Opinion
Why treating the Homesless as victims only makes the problem worse

This article is from Substack
Bestselling author Michael Shellenberger has just published a new book, “San Fransicko” about the homeless crisis in San Francisco. Shellenberger has lived in San Fransisco for 30 years. In “San Fransicko” Shellenberger argues one of the root causes of the homeless crisis sweeping cities all over America (and Canada) is the victimization of homeless people. In this article, Michael Shellenberger talks about the prevalent theory that homeless people are all victims as portrayed by TV Host John Oliver.
Why John Oliver Is Wrong About Homelessness
HBO TV Comedian Repeats Myth that the Homeless Are Just Poor People in Need of Subsidized Housing
The intelligent and hilarious HBO comedian John Oliver last night aired a 25-minute segment on homelessness. In it, he attributed homelessness to poverty, high rents, and NIMBY neighborhood activists who block new housing developments. Oliver showed interviews with homeless people who say they would like to work full-time but are unable to do so because they have to live in homeless shelters.
Unfortunately, Oliver’s segment repeated many myths that are easy to debunk. The vast majority of people we call “homeless” are suffering from serious mental illness, addiction, or both. We do a great job of helping mothers and others who don’t suffer from addiction or untreated mental illness to benefit from subsidized housing, but don’t mandate the psychiatric and addiction care that many “homeless” require. And the best-available, peer-reviewed science shows that “Housing First” agenda Oliver promotes fails on its own terms, worsens addiction, and is one of the main reasons homelessness has grown so much worse.
It’s true that we need more housing and voluntary addiction and psychiatric care, including what is called “permanent supportive housing” for people suffering from mental illness. In my new book, San Fransicko, I advocate for universal psychiatric care, drug treatment on demand, and building of more shelter space for the homeless. And Oliver is right that the U.S. lacks the social safety net that European and other developed nations have.
But Oliver badly misdescribes the problem. For example, he notes that some cities lack sufficient homeless shelter. But he doesn’t acknowledge that it has been “Housing First” homelessness advocates who caused the lack of shelter by demanding that funding be diverted to apartments often costing $750,000 each.
And Oliver promotes policies that have made addiction, mental illness, and homelessness worse. He claims homelessness causes addiction when it is far more often the other way around. And Oliver completely ignores the overwhelming body of scientific research showing that using housing as a reward for abstinence, rather than giving it away as a right, is essential to reducing homelessness by reducing addiction.
Oliver was wrong to encourage more of the same policies that caused homelessness to increase in the U.S. over the last decade, but also wrong for suggesting that anyone who disagreed with him were racist and NIMBY “dicks” who cause violence against homeless people. Oliver closes his segment by ridiculing a white woman who expresses concern about subsidized housing bringing the homeless into her neighborhood.
Why is that? Why does such an intelligent, thoughtful, and compassionate journalist repeat easily-debunked myths about homelessness?
Part of it is just ignorance. Oliver appears to have relied entirely on Housing First advocates and not read anything that questions their narrative. As I document in San Fransicko, homeless advocates are not just small service providers but major academics at top universities including Columbia University and University of California, San Francisco. Those “Housing First” advocates have received hundreds of millions in grants from Marc Benioff, John Arnold, George Soros, and other donors to promote the notion that Housing First works.
Another part of it is ideological. Housing First advocates believe that housing, not shelter, is a right, and that governments have a moral obligation to provide it. They have spent 20 years trying to prove that giving away housing to addicts and the mentally ill works, but the studies show that it fails to address addiction and thus even keep people in apartments at higher rates than other methods. The only thing proven to work is to make housing a reward for good behavior, mostly abstinence but also things like taking one’s psychiatric medicines, and going to work.
The dominant view among progressives of homelessness, drugs, and mental illness stems from victim ideology, which was born in the 1960s. Starting in the late 1960s, progressives attacked any effort to hold people who receive welfare or subsidized accountable as “blaming the victim.” Today, many progressives even view drug dealers as victims.
Victim ideology categorizes people as victims or oppressors, and argues that nothing should be demanded of people categorized as victims. This is terrible for the mentally ill, who often need to be coerced into taking their medicines, so they don’t end up breaking the law, hurting people or themselves, and winding up in prison. And this is terrible for addicts, who need to be arrested, when breaking laws related to their addiction, such as public drug use, shoplifting, and public defecation.
In the end, Oliver’s 25 minute segment on homelessness is a perfect encapsulation of victim ideology and why it is so wrong on both the facts and on ethics. On the facts, Oliver misdescribes a homeless woman who is likely suffering from mental illness and/or drug addiction as merely down on her luck. And Oliver mixes together apparently sober and sane homeless families, temporarily down on their luck, with people are on the street because of addiction and untreated mental illness. Doing so is wrong, analytically, but also wrong, morally, since most addicts and the mentally ill need something very different from just a subsidized apartment unit.
If we are to solve homelessness rather than make it worse, we need intelligent and thoughtful comedians and influencers like Oliver to do their homework, rather than to repeat myths. I researched and wrote San Fransicko, in part, to make it easier for people to get the facts, rather than repeat what we were told, and to see that there’s a better way to help the homeless, whether addicted to drugs, mentally ill, or not.
The good news is that the conversation around drugs and homelessness is changing rapidly because the situation on the ground has grown so much worse. Environmental Progress and the California Peace Coalition are at the very beginning of our efforts to educate journalists, policymakers, and the public. And San Fransicko was published just three weeks ago.
As time passes, many Americans will see the consequence of treating what is fundamentally a problem of untreated mental illness and addiction as a problem of poverty, high rents, and NIMBYs. And some of them, perhaps even comedians like John Oliver, will come to find humor, and humility, from the fact that so many of us got it so wrong.
MacDonald Laurier Institute
Rushing to death in Canada’s MAiD regime

By Ramona Coelho for Inside Policy
Canada legalized Medical Assistance in Dying (MAiD) in 2016, encompassing both euthanasia and assisted suicide. Initially limited to those nearing their natural death, eligibility expanded in 2021 to individuals with physical disabilities, with eligibility for individuals with mental illness in 2027. Parliamentary recommendations include MAiD for children. A recent federal consultation explored extending MAiD to those who lack capacity via advance directives, an approach Quebec has already adopted, despite its criminal status under federal law.
Despite its compassionate framing, investigative journalists and government reports reveal troubling patterns where inadequate exploration of reversible suffering – such as lack of access to medical treatments, poverty, loneliness, and feelings of being a burden – have driven Canadians to choose death. As described by our former Disability Inclusion Minister, Canada’s system at times makes it easier to access MAiD than to receive basic care like a wheelchair. With over 60,000 MAiD cases by the end of 2023, the evidence raises grave concerns about Canada’s MAiD regime.
I am a member of Ontario’s MAiD Death Review Committee (MDRC). Last year, the Chief Coroner released MDRC reports, and a new set of reports has just been published. The first report released by the Office of the Chief Coroner, Waivers of Final Consent, examines how individuals in Track 1 (reasonably foreseeable natural death) can sign waivers to have their lives ended even if they lose the capacity to consent by the scheduled date of MAiD. The second, Navigating Complex Issues within Same Day and Next Day MAiD Provisions, includes cases where MAiD was provided on the same day or the day after it was requested. These reports raise questions about whether proper assessments, thorough exploration of suffering, and informed consent were consistently practised by MAiD clinicians. While MDRC members hold diverse views, here is my take.
Rushing to death, Ignoring Reversible Causes of Suffering
In the same-day or next-day MAiD report, Mrs. B, in her 80s, after complications from surgery, opted for palliative care, leading to discharge home. She later requested a MAiD assessment, but her assessor noted she preferred palliative care based on personal and religious values. The next day, her spouse, struggling with caregiver burnout, took her to the emergency department, but she was discharged home. When a request for hospice palliative care was denied, her spouse contacted the provincial MAiD coordination service for an urgent assessment. A new assessor deemed her eligible for MAiD, despite concerns from the first practitioner, who questioned the new assessor on the urgency, the sudden shift in patient perspective, and the influence of caregiver burnout. The initial assessor requested an opportunity for re-evaluation, but this was denied, with the second assessor deeming it urgent. That evening, a third MAiD practitioner was brought in, and Mrs. B underwent MAiD that night.
The focus should have been on ensuring adequate palliative care and support for Mrs. B and her spouse. Hospice and palliative care teams should have been urgently re-engaged, given the severity of the situation. Additionally, the MAiD provider expedited the process despite the first assessor’s and Mrs. B’s concerns without fully considering the impact of her spouse’s burnout.
The report also has worrying trends suggesting that local medical cultures—rather than patient choice—could be influencing rushed MAiD. Geographic clustering, particularly in Western Ontario, where same-day and next-day MAiD deaths occur most frequently, raises concerns that some MAiD providers may be predisposed to rapidly approve patients for quick death rather than ensuring patients have access to adequate care or exploring if suffering is remediable. This highlights a worrying trend where the speed of the MAiD provision is prioritized over patient-centered care and ethical safeguards.
MAiD without Free and Informed Choice
Consent has been central to Canadians’ acceptance of the legalization of euthanasia and assisted suicide. However, some cases in these reports point to concerns already raised by clinicians: the lack of thorough capacity assessments and concerns that individuals may not have freely chosen MAiD.
In the waiver of final consent report, Mr. B, a man with Alzheimer’s, had been approved for MAiD with such a waiver. However, by the scheduled provision date, his spouse reported increased confusion. Upon arrival, the MAiD provider noted that Mr. B no longer recognized them and so chose not to engage him in discussion at all. Without any verbal interaction to determine his current wishes or understanding, Mr. B’s life was ended.
In the same-day or next-day MAiD report, Mr. C, diagnosed with metastatic cancer, initially expressed interest in MAiD but then experienced cognitive decline and became delirious. He was sedated for pain management. Despite the treating team confirming that capacity was no longer present, a MAiD practitioner arrived and withheld sedation, attempting to rouse him. It was documented that the patient mouthed “yes” and nodded and blinked in response to questions. Based on this interaction, the MAiD provider deemed the patient to have capacity. The MAiD practitioner then facilitated a virtual second assessment, and MAiD was administered.
These individuals were not given genuine opportunities to confirm whether they wished to die. Instead, their past wishes or inquiries were prioritized, raising concerns about ensuring free and informed consent for MAiD. As early as 2020, the Chief Coroner of Ontario identified cases where patients received MAiD without well-documented capacity assessments, even though their medical records suggested they lacked capacity. Further, when Dr. Leonie Herx, past president of the Canadian Society of Palliative Medicine, testified before Parliament about MAiD frequently occurring without capacity, an MP dismissed her, advising Parliament to be cautious about considering seriously evidence under parliamentary immunities that amounted to malpractice allegations, which should be handled by the appropriate regulatory bodies or police. These dismissive comments stand in stark contrast with the gravity of assessing financial capacity, and yet the magnitude is greater when ending life. By way of comparison, for my father, an Ontario-approved capacity expert conducted a rigorous evaluation before declaring him incapable of managing his finances. This included a lengthy interview, collateral history, and review of financial documents—yet no such rigorous capacity assessment is mandated for MAiD.
What is Compassion?
While the federal government has finished its consultation on advance directives for MAiD, experts warn against overlooking the complexities of choosing death based on hypothetical suffering and no lived experience to inform those choices. A substitute decision-maker has to interpret prior wishes, leading to guesswork and ethical dilemmas. These cases highlight how vulnerable individuals, having lost the capacity to consent, may be coerced or unduly influenced to die—whether through financial abuse, caregiver burnout, or other pressures—reminding us that the stakes are high – life and death, no less.
The fundamental expectation of health care should be to rush to care for the patient, providing support through a system that embraces them—not rush them toward death without efforts to mitigate suffering or ensure free and informed consent. If we truly value dignity, we must invest in comprehensive care to prevent patients from being administered speedy death in their most vulnerable moment, turning their worst day into potentially their last.
Dr. Ramona Coelho is a family physician whose practice largely serves marginalised persons in London, Ontario. She is a senior fellow at the Macdonald-Laurier Institute and co-editor of the new book “Unravelling MAiD in Canada” from McGill University Press.
International
UN committee urges Canada to repeal euthanasia for non-terminally ill patients

From LifeSiteNews
The UN Committee on the Rights of Persons with Disabilities has warned against Canada’s euthanasia program, urging the repeal of legislation that allows the killing of non-terminally ill individuals.
Canada’s euthanasia regime has become too radical even for the anti-life United Nations, who recently called on the nation to repeal its law allowing non-terminally ill patients to qualify for death through the state’s “Medical Assistance in Dying” program.
In closing remarks published March 21, the UN Committee on the Rights of Persons with Disabilities argued that Canada should repeal its 2021 MAID expansion legislation that allowed those who are chronically ill but not terminally ill to be put to death by the state.
The committee said that Canada’s regime “establishes medically assisted dying for persons with disabilities based on negative, ableist perceptions of the quality and value of the life of persons with disabilities, including that ‘suffering’ is intrinsic to disability rather than the fact that inequality and discrimination cause and compound ‘suffering’ for persons with disabilities.”
It pointed out that “the concept of ‘choice’ creates a false dichotomy by setting up the premise that if persons with disabilities are suffering, it is valid for the State Party to enable their death.”
In Canada, euthanasia is divided into Track 1 and Track 2 requests. Track 1 requests deal with those whose death is allegedly imminent or foreseeable. Track 2 requests deal with those who are not terminally ill but have lost the will to live due to their having chronic health problems.
The UN committee took specific issue with Track 2 MAID, writing that it is “extremely concerned about the 2021 amendments to the State Party’s Criminal Code through Bill C-7 that expanded the eligibility criteria for obtaining Medical Assistance in Dying (MAID), known as ‘Track 2’ MAiD by removing the ‘foreseeable death’ criteria.”
The committee further recommended that Canada not euthanize its citizens for mental health reasons and abandon additional expansions of the program. Such an expansion is slated to come into effect in 2027.
It is worth noting that while Track 2 cases of MAID are indeed evil, so are Track 1 cases. The Catholic Church infallibly teaches that euthanasia is a grave evil tantamount to murder and must be rejected in all circumstances.
The UN committee’s criticism of Canada’s euthanasia regime comes after many have pointed out that the regime has spawned a culture of death and eugenics in the country, with the disabled and the poor often being those who request or who are even suggested to request death via Track 2 MAID.
In one case, a Nova Scotia grandmother revealed that doctors repeatedly offered her euthanasia while she underwent cancer treatment, making her feel as though she was “better off dead.”
“I felt like a problem that needed to be [gotten] rid of instead of a patient in need of treatment,” she said. “I don’t want to be asked if I want to die.”
Similarly, in May of last year, LifeSiteNews reported on a Canadian man who felt “completely traumatized” and violated that he was offered MAID “multiple times” instead of getting the proper care he needed while in the hospital.
The most recent reports show that MAID is the sixth highest cause of death in Canada. However, it was not listed as such in Statistics Canada’s top 10 leading causes of death from 2019 to 2022.
When asked why MIiD was left off the list, the agency said that it records the illnesses that led Canadians to choose to end their lives via euthanasia, not the actual cause of death, as the primary cause of death.
According to Health Canada, in 2022, 13,241 Canadians died by MAID lethal injections. This accounts for 4.1 percent of all deaths in the country for that year, a 31.2 percent increase from 2021.
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