now identify as leprosy. She then tracks the relationship between the disease and China's social and political spheres (theories of contagion prompted community and statewide efforts at segregation); religious traditions (Buddhism and Daoism ascribed redemptive meaning to those suffering from the disease), and evolving medical discourse (Chinese doctors have contested the disease's etiology for centuries). Leprosy even pops up in Chinese folklore, attributing the spread of the contagion to contact with immoral women. Leung next places the history of leprosy into a global context of colonialism, racial politics, and imperial danger. A perceived global pandemic in the late nineteenth century seemed to confirm Westerners' fears that Chinese immigration threatened public health. Therefore battling to contain, if not eliminate, the disease became a central mission of the modernizing, state-building projects of the late Qing empire, the nationalist government of the first half of the twentieth century, and the People's Republic of China. Stamping out the curse of leprosy was the first step toward achieving hygienic modernity and erasing the cultural and economic backwardness associated with the disease. Leung's final move connects China's experience with leprosy to a larger history of public health and biomedical regimes of power, exploring the cultural and political implications of China's Sino-Western approach to the disease. |
| leprosy book: Leprosy in Premodern Medicine Luke Demaitre, 2007-07 While premodern poets and preachers viewed leprosy as a “disease of the soul,” physicians in the period understood it to be a “cancer of the whole body.” In this innovative study, medical historian Luke Demaitre explores medical and social perspectives on leprosy at a time when judicious diagnosis could spare healthy people from social ostracization and help the afflicted get a license to beg. Extending his inquiry from the first century to late in the eighteenth century, Demaitre draws on translations of academic treatises and archival records to illuminate the professional standing, knowledge, and conduct of the practitioners who struggled to move popular perceptions of leprosy beyond loathing and pity. He finds that, while not immune to social and cultural perceptions of the leprous as degenerate, and while influenced by their own fears of contagion, premodern physicians moderated society's reactions to leprosy and were dedicated to the well-being of their patients. |
| leprosy book: Out of the Shadow of Leprosy Claire Manes, 2013-04-10 In 1924 when thirty-two-year-old Edmond Landry kissed his family goodbye and left for the leprosarium in Carville, Louisiana, leprosy, now referred to as Hansen's disease, stigmatized and disfigured but did not kill. Those with leprosy were incarcerated in the federal hospital and isolated from family and community. Phones were unavailable, transportation was precarious, and fear was rampant. Edmond entered the hospital (as did his four other siblings), but he did not surrender to his fate. He fought with his pen and his limited energy to stay connected to his family and to improve living conditions for himself and other patients Claire Manes, Edmond's granddaughter, lived much of her life gripped by the silence surrounding her grandfather. When his letters were discovered, she became inspired to tell his story through her scholarship and his writing. Out of the Shadow of Leprosy: The Carville Letters and Stories of the Landry Family presents her grandfather's letters and her own studies of narrative and Carville during much of the twentieth century. The book becomes a testament to Edmond's determination to maintain autonomy and dignity in the land of the living dead. Letters and stories of the other four siblings further enhance the picture of life in Carville from 1919 to 1977. |
| leprosy book: The Colony John Tayman, 2010-05-11 In the bestselling tradition of In the Heart of the Sea, The Colony, “an impressively researched” (Rocky Mountain News) account of the history of America’s only leper colony located on the Hawaiian island of Molokai, is “an utterly engrossing look at a heartbreaking chapter” (Booklist) in American history and a moving tale of the extraordinary people who endured it. Beginning in 1866 and continuing for over a century, more than eight thousand people suspected of having leprosy were forcibly exiled to the Hawaiian island of Molokai -- the longest and deadliest instance of medical segregation in American history. Torn from their homes and families, these men, women, and children were loaded into shipboard cattle stalls and abandoned in a lawless place where brutality held sway. Many did not have leprosy, and many who did were not contagious, yet all were ensnared in a shared nightmare. Here, for the first time, John Tayman reveals the complete history of the Molokai settlement and its unforgettable inhabitants. It's an epic of ruthless manhunts, thrilling escapes, bizarre medical experiments, and tragic, irreversible error. Carefully researched and masterfully told, The Colony is a searing tale of individual bravery and extraordinary survival, and stands as a testament to the power of faith, compassion, and the human spirit. |
| leprosy book: The Second Life of Mirielle West Amanda Skenandore, 2021-07-27 The glamorous world of a silent film star’s wife abruptly crumbles when she’s forcibly quarantined at the Carville Lepers Home in this page-turning story of courage, resilience, and reinvention set in 1920s Louisiana and Los Angeles. Based on little-known history, this timely book will strike a chord with readers of Fiona Davis, Tracey Lange, and Marie Benedict. Based on the true story of America’s only leper colony, The Second Life of Mirielle West brings vividly to life the Louisiana institution known as Carville, where thousands of people were stripped of their civil rights, branded as lepers, and forcibly quarantined throughout the entire 20th century. For Mirielle West, a 1920’s socialite married to a silent film star, the isolation and powerlessness of the Louisiana Leper Home is an unimaginable fall from her intoxicatingly chic life of bootlegged champagne and the star-studded parties of Hollywood’s Golden Age. When a doctor notices a pale patch of skin on her hand, she’s immediately branded a leper and carted hundreds of miles from home to Carville, taking a new name to spare her family and famous husband the shame that accompanies the disease. At first she hopes her exile will be brief, but those sent to Carville are more prisoners than patients and their disease has no cure. Instead she must find community and purpose within its walls, struggling to redefine her self-worth while fighting an unchosen fate. As a registered nurse, Amanda Skenandore’s medical background adds layers of detail and authenticity to the experiences of patients and medical professionals at Carville – the isolation, stigma, experimental treatments, and disparate community. A tale of repulsion, resilience, and the Roaring ‘20s, The Second Life of Mirielle West is also the story of a health crisis in America’s past, made all the more poignant by the author’s experiences during another, all-too-recent crisis. PRAISE FOR AMANDA SKENANDORE’S BETWEEN EARTH AND SKY “Intensely emotional…Skenandore’s deeply introspective and moving novel will appeal to readers of American history.” —Publishers Weekly |
| leprosy book: No Matter where the Journey Takes Me Yōhei Sasakawa, 2019 Leprosy has tormented mankind since records began. For much of its long history it was without cure--a disfiguring disease that stigmatized those it affected, isolating them from society. Today there is an effective treatment, but the last mile to achieve a leprosy-free world is the hardest. Now approaching eighty years old, one Japanese philanthropic activist has played a key role in global efforts against leprosy, both as head of a private foundation and as the World Health Organization's 'Goodwill Ambassador for Leprosy Elimination'. In this book, he lays out his personal mission and philosophy, and explains how his father, the politician and philanthropist Ryoichi Sasakawa, influenced his decision to make leprosy elimination his life's work. Yohei Sasakawa has visited more than 100 countries, motivating political leaders, raising awareness via the media, encouraging frontline health workers, and helping to empower persons affected by leprosy and their families to speak out for their rights. His book is a validation of the path taken by a father and son to change the course of leprosy history, and to transform the circumstances of those affected by the disease for the better. |
| leprosy book: Squint Jose P. Ramirez, 2009-09-28 Lying in a hospital bed, José P. Ramirez, Jr. (b. 1948) almost lost everything because of a misunderstood disease. When the health department doctor gave him the Handbook for Persons with Leprosy, Ramirez learned his fate. Such a diagnosis in 1968 meant exile and hospitalization in the only leprosarium in the continental United States—Carville, Louisiana, 750 miles from his home in Laredo, Texas. In Squint: My Journey with Leprosy, Ramirez recalls being taken from his family in a hearse and thrown into a world filled with fear. He and his loved ones struggled against the stigma associated with the term “leper” and against beliefs that the disease was a punishment from God, that his illness was highly communicable, and that persons with Hansen's disease had to be banished from their communities. His disease not only meant separation from the girlfriend who would later become his wife, but also a derailment of all life's goals. In his struggle Ramirez overcame barriers both real and imagined and eventually became an international advocate on behalf of persons with disabilities. In Squint, titled for the sliver of a window through which persons with leprosy in medieval times were allowed to view Mass but not participate, Ramirez tells a story of love and perseverance over incredible odds. |
| leprosy book: Carville Marcia G. Gaudet, 2004-12-02 Personal accounts of life in America's last colony for sufferers of Hansen's disease |
| leprosy book: Jopling’s Handbook Of Leprosy, 6/E Kabir Sardana, Ananta Khurana, 2022-02-28 This is a thoroughly revised, updated and rewritten edition of the book reflecting guidelines and studies till early 2020. It contains original Jopling’s clinical text which has been updated with over 370 images and diagrams. It will serve as a textbook for postgraduate students in dermatology as well as a ready-reckoner for all health personnel dealing with leprosy at various levels. |
| leprosy book: IAL Textbook of Leprosy Hemanta Kumar Kar, Bhushan Kumar, 2010-06-20 |
| leprosy book: The Gift Nobody Wants Paul Brand, Paul W. Brand, Philip Yancey, 1995 Inspirational cassette on the dramatic career of Paul Brand, a famous surgeon |
| leprosy book: Kingdom of the Sick Susan L. Burns, 2019-05-31 In this groundbreaking work, Susan L. Burns examines the history of leprosy in Japan from medieval times until the present. At the center of Kingdom of the Sick is the rise of Japan’s system of national leprosy sanitaria, which today continue to house more than 1,500 former patients, many of whom have spent five or more decades within them. Burns argues that long before the modern Japanese government began to define a policy toward leprosy, the disease was already profoundly marked by ethical and political concerns and associated with sin, pollution, heredity, and outcast status. Beginning in the 1870s, new anxieties about race and civilization that emanated from a variety of civic actors, including journalists, doctors, patent medicine producers, and Christian missionaries transformed leprosy into a national issue. After 1900, a clamor of voices called for the quarantine of all sufferers of the disease, and in the decades that followed bureaucrats, politicians, physicians, journalists, local communities, and leprosy sufferers themselves grappled with the place of the biologically vulnerable within the body politic. At stake in this “citizenship project” were still evolving conceptions of individual rights, government responsibility for social welfare, and the delicate balance between care and control. Refusing to treat leprosy patients as simply victims of state power, Burns recovers their voices in the debates that surrounded the most controversial aspects of sanitarium policy, including the use of sterilization, segregation, and the continuation of confinement long after leprosy had become a curable disease. Richly documented with both visual and textual sources and interweaving medical, political, social, and cultural history, Kingdom of the Sick tells an important story for readers interested in Japan, the history of medicine and public health, social welfare, gender and sexuality, and human rights. |
| leprosy book: The Dark Island Benjamin Kingsbury, 2019 From 1906 to 1925 Quail Island was the site of New Zealands leprosy colony. The colony began by accident, as it were, after the discovery of a leprosy sufferer in Christchurch. As further patients arrived from across the country, it grew into a controversial and troubled institution an embarrassment to the Health Department, an object of pity to a few, a source of fear to many. It was a place that some people wanted to forget, but its stories are worth remembering: among them are stories of remarkable generosity and selflessness, as well as of violence and great suffering. This fascinating narrative from a talented young historian reveals a little-known aspect of New Zealands past. Through the tale of the Quail Island colony, the book shines a light on wider society in that period, both in New Zealand and beyond. Elegantly and engagingly written, The Dark Island heralds the arrival of a significant historical voice. |
| leprosy book: Leprosy and identity in the Middle Ages Elma Brenner, François-Olivier Touati, 2021-04-13 For the first time, this volume explores the identities of leprosy sufferers and other people affected by the disease in medieval Europe. The chapters, including contributions by leading voices such as Luke Demaitre, Carole Rawcliffe and Charlotte Roberts, challenge the view that people with leprosy were uniformly excluded and stigmatised. Instead, they reveal the complexity of responses to this disease and the fine line between segregation and integration. Ranging across disciplines, from history to bioarchaeology, Leprosy and identity in the Middle Ages encompasses post-medieval perspectives as well as the attitudes and responses of contemporaries. Subjects include hospital care, diet, sanctity, miraculous healing, diagnosis, iconography and public health regulation. This richly illustrated collection presents previously unpublished archival and material sources from England to the Mediterranean. |
| leprosy book: The Island at the End of Everything Kiran Millwood Hargrave, 2017-05-04 Ami lives on Culion, an island for people who have leprosy. Her mother is infected. She loves her home - but then islanders untouched by sickness are forced to leave. Ami's desperate to return before her mother's death. She finds a strange and fragile hope in a colony of butterflies. Can they lead her home before it's too late? |
| leprosy book: The Samurai's Garden Gail Tsukiyama, 2008-06-24 The daughter of a Chinese mother and a Japanese father, Gail Tsukiyama's The Samurai's Garden uses the Japanese invasion of China during the late 1930s as a somber backdrop for this extraordinary story. A 20-year-old Chinese painter named Stephen is sent to his family's summer home in a Japanese coastal village to recover from a bout with tuberculosis. Here he is cared for by Matsu, a reticent housekeeper and a master gardener. Over the course of a remarkable year, Stephen learns Matsu's secret and gains not only physical strength, but also profound spiritual insight. Matsu is a samurai of the soul, a man devoted to doing good and finding beauty in a cruel and arbitrary world, and Stephen is a noble student, learning to appreciate Matsu's generous and nurturing way of life and to love Matsu's soulmate, gentle Sachi, a woman afflicted with leprosy. |
| leprosy book: Leprosy in Colonial South India Jane Buckingham, 2002-03-20 British medical treatment similarly was contingent on the leprosy sufferer's co-operation. Confronted with leprosy, law was as weak a 'tool of empire' as medicine. Even the poorest and weakest of the empire had the power to resist.--BOOK JACKET. |
| leprosy book: Handbook of Leprosy W. H. Jopling, A. Colin McDougall, 1988 |
| leprosy book: Leprosy in Medieval England Carole Rawcliffe, 2009 A major reassessment, based on hitherto unpublished manuscript material, of a disease whose history has attracted more myths and misunderstandings than any other. |
| leprosy book: Handbook of Leprosy W. H. Jopling, 1978 |
| leprosy book: Leprosy Leonard Rogers, Ernest Muir, 1925 |
| leprosy book: Uncertainty, Anxiety, Frugality Leo van Bergen, 2018-06-30 The story of leprosy in the Dutch East Indies from the beginning of the 19th century to the middle of the 20th reveals important themes in the colonial enterprise across the territory that is today’s Indonesia. Operating in a territory with only a few hundred Western-trained doctors and a population in the tens of millions, Dutch colonial officials approached leprosy with uncertainty and anxiety. In the early 19th century, the Dutch administration simply removed sufferers from public view: campaigns targetted anyone “looking ugly”. Towards the end of the century, colonial science considered leprosy a hereditary disease of tropical subjects, and therefore undeserving of the colonial government’s limited resources. The leprosariums were emptied. At the start of the 20th century, a growing understanding that leprosy was spread by a bacillus caused a panic that leprosy might spread from the tropics to the colonial metropole. The mixed emotions of pity, fear and revulsion associated with management of the disease intensified, and fed into broader debates on colonial policy. The experts were unsure, and resources were never forthcoming, and despite a view that “bacteria are the same everywhere”, Dutch leprosy treatment in the East Indies mobilized traditional healing practices and relied on home care. Leo van Bergen’s detailed, attentive study to changing policies for treatment and prevention of leprosy (now often called Hansen’s disease) is fascinating medical history, and provides a useful lens for understanding colonialism in Indonesia. |
| leprosy book: The Gift of Pain Paul Brand, Philip Yancey, 2020-08-04 Pain is not something that most of us would count as a blessing; however, renowned surgeon Dr. Paul Brand and award-winning writer Philip Yancey shed fresh light on the purpose of our pain. Wouldn't it be nice to never experience pain or never have to take drugs to deal with pain? Many people think so, but they're missing one key piece of information: Pain is the body's built-in warning system that something is wrong and needs to be fixed. Follow world-renowned physician and surgeon Dr. Paul Brand around the world as he shares his humble beginnings as the son of medical missionaries in India to his medical training in London during the Blitz to his groundbreaking medical research with leprosy patients in the United States and India. His work with leprosy patients is what convinced him that pain truly is one of God's great gifts to us. In these pages he shares what he's learned about pain, its purpose in our lives, the impact it has on our daily lives and overall health, and how we can better respond to it. Perfect for those in the medical field or those looking for a firsthand look into the mystery of pain, this book will give you a new perspective on the gift that none of us want and none of us can do without. You'll never look at pain the same way again. Spanish edition also available. Note: The book includes some frank descriptions of medical procedures, illnesses, and diseases |
| leprosy book: No Ordinary Day Deborah Ellis, 2011-08-10 Shortlisted for the SYRCA 2013 Diamond Willow Award, selected as an American Library Association 2012 Notable Children's Book, a Booklist Editors' Choice, nominated for the OLA Golden Oak Tree Award, and a finalist for the Ruth and Sylvia Schwartz Children's Book Awards: Young Adult/Middle Reader Award, the Governor General's Literary Awards: Children's Text and the Canadian Library Association Book of the Year for Children Award There's not much that upsets young Valli. Even though her days are spent picking coal and fighting with her cousins, life in the coal town of Jharia, India, is the only life she knows. The only sight that fills her with terror are the monsters who live on the other side of the train tracks -- the lepers. Valli and the other children throw stones at them. No matter how hard her life is, she tells herself, at least she will never be one of them. Then she discovers that she is not living with family after all, that her aunt was a stranger who was paid money to take Valli off her own family's hands. She decides to leave Jharia ... and so begins a series of adventures that takes her to Kolkata, the city of the gods. It's not so bad. Valli finds that she really doesn't need much to live. She can borrow the things she needs and then pass them on to people who need them more than she does. It helps that though her bare feet become raw wounds as she makes her way around the city, she somehow feels no pain. But when she happens to meet a doctor on the ghats by the river, Valli learns that she has leprosy. Despite being given a chance to receive medical care, she cannot bear the thought that she is one of those monsters she has always feared, and she flees, to an uncertain life on the street. Correlates to the Common Core State Standards in English Language Arts: CCSS.ELA-LITERACY.RL.4.3 Describe in depth a character, setting, or event in a story or drama, drawing on specific details in the text (e.g., a character's thoughts, words, or actions). CCSS.ELA-LITERACY.RL.5.3 Compare and contrast two or more characters, settings, or events in a story or drama, drawing on specific details in the text (e.g., how characters interact). CCSS.ELA-LITERACY.RL.6.6 Explain how an author develops the point of view of the narrator or speaker in a text. |
| leprosy book: Prevention of Disabilities in Patients with Leprosy H. Srinivasan, World Health Organization, 1993 For health workers |
| leprosy book: Walking Corpses Timothy S. Miller, John W. Nesbitt, 2023-05-15 In Walking Corpses, Timothy S. Miller and John W. Nesbitt contextualize reactions to leprosy in medieval Western Europe by tracing its history in Late Antique Byzantium, which had been confronting leprosy and its effects for centuries. Integrating developments in both the Latin West and the Greek East, Walking Corpses challenges a number of misperceptions about attitudes toward the disease, including that theologians branded leprosy as punishment for sin (rather, it was seen as a mark of God's favor); that Christian teaching encouraged bans on the afflicted from society (in actuality, it was Germanic customary law); or that leprosariums were prisons (instead, they were centers of care, many of them self-governing). Informed by extensive archival research and recent bioarchaeology, Walking Corpses also includes new translations of three Greek texts regarding leprosy, while a new preface to the paperback edition updates the historiography on medieval perceptions and treatments of leprosy. |
| leprosy book: Confessions of a Teenage Leper Ashley Little, 2018-09-11 Cheerleading, mean girls, shopping . . . and leprosy? High school is about to get complicated. For fans of Before I Fall and Exit, Pursued By a Bear. Abby Furlowe has plans. Big plans. She's hot, she's popular, she's a cheerleader and she's going to break out of her small Texas town and make it big. Fame and fortune, adoration and accolades. It'll all be hers. But then she notices some spots on her skin. She writes them off as a rash, but things only get worse. She's tired all the time, her hands and feet are numb and her face starts to look like day-old pizza. By the time her seventeenth birthday rolls around, she's tried every cream and medication the doctors have thrown at her, but nothing works. When she falls doing a routine cheerleading stunt and slips into a coma, her mystery illness goes into overdrive and finally gets diagnosed: Hansen's Disease, aka leprosy. Abby is sent to a facility to recover and deal with this new reality. Her many misdiagnoses mean that some permanent damage has been done, and all of her plans suddenly come tumbling down. If she can't even wear high heels anymore, what is the point of living? Cheerleading is out the window, and she might not even make it to prom. PROM! But it's during this recovery that Abby has to learn to live with something even more difficult than Hansen's Disease. She's becoming aware of who she really was before and what her behavior was doing to others; now she's on the other side of the fence looking in, and she doesn't like what she sees. . . Darkly comic but ultimately touching, Confessions of a Teenage Leper is an ugly duckling tale with a surprising twist. |
| leprosy book: People are Not the Same Eric Silla, 1998 Paper Edition. A compelling account of leprosy in colonial and post-colonial Mali. |
| leprosy book: Holy Bible (NIV) Various Authors,, 2008-09-02 The NIV is the world's best-selling modern translation, with over 150 million copies in print since its first full publication in 1978. This highly accurate and smooth-reading version of the Bible in modern English has the largest library of printed and electronic support material of any modern translation. |
| leprosy book: Lord Foul's Bane Stephen R. Donaldson, 2012-05-16 “Covenant is [Stephen R.] Donaldson's genius!”—The Village Voice He called himself Thomas Covenant the Unbeliever, because he dared not believe in this strange alternate world on which he suddenly found himself. Yet the Land tempted him. He had been sick; now he seemed better than ever before. Through no fault of his own, he had been outcast, unclean, a pariah. Now he was regarded as a reincarnation of the Land's greatest hero—Berek Halfhand—armed with the mystic power of White Gold. That power alone could protect the Lords of the Land from the ancient evil of the Despiser, Lord Foul. Except that Covenant had no idea how to use that power. . . . |
| leprosy book: The Separating Sickness, Maʻi Hoʻokaʻawale Ted Gugelyk, Milton Bloombaum, 1996 |
| leprosy book: The International Campaign Against Leprosy Jo Robertson, 2022-01-14 This book may offer a cautionary tale in the age of Covid-19. The narratives we shape around disease in society are so often about politics, and the competing versions of leprosy eradication’s story are no exception. In one telling, the extra-budgetary funding for anti-leprosy work came with unwarranted interference in the WHO programme, resulting in an over-hasty, acrimonious and ultimately unsuccessful elimination campaign. In another interpretation, a great work of twentieth-century disease control was accomplished, through extraordinary philanthropy, visionary courageousness, and wily and pragmatic diplomacy. In yet another, experienced, self-sacrificing anti-leprosy experts refused to abdicate their professional responsibilities to populist campaigns more concerned with statistics than people, which were risking patients’ health with under-trialled drug therapies and irresponsibly entrusting medication to patients without supervision. None of these bureaucratic, triumphalist or elitist narratives exists independently of the others. None is without credit, and none is to the complete credit of all involved. These competing stories offer uncanny resonances in the ongoing politics of public health, which have only intensified since both the emergence of M. Leprae millennia ago, and the concerted campaign against it in the last seventy years. What could the ‘stories of leprosy’ tell us about our pandemic response? |
| leprosy book: Beyond the Bright Sea Lauren Wolk, 2018-09-18 - Winner of the 2018 Scott O'Dell Award for Historical Fiction - From the bestselling author of Echo Mountain and Newbery Honor–winner Wolf Hollow, Beyond the Bright Sea is an acclaimed best book of the year. An NPR Best Book of the Year • A Parents’ Magazine Best Book of the Year • A Booklist Editors' Choice selection • A BookPage Best Book of the Year • A Horn Book Fanfare Selection • A Kirkus Best Book of the Year • A School Library Journal Best Book of the Year • A Charlotte Observer Best Book of the Year • A Southern Living Best Book of the Year • A New York Public Library Best Book of the Year “The sight of a campfire on a distant island…proves the catalyst for a series of discoveries and events—some poignant, some frightening—that Ms. Wolk unfolds with uncommon grace.” –The Wall Street Journal ★ “Crow is a determined and dynamic heroine.” —Publishers Weekly ★ “Beautiful, evocative.” —Kirkus The moving story of an orphan, determined to know her own history, who discovers the true meaning of family. Twelve-year-old Crow has lived her entire life on a tiny, isolated piece of the starkly beautiful Elizabeth Islands in Massachusetts. Abandoned and set adrift in a small boat when she was just hours old, Crow’s only companions are Osh, the man who rescued and raised her, and Miss Maggie, their fierce and affectionate neighbor across the sandbar. Crow has always been curious about the world around her, but it isn’t until the night a mysterious fire appears across the water that the unspoken question of her own history forms in her heart. Soon, an unstoppable chain of events is triggered, leading Crow down a path of discovery and danger. Vivid and heart-wrenching, Lauren Wolk’s Beyond the Bright Sea is a gorgeously crafted and tensely paced tale that explores questions of identity, belonging, and the true meaning of family. |
| leprosy book: The Seventh Gate Peter Greave, 1976 The autobiography of Peter Greave, born in Calcutta in the time of the Raj. He relates the tragic-comic collapse of his family's fortunes, the sufferings endured of his youth, and then heads towards the ultimate degradation as he contracts leprosy. He enters the ranks of the most outcaste of all and by the time of independence has almost entirely lost his eyesight as well as his reason to live. |
| leprosy book: Histopathological Diagnosis Of Leprosy Cleverson Teixeira Soares, 2021-04-29 Histopathological Diagnosis of Leprosy, is a comprehensive guide to the medical pathology of Hansen's disease, which is a complex and clinically challenging infection caused by Mycobacterium leprae. Readers will find 8 chapters on key topics on the subject including general aspects of leprosy, different forms of leprosy (polar, borderline, etc.), reaction types and complications. The information presented in the handbook will equip the reader with the knowledge required to identify the disease in patients and perform differential diagnosis where required. Key Features: - 8 chapters dedicated to key topics about leprosy and its diagnosis - More than 200 figures featuring over 1000 clinical and histopathological photographs - Complete information about differential diagnosis and reaction phenomena - includes a section dedicated to special and complicated cases - References for further reading - Brings the expertise of renowned physicians to the reader The detailed presentation of the book is of great value to both healthcare professionals (pathologists, dermatologists, physicians) who are involved in the care of leprosy patients, and medical residents who are seeking information about the disease as part of their medical training. |
| leprosy book: Manson's Tropical Diseases E-Book Jeremy Farrar, Peter J Hotez, Thomas Junghanss, Gagandeep Kang, David Lalloo, Nicholas J. White, Patricia J. Garcia, 2023-07-14 For 125 years, physicians have relied on Manson's Tropical Diseases for a comprehensive clinical overview of this complex and fast-changing field. The fully revised 24th Edition, Dr. Jeremy Farrar, along with an internationally recognized editorial team, global contributors, and expert authors, delivers the latest coverage on parasitic and infectious diseases from around the world. From the difficult to diagnose to the difficult to treat, this highly readable, award-winning reference prepares you to effectively handle whatever your patients may have contracted. - Covers all of tropical medicine in a comprehensive manner, general medicine in the tropics, and non-clinical issues regarding public health and ethics. - Serves as an indispensable resource for physicians who treat patients with tropical diseases and/or will be travelling to the tropics, or who are teaching others in this area. - Contains a new section on 21st Century Drivers of Tropical Medicine, with chapters covering Poverty and Inequality, Public Health in Settings of Conflict and Political Instability, Climate Change, and Medical Product Quality and Public Health. - Includes all-new chapters on Surgery in the Topics, Yellow Fever, Systemic Mycoses, and COVID-19. - Covers key topics such as drug resistance; emerging and reemerging infections such as Zika, Ebola, and Chikungunya; novel diagnostics such as PCR-based methods; point-of care-tests such as ultrasound; public health in settings of conflict and political instability; and much more. - Differentiates approaches for resource-rich and resource-poor areas. - Includes reader-friendly features such as highlighted key information, convenient boxes and tables, extensive cross-referencing, and clinical management diagrams. |
Leprosy - World Health Organization (WHO)
Jan 24, 2025 · Leprosy, also known as Hansen disease, is a chronic infectious disease caused mainly by a type of bacteria called Mycobacterium leprae. The disease affects the skin, the …
Leprosy (Hansen disease) - World Health Organization (WHO)
Apr 1, 2025 · Leprosy, also known as Hansen disease, is a chronic infectious disease caused mainly by a type of bacteria called Mycobacterium leprae. The disease affects the skin, the …
Leprosy WPRO - World Health Organization (WHO)
Dec 5, 2023 · Leprosy is an infectious disease caused by Mycobacterium leprae, an acid-fast, rod-shaped bacillus. The disease mainly affects the skin, the peripheral nerves, mucosa of the …
Leprosy (Hansen disease) - World Health Organization (WHO)
Recent strategies to eliminate leprosy promote combating stigma and discrimination, including persons affected by leprosy, building partnerships and coalitions of relevant stakeholders, and …
Global leprosy (Hansen disease) update, 2021: moving towards ...
Sep 8, 2022 · Leprosy is a neglected tropical disease (NTD) caused by Mycobacterium leprae. Since the introduction of multidrug therapy (MDT), the registered prevalence has decreased …
Guidelines for the diagnosis, treatment and prevention of leprosy
Oct 6, 2018 · The Guidelines for the Diagnosis, Treatment and Prevention of Leprosy provide state-of-the-art knowledge and evidence on leprosy diagnosis, treatment and prevention …
麻风病 - World Health Organization (WHO)
Jan 24, 2025 · 麻风是由麻风杆菌引起的一种慢性传染病。该病主要侵犯皮肤、周围神经、上呼吸道粘膜和眼睛。本实况报道介绍了有关麻风 ...
Message for World Leprosy Day 2025 - World Health Organization …
Jan 21, 2025 · The number of leprosy patients worldwide has fallen from around 5 million in the 1980s to less than 200,000 new cases reported each year today. But leprosy still exists. Partly …
Towards zero leprosy. Global leprosy (Hansen’s Disease) strategy …
Apr 15, 2021 · The Global Leprosy Strategy 2021–2030 “Towards zero leprosy” was developed through a broad consultative process with all major stakeholders during 2019 and 2020. …
Lepra - World Health Organization (WHO)
La lepra es una enfermedad ancestral, descrita ya en textos de las civilizaciones de la antigüedad. Se trata de una enfermedad infecciosa crónica, causada por una bacteria llamada …
Leprosy - World Health Organization (WHO)
Jan 24, 2025 · Leprosy, also known as Hansen disease, is a chronic infectious disease caused mainly by a type of bacteria called Mycobacterium leprae. The disease affects the skin, the …
Leprosy (Hansen disease) - World Health Organization (WHO)
Apr 1, 2025 · Leprosy, also known as Hansen disease, is a chronic infectious disease caused mainly by a type of bacteria called Mycobacterium leprae. The disease affects the skin, the …
Leprosy WPRO - World Health Organization (WHO)
Dec 5, 2023 · Leprosy is an infectious disease caused by Mycobacterium leprae, an acid-fast, rod-shaped bacillus. The disease mainly affects the skin, the peripheral nerves, mucosa of the …
Leprosy (Hansen disease) - World Health Organization (WHO)
Recent strategies to eliminate leprosy promote combating stigma and discrimination, including persons affected by leprosy, building partnerships and coalitions of relevant stakeholders, and …
Global leprosy (Hansen disease) update, 2021: moving towards ...
Sep 8, 2022 · Leprosy is a neglected tropical disease (NTD) caused by Mycobacterium leprae. Since the introduction of multidrug therapy (MDT), the registered prevalence has decreased …
Guidelines for the diagnosis, treatment and prevention of leprosy
Oct 6, 2018 · The Guidelines for the Diagnosis, Treatment and Prevention of Leprosy provide state-of-the-art knowledge and evidence on leprosy diagnosis, treatment and prevention …
麻风病 - World Health Organization (WHO)
Jan 24, 2025 · 麻风是由麻风杆菌引起的一种慢性传染病。该病主要侵犯皮肤、周围神经、上呼吸道粘膜和眼睛。本实况报道介绍了有关麻风 ...
Message for World Leprosy Day 2025 - World Health Organization …
Jan 21, 2025 · The number of leprosy patients worldwide has fallen from around 5 million in the 1980s to less than 200,000 new cases reported each year today. But leprosy still exists. Partly …
Towards zero leprosy. Global leprosy (Hansen’s Disease) strategy …
Apr 15, 2021 · The Global Leprosy Strategy 2021–2030 “Towards zero leprosy” was developed through a broad consultative process with all major stakeholders during 2019 and 2020. …
Lepra - World Health Organization (WHO)
La lepra es una enfermedad ancestral, descrita ya en textos de las civilizaciones de la antigüedad. Se trata de una enfermedad infecciosa crónica, causada por una bacteria llamada …
