The Last Children's Plague: Poliomyelitis, Disability, and Twentieth-Century American Culture
Poliomyelitis, better known as polio, thoroughly stumped the medical science community. Polio's impact remained highly visible and sometimes lingered, exacting a priceless physical toll on its young victims and their families as well as transforming their social worlds. This social history of infantile paralysis is plugged into the rich and dynamic developments of the United States during the first half of the twentieth century. Children became epidemic refugees because of anachronistic public health policies and practices. They entered the emerging, clinical world of the hospital, rupturing physical and emotional connections with their parents and siblings. As they underwent rehabilitation, they created ward cultures. They returned home to occasionally find hostile environments and always discover changed relationships due to their disabilities. The changing concept of the child, from an economic asset to an emotional commitment, medical advances, and improved sanitation policies led to significant improvements in child health and welfare. This study, relying on published autobiographies, memoirs, and oral histories, captures the impact of this disease on children's personal lives, encompassing public-health policies, hospitalization, philanthropic and organizational responses, physical therapy, family life, and schooling. It captures the anger, frustration, and terror not only among children but parents, neighbors, and medical professionals alike.
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The Last Children's Plague: Poliomyelitis, Disability, and Twentieth-Century American Culture
Poliomyelitis, better known as polio, thoroughly stumped the medical science community. Polio's impact remained highly visible and sometimes lingered, exacting a priceless physical toll on its young victims and their families as well as transforming their social worlds. This social history of infantile paralysis is plugged into the rich and dynamic developments of the United States during the first half of the twentieth century. Children became epidemic refugees because of anachronistic public health policies and practices. They entered the emerging, clinical world of the hospital, rupturing physical and emotional connections with their parents and siblings. As they underwent rehabilitation, they created ward cultures. They returned home to occasionally find hostile environments and always discover changed relationships due to their disabilities. The changing concept of the child, from an economic asset to an emotional commitment, medical advances, and improved sanitation policies led to significant improvements in child health and welfare. This study, relying on published autobiographies, memoirs, and oral histories, captures the impact of this disease on children's personal lives, encompassing public-health policies, hospitalization, philanthropic and organizational responses, physical therapy, family life, and schooling. It captures the anger, frustration, and terror not only among children but parents, neighbors, and medical professionals alike.
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The Last Children's Plague: Poliomyelitis, Disability, and Twentieth-Century American Culture

The Last Children's Plague: Poliomyelitis, Disability, and Twentieth-Century American Culture

by Richard J. Altenbaugh
The Last Children's Plague: Poliomyelitis, Disability, and Twentieth-Century American Culture

The Last Children's Plague: Poliomyelitis, Disability, and Twentieth-Century American Culture

by Richard J. Altenbaugh

Hardcover(1st ed. 2015)

$109.99 
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Overview

Poliomyelitis, better known as polio, thoroughly stumped the medical science community. Polio's impact remained highly visible and sometimes lingered, exacting a priceless physical toll on its young victims and their families as well as transforming their social worlds. This social history of infantile paralysis is plugged into the rich and dynamic developments of the United States during the first half of the twentieth century. Children became epidemic refugees because of anachronistic public health policies and practices. They entered the emerging, clinical world of the hospital, rupturing physical and emotional connections with their parents and siblings. As they underwent rehabilitation, they created ward cultures. They returned home to occasionally find hostile environments and always discover changed relationships due to their disabilities. The changing concept of the child, from an economic asset to an emotional commitment, medical advances, and improved sanitation policies led to significant improvements in child health and welfare. This study, relying on published autobiographies, memoirs, and oral histories, captures the impact of this disease on children's personal lives, encompassing public-health policies, hospitalization, philanthropic and organizational responses, physical therapy, family life, and schooling. It captures the anger, frustration, and terror not only among children but parents, neighbors, and medical professionals alike.

Product Details

ISBN-13: 9781137527844
Publisher: Palgrave Macmillan US
Publication date: 09/15/2015
Edition description: 1st ed. 2015
Pages: 277
Product dimensions: 6.20(w) x 9.10(h) x 0.90(d)

About the Author

Richard J. Altenbaugh is a Visiting Fellow at St. Edmund s College, University of Cambridge, UK and Professor Emeritus at Slippery Rock University, USA.

Table of Contents

Why Children, Disease, and Disability?
1. The American Plague
2. Many Yellow Caskets
3. After Treatment
4. Wheelchair Gladiators
5. Home Sweet Home
6. The Cripples
7. Polio's Legacy

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