MAiD
Canada’s devastating assisted suicide regime is tearing families apart

From LifeSiteNews
The father stated that his daughter’s ‘capacity to consent to [assisted suicide] is impacted by mental illness’ and that she had likely been ‘unduly influenced by a third party.’
Last year, I noted in First Things that of all the perverse lies told by proponents of euthanasia, one of the worst is their claim that it reduces suffering in society. The precise opposite is true. We have seen this in Canada time and again; heartbroken relatives reaching out to the media to explain how the assisted suicide of a loved one has left them destroyed. Each person who dies at the end of a doctor’s needle leaves loved ones behind; many of them are deeply traumatized by the experience.
Gary Hertgers of British Columbia found out that his sister, Wilma, had died by lethal injection when her building manager called him to inform him that the coroner had just left her apartment. A doctor told the Globe and Mail that he still has nightmares about his father’s euthanasia death, which the family opposed. Two sisters in B.C. found out that their mother had died through euthanasia by text message. Another mother whose troubled son was approved for euthanasia only managed to have that approval rescinded by launching a media campaign.
The CBC is now reporting on a similar story. A desperate father has requested that Court of King’s Bench Justice Colin Feasby in Alberta examine the process that led to two of three doctors approving his daughter for euthanasia (which is referred to in Canada as “MAiD,” or medical assistance in dying). His daughter, who suffers from autism, is only 27 years old. The court has issued a publication ban to protect the identities of the family members and the doctors involved; CBC identified the father as “W.V.” and the daughter as “M.V.”
According to court proceedings, M.V. was approved for euthanasia in December – signoff by two doctors is required to meet the threshold. She was given the date of February 1 to receive the lethal injection. M.V. still lives with her father, who managed to obtain a temporary injunction halting the impending euthanasia (the CBC reported that this “prevent(ed) M.V. from accessing MAiD”) the day before her scheduled death. Her father argued to the court that “M.V. suffers from autism and possibly other undiagnosed maladies that do not satisfy the eligibility criteria for MAiD.”
The daughter’s lawyer, Austin Paladeau, countered by arguing that M.V. is “not trying to withhold or hide anything” by her failure to supply medical documents justifying euthanasia, but that “She’s saying ‘it’s none of (W.V.’s) or the public’s business, I’ve been approved by two doctors, I am entitled to this and, court, it’s none of your business either.’”
Her father, who still cares for her, feels differently; her death is very much his business. His lawyer, Sarah Miller, argued in a brief: “As it stands, AHS (Alberta Health Services) operates a MAiD system with no legislation, no appeal process and no means of review.”
Miller is asking the Calgary judge for a judicial review of M.V.’s approval for euthanasia, and W.V. submitted a 2021 report to the court from a neurologist who stated that M.V. was “normal”; the father also stated that M.V.’s “capacity to consent to MAiD is impacted by mental illness” and that she had likely been “unduly influenced by a third party.” M.V.’s lawyer argued that the issue at stake was medical autonomy itself, stating:
He’s at risk of losing his daughter and while this is sad, it does not give him the right to keep her alive against her wishes. One of the real challenging parts of this process… is what’s actually happening. I completely understand (W.V.) does not want his daughter to die… I represent (M.V.), I don’t want her to die either but that doesn’t play into account here. Even though we have or may have very strong views… at the end of the day this is (M.V.’s) decision.
The judge is grappling with the case. “As a court, I can’t go second guessing these MAiD assessors… but I’m stuck with this: the only comprehensive assessment of this person done says she’s normal,” Feasby stated. “That’s really hard.” He called the case a “vexing” one and, according to the CBC, “reserved his decision on whether he’ll set aside the temporary injunction preventing M.V. from accessing MAiD… the other part of his decision will deal with whether a judicial review will take place, which would examine how doctors came to sign off on M.V.’s MAiD application.”
I hope Feasby makes the right decision. If he does not, a father will face the horror of a doctor coming into his home and giving his daughter a lethal injection against his will – with the entire force of the state endorsing the doctor’s right to do so. At the end of the day, this case is vexing – but it really isn’t hard.
Health
Disabled man needs help as hospital continues to pressure him with assisted suicide

From LifeSiteNews
Roger Foley has been pressured to consider euthanasia while being denied adequate care, prompting a new campaign to cover his medical costs and support his fight to return home.
Roger Foley, an Ontario man, has been forced to turn to charity after being denied sufficient care from hospitals which continue to push euthanasia on him.
On September 30, the Life Care Network launched a LifeFunder to cover medical costs for Roger Foley, a disabled Canadian who is struggling to receive support in an Ontario hospital which is encouraging him to end his life with Medical Assistance in Dying (MAiD).
“Hospital staff have repeatedly offered and pressured me to consider Canada’s infamous assisted suicide program Medical Assistance in Dying (MAiD) while simultaneously obstructing the very services and supports I need to live safely,” Foley revealed in a write-up for the fundraiser.
“Despite my condition, I have fought tirelessly for my rights, dignity, and the ability to return to the community,” he continued.
Foley, who is well known for speaking out against the injustice of Canada’s euthanasia regime, suffers from spinocerebellar ataxia, an incurable brain disease that makes it difficult to move.
As a result of his, he requires caregivers to assist him in eating, drinking, and getting up. According to Foley, his caregivers mistreated him while caring for him at his home. In 2016, Foley was admitted to the London Health Sciences Centre (LHSC) in Ontario for food poisoning and has been there ever since.
Foley revealed that over the past nine years he has repeatedly been offered MAiD despite his desire to be released from the hospital and return home with the help of caregivers.
In May, Foley began enduring even more pain when the LHSC switched out the amber lights in his room for bright bulbs. Foley, who is light sensitive, is now in so much pain that he is unable to be lifted for meals.
“I can only tolerate fluids for a few minutes at a time using makeshift taped-together ski goggles. I am unable to eat solid food or take oral medications,” Foley explained.
“I live in constant pain, severe fatigue, and cognitive decline from dehydration and lack of sleep,” he continued. “Staff continue to impose arbitrary and unsafe ‘rules,’ including denying me side rails during transfers and barging in with bright lights – despite knowing it causes me extreme harm.”
Now Foley is seeking private funding for a Personal Support Worker to assist him with feeding, medication, hydration, and basic hygiene support. Life Care Network, an organization which assists vulnerable Canadians at risk for MAiD, has intervened to raise the necessary funds for Foley’s care.
In an interview with LifeSiteNews, Lino DeFacendis, founder and CEO of Life Care Network, stressed the importance of defending Foley from a medical system which appears to prioritize ending his life with MAiD over providing proper care.
“There needs to be a re-awakening that every life is precious and must be treated with true dignity and compassion no matter how difficult the circumstance,” DeFacendis said.
“Killing oneself via MAiD is never the answer to one’s problems,” he declared.
To support Foley’s medical care, please visit his LifeFunder page.
Alberta
Alberta puts pressure on the federal government’s euthanasia regime

From LifeSiteNews
Premier Danielle Smith is following through on a promise to address growing concerns with Canada’s euthanasia regime.
Alberta Premier Danielle Smith has sent a mandate letter to Justice Minister Mickey Amery directing him to draft and introduce new legislation on euthanasia to ensure better oversight of so-called “medical aid in dying,” or “MAiD” and to prohibit it for those suffering solely from mental illness.
In December of last year, Smith’s United Conservative government indicated that they would seek to address growing concerns with Canada’s euthanasia regime. Mainstream media outlets attacked the move, with the CBC actually reporting that: “Some are concerned new limitations could impact already vulnerable Albertans.”
Premier Smith has now followed through on that promise. The September 25 mandate letter, which lays out directives on a wide range of issues, calls for the justice minister to take steps to protect vulnerable Albertans suffering from mental illness:
As lead, work with relevant ministries to introduce legislation to provide greater oversight and appropriate safeguards for medical assistance in dying and prohibit medical assistance in dying where a person seeks this procedure based solely on a mental illness.
In an email to the CBC, Amery stated that while euthanasia law is under federal jurisdiction, healthcare falls under provincial jurisdiction. The CBC falsely claimed that mental illness “has never been an approved sole eligibility factor for MAID, though the government has considered permitting it.” In fact, the Trudeau government passed Bill C-7, which legalized MAID for those struggling with mental illness, in 2021.
That eligibility expansion has been delayed twice—in 2023 and 2024—and is now slated to come into effect in 2027. Despite those delays, Bill C-7 is still law. MP Tamara Jansen and MP Andrew Lawton are currently championing Bill C-218, the “Right to Recover Act,” which would reverse this and make it illegal to offer or perpetrate euthanasia on someone struggling solely with mental illness.
The CBC’s coverage of this move was predictably repulsive. In addition to their disinformation on euthanasia for mental illness, they reported that “Smith’s letter directing new provincial legislation on MAID comes almost a year after the government surveyed just under 20,000 Albertans on whether they think the province should step in. Nearly half of those surveyed disagreed with putting in more guardrails on MAID decisions.”
“Nearly half” is an unbelievably deceitful way of reporting on those results. In fact, 62% were in favor of legislation for a dedicated agency monitoring euthanasia processes; 55% were in favor of a MAID dispute mechanism allowing families or eligible others to challenge decisions to protect vulnerable people, such as those with disabilities or mental health struggles; and 67% supported restricting euthanasia to those with physical illnesses rather than mental illnesses. The CBC did not report on a single one of those numbers.
Provincial legislation to protect people with mental illnesses is badly needed, although I pray that by the time Justice Minister Amery gets around to drafting it, the Right to Recover Act will be passed in Parliament, and provincial action will be unnecessary. In the meantime, it is increasingly clear that much of Canada’s mainstream press coverage of this issue actively threatens the lives of the suicidal and those struggling with mental illnesses. If their dishonesty and attempts and manufacturing consent were not so routine, they would be breathtaking.
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