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Broadly construed, a disability is an impairment in physical, mental, intellectual, and/or sensory functioning. Disabilities are usually classified as severe, profound, moderate, or mild, depending on the individual’s need for support, which may be lifelong. Specific types of disabilities are diverse and often multifaceted, including intellectual; physical (e.g., hearing, vision, paralysis, epilepsy, muscular dystrophy, cerebral palsy, missing extremities); speech, language, and learning; and psychiatric (e.g., anxiety disorders, schizophrenia, anorexia). A disability can manifest at any time within a person’s life (although developmental disabilities typically manifest before the ages 18–22 years), and it can be visible or invisible, long-term, episodic, or temporary and thus vary in the degree to which it imposes limitations and resists effective treatment. The causes of disabilities are also extensive and may be attributable to genetic abnormalities, congenital infections, perinatal or postnatal trauma, environmental poisons or deprivation, malnutrition, abuse, accidents, lack of parental or child health care, or they may be of unknown origin. This entry provides an historical view of the diagnosis and treatment of disabilities, significant advancements from a global perspective, and progress and future directions for research and practice.

Historically, the perception, attitude, and treatment of individuals with disabilities have been determined by societal norms and/or cultural beliefs. At various points in time and within various cultures, individuals with a disability were considered inferior, possessed by supernatural or evil spirits, the symbol of a curse on an entire family, or the reincarnation of a god. Consequently, treatment of individuals with disabilities ranged from extermination, forced sterilization, institutionalization, neglect, or maltreatment to being treated with acceptance, kindness, and even reverence. On the whole, individuals with disabilities have been seen as incompetent and incapable of decision-making or self-determination. From the 1800s to the mid-1900s, in Western countries, the vast majority of people with disabilities were segregated and hidden in institutions, asylums, hospitals, and attics with only their most basic needs (e.g., food, shelter, and clothing) being met. Services that were provided were based on a medical model of disability (treatment and care based on a medical diagnosis of bodily function or structure such as spinal injury, blindness, etc.), without regard for the environmental and psychological needs of the individual. Most negative attitudes and treatments were based on misconceptions and lack of an informed understanding of specific disabilities and the differing functional capacities of disabled persons.

With advances in medical technologies and diagnostic instruments, changes began to take place in the diagnosis and treatment of persons with disabilities; however, only recently have significant advances been made for the provision of support and resources to enable disabled persons to live to their full potential.

Diagnosis and Treatment: From Medical Model to Biopsychosocial Model

By the mid-1900s, advances in technology, coupled with public activism and advocacy, led to changes in understanding and treating persons with disabilities. Legislation was enacted to provide protections and equal rights to education, employment, and government funding for assistive services and resources. Medical advances and targeted research led to the development of specific diagnostic classifications of disabilities and research on both the origins of disabling conditions and efficacy of individualized treatment both in the United States and abroad. A significant step forward in the international arena was the creation by the World Health Organization of the International Classification of Diseases, a revised classification system which provides consistent diagnostic criteria of both physical diseases as well as mental disorders such as autism, bipolar disorder, and cerebral palsy. Similar efforts in the United States resulted in the creation of the Diagnostic and Statistical Manual for Mental Disorders by the American Psychiatric Association for classifying underlying clinical disorders such as learning disorders and attention-deficit/hyperactivity disorders, general medical conditions including brain injury or physical disorders, environmental factors that contribute to the disorders, and an overall assessment of general functioning. In addition, the American Association on Intellectual and Developmental Disabilities was established to provide diagnostic criteria for mental retardation (since renamed intellectual disability) based on IQ, age of onset, and limitations in overall functioning. The cumulative results of these efforts were dramatic changes in the lives of people with disabilities, with a move toward more community-based services, deinstitutionalization of people into the general community, and residence in group homes or at home with their families. Support services became more available outside the home, as did in-home support and caregiving. Medical treatments were developed to prevent, moderate, or alleviate some symptoms, providing more opportunities for success in education, training, and employment.

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