Mental Retardation!!!!!??!?!?
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So to give an answer to the question that was asked, in the first half of the 20th century, there were not very many choices for a family whose child had a disability. There was no right to a free appropriate public education for “handicapped children” as they were then termed; that did not come about until 1975. There were very few opportunities for people with disabilities to get job training, and housing choices were limited essentially to institutions or living at home until the parents got too old. There was a lot of stigma attached to having a family member with a disability – people ignorantly thought that mental retardation was contagious, or was an indication of poor genes in the family (so siblings might be considered poor choices for marriage), or that the person with mental retardation was a social or sexual deviant and therefore a danger to society – the list goes on. Often people who were considered to be mentally retarded were sterilized against their will, so that they would be unable to “taint the gene pool.” (To put these attitudes into historical perspective, realize that until the Civil Rights Act of 1964, it was LEGAL to discriminate against people on the basis of race, color, or religion.) When my sister was born with Down syndrome in 1965, people – including doctors – referred to her as a “Mongolian idiot” and told my parents that she should be immediately placed in an institution. And that was long after the era you are asking about, so presumably society was far more enlightened by the 60s.
In the old institutions, conditions were often incredibly inhumane. Geraldo Rivera, back when he was actually a journalist, did a powerful documentary (in 1972) on an institution in New York called Willowbrook. Among the horrendous conditions he observed and recorded, residents were kept naked and hosed off when they soiled themselves.
Luckily for my sister, my parents brought her home from the hospital and treated her like they did us 4 older kids. Our family did find some infant-toddler programs and special preschool programs for kids with disabilities, which was very rare in that era. My sister can read well, uses a computer and sends email to her family, has a job, has friends and a boyfriend, and a happy life. Now there are services to help people with developmental disabilities from infancy through old age – everything from heath services, therapies of various sorts, support groups, special education, job training and placement, residential services, assistance with transportation, and most importantly, civil rights.
Plus your terminology is way out of date, haven’t heard mental disabilities referred to with that disgusting term for a long time…and I work in special ed.
Rather than living in institutions with flith and no help, people now have options to live in small settings and are integrated into the community into various jobs. To name a few.
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