Addictions
B.C.’s provincial health officer should be fired
Dr. Bonnie Henry has been British Columbia’s provincial health officer since 2014. She has used her position to advocate for expanded legal access to addictive drugs.
By Rahim Mohamed
If Premier Eby has little faith in Dr. Bonnie Henry’s radical drug legalization agenda, why keep her on the job?
B.C.’s Provincial Health Officer Dr. Bonnie Henry has been one of Canada’s leading advocates for radical “harm reduction” policies — but Premier David Eby cast an unmistakable vote of non-confidence in her judgment last month when he called her position on safer supply a “non-starter.”
Eby’s remarks came just days after Dr. Henry told a parliamentary committee in Ottawa that she supported the “legalization and regulation” of illicit street drugs. The public disagreement suggested a sidelining of the doctor within the provincial government — especially after Eby further distanced himself from her by announcing that he’d appointed a separate medical expert, Dr. Daniel Vigo, to advise him on the province’s toxic drug crisis.
It is great to see that Eby is starting to treat Dr. Henry’s activist-driven recommendations with the scepticism they deserve. But he needs to go farther. The doctor should be fired.
Yet Eby has thus far rebuffed calls to remove Dr. Henry from her post. To the contrary, Eby insists that he has “huge confidence” in her ability to continue on as B.C.’s top public health official, despite his disagreements with her on how to combat the overdose crisis.
To reiterate, the premier’s current position is that he trusts his provincial health officer to effectively do her job, despite being fundamentally and irreconcilably at odds with her over the province’s most pressing public health issue — which, might we remember, kills roughly seven British Columbians each day.
This is not some minor quibble that the premier can simply gloss over with a new advisor and a few scolding words. If Eby cannot abide by Dr. Henry’s views on safer supply, as he claims to be the case, he has a professional and moral obligation to find a new provincial health officer who shares his vision on beating back the scourge of illicit drugs.
And while Dr. Henry’s latest parliamentary remarks alone were egregious enough to justify her firing, what’s even more concerning is that they fell in line with a pattern of ideological and unscientific statements on drug policy.
Two years ago, Dr. Henry stunned many in the recovery community by publicly stating that abstinence “does not work for opioid addiction.”
By implying that it is unrealistic to expect opioid users to kick their habit, and dismissing abstinence-based treatment programs in a carte blanche manner, Dr. Henry not only devalued the lived experiences of scores of British Columbians who’ve recovered from opioid addiction, she also betrayed a profound ignorance of decades of scientific research that shows that ex-addicts can, and often do, attain long-term abstinence from opioid drugs through community-based treatment programs.
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Surrey, B.C.-based addictions specialist Dr. Jenny Melamed said in an email that it was “disingenuous” for Dr. Henry to “differentiate opioid addiction from other forms of addiction with respect to the ability (of addicts) to recover.”
“I have devoted my medical career to working with individuals with addiction. I witness recovery on a daily basis from all addictions,” wrote Dr. Melamed.
Instead of helping drug users obtain recovery, Dr. Henry has fixated on ideological policies that only enable and entrench addiction.
Dr. Henry’s mission to legalize drugs has been particularly concerning. In a 2019 report titled, “Stopping the Harm: Decriminalization of people who use drugs in BC,” she wrote in an executive summary that B.C. cannot “treat its way out of the overdose crisis.” The report recommended that provincial authorities “urgently move to decriminalize people who possess controlled substances for personal use,” following the then-fashionable hands-off approach to drug use.
Her solutions have catastrophically failed in jurisdictions across North America, most recently in the State of Oregon, whose leaders now acknowledge that legalizing hard drugs was a mistake. But Dr. Henry shows no capacity for this sort of hard self-reflection — despite the mayhem that decriminalization, a policy she aggressively championed, caused in B.C. over the last year.
She is instead choosing to double down on an ideological dogma that is fast losing popularity with both experts and lay citizens.
Dr. Henry’s inability to admit she was wrong when confronted with new information is perhaps the most damning indictment of her fitness to lead. British Columbians deserve a provincial health officer who will follow the evidence, especially when it leads them to reconsider strongly held beliefs.
One public figure who hasn’t minced words about Dr. Henry’s unsuitability as B.C.’s top doc has been South Surrey MLA Elenore Sturko, a newly minted BC Conservative, tweeted last week that “David Eby needs to fire Dr. Henry immediately.”
In a phone interview, Sturko said that while Dr. Henry has done some good work as provincial health officer, she believes it’s time to change directions.
“Given the lack of improvement, and the complexity of the overdose public health emergency, I believe that we need a change of approach. Perhaps it’s time to appoint an addictions specialist with front line experience as well as a research background lead this emergency,” Sturko said.
“In a statement last week NDP Premier David Eby said he’s not in agreement with Dr. Henry’s push to legalize drugs,” Sturko added. “If she is focusing her work and response to a public emergency in a direction that isn’t supported by the premier, this conflict will perpetuate his government’s ineffectiveness at saving lives.”
With drug-related deaths on the rise for three consecutive years, B.C.’s near decade-long drug crisis shows no signs of abating. The time for half-measures has long since passed. David Eby must take a clear stand against the failed drug policies of yesteryear by removing Dr. Bonnie Henry from her post as provincial health officer.
The stakes, both political and human, are frankly too high for the premier to keep the intransigent doctor in her current job.
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Addictions
The War on Commonsense Nicotine Regulation
From the Brownstone Institute
Cigarettes kill nearly half a million Americans each year. Everyone knows it, including the Food and Drug Administration. Yet while the most lethal nicotine product remains on sale in every gas station, the FDA continues to block or delay far safer alternatives.
Nicotine pouches—small, smokeless packets tucked under the lip—deliver nicotine without burning tobacco. They eliminate the tar, carbon monoxide, and carcinogens that make cigarettes so deadly. The logic of harm reduction couldn’t be clearer: if smokers can get nicotine without smoke, millions of lives could be saved.
Sweden has already proven the point. Through widespread use of snus and nicotine pouches, the country has cut daily smoking to about 5 percent, the lowest rate in Europe. Lung-cancer deaths are less than half the continental average. This “Swedish Experience” shows that when adults are given safer options, they switch voluntarily—no prohibition required.
In the United States, however, the FDA’s tobacco division has turned this logic on its head. Since Congress gave it sweeping authority in 2009, the agency has demanded that every new product undergo a Premarket Tobacco Product Application, or PMTA, proving it is “appropriate for the protection of public health.” That sounds reasonable until you see how the process works.
Manufacturers must spend millions on speculative modeling about how their products might affect every segment of society—smokers, nonsmokers, youth, and future generations—before they can even reach the market. Unsurprisingly, almost all PMTAs have been denied or shelved. Reduced-risk products sit in limbo while Marlboros and Newports remain untouched.
Only this January did the agency relent slightly, authorizing 20 ZYN nicotine-pouch products made by Swedish Match, now owned by Philip Morris. The FDA admitted the obvious: “The data show that these specific products are appropriate for the protection of public health.” The toxic-chemical levels were far lower than in cigarettes, and adult smokers were more likely to switch than teens were to start.
The decision should have been a turning point. Instead, it exposed the double standard. Other pouch makers—especially smaller firms from Sweden and the US, such as NOAT—remain locked out of the legal market even when their products meet the same technical standards.
The FDA’s inaction has created a black market dominated by unregulated imports, many from China. According to my own research, roughly 85 percent of pouches now sold in convenience stores are technically illegal.
The agency claims that this heavy-handed approach protects kids. But youth pouch use in the US remains very low—about 1.5 percent of high-school students according to the latest National Youth Tobacco Survey—while nearly 30 million American adults still smoke. Denying safer products to millions of addicted adults because a tiny fraction of teens might experiment is the opposite of public-health logic.
There’s a better path. The FDA should base its decisions on science, not fear. If a product dramatically reduces exposure to harmful chemicals, meets strict packaging and marketing standards, and enforces Tobacco 21 age verification, it should be allowed on the market. Population-level effects can be monitored afterward through real-world data on switching and youth use. That’s how drug and vaccine regulation already works.
Sweden’s evidence shows the results of a pragmatic approach: a near-smoke-free society achieved through consumer choice, not coercion. The FDA’s own approval of ZYN proves that such products can meet its legal standard for protecting public health. The next step is consistency—apply the same rules to everyone.
Combustion, not nicotine, is the killer. Until the FDA acts on that simple truth, it will keep protecting the cigarette industry it was supposed to regulate.
Addictions
The Shaky Science Behind Harm Reduction and Pediatric Gender Medicine

By Adam Zivo
Both are shaped by radical LGBTQ activism and questionable evidence.
Over the past decade, North America embraced two disastrous public health movements: pediatric gender medicine and “harm reduction” for drug use. Though seemingly unrelated, these movements are actually ideological siblings. Both were profoundly shaped by extremist LGBTQ activism, and both have produced grievous harms by prioritizing ideology over high-quality scientific evidence.
While harm reductionists are known today for championing interventions that supposedly minimize the negative effects of drug consumption, their movement has always been connected to radical “queer” activism. This alliance began during the 1980s AIDS crisis, when some LGBTQ activists, hoping to reduce HIV infections, partnered with addicts and drug-reform advocates to run underground needle exchanges.
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In the early 2000s, after the North American AIDS epidemic was brought under control, many HIV organizations maintained their relevance (and funding) by pivoting to addiction issues. Despite having no background in addiction medicine, their experience with drug users in the context of infectious diseases helped them position themselves as domain experts.
These organizations tended to conceptualize addiction as an incurable infection—akin to AIDS or Hepatitis C—and as a permanent disability. They were heavily staffed by progressives who, influenced by radical theory, saw addicts as a persecuted minority group. According to them, drug use itself was not the real problem—only society’s “moralizing” norms.
These factors drove many HIV organizations to lobby aggressively for harm reduction at the expense of recovery-oriented care. Their efforts proved highly successful in Canada, where I am based, as HIV researchers were a driving force behind the implementation of supervised consumption sites and “safer supply” (free, government-supplied recreational drugs for addicts).
From the 2010s onward, the association between harm reductionism and queer radicalism only strengthened, thanks to the popularization of “intersectional” social justice activism that emphasized overlapping forms of societal oppression. Progressive advocates demanded that “marginalized” groups, including drug addicts and the LGBTQ community, show enthusiastic solidarity with one another.
These two activist camps sometimes worked on the same issues. For example, the gay community is struggling with a silent epidemic of “chemsex” (a dangerous combination of drugs and anonymous sex), which harm reductionists and queer theorists collaboratively whitewash as a “life-affirming cultural practice” that fosters “belonging.”
For the most part, though, the alliance has been characterized by shared tones and tactics—and bad epistemology. Both groups deploy politicized, low-quality research produced by ideologically driven activist-researchers. The “evidence-base” for pediatric gender medicine, for example, consists of a large number of methodologically weak studies. These often use small, non-representative samples to justify specious claims about positive outcomes. Similarly, harm reduction researchers regularly conduct semi-structured interviews with small groups of drug users. Ignoring obvious limitations, they treat this testimony as objective evidence that pro-drug policies work or are desirable.
Gender clinicians and harm reductionists are also averse to politically inconvenient data. Gender clinicians have failed to track long-term patient outcomes for medically transitioned children. In some cases, they have shunned detransitioners and excluded them from their research. Harm reductionists have conspicuously ignored the input of former addicts, who generally oppose laissez-faire drug policies, and of non-addict community members who live near harm-reduction sites.
Both fields have inflated the benefits of their interventions while concealing grievous harms. Many vulnerable children, whose gender dysphoria otherwise might have resolved naturally, were chemically castrated and given unnecessary surgeries. In parallel, supervised consumption sites and “safer supply” entrenched addiction, normalized public drug use, flooded communities with opioids, and worsened public disorder—all without saving lives.
In both domains, some experts warned about poor research practices and unmeasured harms but were silenced by activists and ideologically captured institutions. In 2015, one of Canada’s leading sexologists, Kenneth Zucker, was fired from the gender clinic he had led for decades because he opposed automatically affirming young trans-identifying patients. Analogously, dozens of Canadian health-care professionals have told me that they feared publicly criticizing aspects of the harm-reduction movement. They thought doing so could invite activist harassment while jeopardizing their jobs and grants.
By bullying critics into silence, radical activists manufactured false consensus around their projects. The harm reductionists insist, against the evidence, that safer supply saves lives. Their idea of “evidence-based policymaking” amounts to giving addicts whatever they ask for. “The science is settled!” shout the supporters of pediatric gender medicine, though several systematic reviews proved it was not.
Both movements have faced a backlash in recent years. Jurisdictions throughout the world are, thankfully, curtailing irreversible medical procedures for gender-confused youth and shifting toward a psychotherapy-based “wait and see” approach. Drug decriminalization and safer supply are mostly dead in North America and have been increasingly disavowed by once-supportive political leaders.
Harm reductionists and queer activists are trying to salvage their broken experiments, occasionally by drawing explicit parallels between their twin movements. A 2025 paper published in the International Journal of Drug Policy, for example, asserts that “efforts to control, repress, and punish drug use and queer and trans existence are rising as right-wing extremism becomes increasingly mainstream.” As such, there is an urgent need to “cultivate shared solidarity and action . . . whether by attending protests, contacting elected officials, or vocally defending these groups in hostile spaces.”
How should critics respond? They should agree with their opponents that these two radical movements are linked—and emphasize that this is, in fact, a bad thing. Large swathes of the public understand that chemically and surgically altering vulnerable children is harmful, and that addicts shouldn’t be allowed to commandeer public spaces. Helping more people grasp why these phenomena arose concurrently could help consolidate public support for reform and facilitate a return to more restrained policies.
Adam Zivo is director of the Canadian Centre for Responsible Drug Policy.
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