Health
1,000 UK doctors condemn medical association’s push to lift puberty blocker ban for minors
From LifeSiteNews
1,000 senior doctors signed an open letter to the British Medical Association after it lobbied for the NHS to lift a ban on puberty blockers for children following the Cass Review, which found the drugs were harmful.
On August 1, the British Medical Association (BMA) – the United Kingdom’s doctors’ union – called on the government to lift the ban on puberty blockers for minors. Weirdly, the BMA also stated that in their view the implementation of NHS England’s Cass Review should be “paused” despite the fact that, as the BBC noted, the review “took four years to carry out and was widely welcomed by the medical establishment in the U.K.” The BMA called the Cass Review’s recommendations – based on “the largest and most comprehensive review” on the subject seen, looking at 237 papers from 18 countries – “unsubstantiated.”
A spokesperson for the Department of Health and Social Care responded to the BMA, firmly rejecting both the request and the claim, stating, “The Cass Review is a robust report backed by clinicians and firmly grounded in evidence. NHS England will be implementing Dr. Cass’s recommendations so that children and young people get the safe, holistic support they need. We do not support a delay to vital improvements from the NHS to gender services.” Even the leftist Guardian ran an editorial criticizing the BMA’s position, stating, “The BMA’s stance on puberty blockers defies the key principle of medicine: first, do no harm.”
READ: FDA official recommends approval of puberty blockers despite suicide risk for gender-confused youth
As it turns out, there are plenty of physicians who are very unhappy with the BMA’s move – and they are now making their voices heard. This week, 1,000 senior doctors from across the U.K. published an open letter addressed to Professor Philip Banfield, chairman of the BMA.
“We write as doctors to say, ‘not in my name,’” the letter reads. “We are extremely disappointed that the BMA council had passed a motion to conduct a ‘critique’ of the Cass Review and to lobby to oppose its recommendations. The passing of the motion was opaque and secretive. It does not reflect the views of the wider membership, whose opinion you did not seek. We understand that no information will be released on the voting figures and how council members voted. That is a failure of accountability to members and is simply not acceptable.”
The open letter further emphasizes that the Cass Review “is the most comprehensive review into healthcare for children with gender related distress ever conducted” and urged the BMA to “abandon its pointless exercise” of attacking and opposing the recommendations. “By lobbying against the best evidence we have, the BMA is going against the principles of evidence-based medicine and against ethical practice.”
Among the signatories to the letter are 23 former or current clinical leaders at royal colleges, as well as the heads and former heads of some royal colleges.
The British Medical Association is the only main medical organization to oppose the Cass Review; all others have backed it. For example, Professor Sir Stephen Powis, NHS national medical director, stated, “These plans set out in detail how we will establish a fundamentally different and safer model of care for children and young people. The work Dr. Cass has undertaken has been invaluable in helping us shape the new service offer, and we have already begun our transformation of these services by opening two new regional centres this year.” Banfield responded on behalf of the BMA council to say that the points made in the letter would be considered during their ongoing evaluation.
As Josephine Bartosch observed, “it is becoming increasingly clear that the BMA is dangerously out of step with the medical consensus. The Cass Review has sent ripples across the world, and from lawsuits in the U.S. to a change of tack across Europe – medics are increasingly acknowledging that what is a crisis in youth mental health cannot be cured by changing bodies.”
Addictions
Activists Claim Dealers Can Fix Canada’s Drug Problem
By Adam Zivo
We should learn from misguided experiments with activist-driven drug ideologies.
Some Canadian public-health researchers have argued that the nation’s drug dealers, far from being a public scourge, are central to the cause of “harm reduction,” and that drug criminalization makes it harder for them to provide this much-needed “mutual aid.” Incredibly, these ideas have gained traction among Canada’s policymakers, and some have even been put into practice.
Gillian Kolla, an influential harm-reduction activist and researcher, spearheaded the push to whitewash drug trafficking in Canada. Over the past decade, she has advocated for many of the country’s failed laissez-faire drug policies. In her 2020 doctoral dissertation, she described her hands-on research into Toronto’s “harm reduction satellite sites”—government-funded programs that paid drug users to provide services out of their homes.
The sites Kolla studied were operated by the nonprofit South Riverdale Community Health Centre (SRCHC) in Toronto. Addicts participating in the programs received $250 per month in exchange for distributing naloxone and clean paraphernalia (needles and crack pipes, for example), as well as for reversing overdoses and educating acquaintances on safer consumption practices. At the time of Kolla’s research (2016–2017), the SRCHC was operating nine satellite sites, which reportedly distributed about 1,500 needles and syringes per month.
Canada permits supervised consumption sites—facilities where people can use drugs under staff oversight—to operate so long as they receive an official exemption via the federal Controlled Drugs and Substances Act. As the sites Kolla observed did not receive exemptions, they were certainly illegal. Kolla herself acknowledged this in her dissertation, writing that she, with the approval of the University of Toronto, never recorded real names or locations in her field notes, in case law enforcement subpoenaed her research data.
Even so, the program seems to have enjoyed the blessing of Toronto’s public health officials and police. The satellite sites received local funding from 2010 onward, after a decade of operating on a volunteer basis, apparently with special protection from law enforcement. In her dissertation, Kolla described how SRCHC staff trained police officers to leave their sites alone, and how satellite-site workers received special ID badges and plaques to ward off arrest.
Kolla made it clear that many of these workers were not just addicts but dealers, too, and that tolerance of drug trafficking was a “key feature” of the satellite sites. She even described, in detail, how she observed one of the site workers packaging and selling heroin alongside crackpipes and needles.
In her dissertation, Kolla advocated expanding this permissive approach. She claimed that traffickers practice harm reduction by procuring high-quality drugs for their customers and avoiding selling doses that are too strong.
“Negative framings of drug selling as predatory and inherently lacking in care make it difficult to perceive the wide variety of acts of mutual aid and care that surround drug buying and selling as practices of care,” she wrote.
In truth, dealers routinely sell customers tainted or overly potent drugs. Anyone who works in the addiction field can testify that this is a major reason that overdose deaths are so common.
Ultimately, Kolla argued that “real harm reduction” should involve drug traffickers, and that criminalization creates “tremendous barriers” to this goal.
The same year she published her dissertation, Kolla cowrote a paper in the Harm Reduction Journal with her Ph.D. supervisor at the Dalla Lana School of Public Health. The article affirmed the view that drug traffickers are essential to the harm-reduction movement. Around this time, the SRCHC collaborated with the Toronto-based Parkdale Queen West Community Health Centre— the only other organization running such sites—to produce guidelines on how to replicate and scale up the experiment.
Thankfully, despite its local adoption, this idea did not catch on at the national level. It was among the few areas in the early 2020s where Canada did not fully descend into addiction-enabling madness. Yet, like-minded researchers still echo Kolla’s work.
In 2024, for example, a group of American harm-reduction advocates published a paper in Drug and Alcohol Dependence Reports that concluded, based on just six interviews with drug traffickers in Indianapolis, that dealers are “uniquely positioned” to provide harm-reduction services, partly because they are motivated by “the moral imperative to provide mutual aid.” Among other things, the authors argued that drug criminalization is harmful because it removes dealers from their social networks and prevents them from enacting “community-based practices of ethics and care.”
It’s instructive to review what ultimately happened with the originators of this movement—Kolla and the SRCHC. Having failed to whitewash drug trafficking, Kolla moved on to advocating for “safer supply”—an experimental strategy that provides addicts with free recreational drugs to dissuade use of riskier street substances. The Canadian government funded and expanded safer supply, thanks in large part to Kolla’s academic work. It abandoned the experiment after news broke that addicts resell their safer supply on the black market to buy illicit fentanyl, flooding communities with diverted opioids and fueling addiction.
The SRCHC was similarly discredited after a young mother, Karolina Huebner-Makurat, was shot and killed near the organization’s supervised consumption site in 2023. Subsequent media reports revealed that the organization had effectively ignored community complaints about public safety, and that staff had welcomed, and even supported, drug traffickers. One of the SRCHC’s harm-reduction workers was eventually convicted of helping Huebner-Makurat’s shooter evade capture by hiding him from the police in an Airbnb apartment and lying to the police.
There is no need for policymakers to repeat these mistakes, or to embrace its dysfunctional, activist-driven drug ideologies. Let this be another case study of why harm-reduction policies should be treated with extreme skepticism.
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Health
NEW STUDY: Infant Vaccine “Intensity” Strongly Predicts Autism Rates Worldwide
Across countries on three continents, a 1% increase in vaccine types before age one corresponded to a 0.47% increase in autism prevalence.
A new cross-national study from Italy’s National Research Council, spanning multiple developed countries across three continents, has identified a remarkably strong association between early-life vaccine intensity and autism prevalence. The number of vaccine types and doses administered before 12 months showed exceptionally high correlations with national autism rates.
A 1% increase in vaccine types before age one corresponded to a 0.47% increase in autism prevalence.
The correlation is enormous — r = 0.87 for vaccine types and r = 0.79 for vaccine doses. In regression models, vaccine intensity alone explained 81% of the variance in autism prevalence across nations.
This is not an isolated signal. It directly corroborates earlier U.S. state-level data from DeLong (2011) — and aligns with the 107 positive-association studies catalogued in the McCullough Foundation’s Landmark Autism Report.
Key Findings
Coccia used cross-national 2021 autism incidence data paired with WHO-reported infant vaccine schedules. Countries were grouped into relatively comparable healthcare and surveillance systems (North America, Europe, and advanced Asian nations) to reduce detection and reporting bias. The primary exposures were:
- number of vaccine types given ≤12 months, and
- total number of doses delivered ≤12 months.
Autism prevalence per 100,000 children served as the outcome, and general vaccination coverage rates were statistically controlled so only vaccine intensity and timing were isolated.
The results were striking but unfortunately expected:
- Countries such as the U.S., Canada, Australia, Japan, South Korea, and Singapore give ~15 vaccine types and 20 doses before age one — and have the highest autism prevalence (~1,273 per 100k).
- Countries like Norway, Finland, Denmark, Italy, and the UK give ~8 vaccine types and 9 doses — and have significantly lower autism rates (~834 per 100k).
- A 1% increase in vaccine types before age one corresponded to a 0.47% increase in autism prevalence.
- The regression model (log–log) explained 81% of the variance.
Coccia then used quadrant mapping to classify nations:
- Critical Risk Zone: high vaccine intensity + high autism (U.S., Canada, Australia, Japan, South Korea, Singapore)
- Protection Zone: low vaccine intensity + low autism (Nordic countries)
- Transitional Zone: countries on track to move upward as vaccine intensity rises (Italy, UK)
The conclusion is clear: Early-timed and compound vaccination strongly tracks with rising autism rates.
How DeLong (2011) Fits In
DeLong’s analysis of CDC data found that each 1% rise in U.S. childhood vaccination coverage was associated with ~680 additional cases of autism and speech/language impairment nationwide.
Where DeLong examined state-level associations between how many children were fully vaccinated and subsequent autism/SLI prevalence, Coccia provides the first true cross-national dose–response analysis — showing that the number of vaccine types and doses given before age one powerfully predicts national autism prevalence.
Both studies point in the same direction:
more vaccination in early life → higher autism prevalence.
How This Strengthens the McCullough Foundation’s Landmark Autism Report
Our Autism Report reviewed 136 vaccine-related studies:
- 107 studies inferred positive associations between vaccination or vaccine components and ASD/NDDs.
- All 12 vaccinated vs unvaccinated studies found better neurodevelopmental outcomes in completely unvaccinated children, including far lower rates of autism.
- Found strong, consistent increases in cumulative vaccine exposure during early childhood and the reported prevalence of autism across successive birth cohorts.
We concluded:
Combination and early-timed routine childhood vaccination constitutes the most significant modifiable risk factor for ASD, supported by convergent mechanistic, clinical, and epidemiologic findings, and characterized by intensified use, the clustering of multiple doses during critical neurodevelopmental windows, and the lack of research on the cumulative safety of the full pediatric schedule.
Coccia independently arrived at a highly similar conclusion:
This study offers a critical contribution to the ongoing discourse on vaccine safety and neurodevelopment by identifying a statistically significant association between early-life vaccine intensity and national autism rates.
All evidence points to the same conclusion:
Early, clustered vaccination is the strongest modifiable driver of rising autism rates.
Epidemiologist and Foundation Administrator, McCullough Foundation
Support our mission: mcculloughfnd.org
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