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1,377
result(s) for
"Intellectual Disability history."
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A rhetoric of remnants : idiots, half-wits, and other state-sponsored inventions
by
Stuckey, Zosha
in
Intellectual disability facilities patients-United States-History
,
Intellectual disability facilities-New York (State)-History
,
Intellectual disability facilities-United States-History
2014
Examines the rhetoric in and around the New York State Asylum for Idiots in Syracuse, New York from 1854 to 1884.
Intellectual disability : a conceptual history, 1200-1900
\"This collection explores the historical origins of our modern concepts of intellectual or learning disability. The essays, from some of the leading historians of ideas of intellectual disability, focus on British and European material from the Middle Ages to the late-nineteenth century and extend across legal, educational, literary, religious, philosophical and psychiatric histories. They investigate how precursor concepts and discourses were shaped by and interacted with their particular social, cultural and intellectual environments, eventually giving rise to contemporary ideas. The collection is essential reading for scholars interested in the history of intelligence, intellectual disability and related concepts, as well as in disability history generally\"-- Provided by publisher.
Who Was Deborah Kallikak?
2012
\"The Kallikak Family\" was, along with \"The Jukes: A Study in Crime, Pauperism, Disease, and Heredity\", one of the most visible eugenic family narratives published in the early 20th century. Published in 1912 and authored by psychologist Henry Herbert Goddard, director of the psychological laboratory at the Vineland Training School for Feebleminded Children in Vineland, New Jersey, \"The Kallikak Family\" told the tale of a supposedly \"degenerate\" family from rural New Jersey, beginning with Deborah, one of the inmates at the Training School. Like most publications in the genre, this pseudoscientific treatise described generations of illiterate, poor, and purportedly immoral Kallikak family members who were chronically unemployed, supposedly feebleminded, criminal, and, in general, perceived as threats to \"racial hygiene.\" Presented as a \"natural experiment\" in human heredity, this text served to support eugenic activities through much of the first half of the 20th century. This article reviews the story of Deborah Kallikak, including her true identity, and provides evidence that Goddard's treatise was incorrect.
Journal Article
'Four Corners and a Void': Idiocy and Childhood Disability in Nineteenth-Century America
2024
Over the second half of the nineteenth century, thousands of Americans were admitted to schools for so-called idiotic children, later known as institutions for the feebleminded and linked to the Eugenics movement. While idiocy is often presumed to be the antecedent of intellectual disability, an analysis of the stories of three hundred children admitted to one such institution over a forty-year period demonstrates an unexpected diversity of appearances, abilities, and behaviors. Within the walls of the institution, idiocy was composed of children whose perceived abilities deviated from the expectations of their social position. Families further shaped the diagnosis of idiocy by negotiating the timing of admission for their children, influenced not only by personal factors, but by shifting educational and employment opportunities, and cultural tolerance of diversity. Consequently, idiocy became the broadest descriptor of disability during the nineteenth century.
Journal Article
California’s Sterilization Survivors: An Estimate and Call for Redress
2017
From 1919 to 1952, approximately 20 000 individuals were sterilized in California’s state institutions on the basis of eugenic laws that sought to control the reproductive capacity of people labeled unfit and defective. Using data from more than 19 000 sterilization recommendations processed by state institutions over this 33-year period, we provide the most accurate estimate of living sterilization survivors. As of 2016, we estimate that as many as 831 individuals, with an average age of 87.9 years, are alive. We suggest that California emulate North Carolina and Virginia, states that maintained similar sterilization programs and recently have approved monetary compensation for victims. We discuss the societal obligation for redress of this historical injustice and recommend that California seriously consider reparations and full accountability.
Journal Article
Beyond Terminology: The Policy Impact of a Grassroots Movement
2013
This article discusses the history of the grassroots movement led by self-advocates and their families to replace the stigmatizing term \"mental retardation\" with \"intellectual disability\" in federal statute. It also describes recent and pending changes in federal regulations and policy to adopt the new terminology for Social Security and Medicaid.
Journal Article
Patenting the PKU Test — Federally Funded Research and Intellectual Property
by
Ankeny, Rachel A
,
Paul, Diane B
in
Bayh, Birch
,
Biomedical Research - economics
,
Biomedical Research - ethics
2013
In 1960, Robert Guthrie invented a new assay to detect phenylketonuria in newborns, inspiring hope for treating mental retardation. But efforts to patent and license the test generated controversy, presaging current debates over commercialization in biomedicine.
In 1960, microbiologist Robert Guthrie and technician Ada Susi invented a bacterial inhibition assay that reliably detected phenylketonuria (PKU) in newborns. The damage caused by PKU, including often profound cognitive impairment, results from an inability to metabolize phenylalanine, an amino acid necessary for protein synthesis and normal growth and development. To be effective, treatment with a low-phenylalanine diet must begin in early infancy, before the onset of irreversible neurologic impairment. Although a ferric chloride urine test for PKU existed in the 1950s, it was unreliable until the infant was 6 to 8 weeks old. The new assay was also more . . .
Journal Article
Why the intellectually disabled in the Evans case continue to hold the DC government neglectful after 40 years: a history of differing views about disability rights
2017
This article is about Washington, DC’s intellectually disabled and the history of their struggle for habilitation rights, which for them includes gainful employment and having a family. Against them has been a conservative local and national government and the US District Court in its rulings over the past 40 years in the
case. The disabled have had only limited success in their expansive interpretation of their rights, but by exploiting differences between the government and court, they have obtained concessions concerning basic food, clothing and shelter. For this reason they advocate for an indefinite continuation of the
litigation.
Journal Article