[Note: Shared for #AutisticHistory archive purposes. This is NOT An Autistic Ally.]
HHS Report to Congress: How Federal Funds For Autism Are Spent
February 28, 2014
WASHINGTON, DC (February 28, 2014) — The U.S. Department of Health and Human Services (HHS) has reported to Congress on how funding dedicated to autism research and services under the Combating Autism Act (CAA) has been allocated and the progress that has been achieved under the law.
“Since the enactment of the Combating Autism Act in 2006, and its reauthorization under the Combating Autism Reauthorization Act of 2011, federal agencies, in partnership with the community, have made significant strides in addressing many of the pressing needs of individuals and families affected by autism spectrum disorder,” HHS reported.
The 2011 law dedicated $231 million a year in federal funding for autism research and services through September of this year to HHS, allocated primarily to the National Institutes of Health, the Centers for Disease Control and Prevention, and the Health Resources and Services Administration.
“Autism Speaks is actively working with our champions in Congress to reauthorize the CAA before September 30, and we will again demand this accountability over how federal dollars are spent on autism activities,” said Liz Feld, president of Autism Speaks. “Progress has been gained in our understanding and treatment of autism, but much more needs to be done. The law should continue to provide structure and transparency for the most efficient and effective use of federal dollars.
“Autism Speaks has provided nearly $200 million for autism research and is funding breakthrough science that can make a difference for our community,” she said, “but autism is an issue that covers the lifespan and we need a national strategy now to meet the employment, housing and community integration needs of all those affected.
“But we can’t do this alone. We need a strong federal partner to address what is a national epidemic.”
Among the advances cited by HHS between 2010 and 2013 were:
- the new prevalence estimate of 1 in 88 children, along with a finding that more children are being diagnosed by age 3, creating critical opportunities for early intervention
- expanded outreach to underserved populations to access diagnoses
- new findings on risk factors, including environmental risk factors such as nutrients, air pollutants, pesticides, and paternal age
- studies of conditions that often co-occur with ASD, such as gastrointestinal disorders, sleep disruptions, and epilepsy, are contributing to intervention strategies
- efforts to develop and evaluate educational interventions, as well as provide guidance for schools on how to make school environments safe and conducive to learning for students with disabilities
“While the collaborative efforts of federal and state agencies and community partners have resulted in many research advances and improvements in services over the past seven years, all acknowledge the growing needs of the community and the work that remains to be done,” HHS concluded. “Continued collaborative efforts between the public and private sectors will be essential to drive the innovations that will lead to improved identification, interventions, services, and policies that will enhance the lives of people with ASD and their families.”
The Autism Community Is Not The Autistic Community
More With Autism Votes
Autistic people have fought the inclusion of ABA in therapy for us since before Autism Speaks, and other non-Autistic-led autism organizations, started lobbying legislation to get it covered by insurances and Medicaid.
ABA is a myth originally sold to parents that it would keep their Autistic child out of an institution. Today, parents are told that with early intervention therapy their child will either be less Autistic or no longer Autistic by elementary school, and can be mainstreamed in typical education classes. ABA is very expensive to pay out of pocket. Essentially, Autism Speaks has justified the big price tag up front will offset the overall burden on resources for an Autistic’s lifetime. The recommendation for this therapy is 40 hours a week for children and toddlers.
The original study that showed the success rate of ABA to be at 50% has never been replicated. In fact, the study of ABA by United States Department of Defense was denounced as a failure. Not just once, but multiple times. Simply stated: ABA doesn’t work. In study after repeated study: ABA (conversion therapy) doesn’t work.
What more recent studies do show: Autistics who experienced ABA therapy are at high risk to develop PTSD and other lifelong trauma-related conditions. Historically, the autism organizations promoting ABA as a cure or solution have silenced Autistic advocates’ opposition. ABA is also known as gay conversion therapy.
The ‘cure’ for Autistics not born yet is the prevention of birth.
The ‘cure’ is a choice to terminate a pregnancy based on ‘autism risk.’ The cure is abortion. This is the same ‘cure’ society has for Down Syndrome.
This is eugenics 2021. Instead of killing Autistics and disabled children in gas chambers or ‘mercy killings’ like in Aktion T4, it’ll happen at the doctor’s office, quietly, one Autistic baby at a time. Different approaches yes, but still eugenics and the extinction of an entire minority group of people.
Fact: You can’t cure Autistics from being Autistic.
Fact: You can’t recover an Autistic from being Autistic.
Fact: You can groom an Autistic to mask and hide their traits. Somewhat. … however, this comes at the expense of the Autistic child, promotes Autistic Burnout (this should not be confused with typical burnout, Autistic Burnout can kill Autistics), and places the Autistic child at high risk for PTSD and other lifelong trauma-related conditions.
[Note: Autism is NOT a disease, but a neurodevelopmental difference and disability.]
Fact: Vaccines Do Not Cause Autism.