Health
Doctor withholds results of study that fails to show transitioning improves kids’ health

From LifeSiteNews
A prominent doctor has been refusing to release the findings of a federally funded “transgender youth” study she began in 2015 because the results did not match the conclusions she hoped for, according to an explosive report in The New York Times.
The Times reported that Johanna Olson-Kennedy, medical director of the Center for Trans Youth Health & Development at Children’s Hospital in Los Angeles, “recruited 95 children from across the country and gave them puberty blockers,” then “followed the children for two years to see if the treatments improved their mental health.” She told the National Institutes of Health (NIH) that she expected to find that the kids would show “decreased symptoms of depression, anxiety, trauma symptoms, self-injury, and suicidality, and increased body esteem and quality of life over time.”
However, the study did not show the children doing better than they started. “Before receiving the drugs, around one-quarter of the group reported depression symptoms and significant anxiety, and one quarter reported ever having thoughts of suicide,” the Times says. “Eight percent reported a past suicide attempt.”
In an interview with the Times, Olson-Kennedy attempted to argue that the children’s starting point actually wasn’t so bad after all, and therefore the lack of change was not concerning: “They’re in really good shape when they come in, and they’re in really good shape after two years.” On follow-up, she claimed her “good shape” comment was referring to data averages, and her conclusion about the full data was still pending.
Regardless, in the nine years since the study commenced, Olson-Kennedy has still yet to publish any of the data for outside observers to analyze for themselves, which she justified by claiming, “I do not want our work to be weaponized. It has to be exactly on point, clear and concise. And that takes time.”
NEW: Azeen Ghorayshi reports in the @nytimes that prominent gender clinician Johanna Olson-Kennedy of @ChildrensLA has refused to publish data from a study on puberty blockers, fearing that the unimpressive results will be "weaponized" by critics of "gender-affirming care." 🧵 pic.twitter.com/DREXSNsFYk
— Leor Sapir (@LeorSapir) October 23, 2024
https://t.co/st0O6ox763 https://t.co/WZbnXv6DO2
— Leor Sapir (@LeorSapir) October 23, 2024
A significant body of evidence shows that “affirming” gender confusion carries serious harms, especially when done with impressionable children who lack the mental development, emotional maturity, and life experience to consider the long-term ramifications of the decisions being pushed on them, or full knowledge about the long-term effects of life-altering, physically transformative, and often-irreversible surgical and chemical procedures.
Studies find that more than 80% of children experiencing gender dysphoria outgrow it on their own by late adolescence, and that even full “reassignment” surgery often fails to resolve gender-confused individuals’ heightened tendency to engage in self-harm and suicide — and may even exacerbate it, including by reinforcing their confusion and neglecting the actual root causes of their mental strife.
Many oft-ignored “detransitioners,” individuals who attempted to live under a different “gender identity” before embracing their sex, attest to the physical and mental harm of reinforcing gender confusion as well as to the bias and negligence of the medical establishment on the subject, many of whom take an activist approach to their profession and begin cases with a predetermined conclusion that “transitioning” is the best solution.
“Gender-affirming” physicians have also been caught on video admitting to more old-fashioned motives for such procedures, as with a 2022 exposé about Vanderbilt University Medical Center’s Clinic for Transgender Health, where Dr. Shayne Sebold Taylor said outright that “these surgeries make a lot of money.”
In December, the U.S. Supreme Court will begin considering arguments about the permissibility of state laws prohibiting the gender “transitioning”” of minors.
Health
Dr. Pierre Kory Exposes the Truth About the Texas ‘Measles Death’ Hoax

“She did not die of measles by any stretch of the imagination. In fact, she died of pneumonia. But it gets worse than that…”
Turn on the news today, and you’ll hear about a measles outbreak in Texas. The headline? A 6-year-old girl has “died from measles.” The coverage is nonstop. And the goal is simple: to make you angry and afraid.
But here’s what they’re not telling you.
That little girl should still be alive. She should be at home with her mom, dad, and siblings. But their unconscionable loss, which is being heavily politicized, is not what the mainstream has led us to believe. Her death was the result of medical error. Plain and simple.
And you should be angry.
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When this case first made the news, little was known. But those who know it’s okay to ask questions began asking them.
Was she vaccinated for measles? If so, was the vaccination done recently or while she was ill? What treatment did she receive, if any? Was she infected with the wild type, or was this due to a leaky vaccine? Did she die with measles or from it?
Children’s Health Defense (CHD) stepped up and interviewed the mourning parents to uncover the truth about what really happened to their 6-year-old daughter.
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Parents of Child Who Died During Texas Measles Outbreak Speak Out |
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This article originally appeared on The Defender and was republished with permission. | |
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The emotional interview reveals the child was not vaccinated for measles. She fell ill, and while the spots faded quickly, her breathing was affected. Her parents became concerned and took her to the emergency room at Covenant Children’s Hospital in Lubbock, Texas.
It was all downhill from there. And before long, their daughter was gone.
Dr. Pierre Kory Shares Disturbing Information
In a display of journalistic integrity, CHD obtained the 6-year-old’s medical records from her parents. Dr. Pierre Kory, a critical care physician, had a chance to analyze the records and shared his thoughts with CHD.
According to Dr. Kory, the child “did not die of measles by any stretch of the imagination. In fact, she died of a pneumonia. But it gets worse than that, because she didn’t really die of pneumonia. She died of a medical error.”
Let that sink in.
Loving parents just lost their young child due to a medical error. But not only that, their story is being twisted and used to spread fear about measles and to push the measles vaccine—two things this family does not appear to agree with.
As it turns out, their four other children came down with measles following their sister’s death. All four were treated with cod liver oil (vitamin A) and budesonide (a steroid). And all four recovered quickly. No vaccination necessary.
Kory calls the case “absolutely enraging.”
“When you admit someone to the hospital for pneumonia, what you need to do is you treat what’s called empirically, meaning you put them on antibiotics that you think will cover the most common organism.”
Covenant Children’s Hospital failed to do this.
“I mean, this is like medicine 101. You put them on two antibiotics to cover all the possibilities. It’s a grievous error, and it’s an error which led to her death.”
Not only did Covenant Children’s Hospital fail to provide the appropriate antibiotics, when they noticed their error, they dragged their feet and delayed another 10 hours.
“By that time, she was already on a ventilator. And approximately 24 hours later, actually less than 24 hours later, she died.”
And she did not pass away peacefully. According to Kory, “she died rather catastrophically.”
“I can only surmise that she died of a catastrophic pulmonary embolism.”
Kory calls the whole thing “disturbing.”
And it is. What happened to this young girl at Covenant Children’s Hospital was indeed disturbing. But the way this tragedy is being portrayed in the media and used inappropriately and inaccurately to cause fear and push the measles vaccine is downright disgusting.
Gone are the days when people seek help from local media to expose injustices. The media machine has one job and it isn’t to help you.
This young girl should still be here. Hugging her parents and giggling with her siblings. Enjoying the start of Spring and looking forward to celebrating Easter.
Instead, the media is exploiting this family’s unimaginable loss to push an agenda, and social media is swirling with nasty criticisms.
We can only hope this poor family receive justice and support as they combat the unwarranted attacks on their character, choices, and way of life.
“Pray. Just pray for us. That’s the best you can do, for now,” the father said.
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Addictions
There’s No Such Thing as a “Safer Supply” of Drugs

By Adam Zivo
Sweden, the U.K., and Canada all experimented with providing opioids to addicts. The results were disastrous.
[This article was originally published in City Journal, a public policy magazine and website published by the Manhattan Institute for Policy Research. We encourage our readers to subscribe to them for high-quality analysis on urban issues]
Last August, Denver’s city council passed a proclamation endorsing radical “harm reduction” strategies to address the drug crisis. Among these was “safer supply,” the idea that the government should give drug users their drug of choice, for free. Safer supply is a popular idea among drug-reform activists. But other countries have already tested this experiment and seen disastrous results, including more addiction, crime, and overdose deaths. It would be foolish to follow their example.
The safer-supply movement maintains that drug-related overdoses, infections, and deaths are driven by the unpredictability of the black market, where drugs are inconsistently dosed and often adulterated with other toxic substances. With ultra-potent opioids like fentanyl, even minor dosing errors can prove fatal. Drug contaminants, which dealers use to provide a stronger high at a lower cost, can be just as deadly and potentially disfiguring.
Because of this, harm-reduction activists sometimes argue that governments should provide a free supply of unadulterated, “safe” drugs to get users to abandon the dangerous street supply. Or they say that such drugs should be sold in a controlled manner, like alcohol or cannabis—an endorsement of partial or total drug legalization.
But “safe” is a relative term: the drugs championed by these activists include pharmaceutical-grade fentanyl, hydromorphone (an opioid as potent as heroin), and prescription meth. Though less risky than their illicit alternatives, these drugs are still profoundly dangerous.
The theory behind safer supply is not entirely unreasonable, but in every country that has tried it, implementation has led to increased suffering and addiction. In Europe, only Sweden and the U.K. have tested safer supply, both in the 1960s. The Swedish model gave more than 100 addicts nearly unlimited access through their doctors to prescriptions for morphine and amphetamines, with no expectations of supervised consumption. Recipients mostly sold their free drugs on the black market, often through a network of “satellite patients” (addicts who purchased prescribed drugs). This led to an explosion of addiction and public disorder.
Most doctors quickly abandoned the experiment, and it was shut down after just two years and several high-profile overdose deaths, including that of a 17-year-old girl. Media coverage portrayed safer supply as a generational medical scandal and noted that the British, after experiencing similar problems, also abandoned their experiment.
While the U.S. has never formally adopted a safer-supply policy, it experienced something functionally similar during the OxyContin crisis of the 2000s. At the time, access to the powerful opioid was virtually unrestricted in many parts of North America. Addicts turned to pharmacies for an easy fix and often sold or traded their extra pills for a quick buck. Unscrupulous “pill mills” handed out prescriptions like candy, flooding communities with OxyContin and similar narcotics. The result was a devastating opioid epidemic—one that rages to this day, at a cumulative cost of hundreds of thousands of American lives. Canada was similarly affected.
The OxyContin crisis explains why many experienced addiction experts were aghast when Canada greatly expanded access to safer supply in 2020, following a four-year pilot project. They worried that the mistakes of the recent past were being made all over again, and that the recently vanquished pill mills had returned under the cloak of “harm reduction.”
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Most Canadian safer-supply prescribers dispense large quantities of hydromorphone with little to no supervised consumption. Patients can receive up to 40 eight-milligram pills per day—despite the fact that just two or three are enough to cause an overdose in someone without opioid tolerance. Some prescribers also provide supplementary fentanyl, oxycodone, or stimulants.
Unfortunately, many safer-supply patients sell or trade a significant portion of these drugs—primarily hydromorphone—in order to purchase more potent illicit substances, such as street fentanyl.
The problems with safer supply entered Canada’s consciousness in mid-2023, through an investigative report I wrote for the National Post. I interviewed 14 addiction physicians from across the country, who testified that safer-supply diversion is ubiquitous; that the street price of hydromorphone collapsed by up to 95 percent in communities where safer supply is available; that youth are consuming and becoming addicted to diverted safer-supply drugs; and that organized crime traffics these drugs.
Facing pushback, I interviewed former drug users, who estimated that roughly 80 percent of the safer-supply drugs flowing through their social circles was getting diverted. I documented dozens of examples of safer-supply trafficking online, representing tens of thousands of pills. I spoke with youth who had developed addictions from diverted safer supply and adults who had purchased thousands of such pills.
After months of public queries, the police department of London, Ontario—where safer supply was first piloted—revealed last summer that annual hydromorphone seizures rose over 3,000 percent between 2019 and 2023. The department later held a press conference warning that gangs clearly traffic safer supply. The police departments of two nearby midsize cities also saw their post-2019 hydromorphone seizures increase more than 1,000 percent.
The Canadian government quietly dropped its support for safer supply last year, cutting funding for many of its pilot programs. The province of British Columbia (the nexus of the harm-reduction movement) finally pulled back support last month, after a leaked presentation confirmed that safer-supply drugs are getting sold internationally and that the government is investigating 60 pharmacies for paying kickbacks to safer-supply patients. For now, all safer-supply drugs dispensed within the province must be consumed under supervision.
Harm-reduction activists have insisted that no hard evidence exists of widespread diversion of safer-supply drugs, but this is only because they refuse to study the issue. Most “studies” supporting safer supply are produced by ideologically driven activist-scholars, who tend to interview a small number of program enrollees. These activists also reject attempts to track diversion as “stigmatizing.”
The experiences of Sweden, the United Kingdom, and Canada offer a clear warning: safer supply is a reliably harmful policy. The outcomes speak for themselves—rising addiction, diversion, and little evidence of long-term benefit.
As the debate unfolds in the United States, policymakers would do well to learn from these failures. Americans should not be made to endure the consequences of a policy already discredited abroad simply because progressive leaders choose to ignore the record. The question now is whether we will repeat others’ mistakes—or chart a more responsible course.
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