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March 2026

Alberta government proposes new safeguards for medically assisted dying

By | Latest News

In just four years, deaths from assisted suicide/assisted dying in Alberta, Canada, increased by 109 percent. This is the reality Premier Danielle Smith’s government in Alberta faced when she introduced Bill 18, the Safeguards for Last-Resort Termination of Life Act, on 18 March 2026. It is also a reality that New Zealanders should pay close attention to, because Canada’s assisted suicide trajectory is linked to New Zealand’s story. It acts as a warning.

So what does the Bill actually do?

  • Restrict who qualifies – Only adults 18 and over whose natural death is likely within 12 months (Track 1) would be eligible. Track 2 MAID — for those not facing imminent death — would be banned entirely. Also prohibited: MAID for those under 18, those lacking decision-making capacity, those whose sole condition is mental illness, and advance requests.
  • Tighten the assessment process. Before assessing a patient, doctors and nurse practitioners must make reasonable efforts to contact every primary care provider the patient has seen in the past 12 months, and review all of the patient’s health and personal information.
  • Require a family witness – A family member — defined as a parent, spouse or partner, child, sibling, grandparent, or grandchild — must be present when MAID is administered, unless the provider determines one is not reasonably available.
  • Restrict what providers can say and do – Health professionals cannot raise MAID as an option with patients — the patient must bring it up first. Referrals out of province for MAID assessments would be banned. Public display of MAID information within healthcare facilities (such as posters) would also be prohibited.
  • Mandate training and enforce compliance – All MAID assessors and providers would need to meet new training requirements. Sanctions — starting with remedial training and escalating to suspension or loss of the right to provide MAID — would apply to any provider who breaches the legislation.
  • Protect conscientious objectors – Individual doctors and nurse practitioners would have an explicit legal right to refuse to participate in MAID. Certain facilities — including faith-based ones — would have the right to refuse MAID on their premises entirely, and could establish a 150-metre exclusion zone around their building where MAID services would not be permitted.

Should the bill pass, Alberta would become the first Canadian jurisdiction to place these kinds of limits on federally permitted assisted suicide deaths. The legislation would also proactively limit access to MAID in situations where the federal government has indicated it might implement changes.

Critics are framing this legislation as cruel because it forces suffering people to live against their will. However, supporters of the bill say otherwise.

Inclusion Alberta CEO Trish Bowman stated that MAID was sometimes causing medical systems to offer death as an alternative to supporting people with disabilities, rather than providing the necessary support for a better quality of life. She mentioned that Alberta’s limits could help save lives.

“We know it reinforces incredibly negative and dangerous stereotypes about the value and worth of the lives of people with disabilities. And so we’re very pleased to see this legislation today that serves to protect them,” Bowman said.

Krista Carr, CEO of Inclusion Canada, says she hopes other provinces follow Alberta’s example. However, she said the limits should also compel governments to invest more into programs and support that improve the quality of life for people with disabilities.

Canadian Mental Health Association research librarian Robert Olson called the legislation “heartening” and noted that their organisation opposes the expansion of MAID to people with mental illness.

Dr. Ramona Coelho, an Ontario family doctor who spoke at the bill’s introduction, has documented something deeply troubling in her practice: marginalised patients — people struggling with poverty, social isolation, inadequate housing — being offered assisted death instead of the comprehensive care that could actually ease their suffering. “Patient suffering can be addressed,” she said, “and their lives can greatly improve if we take that time.”

This is the heart of the bill. A refusal to let the medical system off the hook by offering death where it should be offering care.

Canada introduced medical assistance in dying in 2016, initially for the terminally ill only. By 2021, a court ruling expanded eligibility to include people who were not dying imminently. By 2024, Quebec began allowing advance requests — meaning people could arrange their death while still lucid, for a future date. And by March 2027, the federal government is scheduled to allow assisted suicide for people whose sole underlying condition is a mental illness.

Read that again. Mental illness. Alone. As grounds for an assisted suicide death.

New Zealand’s End of Life Choice Act came into force in November 2021, limiting assisted dying to adults with a terminal illness likely to end their life within six months. Canada started with similar bones.

Our law may be due for change. The pressure to expand eligibility to non-terminal conditions, to those suffering from psychological conditions, to younger people, will come. It always does. The Canadian experience shows us exactly where that pressure leads when it is not resisted.

Alberta’s Bill 18 is significant because it reflects a government willing to oppose and take action on the MAID programme, which has shown itself to be spiralling out of control – not just in Alberta but across Canada.

The solution to suffering isn’t a faster, cheaper, tidier way out. It is investing in palliative care, mental health services, disability support, and resources to assist families supporting loved ones through difficult times. That is the alternative Alberta’s own critics of the bill acknowledged was missing. That is what our most vulnerable truly need.

Now, the “slippery slope” in the euthanasia debate, whether here at home or internationally, was not merely a scare tactic; it functions as a roadmap, and we are witnessing it happen in real time. Perhaps, the better metaphor is that the slope is no longer slippery—it’s a cliff.

New Zealand must pay attention and take note.

*Written by Family First staff writers*

Scottish Parliament chooses life as assisted dying bill falls

By | Latest News

On the 17th March 2026, the Scottish Parliament rejected the Assisted Dying for Terminally Ill Adults (Scotland) Bill at Stage 3, with 69 MSPs voting against, 57 voting in favour, and one abstention. The bill, introduced by Liberal Democrat MSP Liam McArthur, would have permitted terminally ill, mentally competent adults with a prognosis of six months or less to request assistance to end their lives, subject to safeguards.

In May 2025, the legislation passed Stage 1 with a vote of 70 to 56, approving its core principles. Stage 3 involved extensive debate across multiple sessions, with over 300 amendments discussed, including a late change to limit eligibility to those with a six-month prognosis.

Supporters, including McArthur and Scottish Conservative MSP Sandesh Gulhane (a practising GP who chaired the bill’s medical advisory group), argued that the bill was carefully drafted with solid safeguards. They claimed it would offer compassion and dignity to those facing terminal illness, ease severe suffering, prevent unsafe travel abroad for assisted dying, and ensure proper oversight rather than unchecked deaths.

Gulhane stated: “Choice matters. This bill represents years of work, consultation and scrutiny. It offers compassion, safeguards and dignity for those facing the end of life.”

Opponents, including disabled MSP Jeremy Balfour and some SNP and Conservative members, raised concerns about risks of coercion, especially for disabled or vulnerable people, potential pressure on individuals to avoid being a burden, and changes to the doctor-patient relationship. They argued that no safeguards could fully eliminate the risk of abuse.

Balfour, who was born without a left arm and with a shortened right arm, said disabled people felt “terrified” by the proposals and warned that the bill could open Pandora’s box with insufficient protections against coercion. “I’m begging you to consider the consequences for the most vulnerable,” he said.

Many MSPs opposing the bill emphasised the need to prioritise improvements in palliative care, social care, and protections for vulnerable groups before any change to the law.

After the vote, campaign groups on both sides issued statements. Dignity in Dying expressed disappointment but reaffirmed its commitment to pursuing reform, citing strong public support in some polls. Opponents like Right To Life UK and CARE for Scotland welcomed the result, viewing it as a safeguard for vulnerable individuals.

The bill was subject to a free (conscience) vote, with no party whips. This marks the latest in several unsuccessful attempts to introduce assisted suicide legislation in Scotland, though it progressed further than previous efforts. Attention may now (and should) shift towards improving palliative care.

*Written by Family First staff*

New Zealand is paying more to end lives than care for them

By | Latest News

A frontline New Zealand GP has exposed a troubling financial incentive at the heart of our end-of-life system — assisted dying pays up to six times more than palliative care. According to an article in Doctor NZ, Fiordland Medical Practice specialist GP Stephen Hoskin has written to Deputy Prime Minister David Seymour, raising urgent questions about why the system is structured this way, and who is responsible for fixing it.

The numbers are stark. Under his PHO, Dr Hoskin can claim $517.50 per patient for providing palliative care in the community. This covers every visit, every call, every hour spent supporting a dying person and their family. By contrast, the Te Whatu Ora website indicates a GP could claim up to $3,080 for a single assisted death. This isn’t a technical error either. This is a system that has been built (unintentionally or not) to reward ending lives over supporting them.

This isn’t a claim from a lobby group. It’s the assessment of a working rural doctor. Dr Hoskin describes the situation as “deeply concerning and unethical,” warning that even well-meaning doctors carry unconscious biases. When a patient raises assisted dying, and a doctor knows they could earn six times more by proceeding rather than redirecting towards palliative care, can we truly say that the consultation is unbiased? Dr Hoskin doesn’t think so, and neither should we.

The rural health disparities make this worse. Some palliative care visits in rural New Zealand are reimbursed at under $50 — less than the cost of a standard GP consultation, and a fraction of what urban patients may receive. Why doesn’t a dying person in Fiordland deserve the same quality of end-of-life support as someone in Wellington?  Despite the Government spending $119 million on hospice care for 2025/26, these disparities persist.

Before the End of Life Choice Act was passed, and again during its three-year review, pro-life advocates and organisations, including Family First NZ, warned that financial disparities and perverse incentives would follow. Those concerns were dismissed as scaremongering. Well, it looks like this recent exposure by Dr Hoskin confirms what we have always said — the system is not neutral. It structurally incentivises death over palliative care, and it has been doing so since the Act came into force in November 2021.

And it appears from the deflection in responses from Seymour to the Health Minister to Te Whatu Ora, no one is taking accountability for a system that Dr. Hoskin describes as “deeply concerning and unethical. While Te Whatu Ora recognises that palliative care funding is “inconsistent across New Zealand” and mentions a National Palliative Care Work Programme but provides no timeline or specific commitments.

Three deflections. Zero answers. Nobody owns this.

And the push to expand the system continues regardless. A proposed amendment bill, lodged by ACT’s Todd Stephenson, wants to make it easier for doctors to raise assisted dying directly with patients — removing one of the few remaining safeguards in the current legislation. Even more troubling, the bill includes removing the 6-month prognosis time-limit and looks to pressure palliative care facilities to participate in assisted dying services. Organisations built around the sanctity of life and caring for the dying could be compelled to facilitate death instead. Combined with the financial incentives already baked into the system, this expansion should alarm every New Zealander who cares about protecting the elderly, the vulnerable, and the dying.

A society’s priorities are revealed by what it funds. Right now, New Zealand is paying more to end lives than to cherish them.

Source: New Zealand Doctor Rata Aotearoa. All quotes and figures cited are drawn from their original reporting.


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