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Showing posts with label autism. Show all posts
Showing posts with label autism. Show all posts

Saturday, June 24, 2023

Myths, Misinformation, and RFK Jr.


Julia Shapero at The Hill:
Democratic presidential candidate Robert F. Kennedy Jr. suggested Wednesday that Russia has been “acting in good faith” in various efforts to end the war in Ukraine and placed blame on the U.S. for the 16-monthlong conflict.

Kennedy said in an interview on SiriusXM’s “The Briefing with Steve Scully” that Russian President Vladimir Putin has “repeatedly said yes” to negotiations.

Joan Walsh at The Nation:

I’ve been doing my best to ignore the farcical presidential candidacy of Robert F. Kennedy Jr. His noxious views on vaccines, the origin of AIDS, the alleged dangers of wi-fi and other forms of junk science deserve no wide hearing. Polls showing he’s favored by 20 percent of likely Democratic voters over President Biden are almost as laughable as Kennedy’s views. It’s early; he’s got iconic American name recognition; and there’s almost always an appetite, among Democrats anyway, for anybody but the incumbent. His lies have been thoroughly debunked by Judd Legum at Popular Info, Michael Scherer in The Washington Post, Naomi Klein in The Guardian, and Brandy Zadrozny on NBC News.

But I’ve come to believe I have a responsibility to write about Kennedy because of my own shameful role in sending his toxic vaccine views into public discourse: I was the Salon editor, in partnership with Rolling Stone, who 18 years ago published his mendacious, error-ridden piece on how thimerosal in childhood vaccines supposedly led to a rise in autism, and how public health officials covered it up. From the day “Deadly Immunity” went up on Salon.com, we were besieged by scientists and advocates showing how Kennedy had misunderstood, incorrectly cited, and perhaps even falsified data. Some of his sources turned out to be known crackpots.
///
But as subsequent articles and books continued to debunk Kennedy’s conspiracy theory, it felt irresponsible to leave it up. Six years later, in 2011, my successor as editor in chief, Kerry Lauerman, in consultation with me and others, decided we should take it down. Rolling Stone later did the same. (In the interests of transparency, we preserved the corrections page.)

Jake Tapper at CNN:

Go back to 2005. I was a reporter with ABC News and Salon.com reached out to see if we were interested in doing a TV spot tied to the publication of the Kennedy Jr. piece. I interviewed him via phone, with a TV crew in his office, and prepared a spot for “World News Tonight with Peter Jennings.”

In Kennedy’s bizarre retelling a few days ago (the relevant part starts at 27:55 into the interview), I worked with him “for three weeks doing this incredible documentary” (no and no) about his Rolling Stone story – please note he makes zero mention of the article having since been retracted and disappeared – and then “the night before the piece was supposed to run, he called me up and said, ‘The piece just got killed by corporate.’” (I didn’t say that in any way and the piece wasn’t killed.) “All my career, I have never had a piece killed by corporate and I’m so mad,” he said I said. (I hadn’t. I had been at ABC News for two years. I had had plenty of pieces killed. Not once did “corporate” play a role in killing any of them.)

 




 

Thursday, November 24, 2022

Saturday, April 2, 2022

World Autism Awareness Day

 California Assembly Member Suzette Valladares:

From President Biden:

On World Autism Awareness Day, we reaffirm our commitment to ensuring that the more than 5 million Americans who live with autism are able to make the most of their talents and participate fully in our society, and we celebrate the contributions autistic Americans have made to our families, our communities, our Nation, and the world.

We have made significant progress in improving access to opportunity for people with developmental disabilities in recent years. However, many autistic individuals still experience gaps in employment and income. The COVID-19 pandemic has compounded these inequities, creating unique challenges and strains for people with autism and their families.

That is why my Administration is committed to addressing the systemic barriers people with autism face in their daily lives. The pandemic upended school routines for children and students living with disabilities. That is why the Department of Education is working tirelessly to accelerate pandemic recovery for special education programs. In addition, the Department of Health and Human Services and the Department of Housing and Urban Development are committed to ensuring individuals with disabilities have access to affordable housing as we come through this pandemic.

In order to improve quality of life for people with autism and their families in every community, my Administration is committed to funding cutting-edge research to help us better understand, diagnose, and treat autism, including funding research at the National Institutes of Health and the Centers for Disease Control and Prevention that seeks to better understand the underlying mechanisms of autism from childhood through early adulthood, improve methods of early identification and diagnosis, and develop innovations in the delivery of interventions and services.

My Administration remains committed to reducing barriers in access to early diagnoses, interventions, and services for people with autism — regardless of race, gender, ethnicity, culture, or geography — and to incorporating the lived experiences of individuals with autism into their research. Last June, when I signed the Executive Order on Diversity, Equity, Inclusion, and Accessibility in the Federal Workforce, I promised to cultivate a Federal workforce that draws from the full diversity of the Nation. One of the ways we are delivering on that promise is through a partnership between the Department of Labor and the Administration for Community Living, which is expanding access to competitive, integrated employment opportunities for people with disabilities, including autism.

In addition, my Administration will continue to build on the work done by the Interagency Autism Coordinating Committee, the National Autism Coordinator, and others to make certain that autistic Americans have access to the care, services, and support they need, so they can pursue their educational, career, and life interests without discrimination.

Today and every day, we honor autistic people and celebrate the meaningful and measureless ways they contribute to our Nation. We applaud the millions of educators, advocates, family members, caregivers, and others who support them. As we continue to build a better America, we reaffirm our promise to provide Americans with autism the support they need to live independently, fully participate in their communities, and lead fulfilling lives of dignity and respect.

NOW, THEREFORE, I, JOSEPH R. BIDEN JR., President of the United States of America, by virtue of the authority vested in me by the Constitution and the laws of the United States, do hereby proclaim April 2, 2022, as World Autism Awareness Day. I call upon all Americans to learn more about autism to improve early diagnosis, to learn more about the experiences of autistic people from autistic people, and to build more welcoming and inclusive communities to support people with autism.

IN WITNESS WHEREOF, I have hereunto set my hand this first day of April, in the year of our Lord two thousand twenty-two, and of the Independence of the United States of America the two hundred and forty-sixth.


Wednesday, May 12, 2021

Antivax and QAnon

Alex Kaplan at Media Matters:

Multiple online influencers known for spreading misinformation about the coronavirus and vaccines have been appearing on shows supporting the QAnon conspiracy theory, where they have continued to spread this misinformation.

Supporters of QAnon -- some of whom have been tied to violent incidents and participated in the January 6 insurrection at the United States Capitol -- have also played a significant role in spreading misinformation about the coronavirus pandemic since it began. In recent months, as coronavirus vaccines -- which are safe and effective -- have been released, QAnon supporters have turned their attacks on the vaccines, spreading numerous false claims about them.

In recent months, anti-vax influencers have appeared on multiple different QAnon shows, apparently noticing in QAnon supporters an audience primed to be receptive to their message. At least two are part of the so-called “Disinformation Dozen,” influencers identified in a report by the Center for Countering Digital Hate as the originators of an estimated 65% of vaccine misinformation spread on Facebook and Twitter.


Tuesday, April 30, 2019

Measles and the Antivax Movement

 Donald G. McNeil Jr.n at NYT:
Measles continues to spread in the United States, federal health officials said on Monday, surpassing 700 cases this year as health officials around the country sought aggressive action to stem the worst outbreak in decades.
In New York, an epicenter of the outbreak, city officials closed two more schools for Orthodox Jewish children for failing to comply with an order to exclude unvaccinated children.
In California, hundreds of students and staff members at two universities remained under quarantine following possible exposure to the virus.
And with measles spreading globally, officials at the Centers for Disease Control and Prevention have urged Americans traveling abroad to make sure they are immunized against the disease. On Monday, the agency renewed an urgent call for parents to get their children vaccinated.
Bryan Llenas at Fox News:
"The biggest challenge we face right now is misinformation and myths about the vaccine. It's important that parents realize that the vaccine is safe and effective," Dr. Nancy Messonnier, director of the National Center for Immunization and Respiratory Diseases, told Fox News.

Anti-vaccination propaganda targeted specifically to parents has popped out throughout Hasidic communities in Williamsburg, Brooklyn and in Rockland County, N.Y. and it appears to have convinced some mothers that the vaccines are more dangerous than the disease. The vast majority of the 704 confirmed measles cases in 22 states are located in these communities, according to the Centers for Disease Control's (CDC) latest data, released Monday. Of those cases, 432 are in Brooklyn.
An anti-vaccination organization known as PEACH has published a 40-page booklet, filled with misinformation and discredited science about why it says vaccines are unsafe. Among the many discredited claims are that vaccines cause autism and are made of aborted fetuses.

Friday, December 1, 2017

Autism and Medical Marijuana in Minnesota

In The Politics of Autism, I discuss alternative treatments.

From the Minnesota Department of Public Health:
Minnesota Commissioner of Health Dr. Ed Ehlinger today announced the decision to add autism spectrum disorders and obstructive sleep apnea as new qualifying conditions for the state’s medical cannabis program.
“Any policy decisions about cannabis are difficult due to the relative lack of published scientific evidence,” said Commissioner Ehlinger. “However, there is increasing evidence for potential benefits of medical cannabis for those with severe autism and obstructive sleep apnea.”
This year, as in years past, the Minnesota Department of Health used a formal petitioning process to solicit public input on potential qualifying conditions. Throughout June and July, Minnesotans were invited to submit petitions to add qualifying conditions. The process included public comments, a citizens’ review panel and a set of research summaries for each condition prepared by Minnesota Department of Health staff.
Petitioners put forward a total of 10 conditions for consideration this year, including anxiety disorders, autism, cortico-basal degeneration, dementia, endogenous cannabinoid deficiency syndrome, liver disease, nausea, obstructive sleep apnea, Parkinson’s disease and peripheral neuropathy. There were also petitions to add cannabis delivery methods including infused edibles and vaporizing or smoking cannabis flowers. These requests were not approved.
Autism spectrum disorder is characterized by sustained social impairments in communication and interactions, and repetitive behaviors, interests or activities. Patients certified for the program because of autism must meet the DSM-5 (Diagnostic and Statistical Manual of Mental Disorders – 5th edition) for autism. The health department’s autism research brief (PDF) found a growing body of research indicating that the human body’s endocannabinoid system may play a role in autism symptoms. In support of adding autism, the review panel report (PDF) noted the lack of effective drug treatments, the potentially severe side effects of current drug treatments and anecdotal evidence of Minnesota children with autism already receiving benefits from medical cannabis taken for other qualifying conditions.
...
Under current state rules, patients certified to have autism or obstructive sleep apnea will be newly eligible to enroll in the program on July 1, 2018 and receive medical cannabis from the state’s two medical cannabis manufacturers beginning Aug. 1, 2018. As with the program’s other qualifying conditions, patients will need advance certification from a Minnesota health care provider. More information on the program’s certification process is available from the Office of Medical Cannabis.

Sunday, September 24, 2017

Pretty Much Everybody Hates Graham-Cassidy

There is a remarkable consensus against the Graham-Cassidy health bill.  Groups and interests that usually disagree are united in opposition. From America's Health Insurance Plans:
The following statement was jointly released on September 23, 2017 by the American Medical Association, American Academy of Family Physicians, American Hospital Association, Federation of American Hospitals, America’s Health Insurance Plans, and the BlueCross BlueShield Association regarding the Graham-Cassidy-Heller-Johnson legislation.
We represent the nation’s doctors, hospitals, and health plans. Collectively, our organizations include hundreds of thousands individual physicians, thousands of hospitals, and hundreds of health plans that serve tens of millions of American patients, consumers, and employers every day across the United States.
While we sometimes disagree on important issues in health care, we are in total agreement that Americans deserve a stable healthcare market that provides access to high-quality care and affordable coverage for all. The Graham-Cassidy-Heller-Johnson bill does not move us closer to that goal. The Senate should reject it.
We agree that the bill will cause patients and consumers to lose important protections, as
well as undermine safeguards for those with pre-existing conditions. Without these
guaranteed protections, people with significant medical conditions can be charged much
higher premiums and some may not be able to buy coverage at all.
We agree that the bill will result in dramatic cuts to Medicaid and a funding cliff in the
future, fundamentally changing the way that states provide coverage for some of our most vulnerable citizens. This means that millions of patients will lose their coverage and go without much-needed care.
We agree that the individual insurance market will be drastically weakened, making
coverage more expensive and jeopardizing Americans’ choice of health plans. By not
providing all states with sufficient funds to support working families who need help buying coverage, millions will go without it.
We agree that the bill’s current implementation timelines are not workable. State and
industry leaders will need to completely transform their individual insurance markets and
Medicaid programs in little more than a year – an impossible task.
Health care is too important to get wrong. Let’s take the time to get it right. Let’s agree to
find real, bipartisan solutions that make health care work for every American.
At The Washington Post, Christopher Ingraham provides a partial list of groups against the bill:






Tuesday, December 27, 2016

Pennsylvania, Texas and Special Education

Reposted from Autism Policy and Politics:

In The Politics of Autism, I discuss special education.  Some states do a reasonably good job, but Texas is not one of them.

At The Houston Chronicle, Susan Carroll and Brian M. Rosenthal report on a girl with Asperger's who made great progress after her dad moved from Texas to Pennsylvania. (h/t FRL)
Pennsylvania does not have a special education enrollment target — no state does, other than Texas — but it does fund special ed in an unusual way.
The state assumes that roughly 16 percent of students need special ed and funds all school districts at that rate, regardless of how many special ed kids they actually have.
The state's rationale for choosing that number was simple — it was the state average at the time, according to Casey Smith, an education department spokesman. But before implementing the system, officials also called in experts and hosted public forums across the state, Smith said.
That approach is far different than what took place in Texas, when a small group of officials set a benchmark well below the state average without consulting the public, the federal government or any researchers.
The Pennsylvania system is good because it does not incentivize either under-identification or over-identification, several experts said.
Pennsylvania law also is praised for requiring schools to respond to verbal requests from parents for special education evaluations, instead of only written requests.
As a result, about 17 percent of students receive special education,  a 1.5 percentage point increase from 2004, according to the latest federal data.

Wednesday, February 17, 2016

The Irony of Red Tape

Reposted from Autism Policy and Politics:

"Every restraint and requirement originates in somebody's demand for it." -- Herbert Kaufman, Red Tape.

In The Politics of Autism, I discuss the red tape that pervades all aspects of the issue, from special education to  insurance to health care.

The Government Accountability Office reports that the US Department of Education tried pilot projects to reduce paperwork in special education. But states have been reluctant to take part -- because the pilot projects involve too much paperwork.
Despite Education’s efforts, no state applied to participate in either of the pilot programs. NASDSE [National Association of State Directors of Special Education] officials told us that the application requirements were much too resource-intensive for the potential value they would bring, and implementation of either pilot program would most likely require require additional staff that federal funding would not cover. Several states wrote letters to Education explaining their reasons for not applying for and implementing the Paperwork Waiver Program in particular, noting that the program would require more paperwork and staff, but provide little in the way of additional federal funds. For example, New York’s letter listed as key reasons for not participating the extensive requirements for participation, limited funding for the pilots, and the staff commitment necessary for both development of the proposals and ongoing oversight of the pilot projects. In a similar letter, Rhode Island noted that implementing the Paperwork Waiver Program would likely result in more paperwork—not less—as well as taking more time from staff.
A summary of the report:
In response to the 2004 reauthorization of the Individuals with Disabilities Education Act (IDEA)—the primary federal law governing education of children with disabilities—the Department of Education (Education) attempted to reduce administrative burden by creating pilot programs and publishing model paperwork forms, but states have used these tools sparingly. Specifically, Education created pilot programs allowing states to use multi-year rather than annual individualized education programs (IEP) to describe services to meet each student’s needs, and to waive certain federal paperwork requirements. However, no state applied for these pilots, citing a perceived lack of benefit, and inadequate funding to implement and evaluate the pilots. As required by law, Education also published templates, known as model forms, to help states streamline the process of preparing IEPs and comply with parent notice requirements in IDEA. Although some states and school districts adopted at least one of these model forms, they have used others primarily as a starting point to develop their own forms. State and district officials told GAO this allowed them to meet federal as well as state and local requirements, and provided better protection against potential litigation. Stakeholders were mixed in their views about the effects of other provisions intended to reduce administrative burden. For example, several stakeholders viewed a provision allowing states to use more grant funds for paperwork reduction activities as helpful; others said the effect of a provision eliminating benchmarks and short-term objectives for IEPs was largely negligible.
Stakeholders across 9 focus groups—3 each with state administrators, local administrators, and educators—said that state-imposed requirements contribute to the administrative and paperwork burden, but their views on the burdens and benefits of federal IDEA requirements varied somewhat. For example, in focus groups, educators expressed concerns about monitoring and documenting student progress, while local and state administrators expressed concerns, respectively, about IEP implementation and federal reporting requirements. Consistent with prior research, many educators in these focus groups estimated they spend roughly one to two hours daily on administrative tasks, and expressed concern about this taking time away from the classroom. Despite perceived burdens, stakeholders widely acknowledged that IDEA’s requirements play an important role in accountability. For example, educators said the requirements provide information about student strengths and limitations that help them assist the student, while state administrators said requirements aid planning and program development.
Education, states, and school districts have reduced administrative burdens by adopting new technology and using certain resource strategies. For example, several state administrators said Education’s electronic data submission system has made it easier to complete federally-required state performance plans. During fall 2014, Education launched a new electronic reporting system intended to, among other things, consolidate data collections and ease data entry. Some schools and districts have also adopted resource strategies, such as hiring data clerks to reduce administrative burdens, but these strategies can be costly.

Sunday, September 20, 2015

Autism and the Campaign

Yesterday morning, The Hill ran the piece below, which deals with some of the topics I cover iThe Politics ofAutism.

During the recent GOP debateDonald Trump suggested that kids are developing autism because they are getting too many shots too soon. “Just the other day, two years old, two and a half years old, a child, a beautiful child went to have the vaccine, and came back, and a week later got a tremendous fever, got very, very sick, now is autistic.”

Curiously, Trump used almost the same words three years ago. “It happened to somebody that worked for me recently,” he said on Fox News in 2012. “I mean, they had this beautiful child, not a problem in the world, and all of the sudden they go in and they get this monster shot…then all of the sudden the child is different a month later.”

Wherever this mysterious anecdote came from, Trump was talking nonsense. Multiple scientific studies have shown that there is no connection between autism and the vaccine schedule, or any individual vaccine. The idea of such a linkage has been circulating for years because of a 1998 study that turned out to be fraudulent. The British medical journal that ran the piece later retracted it, and its lead author lost his medical license.

Trump is hardly the first politician to spout misinformation – but in this case, it is downright dangerous. If parents take him seriously and delay vaccinations, their children could catch the diseases that the vaccines prevent. And some of these diseases can be deadly.

Trump also erred on the broader issue of autism. “Autism has become an epidemic,” he said. “Twenty-five years ago, 35 years ago, you look at the statistics, not even close. It has gotten totally out of control.” Trump unintentionally fingered a reason why we have to be cautious about declaring an “epidemic.” Thirty-five years ago was when the American Psychiatric Association’s manual first listed autism as a distinct category. And twenty-five years ago was when federal law first required the Education Department to gather national data on the number of students with autism.

When you start counting something, you usually find more of it. In this case, much of the apparent increase in autism involves better identification of people who previously would have gotten a different label. Scientists at Penn State University found no overall increase in the number of students in special education. As the number of students with an autism label has gone up, the number with an intellectual disability label has gone down.

Aside from improvements in reporting, has there also been any true increase in the prevalence of autism? Nobody knows for sure, in part because we lack good data from the past. Indeed, the most important thing for presidential candidates to know about autism is how much we don’t know.

Vaccines are one of the few purported causes that scientists have ruled out. Autism tends to run in families, so genetics probably has something to do with it. Beyond that, the possibilities include such disparate things as paternal age, maternal age, pollution, and immune responses to viruses. And until scientists know what causes autism, when and how it starts in the developing body, and how it expresses itself over time, they will have difficulty in devising medical responses. Studies show that certain behavioral and educational programs can help with symptoms, but there is little research showing how much these interventions can improve quality of life in the long run.

Information on the workings of autism policy is just as sparse. In a recent article, autism experts Paul T. Shattuck and Anne M. Roux asked us to picture a big company that tried to do business without financial statements, that is, without data on sales, spending, customer experience, or assets. Such a firm would fail. “Yet, this state of affairs is commonplace in many autism services. At a population level, we are almost completely unable to clearly describe the resources expended on services or measurable indicators of the population outcomes we hope to influence -- including the employment rate.”

So the major lesson is that we need more research – not just on biology, but on effective ways in which policy can help autistic people in the here and now. Presidential candidates should address this issue. Above all, they need to tell the truth.

Pitney, professor of government at Claremont McKenna College, is the author of The Politics of Autism: Navigating the Contested Spectrum (Rowman and Littlefield).

Sunday, August 23, 2015

New Book: The Politics of Autism

A number of posts have discussed the politics of autism.  I have a new book on the topic:


FOR RELEASE AUGUST 2015

Contact Jacqline Barnes 301-459-3366 x5515
jbarnes@rowman.com

“Autism matters to everyone. Pitney leaves his reader understanding why this is true and why solutions have proven elusive. The Politics of Autism expertly maps the complex terrain of policy designed to address society’s challenges attributed to autism and provides a solid foundation from which to move forward.”
—Dana Lee Baker, School of Politics, Philosophy and Public Affairs, Washington State University

In the first book devoted exclusively to the contentious politics of autism, noted political scientist and public policy expert John J. Pitney, Jr., explains how autism has evolved into a heated political issue disputed by scientists, educators, social workers, and families. Nearly everything about autism is subject to debate and struggle, including its measurement and definition. Organizational attempts to deal with autism have resulted in not a single “autism policy,” but a vast array of policies at the federal, state, and local levels, which often leave people with autism and their families frustrated and confused.

Americans with autism are citizens, friends, coworkers, sons, daughters, fathers, and mothers. No longer simply the objects of public policy, they are active participants in current policy debates. Pitney’s fascinating look at how public policy is made and implemented offers networks of concerned parents, educators, and researchers a compass to navigate the current systems and hope for a path towards more regularized and effective policies for America’s autism community.

Features

  • The first book to focus exclusively and comprehensively on the politics of autism in the USA
  • Offers a vivid case study of how our political system deals with policy uncertainty
  • Useful to scholars, especially in college classes, but also accessible to general readers


John J. Pitney, Jr., is the Roy P. Crocker Professor of American Politics at Claremont McKenna College. He received his B.A. from Union College and his Ph.D. in political science at Yale. He is the author of The Art of Political Warfareand the coauthor of several books, including Epic Journey: The 2008 Elections and American Politics and After Hope and Change: The 2012 Elections and American Politics.

www.rowman.com

August 2015  180 pages  978-1-4422-4960-8  $38.00 Cloth
August 2015  180 pages  978-1-4422-4961-5  $37.99 eBook

Thursday, December 20, 2012

The Shooting, The Media, and Autism

A previous post noted the many mistakes in media coverage of the Newtown shooting. Almost as soon as news broke of the tragedy in Connecticut, some news organizations began quoting speculation that the killer might have had autism.  

In a string of heated interviews that sought to get both sides of the post-Sandy Hook debates on gun ownership and mental illness, CNN's Piers Morgan booked a guest who suggested autistic people may be more prone to acting out violent fantasies. Asperger's was a central component of 60 Minutes's report on Lanza Sunday night, including a statement from an advocacy group that insisted those with Asperger's are more likely to be victims of violence than proponents of it. Media critics have also singled out Fox News and The New York Times as outlets that have overplayed the connection between Lanza's action and any developmental disorders he may have had. (A high school advisor also said Lanza had a rare condition in which he couldn't feel pain).
In our textbook, we discuss ombudsmen, or  in-house media critics.  Margaret Sullivan is "public editor" at the New York Times and she has questioned her paper's coverage.  In particular, one story had this vague reference:
Several said in separate interviews that it was their understanding that he had a developmental disorder. They said they had been told that the disorder was Asperger’s syndrome, which is considered a high functioning form of autism.
“It’s not like people picked on him for it,” Mr. Baier said. “From what I saw, people just let him be, and that was that.”
Law enforcement officials said Friday that they were closely examining whether Mr. Lanza had such a disorder.
When Sullivan questioned reporter David Halbfinger and Metro editor Carolyn Ryan , they were defensive.
Critics, though, say that if you want to understand how such a statement might be taken, try this hypothetical substitution: “Law enforcement officials said they were closely examining whether Mr. Lanza is gay.” There is, for a reasonable person, the suggestion of cause and effect. It is very unlikely that that sentence would have appeared in The Times without further explanation.
References to Asperger’s have now appeared in several Times articles, all based on anonymous sources or on named sources who were reporting what they had heard from someone else. It has been, in short, repeated conjecture by those who don’t know. [emphasis added] On Monday, The Associated Press reported that a divorce mediator, who was named, was told by the Lanzas that their son had Asperger’s, and The Times began reporting that on The Lede blog. The blog post did a great deal to explain the issue clearly and responsibly.
For discussion of how some activists and writers are trying to correct the record, see The Columbia Journalism Review and Autism Policy and Politics (another blog that I run).

Tuesday, July 24, 2012

Bad Journalism and the Aurora Shooting

An earlier post described a hasty, false report linking the Colorado shooter to the tea party.

Bad journalism continues.  At MSNBC, Joe Scarborough speculated -- without a scrap of supporting evidence -- that the shooter has Asperger Syndrome.

At Politico, Dylan Byers writes:
Arlene Holmes, the mother of Colorado theater shooting suspect James Holmes, has suggested that ABC News mischaracterized her when it reported that her initial statement to the reporter, "you have the right person," was a reference to her son.
"This statement is to clarify a statement made by ABC media. I was awakened by a call from a reporter by ABC on July 20 about 5:45 in the morning. I did not know anything about a shooting in Aurora at that time," Holmes said in a statement this afternoon, read to the national press by attorney Lisa Damiani. "He asked if I was Arlene Holmes and if my son was James Holmes who lives in Aurora, Colorado. I answered yes, you have the right person. I was referring to myself."
"I asked him to tell me why he was calling and he told me about a shooting in Aurora," she continues. "He asked for a comment. I told him I could not comment because I did not know if the person he was talking about was my son, and I would need to find out."
In the first paragraph of its initial report on Friday, ABC News reported that it had identified the correct James Holmes because his mother "told ABC News her son was likely the alleged culprit, saying, 'You have the right person.'"
If Arlene Holmes' latest statement is true, it means that she did not tell ABC News her son was likely the alleged culprit, calling into question the reporting of a network that has already been marred by one inaccuracy.
HotAir follows up:
Update: ABC says it didn’t happen the way Holmes says it did — and no, there’s no recording of the conversation:
ABC News phoned Arlene Holmes at 5am PST, at her home in San Diego, Calif., according to notes and email records by ABC News producer Matthew Mosk, who placed the call…
Mosk said today that he awoke Arlene Holmes and informed her that a man, he believed was her son had been arrested in Aurora and asked to confirm their relationship.
“You have to tell me what happened… You have to tell me what happened,” the woman on the phone said, according to Mosk. Mosk said he told her that ABC News had learned the 24-year-old had been identified by police as the lone suspect in the mass killing in Aurora, Colo and that the details of the events were still taking shape.
“You have the right person,” was her response, he said. “I need to call the police. I need to fly to Colorado.”
That contradicts Holmes’s claim that she didn’t know anything about the shooting before her “right person” comment — but even here, according to ABC’s own account, the quote is totally ambiguous. Was she saying that James Holmes was the “right person,” i.e. the shooter, or merely that she was his mother? Why did ABC leap to assume the former instead of the latter?

Tuesday, May 29, 2012

The Young Marines

Daniel de Vise writes at The Washington Post:
Bob Nobles and Cornell Wright might not have a chance to serve their country when they are adults. No matter: They are serving it now.
“Good morning, Young Marines,” barked 1st Sgt. Vivian Price-Butler, greeting Bob and Cornell and eight other boys Friday morning in her small classroom at Kennedy Krieger High School.

“Good morning, First Sergeant,” they replied in unison, standing straight and still.
The Young Marines is an education and service program reaching 10,000 youths around the nation and overseas. Of its more than 300 units, only one is dedicated to students with special needs.
Founded in 1993, the Kennedy Krieger program serves 24 students at a high school for children who cannot be accommodated in traditional schools. Bob, a 16-year-old sophomore from New Windsor, has autism. Cornell, a 17-year-old junior from Glendale, has an intellectual disability. Other students have cerebral palsy, Down syndrome or brain injuries.
Price-Butler, known affectionately as First Sergeant around the Baltimore school, is not a trained teacher. Yet, 10 or 20 years from now, she is the Kennedy Krieger educator most likely to be getting e-mails and baby pictures from Bob and Cornell and the other Young Marines.

Monday, February 6, 2012

Military Kids with Autism

What do the armed forces have to do with health care? The US military health care system is among the world's largest, serving more than 9.2 million people, including active duty personnel and families, retirees and their families, and eligible veterans.  The following item, reposted from Autism Policy and Politics, explains one of the many issues arising from this system.


Jean Winegardner writes at The Washington Times:
Last Tuesday, Scott Campbell stood up during the public comment section of a congressional briefing for H.R. 2288, the Caring for Military Children with Autism Act (CMKAA) and spoke about his lung cancer. Doctors discovered it during his retirement physical, requiring him to stay on active duty for treatment.
That active duty, following 28 years of service, allowed his son, a 13-year-old severely affected by autism, to continue his applied behavior analysis (ABA) treatments and to have them paid for by his military insurance.
"I was glad I got lung cancer," he said, letting the irony of his words seep into the room, "because it meant my son could get treatment."
Campbell was addressing a situation that affects military parents of children with autism across the country. ABA therapy, which is often recommended to to treat autism, is not covered under TRICARE standard, the basic military insurance. Military families must seek coverage under the Extended Health Care Option (ECHO) which is only available after enrollment in the Exceptional Family Member Program (EFMP).
Once enrolled, coverage caps limit ABA therapy at an average of 11 hours per week, less than the 25-40 hours that is often recommended for young recently diagnosed children. Furthermore, ECHO is not available to retirees, even those forced to retire due to injury or disease.
...
The Caring for Military Kids with Autism Act would remove ABA treatment from ECHO, placing it under TRICARE Standard as medically necessary, removing the dollar cap on care, as well as making the therapy accessible to all eligible retiree dependents.
A CMKAA website is here.

Autism Speaks has a video clip of the briefing, along with messages from affected moms:

An MSNBC report:



Tuesday, January 3, 2012

Social Media, The Presidential Race, and a 9-Year-Old with Autism

Social media allow citizens to influence campaign discussions. Lin Wessels has been recording her son's encounters with Republican presidential candidates campaigning for the Iowa caucuses.  She has posted the results on Facebook, Twitter, and YouTube.


Reposted from Autism Policy and Politics:

Sam Wessels, a nine-year-old Iowan with autism, has been asking presidential candidates about their positions on autism.  A previous post showed his encounter with Ron Paul.  Others are below.


Mitt Romney:

 

Rick Santorum:




Newt Gingrich:



Michele Bachmann:

Sunday, May 8, 2011

Federalism Stays Hot

Previous posts have confirmed a point that we make in the textbook: issues of federalism continue to pervade public policy disputes. The New York Times reports:

Marijuana remains illegal under federal law, but that has not stopped a fuzzy industry of marijuana farms and dispensaries from rising to serve the 15 states that allow the drug to be used for medical purposes. Under President Obama, the federal government had seemed to make a point of paying little attention — until now.

Gov. Christine Gregoire of Washington reversed her stance on an expansive marijuana bill.

As some states seek to increase regulation but also further protect and institutionalize medical marijuana, federal prosecutors are suddenly asserting themselves, authorizing raids and sending strongly worded letters that have cast new uncertainty on an issue that has long brimmed with tension between federal and state law.

The New York Times also reports:

Companies looking to do business in secret once had to travel to places like the Cayman Islands or Bermuda.

Today, all it takes is a trip to Vermont.

Vermont, and a handful of other states including Utah, South Carolina, Delaware and Hawaii, are aggressively remaking themselves as destinations of choice for the kind of complex private insurance transactions once done almost exclusively offshore. Roughly 30 states have passed some type of law to allow companies to set up special insurance subsidiaries called captives, which can conduct Bermuda-style financial wizardry right in a policyholder’s own backyard.

Captives provide insurance to their parent companies, and the term originally referred to subsidiaries set up by any large company to insure the company’s own risks. Oil companies, for example, used them for years to gird for environmental claims related to infrequent but potentially high-cost events. They did so in overseas locations that offered light regulation amid little concern since the parent company was the only one at risk.

Now some states make it just as easy. And they have broadened the definition of captives so that even insurance companies can create them. This has given rise to concern that a shadow insurance industry is emerging, with less regulation and more potential debt than policyholders know, raising the possibility that some companies will find themselves without enough money to pay future claims. Critics say this is much like the shadow banking system that contributed to the financial crisis.

But lest anyone think that states are uniformly going easy on the insurance industry, a development from Virginia reminds of of an issue where regulations are getting tighter. Governor Bob McDonnell signed legislation requiring coverage of autism spectrum disorders. The organization Autism Speaks reports:

In addition to Virginia, twenty-five states – Arizona, Arkansas, Colorado, Connecticut, Florida, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Massachusetts, Missouri, Montana, Nevada, New Hampshire, New Jersey, New Mexico, Pennsylvania, South Carolina, Texas, Vermont, West Virginia and Wisconsin – have enacted autism insurance reform legislation. Several other state legislatures are considering similar legislation during the 2011 session.


Tuesday, March 1, 2011

One Student Makes a Difference

The Daily Press (Newport News, Virginia) reports:
When other kids stayed home from school during a snow day last month, Robert Maino headed with his mother to the halls of the General Assembly.

The debate around the autism bill fascinated him, so his mother encouraged him to write a letter thanking the bill's supporters.

He took it a step further, writing to both those who supported and those who voted against the bill requiring insurance companies to cover a form of autism treatment. Maino, an 18-year-old from Mechanicsville and an upcoming Christopher Newport University freshman, has Asperger's syndrome, a mild form of autism.

His letter captured the attention of legislators, who invited him to speak.

His story about his struggles and how early intervention paid off helped put a face on the bill, which supporters spent four years trying to get passed.

"They hadn't heard from somebody who lived it," said Marybeth Maino, Robert's mother.
After the bill passed, he wrote the legislators:

I want to extend my sincerest thanks for your support of the Autism Insurance Reform Bill. I am a 17 year old that has been living with Autism my whole life and I know from personal experience that early intervention is one of the most vital steps in a child's life with autism. Because of my parents, I have been fortunate enough to receive such treatment from an early age and have gone through countless therapies and behavioral counselors to get to where I am today. Because my parents took the personal burden of having to give up so much of their livelihood to give me this blessing, I am now an independent advocate of autism awareness and I spend a good portion of my time volunteering and working to help assist children like myself. Without this intervention on my parent's part, I would most likely not be graduating high school. Instead, I will be graduating high school in June and have been accepted into the President's Leadership Program at Christopher Newport University. I sincerely believe that this bill, once put into action, will make a difference for all those children that don't have it as well off as I did, and make their lives and those that care for them much easier.