56 episodes

Autism Confidential shines a light on the hottest issues in the world of autism, including topics often shunned by conventional media. Who cares for autistic adults after their parents die? How can we fix our broken care system? What interventions help, or hurt? Join hosts Jill Escher, Amy Lutz and others from the National Council on Severe Autism as they take on the hardest questions of autism with leading thinkers and doers.

Autism Confidential Autism Confidential Podcast

    • Business
    • 4.8 • 20 Ratings

Autism Confidential shines a light on the hottest issues in the world of autism, including topics often shunned by conventional media. Who cares for autistic adults after their parents die? How can we fix our broken care system? What interventions help, or hurt? Join hosts Jill Escher, Amy Lutz and others from the National Council on Severe Autism as they take on the hardest questions of autism with leading thinkers and doers.

    Episode #056 - Sounding Off About Autism Month

    Episode #056 - Sounding Off About Autism Month

    Autism Confidential returns to its usual podcast format for a discussion about April, Autism Month featuring host Jill Escher and guest Thomas McKean, a pioneering autism self-advocate. Jill and Tom discuss: Biden's signing of a proclamation declaring April "Autism Acceptance Month," historical background about Autism Month, some op-eds offering a dissenting view from the rah-rah rosy tone of April, acceptance of our kids v acceptance of autism, the very broken definition of "autism," and of course, guitar!

    Links to material discussed in the podcast:

    https://www.disabilityscoop.com/2024/04/03/white-house-embraces-autism-acceptance-over-awareness/30811/

    https://www.cdc.gov/ncbddd/autism/toolkit.html#:~:text=April%20is%20Autism%20Acceptance%20Month,and%20connectedness%20throughout%20the%20community

    https://www.post-gazette.com/opinion/insight/2024/04/07/profound-autism-awareness-month-neurodivergence-disorder-labels/stories/202404070031

    https://www.newsweek.com/i-love-my-child-i-hate-his-autism-1888870

    Amie, by Pure Prairie League: 

    https://youtu.be/lPgNbFni0oI?si=JWwD6swVhTyMn7jx

    • 59 min
    Episode #055 - Karen Fessel: Insurance Coverage for Severe Autism

    Episode #055 - Karen Fessel: Insurance Coverage for Severe Autism

    Karen Fessel, executive director of the Mental Health and Autism Insurance Project, returns to our National Council on Severe Autism webinar series to explain how insurance coverage works for children and adults with severe autism. She goes into detail about the governing laws and about how you can fight at several levels to obtain the coverage your child needs. Followed by Q&A with the audience.

    Links: https://mhautism.org

    • 1 hr 17 min
    Episode #054 - Discrimination by Design: How Policies Threaten the Most Severely Disabled

    Episode #054 - Discrimination by Design: How Policies Threaten the Most Severely Disabled

    Featuring: Ashley Kim, Together for Choice

    Jackie Ceonzo, SNACK* NYC

    Note: For a video recording with slides, please see NCSAutism.org/webinars.


    There is a nationwide shortage of long term supports and services available and it disproportionately affects adults with intellectual/developmental disabilities in need of 24/7 support. The need for such housing has been ignored and gone unanswered for decades by many responsible for the well-being of this population.
    While Congress expected that the ADA’s integration mandate would be interpreted in a manner that ensures that individuals who are eligible for institutional placement are able to exercise a right to community-based long-term services and supports, that expectation has not been fulfilled.


    We believe that people with disabilities should have the right to choose where they live, work, and receive services that are appropriate for their needs and preferences without those responsible for making choice a reality blocking that path with red tape.


    Links:
    Togetherforchoice.org
    SNACKNYC.com

    • 1 hr 23 min
    Episode #053 - Seizures and Epilepsy in Severe and Profound Autism

    Episode #053 - Seizures and Epilepsy in Severe and Profound Autism

    This episode features Stephanie M. Morris , MD, is Medical Director, Center for Autism Services, Science and Innovation (CASSI) At Kennedy Krieger Institute, Baltimore. She is a neurologist with special qualifications in child neurology, and is also an assistant professor in the Department of Neurology at the Johns Hopkins University School of Medicine. She works with kids with autism and I/DD and especially genetic conditions such as Fragile X syndrome and Neurofibromatosis Type 1 (NF1).


    In this webinar, Dr. Morris explains what seizures and epilepsy are, the different types, the high prevalence of seizures in autism, particularly in severe autism, various treatment approaches, and accessing care.
    Moderated by Jill Escher, president, NCSA


    For more information, please see NCSAutism.org

    • 1 hr 22 min
    Episode #052 - National Council on Severe Autism Webinar, February 15, 2024

    Episode #052 - National Council on Severe Autism Webinar, February 15, 2024

    National Council on Severe Autism Webinar, February 15, 2024, featuring:
    Jill Escher, Escher Fund for Autism
    Walter Zahorodny, PhD, Rutgers University
    This webinar examines the most important and poorly understood phenomenon in autism — the sharply escalating rates over the past several decades. The speakers explain:
    • The overwhelming evidence for a true increase in autism in the U.S., including specifically California (Escher) and New Jersey (Zahorodny), an increase that is likely between 2,000-5,500%
    • The evidence for a true increase in other high-income countries (and lower rates in lower-income countries)
    • The lack of evidence for commensurate autism rates in older birth cohorts
    • The flaws in the arguments that certain studies (eg, Hansen or Brugha) show there has been no increase in autism
    • Autism rates are still increasing, and no one understands why
    • The tired, unsupported rationalizations that the autism increase stems from awareness and diagnostic shifts
    • An emerging hypothesis that could help explain at least part of the surge, and the 6 key findings from autism research
    • The reasons for widespread denial of the increase in autism


    Links:


    JillEscher.com
    EscherFund.org

    Autism Epidemic, Autism Research, Autism Genetics, Autism Epigenetics, CDC ADDM Network, Developmental Disabilities, Aspergers, Autistic Disorder, Gene-Environment Interaction, Heritable Impacts of General Anesthesia, Sevoflurane

    • 1 hr 41 min
    Episode #051 - The Reauthorization of the Autism CARES Act

    Episode #051 - The Reauthorization of the Autism CARES Act

    This episode features Alison Singer, president of Autism Science Foundation, and Craig Snyder of IKON Consulting, discussing why the Autism CARES Act should be reformed before it is re-authorized. This federal legislation sunsets on September 30, 2024 and efforts are underway to continue it with another budget authorization. But the CARES Act has glaring shortcomings: it has turned away from the most important questions in autism; it has sidelined the most severely affected part of the autism population; it serves the needs of entrenched interests rather than the urgent needs of the American people.

    Please listen to Alison and Craig discuss:

    • The history of the act, which started as The Combating Autism Act

    • The problems with the IACC, the Interagency Coordinating Committee created by the Act

    • The failure of the CARES Act to effect meaningful change, all while autism rates continue to climb and supports and services become more difficult to obtain

    • How the CARES Act should explicitly require efforts to address profound autism; why the NIH needs an Office of Autism Research, not an IACC

    What our community can do to help reform the CARES Act, and more

    Link:NCSA Letter re CARES Act Reauthorization. Includes link to ASF white paper: https://www.ncsautism.org/blog//ncsa-submits-concerns-about-the-autism-cares-act-reauthorization-now-is-the-time-for-bold-action

    • 1 hr 18 min

Customer Reviews

4.8 out of 5
20 Ratings

20 Ratings

Rob Schmoldt ,

Thank You

Thank you for this discussion on a universally difficult and complex topic. I have a 20-year old adult son living with my wife and I in California. He has severe Autism and IDD. This podcast offers key insight and perspective for us to more effectively plan for his and our future.

MyElectricTypewriter ,

Eugenics 101

For those who are looking for content related to members of the Autistic community with the most intensive support needs (whether that describes you or someone you care for), steer clear of this podcast.

Autism Confidential is a project of the National Council on Severe Autism (NCSA), a vile organization full of parents of Autistic children with intensive support needs who believe (among other abhorrent things) the following.

1) It’s a moral imperative to wipe the autistic neurotype (and, thus, Autistic people) out of the human gene pool (they explicitly stated this in a 2021 Medium post). Anyone who calls this belief what it is - eugenics - is no more than an “anti-preventionist” hater.

2) All Autistic individuals are either not disabled enough or too disabled to have a valid opinion on issues that impact themselves and their communities. Parents and caregivers of Autistic people with intensive support needs (and charlatans, like applied behavior analysis practitioners) are the only people who deserve a seat at the table with those with the power to allocate funding and set research priorities related to the Autistic community.

3) Speaking Autistic individuals with minimal support needs and no co-occurring intellectual disabilities are not really Autistic and are stealing their children’s labels and resources. Only Autistic people who are non-speaking, have intensive support needs and/or are intellectually disabled deserve a clinical autism diagnosis and any kind of support, resources or accommodations.

4) Although they flatly reject other conspiracy theories regarding the autistic neurotype (like the thoroughly debunked vaccine connection), they unapologetically traffic in conspiracy theories regarding unproven environmental causes (especially their president, Jill Escher).

5) The autistic neurotype should never be treated as a natural variation of the human experience. Autistic people should be treated as diseased burdens instead.

6) Instead of researching and paying for legitimate and ethical ways to support Autistic people, we should just pour all funding into pseudoscientific and abusive compliance training masquerading as support (e.g., applied behavior analysis).

7) Instead of researching and paying for ways to keep Autistic people with intensive support needs (including those who engage in aggressive or self-injurious behavior) in their own homes (or their family homes), we should force them into segregated housing or institutions.

8) Non-speaking or minimally speaking Autistics with intensive support needs are incapable of any complex form of communication or self-advocacy. They shouldn’t be granted access to alternative means of communication or be allowed access to independent or shared decision-making.

I could go on, but I would be here all day. If any of the points above fill you with disgust, please avoid this podcast and anything else with the NCSA’s fingerprints on it. If you agree with even a single point listed above, congratulations on finding like-minded bigots to commiserate with.

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