Autism-From Denial to Hope
Bell, Peter, Behavioral Healthcare
In 15 years, the ranks of autism researchers have swelled from fewer than 25 to more than 700 BY PETER BELL
A recently as 1990, autism was considered a rare and hopeless disorder. The prevalence was thought to be 1 in every 2,500 children; little was known about the efficacy of treatments; and fewer than 25 scientists called themselves autism researchers.
Today in America, autism affects as many as 1 in every 166 children (including all autism disorders, such as Asperger's disorder). On average a family receives the devastating diagnosis of autism every 21 minutes. Once believed to be caused by cold and distant mothers, autism is now among the most common and severe developmental disabilities facing children in the United States. Indeed, autism is a national health crisis that costs the U.S. economy an estimated $90 billion annually and is more prevalent among children than juvenile diabetes, cystic fibrosis, and childhood cancer combined.
Although parents and healthcare professionals have shown that autism is amenable to treatment and more rigorous scientific research is moving forward, the disorder remains a major public health problem with virtually no medically proven treatments, no curative protocols, and no clear scientific understanding of why it is so pervasive and so devastating.
I recently participated in a Brookings Institution roundtable discussion about the history of autism and where we are today. To illustrate the dramatic changes in how society and the medical community have understood and addressed autism, I suggested there have been three distinct ages defining the disorder.
Age of Denial: 1940s-1960s
Autism was first characterized in 1943 by a child psychiatrist at Johns Hopkins University, Leo Kanner, MD. In a landmark paper, Dr. Kanner described 11 children from his practice who presented with limited speech, lack of emotional connection, and an obsessive desire for sameness. For some time, autism was thought to be a form of childhood schizophrenia with no link to biologic factors. This denial lasted well into the 1960s. Tragically, the idea that autism was caused by so-called "refrigerator mothers" who raised their children in a nonstimulating environment was pervasive during this period and produced disastrous misconceptions that still linger today.
Age of Defeat: 1960s-1980s
Once the medical community determined that autism has a biologic origin, the next 30 years were characterized by defeat. Parents were told that nothing could be done to improve the quality of life for their children. Autism was considered a lifelong disorder that couldn't be treated and eventually required some rorm of institutionalization. Few scientists were involved in autism research, and most of the research was of marginal quality. Families affected by autism had almost no support and little recourse against the disorder.
Age of Hope: 1990s-Present
Beginning in the early 1990s, autism entered the age of hope. The medical community finally began to understand that autism is a complex biologic disorder that could be treated by addressing the distinct challenges associated with it. As autism began to enter our popular culture through the media and entertainment (including movies such as Rain Man), people began to think about autism as a real disorder. The more public and real the disorder became, the more parents began to hope that a cure for autism would come during their children's lifetime. This age represents a …
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Publication information: Article title: Autism-From Denial to Hope. Contributors: Bell, Peter - Author. Magazine title: Behavioral Healthcare. Volume: 26. Issue: 7 Publication date: July 2006. Page number: 16+. © 2009 Vendome Group LLC. Provided by ProQuest LLC. All Rights Reserved.
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