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In the last 40 to 50 years, many changes have taken place in the way persons with disabilities are managed and treated in our society. Additionally, a variety of medical treatment modalities have seen advances. People with these conditions are more likely to live in the community rather than in institutions, and they receive oral healthcare from community-based private practitioners rather than from government-run health facilities. As a result of this notion, disabled people were viewed by society as ill, flawed, and deviant until the twentieth century. As a result, these individuals have been seen with a mixture of terror and sympathy by society throughout time. According to popular view, these individuals were unable to contribute to or participate in society and so needed welfare or benevolent groups. Autism and/or epilepsy were the most common conditions treated at home by families until the late 1800s. In the past, those with severe and profound disabilities did not have the same longevity as those who are healthy now. In the latter half of the nineteenth century, state and local governments began to set up facilities for people with developmental disabilities. There are a large number of these facilities located outside of town. Societal sentiments helped this method of management separation. ‘ Sadly, people are further stigmatized when they are isolated from the rest of society.
An epileptic farm colony for the mentally ill was founded in Gainesville in the early 1920s. Using the “custodial” concept, residents were supervised. They were not allowed to participate in community events. Segregation from the rest of society is clearly stigmatizing. Society’s perceptions of people with disabilities have influenced the word used to describe them.

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