MAiD
Disability groups files legal challenge against Canada’s euthanasia regime

From LifeSiteNews
‘Instead of providing the support and resources we need to live, our government is offering death,’ a coalition of disability advocacy groups said in a press release about its legal challenge to Canada’s euthanasia regime.
A coalition of Canadian disability advocacy groups have banded together to file a “Charter Challenge” against the federal government for allowing the euthanasia of people who are not terminally ill but suffer from chronic illness or disability.
The coalition said its legal challenge, which is before the Ontario Superior Court of Justice, “is about protecting the equality and human rights of all people with disabilities in Canada,” as set out in the nation’s Charter of Rights and Freedoms.
“Instead of providing the support and resources we need to live, our government is offering death. It’s unacceptable, and we won’t stand for it,” noted National Chairperson of the Council of Canadians with Disabilities (CCD) Heather Walkus in a press release for the coalition released on September 27.
The coalition is made up of the CCD, Inclusion Canada, Indigenous Disability Canada (IDC/BCANDS), DAWN Canada, and two people who were harmed by Canada’s so-called “Track 2 MAiD” allowances.
The group said it “opposes” Track 2 of Canada’s Medical Assistance in Dying (MAiD) law, “which provides assisted suicide to people with a disability who are not dying, or whose death is not ‘reasonably foreseeable.’”
The group is claiming in its court challenge that making MAiD available to people who are not dying but may have a serious medical condition is a violation of their “fundamental rights” to liberty and security of the person.
According to Inclusion Canada’s Executive Vice-President Krista Carr, people in Canada “are dying” as a consequence of the current law.
“We are witnessing an alarming trend where people with disabilities are seeking assisted suicide due to social deprivation, poverty, and lack of essential supports,” noted Carr.
“This law also sends a devastating message that life with a disability is a fate worse than death, undermining decades of work toward equity and inclusion. It’s time to put an end to helping people with disabilities commit suicide and start supporting them to live.”
When MAiD was first legalized by the Liberal government of Prime Minister Justin Trudeau in 2016 it was restricted to those whose death was considered “reasonably foreseeable.” While euthanasia is tantamount to murder and thus gravely immoral even in cases of terminal illness, as taught by the Catholic Church, the law was loosened further in 2021 with the allowance of “Track 2” cases.
In its press release, the coalition noted that “Track 2 MAiD” has resulted in “premature deaths and an increase in discrimination and stigma towards people with disabilities across the country.”
“While they are not challenging MAiD Track 1 in this case, they recognize that it too can pose significant problems for people with disabilities. Track 2 MAiD has had a direct negative impact on the lives of people with disabilities.”
The coalition, which supports “Track 1” cases, is “urging the court” to “strike down Track 2 of Canada’s MAiD law, arguing that providing assisted death solely on the basis of disability is unconstitutional.”
Despite the immorality of euthanasia in general, and the extra threat posed by Canada’s additional allowance of “Track 2” cases, euthanasia advocates continue to insist the laws be further expanded.
LifeSiteNews recently reported how the Quebec government said it will soon allow early “advance” requests for euthanasia despite it being disallowed by current federal law. If such a practice were allowed, it would mean a person in Quebec could “agree” to be killed at some point in the future, and thus would not have to give consent at the time of their actual death.
Beyond current “Track 2” cases, Trudeau’s Liberal government has even tried to expand euthanasia to those suffering solely from mental illness.
In February, after pushback from pro-life, medical, and mental health groups as well as most of Canada’s provinces, the federal government delayed the mental illness expansion until 2027.
Overall, the number of Canadians killed by lethal injection under the nation’s MAiD program since 2016 stands at close to 65,000, with an estimated 16,000 deaths in 2023 alone. Many fear that because the official statistics are manipulated the number may be even higher.
MAiD
Disability rights panel calls out Canada, US states pushing euthanasia on sick patients

From LifeSiteNews
Physician-assisted suicide programs in the US and Canada are discriminating against patients with serious medical conditions according to a panel discussion at the Religion News Association.
Physician-assisted suicide programs in the United States and Canada are discriminating against patients with serious medical conditions even when their cases are not terminal, in many cases pushing to end their lives for financial reasons rather than medical.
Catholic News Agency reported that a panel of disability-rights advocates recently examined the landscape of the issue during the Religion News Association’s 2025 annual conference. During the panel, Patients Rights Action Fund (PRAF) executive director Matt Vallière accused state euthanasia programs of discriminating against patients with life-threatening conditions in violation of the Americans with Disabilities Act, noting that when a state will “will pay for every instance of assisted suicide” but not palliative care, “I don’t call that autonomy, I call that eugenics.”
Inclusion Canada CEO Krista Carr, meanwhile, discussed her organization’s lawsuit against the expansion of Canada’s medical assistance in dying (MAID) program to “people with an incurable disease or disability who are not dying, so they’re not at end of life and their death is not reasonably foreseeable.”
More astonishingly, she added, this “funded right” to lethal injection is slated to be expanded to mental illness in 2027.
“By setting out a timeline of three years, it’s an indication that the systems need to move towards readiness in two years. There’s the opportunity to do another review, and to assess the readiness of the system through a parliamentary process,” Health Minister Mark Holland said in February of the move, which Dying with Dignity Canada presents as a matter of “equality” for “those whose sole underlying condition is a mental illness.”
“It’s being called a choice,” but “it’s not a choice,” Carr said. Rather, these programs are pushing the “choice” on patients in “a desperate situation where they can’t get the support they need.”
As LifeSiteNews recently covered, the “most recent reports show that (medical assistance in dying) 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.”
In America, nine states plus the District of Columbia currently allow assisted suicide.
Support is available to talk those struggling with suicidal thoughts out of ending their lives. The American Suicide & Crisis Lifeline and the Canadian Suicide Crisis Helpline can both be reached by calling or texting 988.
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.
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