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Category Archives: Research and Data Collection
ASAN supports research that focuses on improving the daily lives of Autistic people, conducted with respect for privacy and the rights of the individual. Other category archives, along with past entries sorted by date and tag, can be accessed via the sitemap.
ASAN Statement on 2018 CDC Prevalence Data
Today, the Centers for Disease Control released the Autism and Developmental Disabilities Monitoring (ADDM) Network report, which estimates the prevalence of autism in certain areas. The results indicate that better recognition of autism, and an encouraging reduction of racial and gender disparities in diagnosis, have caused rates of diagnosis...
Posted in Research and Data Collection, News, Statement
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Tagged research, statement, CDC, nhis, national health interview survey, centers for disease control, prevalence, autism, autism prevalence
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Comments for October 26 IACC Meeting
These comments are available as a PDF here. Thank you for the opportunity to submit written comments. The Autistic Self Advocacy Network (ASAN) continues to be deeply concerned by the allocation of autism research funding. According to the Office of Autism Research Coordination (OARC), the vast majority of NIH...
Posted in Research and Data Collection, News, Policy
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Tagged IACC, research, comment, comments, autism research funding, oarc, office of autism research coordination, NIH
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ASAN Expresses Concern over New Autism Research Funding Numbers
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The Autistic Self Advocacy Network is deeply concerned by numbers released today by the Office of Autism Research Coordination (OARC) showing that autism research funding around services and adult issues has continued to drop from already low levels over the course of the last several years. Based on data from...
Posted in Research and Data Collection, Policy
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Tagged research, self advocacy, supports
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ASAN Statement on CDC’s New Autism Prevalence Data
The Autistic Self Advocacy Network issued the following statement about the Center for Disease Control’s new Autism Spectrum Disorder (ASD) prevalence data on November 19, 2015. The latest CDC numbers reflect better understanding and diagnosis of autism. The data remains in line with studies showing that autistic people are...
Posted in Research and Data Collection, News
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Tagged research, diagnosis
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ASAN Releases New Resource On Medicaid Coverage for Autism Services
ASAN has released a new resource for its toolkit on health coverage for autism-related services. The resource, which is aimed at Medicaid plan administrators, will help plan administrators develop and expand coverage for autism services such as communication supports, occupational therapy, and speech therapy. ASAN released a resource on...
Posted in Community Services and Supports, Research and Data Collection, Therapies and Health Care, News, Publications, Policy
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Tagged health care, Medicaid, services, supports, therapies
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Secretary Burwell Appoints ASAN Director of Public Policy Sam Crane to IACC
October 28, 2015 Today, the Department of Health and Human Services announced its Secretary Sylvia M. Burwell’s appointment of ASAN Director of Public Policy Sam Crane to the Interagency Autism Coordinating Committee (IACC). The IACC is a Federal advisory committee that coordinates research and services programs within the Department...
Posted in Community Services and Supports, Research and Data Collection, Self Advocacy and Representation, ASAN in the News, Policy
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Tagged representation, research, self advocacy, policy
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ASAN Statement on GOP Primary Debate Comments on Autism and Vaccination
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Despite a wealth of scientific evidence debunking any link between autism and vaccinations, tonight’s Republican primary debate featured prominent commentary from a leading candidate repeating inaccurate information suggesting a link. The Autistic Self Advocacy Network is disappointed that long after the science has spoken, politicians and pundits continue to...
Posted in Disability Rights and Neurodiversity, Research and Data Collection, Self Advocacy and Representation, Press, Blog
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Tagged ignorance, research
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ASAN Statement Praising Department of Education’s Results Driven Accountability System
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Last week, the US Department of Education announced a new accountability framework for state compliance with the Individuals with Disabilities Education Act (IDEA). This new accountability framework, entitled Results-Driven Accountability, includes for the first time the use of independent outcome data from the National Assessment of Educational Progress (NAEP)...
Posted in Inclusive Education and College, Research and Data Collection, Policy
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Tagged disability, education
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Community Concerns Regarding the Google-Autism Speaks Ten Thousand Genomes Program (AUT10K)
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In response to the recent announcement of the new Google-Autism Speaks collaboration to produce, expand and analyze the world’s largest private collection of DNA samples of autistic children and adults, many in the autistic community have expressed significant concerns regarding the initiative. The program, entitled the Autism Speaks Ten...
Posted in Research and Data Collection, Self Advocacy and Representation, Therapies and Health Care, News
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Tagged representation, research
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ASAN Comments on the Clinical Use of Human Germline Genome Editing
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