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NIH, CMS partner on autism research

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From The Center Square

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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

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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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Autism

RFK Jr. Completely Shatters the Media’s Favorite Lie About Autism

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The Vigilant Fox's avatar The Vigilant Fox

They say autism is rising because of “better diagnosis”—but RFK Jr. just blew that narrative wide open. He brought the hard data and dropped one undeniable truth the denialists can’t explain.

HHS Secretary Robert Kennedy Jr. appeared on Hannity Thursday evening and unloaded on the predominant autism narrative. It started with a bombshell reveal from Kennedy’s own childhood.

Hannity asked: “What was the number when you were a kid—and what do you think is going on?”

Kennedy replied: “There’s really good data on that.”

He pointed to one of the largest studies ever conducted—900,000 children in Wisconsin, published in a top-tier medical journal.

“It looked at 900,000 kids. It was published in a high-gravitas journal, peer-reviewed study, and they found the rate to be 0.7 out of 10,000.”

That’s less than 1 in 10,000. Today? It’s around 1 in 31.

Let that sink in.

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That’s when Kennedy sounded the alarm on what’s happening now—and why it’s so catastrophic. He said the rise isn’t just in frequency—it’s in severity.

“Two years ago, it was 1 in 36. The CDC data we released this week shows 1 in 31,” Kennedy said.

“The worst state is California,” Kennedy continued, “which actually has the best collection methodologies. So they actually, probably reflect what we’re seeing nationwide.”

“In California, it’s 1 in every 20 kids, and 1 in every 12.5 boys,” he explained.

Even worse, he said the numbers are likely underreported in minority communities. And for many kids, the symptoms are devastating:

“About 25% of the population of those kids with autism, about 25% of them are nonverbal, nontoilet trained,” Kennedy explained.

“They have all of these stereotypical behaviors, the head banging, biting, toe walking, stimming, and that population is growing higher and higher.”

“It’s becoming a larger percentage, so we’re seeing many more cases that are now linked to severe intellectual disability.”

He says it’s a glaring red warning sign—and it’s past time to start acting on it.

And this was the moment that Kennedy took a flamethrower to the media narrative about autism. He shattered the core excuse we’ve all been fed—that this epidemic isn’t real, that it’s just a change in how we count it.

He’s not buying it.

“The media has bought into this industry canard, this mythology, that we’re just seeing more autism because we’re noticing it more. We’re better at recognizing it or there’s been changing diagnostic criteria.”

But the scientific literature, Kennedy said, says otherwise.

“There is study after study in the scientific literature going back, and they decided that the literature going back says decades that says that’s not true.”

He then cited a major investigation by California’s own lawmakers.

“In fact, the California legislature… asked the Mind Institute at UC Davis to look exactly at that topic. They [asked], is it real or are we just noticing it more? The Mind Institute came back and said, ‘Absolutely this is a real epidemic. This is something we’ve never seen before.’

And he made it painfully clear:

“Anybody with common sense, Sean, would notice that, because the autism—this epidemic is only happening in our children. It’s not happening in people who are our age. And if it was better recognition, you’d see it in 70-year-old men.”

But we don’t.

And after laying out the data, dismantling the media narrative, and exposing the severity of the crisis, Kennedy concluded with a clarion call to get to the bottom of this epidemic.

That’s why he says it’s time to dig deeper—leave no stone unturned, and we may have answers sooner than you think.

“President Trump asked me to find out what’s causing it,” he told Hannity.

“And I am approaching that agnostically. We are looking at everything, we are going to do, we’re going to be very transparent in how we design the studies.”

To get real answers, he’s farming the research out to top institutions across the country—with full transparency from day one.

“We’re going to farm the studies out to 15 premier research groups from all over the country. And we’re going to be transparent about our protocols, about the data sets, and then every study will have to be replicated.”

The list of possible factors is long—and nothing is being ruled out, Kennedy explained.

“We’re going to look at mold. We’re going to look at the age of parents. We’re going to look at food and food additives. We’re going to look at pesticides and toxic exposures. We’re going to look at medicines. We’re going to look at vaccines. We’re going to look at everything.”

When asked how long it would take, Kennedy didn’t miss a beat.

“I think we’ll have some preliminary answers in six months. It will take us probably a year from then before we can have definitive answers because a lot of the studies will not go out until the end of the summer.”

For the first time in decades, someone is asking the hard questions—and demanding real answers.

This time, nothing is off-limits.


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