Out of the Shadow of Leprosy

The Carville Letters and Stories of the Landry Family

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Pub Date May 07 2013 | Archive Date Apr 24 2013

Description

A first-hand account of the trauma and impact on one family facing leprosy

In 1924 when thirty-two-year-old Edmond Landry kissed his family good-bye 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.

A first-hand account of the trauma and impact on one family facing leprosy

In 1924 when thirty-two-year-old Edmond Landry kissed his family good-bye and left for the leprosarium in Carville...


Advance Praise

“In the process of describing these ‘half-lives’ of the quarantined leprosy patients of days past to others, it appears that Claire herself has found an intimacy with those great-aunts and uncles and grandfather who lived the public secret of a leprosy diagnosis, achieving a release of sorts, for her whole family –not only the members who were quarantined by a diagnosis of a feared and criminalized disease. She has offered us a way to reach into a particular time and place and feel with them, as they live an unexpected life in the shadow of leprosy.”

--Elizabeth Schexnyder, Curator of National Hansen’s Disease Museum

“Throughout the world, one of the greatest challenges facing the Hansen’s disease/leprosy community is ensuring that individuals whose lives have been affected by this disease are afforded their rightful place in the history of their families, their countries and the world. By sharing the letters that her family kept from their relatives who had been taken from them together with powerful family photographs, Claire Manes provides us with an important, very personal perspective on the social response to those who had leprosy in the days when people were forcibly relocated to places like Carville. Even more important, she shows how the bonds of family ultimately prove stronger than any disease or society’s reaction to it.”

--Anwei Skinsnes Law, International Coordinator of IDEA, the largest international human rights advocacy organization by and for people who have personally faced the challenges of leprosy, also known as Hansen’s disease

“In the process of describing these ‘half-lives’ of the quarantined leprosy patients of days past to others, it appears that Claire herself has found an intimacy with those great-aunts and uncles and...


Available Editions

EDITION Hardcover
ISBN 9781617037764
PRICE $28.00 (USD)

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