Before modern disability
terminology developed, words such as “idiot,” “imbecile,” and “feeble-minded”
were used in medical, legal, educational, and social contexts to classify
people who were considered to have intellectual or developmental impairments.
These words may look
shocking today because they eventually became insults, but their original
historical use was different. Over time, however, they became strongly
associated with stigma, institutionalisation, discrimination, and negative
assumptions about people's abilities.
Idiot — historically used
in some classification systems for people considered to have the most
significant intellectual impairments.
Imbecile — historically
used for a less severe level of impairment than “idiot.”
Feeble-minded — a broad
and often poorly defined term used for people considered to have intellectual
or developmental limitations.
Moron — introduced in the
early 20th century, particularly through the work of psychologist Henry H.
Goddard, for people classified at what was then considered a higher level of
intellectual ability.
⚠️
The problem with these classifications
Historical classifications
were often based on much more than what we would consider appropriate
assessment today. People could be judged according to:
School performance
Communication abilities
Self-care skills
Behaviour and social
conformity
Physical or motor
characteristics
Whether they met
expectations for their age and culture
This meant that social
prejudice could become mixed with medical or psychological judgment.
Someone poor,
behaved differently, had difficulty communicating, or failed to meet social
expectations could be treated as though they were inherently less capable.
🧠From labels to modern terminology
Over the 20th century,
terminology changed considerably. “Mental retardation” eventually replaced some
of the older terminology in professional settings, but that term itself became
increasingly unacceptable because it was used as an insult and carried substantial
stigma.
Today, “intellectual
disability” is the accepted term in most professional and legal contexts.
The historical lesson is
important:
A diagnostic or
classification label can change over time, but the way society uses that label
can have lasting consequences for people's dignity, opportunities, and rights.
This connects directly
with your earlier point about the danger of labelling. A label that was
originally intended as a professional classification can eventually become a
word used to insult, bully, stereotype, or dehumanise people.
📚 Disability in the 20th Century
History can be understood
in three broad stages:
1. Early 20th century —
Segregation and control
People with disabilities
were frequently viewed through a medical, institutional, or eugenic lens.
Many people were placed in
institutions away from their communities.
Eugenic ideas portrayed
some disabilities as undesirable traits that should be prevented from being
passed on.
Forced sterilisation
occurred in the United States and elsewhere.
Some communities even used
laws to restrict visibly disabled people from appearing in public.
People were often given
very little choice about where they lived, worked, or received services.
This period demonstrates
how attitudes and social policies can create enormous barriers, even when those
policies are presented as being for someone's "care."
2. Mid-20th century —
Rehabilitation and emerging advocacy
The World Wars changed
public awareness of physical disability because many injured veterans returned
home needing rehabilitation, employment, housing, and accessibility.
This helped increase
attention to:
Rehabilitation
Employment
Prosthetics and assistive
technology
Community support
Disability organizations
Economic assistance
However, rehabilitation
was not the same as disability rights. The focus was often still on changing or
"fixing" the individual rather than changing society.
3. Late 20th century —
Disability rights and independent living
This is where there was a
major shift.
Disabled activists
increasingly argued:
People with disabilities
should have control over their own lives and should not have to be
"fixed" before they can participate in society.
The Independent Living
Movement emphasised choice, autonomy, community living, personal assistance,
and equal participation.
The Rehabilitation Act of
1973, particularly Section 504, was an important U.S. milestone because it
prohibited disability discrimination in programs receiving federal financial
assistance.
Then came the Americans
with Disabilities Act (ADA) of 1990, which established broad federal
protections against disability discrimination in areas including employment,
state and local government services, public accommodations, transportation, and
telecommunications.
🔄 The change in thinking
You can summarise the
overall historical change like this:
Institutionalization
↓
Rehabilitation
↓
Advocacy
↓
Independent Living
↓
Civil Rights
↓
Accessibility and
Inclusion
And this connects directly
with the models of disability you've been studying.
Earlier approach Rights-based approach
"What is wrong with
the person?" "What barriers
exist?"
Institutional care Community living
Dependence Independence and choice
Professionals make
decisions Person participates in
decisions
Rehabilitation Accessibility
Segregation Inclusion
Pity/charity Equality and rights
One particularly important
lesson is that legal change doesn't automatically eliminate prejudice. Laws can
remove discriminatory barriers, but attitudes, stereotypes, inaccessible
environments, and social exclusion can continue.
That's why modern
disability practice combines rights + accessibility + Universal Design +
person-centred support + respect for lived experience. Key points from the source
1. Eugenics and
segregation
Early 20th-century society
included strong eugenic beliefs. Some influential people believed disability
and other differences were threats to the "health of the nation."
This contributed to the segregation of disabled people and the belief that
society should prevent or eliminate perceived "defects."
2. World War I changed
some attitudes
The return of almost two
million newly disabled British ex-service personnel challenged the idea that
disabled people were simply a "burden." These men had been injured
while serving their country and were often regarded as heroes. This contributed
to advances in prosthetics, plastic surgery, rehabilitation, employment
initiatives, and specialist housing.
However, there was an
important inequality: disabled civilians did not necessarily receive the same
recognition or opportunities as disabled veterans.
3. Institutional
"colonies"
People with learning
disabilities were still placed in isolated rural institutions, described at the
time as "colonies." These were largely self-contained communities
with housing, farms, laundry, bakeries, recreation facilities, and other
services. People could be strictly segregated according to sex, age, and
perceived ability.
This is a powerful example
of the difference between being provided with services and actually having
choice, independence, and inclusion.
4. Disabled children
Historic England explains
that between 1900 and 1945, as many as half a million children had physical or
sensory disabilities, with poverty and disease being significant factors.
Children could attend specialist schools, but some educational approaches were
harsh, and many were trained for low-skilled work because society assumed they
would not be able to obtain ordinary employment.
5. World War II created
another change
When World War II began,
many workers left employment to join the armed forces. The resulting Labour
shortage led the Ministry of Labour to recruit people who had previously been
considered unfit for work. This again challenged assumptions about what
disabled people could contribute.
🔄 The really important lesson
This source shows that
disability history isn't simply a story of "people were discriminated
against, and then everything got better."
There were contradictions:
People could be considered
heroes when they became disabled through military service, while disabled
civilians were still segregated and viewed as dependent or defective.
That distinction is
important when studying the social model of disability. It shows how much
disability is influenced by society's attitudes, expectations, policies,
employment practices, education, and physical environments, rather than being
determined solely by an individual's impairment.
It also connects directly
to your earlier section on labeling: the historical terminology used for
disabled people wasn't neutral. Words such as "mentally deficient"
and "crippled" reflected the attitudes and classifications of the period,
and some later became stigmatizing insults.
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