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Autism

RFK Jr. Exposes a Chilling New Autism Reality

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8 minute read

The Vigilant Fox's avatar The Vigilant Fox

Autism rates are exploding. The “experts” say they’re clueless. But Kennedy believes he knows exactly where to look.

HHS Secretary RFK Jr. just held a press conference to respond to the CDC’s latest numbers on autism rates in the United States.

The findings were impossible to ignore, and Kennedy didn’t sugarcoat just how dire the situation had become.

He revealed that 1 in 31 American children are now diagnosed with autism.

For boys, the numbers are even worse—1 in 20.

And in California, where data tracking is considered the most thorough in the country, the rate may be as high as 1 in 12.5 boys. According to Kennedy, that figure likely reflects a national trend.

Just two years ago, the national rate was 1 in 36. Now, it’s jumped dramatically—and Kennedy says he’s determined to find out why.

“The ASD prevalence rate in 8-year-olds is now 1 in 31. Shocking. There is an extreme risk for boys. Overall, the risk for boys of getting an autism diagnosis in this country is now 1 in 20.

“And as high in California, which has the best data collection.

“So it probably also reflects the national trend—1 in 12.5 boys. This is part of an unrelenting upward trend. The prevalence two years ago was 1 in 36,” Kennedy lamented.

He didn’t hold back in calling out the media and powerful industries, accusing them of covering up environmental factors that are contributing to the crisis.

Kennedy blasted the “epidemic denialists,” pointing to a 1992 ADDM report as proof that autism rates have exploded nearly fivefold in just three decades. Back then, the rate was 1 in 150. Today, it’s 1 in 31.

“It’s clear that the rates are real,” Kennedy stressed.

“Year by year there is a steady, relentless increase. I want it because this epidemic denial has become a feature in the mainstream media and it’s based on an industry canard.

“Obviously there are people who don’t want us to look at environmental exposures,” he said.

He also took direct aim at the claim that today’s rising autism rates are simply the result of better awareness or improved diagnosis.

To prove his point, Kennedy cited a peer-reviewed 1987 study from North Dakota, where researchers attempted to identify every child in the state with a developmental disorder.

They didn’t cut corners. They analyzed medical records, confirmed diagnoses, and even conducted in-person evaluations across a population of 180,000 children. Then, they followed that same group for 12 years.

If you still believe autism rates are only rising because doctors are “getting better at diagnosing it,” Kennedy said, you’d have to believe that the original researchers somehow missed nearly all the cases—98.8 percent of them.

But that’s not what happened.

“They went back in 2000 and found that they had missed exactly one child,” he said.

“They weren’t missing all these cases. The epidemic is real.”

Then came one of the most infuriating parts of the press conference: Kennedy revealed how autism research funding has been misdirected for years.

He said the National Institutes of Health (NIH) has pumped 10 to 20 times more money into studying genetic causes of autism than into researching environmental ones.

That, Kennedy said, is a dead end.

“This is a preventable disease. We know it’s an environmental exposure. It has to be. Genes do not cause epidemics,” he argued.

That’s why Kennedy says he’s redirecting resources toward the kind of research that’s long been neglected—into environmental factors.

“And that’s where we’re going to find the answer,” he added.

The most emotional moment came at the end, when Kennedy spoke from the heart about what this epidemic is doing to children—and to families.

“These are children who should not be suffering like this,” he said.

“These are kids who, many of them, were fully functional and regressed because of some environmental exposure into autism when they’re two years old. These are kids who will never pay taxes, they’ll never hold a job, they’ll never play baseball, they’ll never write a poem, they’ll never go out on a date.

Many of them will never use a toilet unassisted.”

“We have to recognize we are doing this to our children and we need to put an end to it,” Kennedy declared.


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Autism

NIH, CMS partner on autism research

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From The Center Square

By 

Officials at the the National Institutes of Health and the Centers for Medicare & Medicaid Services announced a partnership Wednesday to research “root causes of autism spectrum disorder.”

As part of the project, NIH will build a real-world data platform enabling advanced research across claims data, electronic medical records and consumer wearables, according to the agencies.

“We’re using this partnership to uncover the root causes of autism and other chronic diseases,” said HHS Secretary Robert F. Kennedy Jr. “We’re pulling back the curtain – with full transparency and accountability – to deliver the honest answers families have waited far too long to hear.”

CMS and NIH will start this partnership by establishing a data use agreement under CMS’ Research Data Disclosure Program focused on Medicare and Medicaid enrollees with a diagnosis of autism spectrum disorder or ASD.

“This partnership is an important step in our commitment to unlocking the power of real-world data to inform public health decisions and improve lives,” NIH Director Dr. Jay Bhattacharya said. “Linking CMS claims data with a secure real-world NIH data platform, fully compliant with privacy and security laws, will unlock landmark research into the complex factors that drive autism and chronic disease – ultimately delivering superior health outcomes to the Americans we serve.”

Researchers will focus on autism diagnosis trends over time, health outcomes from specific medical and behavioral interventions, access to care and disparities by demographics and geography and the economic burden on families and healthcare systems, according to a news release.

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Autism

UK plans to test children with gender confusion for autism

Published on

From LifeSiteNews

By Jonathon Van Maren

All children referred to a ‘gender clinic’ in the UK will soon be screened for autism and other ‘neurodevelopmental conditions’ due to the high rate of autism among gender-confused people.

According to The Telegraph, the National Health Service has drafted plans to test all children who believe they are “transgender” for autism due to findings in the Cass Review, which noted that “mental health conditions were disproportionately common among children and young people with gender dysphoria.” 

“Every child referred to a gender clinic will be ‘screened for neurodevelopmental conditions’ such as autism and ADHD under new guidance,” The Telegraph reported. “Medics will also evaluate each child’s mental health, their relationship with their family and their sexual development, including whether they are experiencing same-sex attraction.”  

Many parents, experts, and psychiatrists have been calling for such screenings for years, but transgender activists pushing the so-called “gender-affirming care” model refused to consider the intersection of autism and other factors and gender dysphoria. Consequently, many parents have seen their autistic children sucked into the gender ideology; the newsletter Parents with Inconvenient Truths about Trans has published heartbreaking stories almost weekly.  

The NHS will now be moving away from the “medical model” or “gender-affirming care” to a “holistic” approach. This new guidance will be released for public consultation shortly and come into effect later in 2025. According to The Telegraph: 

However, some groups criticized a “serious flaw” in the policy as it leaves an open door to the use of cross-sex hormones. They also condemned its absence of recognition of the wider societal issues to which children are exposed. The new NHS Children and Young People’s Gender Service will explore eight key areas of a child’s life. 

To assess “development”, doctors will take a “detailed history” of the child’s social, cognitive and physical growth, particularly because of the “substantial” changes that take place during puberty. They will screen children for autism and learning disabilities and look into whether further “cognitive assessments” are necessary. 

The specification says: “Given the high prevalence of neurodiversity identified within this population, all those attending the NHS Children and Young People’s Gender Service should receive screening for neurodevelopmental conditions.” The “multidisciplinary team” of experts, including a consultant specializing in neurodevelopmental disorders, will create a treatment plan for each individual depending on their diagnosis. 

If, during the screening, a “neurodevelopmental condition” is identified, a referral to the Paediatric Neurodevelopmental Service or Paediatric ASD Service will be likely, according to the guidance. Physicians will seek to determine whether the child’s symptoms are a result of underlying conditions or gender dysphoria, and their conditions will be reviewed longer term. Dr. Michael Craig, the clinical lead from the NHS National Autism Unit from 2007 to 2023, “previously estimated half of patients seen by Tavistock’s clinic had autism after observing sessions.”  

Hilary Cass observed the same trend, noting that one study found that autism was a “common denominator” in people identifying as transgender, with a recent study determining that gender-confused people were three to six times more likely to be autistic. The spike in girls identifying as transgender, Cass noted, was in part due to “undiagnosed autism, which is often missed in adolescent girls.” The new NHS guidance noted that there has been a “reluctance to explore or address” mental health issues, in part because gender dysphoria has not been classified as a mental illness under the “gender-affirming care” model. 

The new holistic NHS approach will also include examining the social context of children struggling with gender dysphoria: 

Another key area is dubbed “family context”, with medics being tasked to paint a picture of each child’s upbringing and familial relationships. The specification noted that “there is evidence of an increased frequency of family parental physical and/or mental ill health and other family stressors in this group”.

Under the section titled sexual development, knowledge and sexual orientation, it said “clinicians should seek to understand the child/young person’s emerging sexuality and sexual orientation”. If this has been a previous issue, doctors should consider whether the child was exposed to “adversity and trauma”. They will also examine the children’s physical health needs and the impact of any long-term conditions, along with their broader well-being, school relationships and educational attainment.

Critics of “gender-affirming care” have been enthusiastic about this proposed guidance, with Dr. Louise Irvine of the Clinical Advisory Network on Sex and Gender telling The Telegraph that: “The new service recognizes that many also experience mental health, neurodevelopmental and/or personal, family or social complexities in their lives. The challenge will be to ensure NHS services can provide prompt access to appropriate service for any identified needs as waiting lists are currently very long.” Irvine did note the “serious flaw” in the guidance being that it “leaves the door open for referral of children and young people under 18 for cross-sex hormones,” which she called unscientific and “irresponsible.” 

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Jonathon Van Maren

Jonathon’s writings have been translated into more than six languages and in addition to LifeSiteNews, has been published in the National PostNational ReviewFirst Things, The Federalist, The American Conservative, The Stream, the Jewish Independent, the Hamilton SpectatorReformed Perspective Magazine, and LifeNews, among others. He is a contributing editor to The European Conservative.

His insights have been featured on CTV, Global News, and the CBC, as well as over twenty radio stations. He regularly speaks on a variety of social issues at universities, high schools, churches, and other functions in Canada, the United States, and Europe.

He is the author of The Culture WarSeeing is Believing: Why Our Culture Must Face the Victims of AbortionPatriots: The Untold Story of Ireland’s Pro-Life MovementPrairie Lion: The Life and Times of Ted Byfield, and co-author of A Guide to Discussing Assisted Suicide with Blaise Alleyne.

Jonathon serves as the communications director for the Canadian Centre for Bio-Ethical Reform.

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