Tuesday, July 20, 2021

Netherlands public prosecutor questions euthanasia rules for people who cannot consent.

Alex Schadenberg
Executive Director, Euthanasia Prevention Coalition.

Last November I published an article reporting that based on the Netherlands Supreme Court decision in April 2020, concerning the euthanasia death of an incompetent woman with dementia who resisted, that the five regional euthanasia review committee's in the Netherlands agreed to rules to expand euthanasia for people with dementia.

The Dutchnews.nl published an article on July 20, 2021 based on a report in the Trouw news stating that the public prosecutor questions the new euthanasia rules for people with dementia who cannot consent. The article reports that the dispute centres on who has the last word about euthanasia - the courts or the committees - and how are decisions made concerning someone with dementia who can longer ask for euthanasia.

The article reports that the new guidelines state that:

"In giving euthanasia to a patient who is no longer mentally competent as a result of advanced dementia, it is not necesary for the doctor to agree with the patient the time or manner in which euthanasia will be given... (since) this kind of discussion is pointless because such a patient will not understand the subject."
The public prosecution department chief Rinus Otte says this goes too far. Otte told the Trouw that this is not in line with the law and doctors can still face prosecution for murder.

According to the article, Trouw reported that the regional euthanasia review committee's are in talks to revise the code and a new version of the code will be published by the end of the year.

As I have stated before euthanasia for people with dementia justifies non-voluntary euthanasia. If it is lawful to kill someone with dementia who cannot request it, but indicated at some point in the past support for this type of death, then soon it will become cruel to not lethally inject someone with dementia who never asked for it.

This is an important issue since Canada's federal government and the Québec government have both established committee's to discuss the further expansion of euthanasia in Canada

One area being discussed for expansion in Canada is permitting euthanasia for people who are incompetent (dementia) but previously requested it in their advanced directive.

The dispute between the public prosecutor and the regional review committee's will likely cause Netherlands physicians to refuse to do euthanasia for incompetent people with dementia in order to avoid a possible prosecution.

Once euthanasia is legal, there is no limit for its use. Limiting euthanasia to competent people who make a clear request is discrimination for incompetent people who cannot make a request.

The dispute, the paper said, centres on deciding who has the last word about euthanasia – the courts or the committees – and about how far doctors can go to help someone to die who is no longer able to ask for it.

Read more at DutchNews.nl:
The dispute, the paper said, centres on deciding who has the last word about euthanasia – the courts or the committees – and about how far doctors can go to help someone to die who is no longer able to ask for it.

Read more at DutchNews.nl:
The dispute, the paper said, centres on deciding who has the last word about euthanasia – the courts or the committees – and about how far doctors can go to help someone to die who is no longer able to ask for it.

Read more at DutchNews.nl:

Constitutional Challenge Brief Filed in New Jersey Euthanasia Appeal


BELLEVUE, WA, USA, July 20, 2021 /EINPresswire.com/

Attorney Margaret Dore, President of Choice is an Illusion, which has fought against assisted suicide and euthanasia legalization throughout the United States, and internationally, has released the following statement in connection with the filing of a constitutional challenge amicus brief, which seeks to invalidate New Jersey’s Medical Aid in Dying for the Terminally Ill Act. The case, Petro et al v. Grewal, is pending in the Superior Court of New Jersey Appellate Division, A-003837-19.

“‘Aid in dying’ is a euphemism for physician-assisted suicide, assisted suicide and euthanasia. The amicus brief argues that the Medical Aid in Dying for the Terminally Ill Act is stacked against the individual, not limited to people near death and unconstitutional due to the way it was enacted.

“The Act is based on similar acts in Oregon and Washington State. Oregon’s act went into effect in 1997. Washington’s nearly identical act went into effect in 2009.

“All three acts apply to persons with a six month or less life expectancy. Such persons may in fact have years or decades to live.

“A well known example is Jeanette Hall. In 2000, she made a settled decision to use Oregon’s act. Her doctor convinced her to be treated for cancer instead, such that she is alive today, twenty-one years later.

“The New Jersey Constitution protects against the enactment of misleading legislation, which is what occurred here. The Act’s title and findings are misleading with regard to the Act's content, which renders the Act unconstitutional.

“The New Jersey Legislature understood that it was enacting a strictly voluntary law limited to dying people. Per the Act’s title, it was not clear that the Act would legalize assisted suicide and euthanasia.

“Per the Attorney General, the Act applies ‘only to those individuals, both patients and providers, who voluntarily elect to participate in the Act’s provisions.’ As for the trial judge, he was not persuaded that the Act specifically provides for assisted suicide and euthanasia. But the Act is not required to be voluntary. The Act is about assisted suicide and euthanasia.

“The Act's title also uses the phrase, ‘aid in dying,’ which means assisted suicide and euthanasia.

“The Act has no required oversight over administration of the lethal dose. No doctor, not even a witness, is required to be present at the death.

“The drugs used are water and/or alcohol soluble, such that they can be injected into a sleeping or restrained person without consent. Even if the patient struggled, who would know?

"Persons assisting a suicide or engaging in euthanasia can have an agenda. Consider Tami Sawyer, trustee for Thomas Middleton in Oregon where assisted suicide is legal. Two days after his death by assisted suicide, she sold his home and deposited the proceeds into bank accounts for her own benefit.

“Consider also Graham Morant, who was convicted of counseling his wife to kill herself in Australia. His motive: to get the life insurance.

“The New Jersey Act has a formal application process to obtain the lethal dose. Once the lethal dose is issued by the pharmacy, there is no oversight. No witness, not even a doctor is required to be present at the death. If the patient objects or even struggles, who would know?

“Deaths pursuant to the Act, are reported as natural on the death certificate. With this situation, a patient’s heir, who participates in the patient’s death, is allowed to inherit.

“With passage of the Act, New Jersey residents with money, meaning the middle class and above, have been rendered sitting ducks to their heirs and other financial predators. Passage of the Act has created a perfect crime.”

For more detailed information, read Margaret Dore's brief.

Link to the media release (Link).

Margaret Dore
Choice is an Illusion
+1 206-697-1217

Monday, July 19, 2021

Jean Echlin RN: We honour her life. We mourn her death.

Alex Schadenberg
Executive Director, Euthanasia Prevention Coalition


We celebrate the life and mourn the death of Jean Echlin RN MScN, was a past President and founding Vice President of the Euthanasia Prevention Coalition.

Jean is a past director of the Hospice of Windsor and was awarded the Dorothy Ley award, in 2005, for excellence in palliative care in Ontario

Jean was an extraordinary woman who I first met through Mark Pickup. Mark is a disability writer and activist who told me, many years ago, that Jean Echlin was the most compassionate woman. After meeting Jean, I had to agree, Jean was the most compassionate and caring woman I have ever known.

When I started to found the Euthanasia Prevention Coalition (EPC), I was looking for a few people who would be committed to the cause, who had incredible experience and would be willing to work together. I found those qualities in Dr Barrie deVeber as the founding EPC President and Jean Echin as VP.

Jean was more than just a partner in the cause, she was a speaker, a writer, a leader and a truly compassionate and caring woman. She actually made me feel like I was her son.

Jean believed in caring for people and never killing.

In October 2010, Jean Echlin and Joanne St. Pierre wrote the booklet - Palliative Care Not Euthanasia, as a submission to the Parliamentary Committee on Palliative and Compassionate Care, an all party committee formed in response to the defeat of euthanasia Bill C-384 by a vote of 228 to 59.

EPC will send you a copy of the booklet Palliative Cre Not Euthanaisa when you make a donation in memory of Jean Echlin (Donation Link).

Jean understood that the legalization of euthanasia would affect medical professionals. She wrote in October 2008 the following:
Professional health care relationships with doctors, nurses, patients and family members float on a sea of trust. Asking professional health care providers to kill, or give the means to kill, will destroy this trust relationship. I emphatically believe that we have no right to ask our professional care givers to provide us with death. Neither should our health care providers ever feel obligated to comply with this narcissistic request.
In November 2011, Jean wrote about her concerns related to the Carter court case in BC that led to the legalization of euthanasia in Canada. Jean wrote:
With the advent of Carter versus the Attorney General of Canada, Canada's laws prohibiting euthanasia and assisted suicide are being challenged again. This despite the fact that our federal Parliament vetoed Bill C-384 that sought to legalize assisted suicide and euthanasia by an overwhelming vote of 228 to 59 in 2010.

If the pro-killing side gets its way, five people on the Supreme Court can overrule Parliament and demand change in the Criminal Code that forbids euthanasia and assisted suicide. What would this scenario do to our democratic process and the rights of a majority of Canadians?

Who would be at risk? You are. So is everyone in this country.
In March 2013, Jean responded to a story of an elderly woman who died by suicide and was being lauded as courageous. Jean wrote:
In February of this year, a national paper printed an extraordinary posthumous letter from a 91 year old woman who died by suicide because she was tired of living. She wanted to end her life with dignity. Though most of the (published) responses thought she was courageous, I disagree. I believe there is more to the issue when anyone contemplates suicide.

Ultimately suicide in the elderly is a failure. We must ask ourselves, is it because pain and suffering were not addressed? Did individuals thinking of suicide, and their families, not have access to help and support? Is it because of societal ambivalence about mental health issues or stigma about the elderly? Is it due to encouragement and even pressure by pro-suicide groups like Dying with Dignity? What is the future of this legacy?

Aging brings challenges. These may include loss of independence, chronic discomfort/ pain, even chronic illness. Do these problems mean our lives are no longer of value?

As someone advanced in years living with chronic pain, and who has been with hundreds of people at the end of their lives, I know that aging is a daily struggle with its own share of joy and hope. I believe advancing in years does not diminish the value of our contributions.
In April 2016, in response to the Bill C-14, the bill that legalized euthanasia in Canada, Jean wrote to the Minister of Justice stating:
How dare we ask our doctors and nurses to put patients to death when a safer option exists. Healthcare providers must never assume the role of killers or refer to another who will provide the "death management." Trust and legal issues will make more problems for our sick and elderly. 
EPC will send you a copy of the booklet Palliative Care Not Euthanasia when you make a donation in memory of Jean Echlin (Donation Link).

Jean Echlin R.N., MScN. was a pioneer in Hospice Palliative Care. In 2005, the Ontario Palliative Care Association (OPCA) recognized her 26 year contribution to hospice palliative care by selecting her for the prestigious "Dorothy Ley Award of Excellence" for her part in "fostering the true spirit of Palliative Care in Ontario." Echlin formerly served on faculty, University of Windsor’s Faculty of Nursing, and was director of nursing at Windsor Regional Hospital’s Metropolitan Campus. As coordinator and clinical nurse specialist, then Executive Director, Jean was instrumental in the development of the Hospice of Windsor & Essex County Inc. which is recognized as exemplary in Canada. In 1988, Jean moved to London, Ontario and established the Palliative Care Consultation Team in the heart of tertiary care at University Hospital, London Health Sciences Centre. She was also recognized as a distinguished public speaker, educator and free-lance writer. Jean was a nurse consultant; former President and founding VP of the Euthanasia Prevention Coalition; served on the Advisory Council of the deVeber Institute of Bioethics and Social Research; is a member of the Honour Society of Nursing and member Emeritus of the Registered Nurses Association of Ontario.

Friday, July 16, 2021

Disability advocates say Assisted Dying Bill poses significant dangers for disabled people

Press release from the APPG for Dying Well - July 16, 2021

Disability advocates say Meacher’s Bill poses significant dangers for disabled people - Founder of Not Dead Yet UK, Baroness Jane Campbell

Founder of Not Dead Yet UK, Baroness Jane Campbell of Surbiton, leads an organisation of disabled people and individuals with progressive and terminal medical conditions campaigning against a change in the law on assisted suicide. Speaking to the All-Party Parliamentary Group for Dying Well, Baroness Campbell argued that in countries where assisted suicide has been legalised, disabled individuals who are identified as potential beneficiaries of an assisted death do not receive the equal right to live with dignity and respect. A change in the law, she said, is “far too dangerous” without greater state investment in support for disabled individuals “not only to live or survive, but to thrive”.

Baroness Jane Campbell
Baroness Campbell continued, “We respect, and we understand so well from our own experience, why some individual disabled and terminally ill people want the right for someone to assist them to end their life. But, contrary to popular belief, this is not the general view held by the majority of people with lived experience of progressive medical conditions. They tell me, until such time that disabled and terminally ill people have enough support to thrive with dignity in society, we cannot contemplate a bill that has the opposite effect.”

During the online meeting chaired by Danny Kruger MP and Baroness Campbell, three presenters, all of whom are disabled, questioned whether the proposed assisted dying legislation stands up to public safety standards.

Dr. Miro Griffiths, a Research Fellow at the University of Leeds, discussed the legalisation of assisted suicide in light of the social injustice and marginalisation experienced by disabled people, which has been exacerbated by the Covid-19 pandemic. He stated, “My argument is that it is not a safe time to be introducing this bill because of the historical legacy of injustice experienced by disabled people, but also because currently we are going through a pandemic which has exacerbated the marginalisation experienced by disabled people.”

Dr. Peter Scott Morgan, a leading robotics and AI scientist living with late-stage ALS, showcased his avatar which has given him back his ability to speak and express himself. As someone with severe Motor Neuron Disease who was given less than six months to live nearly four years ago, he invited the APPG to question “the apparently self-evident truth that, with an untreatable condition such as late stage Motor Neuron Disease (MND), with someone diagnosed as being within six months of death, there is no reasonable expectation that the patient can not only survive, but thrive, for many years with an increasing quality of life.”

Dr Scott Morgan stated his opposition against the legalisation of assisted dying, referring to “uncertainty between being terminal and simply being disabled, and danger that some with extreme disability may unnecessarily kill themselves in anticipation of what they incorrectly believe will inevitably happen”.

Chair of the Research Institute for Disabled Consumers, Philip Friend, raised further concerns that the Meacher Bill contains inadequate safeguards, opening the door to significant dangers for disabled people. Addressing parliamentarians, he urged, “it is our concern that you should not focus on personal choice or personal morality, but focus on public safety. This has to be the primary consideration in all letters, all legislation. What we want you to do is to help disabled people to thrive, not to die.”

ENDS

Notes to Editors

The APPG for Dying Well has the support of more than 70 MPs and Peers including: the former Conservative Party leader Sir Iain Duncan Smith MP; disability rights campaigners Baroness Campbell; Baroness Tanni Grey-Thompson; and Lord Alton; former Labour Minister Stephen Timms MP; former Leader of the Liberal Democrats Tim Farron MP; former BMA president Baroness Hollins and more than 60 other cross-party parliamentarians.

For media inquiries, please contact:

Alistair Thompson Alistair@teambritanniapr.com

Bioethicists Propose Time-Delayed Suicide Implant for Dementia Patients

The following article was published by National Review online on July 16, 2021.

Article: Assisted suicide lobby researchers promote suicide devices for people with dementia (Link).

By Wesley Smith

Bioethicists are looking for ways to eliminate people diagnosed with dementia when they become incapacitated. Belgium and the Netherlands permit advance orders to be euthanized. Another proposal gaining traction in bioethics would force caregivers to starve patients to death.

And here’s a new idea: Writing in the Hastings Center Report — the world’s most prominent bioethics journal — two prominent bioethicists propose the implantation of a time-release suicide device that will cause future death at the time of the patient’s choosing. They call the hypothetical device an “advance directive implant, or ADI” (bioethicists sure love their acronyms). From, “Ending One’s Life in Advance:”

The ADI would require extensive engineering and may not be feasible with current technologies. Still, we suspect it could become feasible in the near future. We imagine the ADI as something like a computerized subdermal implant containing a lethal dose of a medication or combination of medications. Release of these medications would occur rapidly after a predetermined interval or after some specific event had occurred. The ADI would likely require a long-lasting battery, computerized control, and a pump or microfluidic mechanism. . . .

It is crucial that the ADI be easily and immediately removable. After all, even those certain of their wish to obtain it would still like the option of changing their minds, at least prior to the onset of dementia, whether for personal reasons or because an effective treatment for their condition has been developed.
Yeah, good luck with that, guys.

And, of course, the usual sop of safeguards to protect against abuse:
The permissibility of ADIs would, first, depend on reasonable standards of care and preimplantation assessment criteria. One would not want healthy adults with minimal risk of dementia to receive them; one would not want them to be implanted under external pressure, forcibly, or surreptitiously; one would not want them to be implanted in persons whose decision-making capacities are impaired by depression. One possible set of criteria would be those used for physician aid-in-dying in Oregon: that the requestor be an adult; able to make and communicate health care decisions; seen by at least two physicians who concur in the diagnosis, prognosis, and assessment of decision-making capacity; not suffering impaired judgment due to a psychiatric or psychological disorder, not coerced, and informed of alternatives.
I don’t have space to get deeply into it here, but the Oregon safeguards are a joke. If one doctor says no, the suicidal patient can just go doctor shopping. There is no state oversight prior to death, the system relies on doctors’ self-reporting, and there are rarely any referrals to psychologists.

Why engage this supposed “thought experiment” — which is actually much more than that? Here’s a good hint (my emphasis):
Perhaps the greatest advantage of ADIs is that they would reduce the distress that living and dying with dementia imposes on others. This is true in two senses. First, there is the obvious sense that ADIs would tend to shorten the period in which the person living with dementia represents a burden for others. . . . ADIs would also reduce the distress that dementia imposes on others because the device, relatively free of any external input or activity, mostly immune to the judgments, misgivings, and second-guessings of family members, physicians, and friends, would absolve people of many of the burdens of judgment once the patient developed advanced dementia.
In other words, we should let the patient put him or herself out of our misery.

The authors describe the ADI as a means of “getting the better of Alzheimer’s.” No, it is softening the ground for authorizing direct killing of such patients. And no, this proposal isn’t satirical or a form of “what if” musing to start a philosophical salon conversation:
As we said at the outset, whether this consideration of the ADI is understood as a conjecture, as a hypothetical exploration, as a real-life thought experiment, or as a proto-proposal, we think it important to take this seemingly radical idea seriously. We may not currently have the technology to realize it, and perhaps not the social conditions that would allow it to be used without abuse.

It may even be hard to conceive of this idea: “Horrible,” said one friend, “even if I agree with the conclusion.” But we think it is an important idea nevertheless: it makes us see what is so problematic about how we respond to dementia in our current world, forcing some to suffer a future they dread and burdening others with acting for them. No one, really, wants to live with dementia: for most of us, it is bad to lose the memories and cognitive capacities that contribute to who we are and that enable us to do many of the things we care about.
There it is! “No one [they left out the implied “should”] wants to live with dementia.” That’s the dehumanizing message people facing this difficult circumstance constantly hear, stripping them of their intrinsic human equality.

Articles like this — particularly when published in influential journals — are insidious because they normalize the noxious idea that dementia patients’ lives are not worth protecting or living. Instead, we should continually assure those who face this crucible that we love them, want them, and will care for them — no matter what.

And don’t any reader tell me that I don’t know how difficult Alzheimer’s can become. My mother died of the disease, spending the last five months of her life living in my wife’s and my home, with quality hospice care. Was it easy? No! But so damn what? Part of the essence of true humanity is caring and loving each other — no matter how taxing and emotionally devastating — especially when a person is so ill or injured they can’t take care of themselves. That’s the best part of who we should be.

The movement to eliminate suffering by eliminating the sufferer is becoming a cult.

Thursday, July 15, 2021

Assisted suicide researchers want suicide devices for people with dementia.

Alex Schadenberg
Executive Director, Euthanasia Prevention Coalition

Just as you thought the assisted suicide lobby has gone too far, long-time assisted suicide lobby leader and researcher, Margaret Pabst Battin opens the debate for developing a suicide device for people with dementia.

The Hastings Center Report published an article (May 2021) by Margaret Pabst Battin and Brent M Kious titled: Ending One's Life in Advance. (Link to the article).

Battin has studied and promoted euthanasia and assisted suicide since the 1980's. Battin is the same philosopher who argues that assisted suicide is not a suicide. Her new article concerns the following question:

People newly diagnosed with progressive dementia may not want to live through its later stages, but the options for those who wish to choose an earlier death are inadequate and can be dependent on others’ cooperation. What if, while still competent, these people could opt for implantation of a device that would achieve their goals—timed to release a painless, fatal drug at a future point they have selected?
Pabst and Kious justify their promotion of suicide devices for people with dementia by stating:
  • to have control over how we die; 
  • to avoid pain and suffering;
  •  not to burden family members with overwhelming care needs; 
  • not to impose overwhelming medical or other financial costs; 
  • not to lose what we may experience as still-good life in the early and middle stages of progressive dementia; 
  • not to impose painfully difficult decisions on our family members or loved ones—for example, between caring for us or facing unsupportable financial burdens; 
  • not to have to ask our doctors to do what might violate their oaths or personal commitments or be emotionally unbearable for them; or 
  • not to have to turn to preemptive suicide to avoid all of the above.

Talking about considering life with dementia as not worth living.  

I recently spoke to a woman who felt that she was being pushed to have her father, with dementia, die by dehydration. This woman loved and respected her father and did not consider his life as not worth living.

Pabst and Kious ask the question?

Suppose there is a simple medical device, based on the triple technology of the timed-release capsule, the subdermal contraceptive implant, and a painless, quick-acting euthanasia drug developed in the Netherlands, where euthanasia is legal: it’s a delayed-onset, rapid-acting, painless euthanasic implant. Anybody newly diagnosed with Alzheimer’s or other irreversible progressive dementia, while still lucid and competent, can request one.
When evaluating the concept of killing by inserting a time delayed suicide device into a person with dementia creates significant concerns. For instance:
  1. Implanting a suicide device into a person with dementia creates a belief that living with dementia is worse than death. This is based on a eugenic ideology that certain lives are not worth living. The assisted suicide lobby will counter that argument by saying its about choice, but that negates the reality that someone has agreed to implant the device. 
  2. Who decides that the person qualifies to have a suicide device implanted? Similar to assisted suicide the death lobby will argue the decision is based on choice. Considering the fear mongering used by Battin and Kious in this article to justify killing, is it truly based on a "choice". 
  3. What happens if the person changes their mind? Once a person is deemed incompetent, they will lose the right to change their mind with the inevitable outcome being death without consent.

Finally, why limit the death device to people with dementia?

Whether it be assisted suicide by mixing a lethal drug cocktail into apple sauce or assisted suicide by suicide device, clearly Battin and Kious are pushing the death envelope and, in turn, dehumanizing people living with dementia.

In a previous article Battin suggests that suicide is different than assisted suicide. Her arguement concerning suicide is philosophically based. This article is clearly justifying suicide for people with dementia. 

As stated earlier, just as you thought things were bad, Battin comes along to justify more killing.

Wednesday, July 14, 2021

Assisted Dying Expansion Aided by Legislation, Public Attitudes

Alex Schadenberg
Executive Director, Euthanasia Prevention Coalition

Lee Harding, writing for the Epoch Times, interviewed me about the expansion of (MAiD) euthanasia in Canada for an article that was published on July 13.
Harding reports on the 2020 Health Canada euthanasia report which indicated that there was a 35% increase in assisted deaths in Canada in 2020. Harding writes.
In 2020, 7,595 Canadians received medical assistance in dying (MAiD). This was an over 34 percent increase from 2019’s 5,660 figure, but 2.7 times the 2017 number of 2,838, the first full year assisted suicide was legal in Canada. The statistics were published in Health Canada’s second annual report on MAiD released at the end of June.

In addition to the increase in assisted deaths, MAiD opponents were disturbed by circumstances in which the procedure was delivered last year, including some that may not have been legal. Taking data from the Health Canada report, the Euthanasia Prevention Coalition found that:
  • 4,120 Canadians chose MAiD because they had cancer, yet it was without discussion with an oncologist about their choice;
  • 2,532 people died by MAiD less than 10 days after requesting it, including 905 whose deaths were not imminent but had the then-legally required 10-day reflection period waived because two practitioners determined that they could lose their decision-making capacity within that 10-day period;
  • 1,253 had non-terminal conditions; and
  • 59 people were assessed by the practitioner as having requested a lethal injection without directly consulting with the person.
Alex Schadenberg
Harding asked me about the effect that the euthanasia expansion Bill C-7 will have on MAiD in Canada. Harding reported:
These numbers are expected to rise yet again in 2021 due to Bill C-7, which became law on March 17, says Alex Schadenberg, founder of the Euthanasia Prevention Coalition.

“The effect of Bill C-7 will be a lot more death, but also the fact that the culture is being inundated with the concept that this is a good thing,” he said in an interview.
Harding then reported what I stated about the problem with cultural loneliness.
Schadenberg is disturbed that 1,412 Canadians requested MAiD in 2020 because they felt isolated and lonely.

“The euthanasia mentality really takes off in a culture of loneliness and isolation, and that’s what we have in our culture, more so than ever before—and it’s only getting worse,”
Angelina Ireland
Harding follows his interview with me by speaking to Angelina Ireland, the President of the Delta Hospice Society who stated:
the medical system has an increasing bias in favour of MAiD instead of supporting people until their natural death.

“We need to call for perhaps a provincial or national inquiry as to what is going on out there with elderly people, with sick people … vulnerable people. People are coming up to them, nurses, doctors, recommending they just MAiD themselves.”
Sadly, the Canadian government's current review of the euthanasia law is oriented to further expansions of euthanasia rather than investigating how the law is actually working in Canada.

Tuesday, July 13, 2021

Colombia's Health Ministry sets euthanasia guidelines.

Alex Schadenberg
Executive Director, Euthanasia Prevention Coalition

In 1997 Colombia's Constitutional Court ruled that: "the State cannot oppose the decision of an individual who does not wish to continue living and who requests help to die when suffering from a terminal illness that causes unbearable pain, incompatible with his idea of dignity".

Since that time, euthanasia has been technically legal in but rarely done in Colombia.

An article by Merco Press reports that Colombia's Health Ministry has set out guidelines for euthanasia. According to the Merco Press article:
Colombia's Health Ministry has issued Resolution 971, setting out the guidelines regarding the carrying out of euthanasia procedures, which has sparked some controversy among national lawmakers.

According to the document from the health authorities of the only country in South America so far to have legalized the right to death with dignity, the patient must make this request directly (verbal or written) or indirectly, through an advance directive document (DVA). The request must be voluntary, informed, unequivocal and persistent.

The resolution states that patients wishing to exercise their right to die with dignity will have to submit ”a clinical condition at the end of life, (...) present secondary suffering, be in a position to express the request directly.”

Once the patient makes the request, the doctor must immediately include it in the medical record and activate the interdisciplinary scientific committee that will study the request within the first 24 hours.

The document also establishes that “health providers (IPS) that have enabled the medium or high complexity hospitalization service for oncological hospitalization, institutional care for chronic patients or home care for chronic patients, that have protocols of management for palliative care, will make up within each entity a scientific-interdisciplinary committee for the right to die with dignity through euthanasia.”

The committee must study the applications within the first 10 days and will be made up of a lawyer, a doctor with the speciality of the pathology suffered by the patient and a psychiatrist or clinical psychologist, and when the committee is formed, it must be declared that none is a conscientious objector.

Eugenics: The root of the assisted dying movement.

Alex Schadenberg
Executive Director, Euthanasia Prevention Coalition

In response to attacks against the Care Not Killing Alliance in the UK, Jamie Gillies, in spiked-online focuses on the eugenics roots of the assisted dying movement. Gillies writes about Killick Millard who founded the leading assisted dying group in the UK. Gillies states:
Scotland’s media class seems quite happy to spare prominent groups on the other side of the assisted-suicide debate from scrutiny. The Record, for instance, has failed to mention that Dignity in Dying, the group leading the charge for assisted suicide in the UK, was founded and funded by eugenicist politician Killick Millard.

Millard is said to have been ‘informed by a coherent philosophy… underpinned by eugenic ideas about the importance of maintaining the calibre of the racial stock’. He was what, in modern terms, we might call ‘ableist’, arguing in 1931 that the ‘feeble-minded and mentally deficient’ – those with mental-health problems – ‘should be sterilised’.

And he was also anti-working class. In 1911, in an essay on poverty, Millard celebrated the fact that ‘slum dwellers’ had a high rate of infant mortality, stating that ‘this consideration goes a long way towards allaying the fear that the falling birth-rate of the superior classes, and the comparatively high birth-rate of the very lowest class, threatens the quality of the race’.

It must be noted that in March 2020, a UN disability rights expert stated that she is concerned about euthanasia, assisted suicide and the new eugenics.

The American media also ignore the fact that the leading assisted suicide lobby group in the US, was also founded by hard core eugenics proponents.

Historian, Ian Dowbiggin, in his ground breaking book: A Merciful End: The Euthanasia Movement in Modern America. proves beyond a doubt that the founders of the euthanasia lobby were wedded to the eugenics movement. His book was so clear that Compassion and Choices appears to have destroyed its historical archives.

In November 2015 Dowbiggin wrote about his concern that the historical records of the euthanasia lobby were destroyed. He wrote:
One thing is clear: if the euthanasia movement’s records have indeed been destroyed, a lot of history has vanished, Orwell-like, down a cavernous memory hole. And with it, information the right-to-die movement doesn’t want you to know.

I should know, because I saw these records and I know what was in them. I wrote up my findings in my 2003 book on the history of the movement, published by Oxford University Press.

The story of my involvement in these valuable records begins about fifteen years ago when I was given permission to explore the archives of what used to be called Partnerships for Caring, Inc. PFC was a successor organization to the defunct Euthanasia Society of America (ESA). The ESA records, housed in a law firm in Baltimore, consisted of 15 large cardboard boxes holding correspondence, financial records, press releases, published materials and minutes of meetings, much of it uncatalogued.

There were literally thousands of items in these boxes documenting the entire 20th c. history of the U.S. and non-American activists who advocated the legalization of various forms of euthanasia. The ESA archive contained materials relating to the careers of noteworthy social activists such as Derek Humphry, the founder of the Hemlock Society (now called Compassion and Choices), Joseph Fletcher, the founder of “situation ethics,” Alan Guttmacher (after whom the population-control Guttmacher Institute in New York City is named), and the birth control pioneer Margaret Sanger who, unbeknownst to all her biographers, was also a vocal proponent of legalized euthanasia.

Not only did these activists urge governments to permit voluntary mercy-killing and physician-assisted suicide, many also supported the involuntary mercy-killing of handicapped people. For example, despite his knowledge of widespread Nazi murder of people with disabilities, in 1943 the ESA’s president thought it was a good idea to legalize euthanasia in time for returning veterans who suffered from mental and physical wounds.

Dowbiggin then explains how he learned that the euthanasia lobby destroyed their history. Dowbiggin states:

But the story did not end there. About five years after the book’s publication, I was contacted by a US graduate student researching the history of euthanasia. She told me that in trying to track down the ESA records she had been informed that the collection had been intentionally destroyed.

 Just this year another US graduate student got in touch with me, also trying to locate the ESA archives. She too has been told the records no longer exist, although she is still investigating.

Of course, it might be that the ESA records are sitting somewhere safe and sound. Yet why do groups like Compassion and Choices ignore my own requests for information? Why, when a published scholar in the history of medicine enquires about the whereabouts of this important archive, is there a resounding silence?


The euthanasia lobby, world-wide, was intertwined with the eugenics movement and its leadership continues to be suspicious in its ideology today.

Let's be clear. Removing the requirement of consent at the time of death, extending euthanasia to people with dementia, and in the Netherlands, the approval of the Groningen Protocol, which permits killing of babies with disabilities, are all eugenic ideolical positions.

Friday, July 9, 2021

Should psychiatrists assist the suicide of their patients, even if it is legal?

This article was published by the Psychiatric Times on July 8, 2021

Alex Schadenberg
Executive Director, Euthanasia Prevention Coalition

Doctors Ronald W. Pies, MD, Mark S. Komrad, MD, Cynthia M.A. Geppert, MD, MA, MPH, MSBE, DPS, and Annette Hanson, MD tackle the difficult question in the Psychiatric Times, that being should psychiatrists assist the suicide of their patients, even if if is legal?

All of the writers have been published on issues concerning their professional obligations and why psychiatrists should never participate in assisted suicide, but now they have written about a more nuanced questions concerning the participation in acts of suicide.

This article is a response to the article "A New Question in End-of-Life Ethics" by Strouse, Battin, Bostwick, et al. Their article in turn addresses an earlier essay on suicidal ideation and behavior in oncology patients.

The response by Pies et al breaks down their concerns into several key issues.

Dr Ronald Pies
The first issue is - What is legal vs what is right. Pies et al state:

The mere fact that some state legislatures have passed statutes redefining suicide, such that MAID is not suicide, does not prove that this redefinition is conceptually or ethically justified...

While redefining suicide averts legal liability for physicians providing MAID, it does not change the essentially unethical nature of the act itself. The term medical aid in dying fundamentally means helping patients kill themselves. This is why the American College of Physicians rejects the term and explicitly endorses the term physician-assisted suicide/PAS. Perhaps even more significant, following a comprehensive evaluation by the Council on Ethical and Judicial Affairs, the American Medical Association (AMA) House of Delegates rejected the term aid in dying and elected to retain the term physician assisted suicide in all AMA documents and references. Indeed, the process typically described as MAID in no sense aids dying; on the contrary, it rapidly converts an ill individual into a dead one. This is substantively different than the withdrawal of heroic but nonbeneficial or inappropriate measures, such as the use of ventilators that merely prolong the dying process in the final stages of a terminal illness.

Finally, statutorily declaring that self-induced death via a physician’s assistance is not suicide may soothe the consciences of legislators and allow payouts on life insurance policies; but, perversely, it may also incentivize some terminally ill patients to kill themselves.
Dr Annette Hanson
Pies et al then clarify that Taking One's Own Life is Suicide:
Redefining suicide to exclude PAS in the context of terminal illness represents a radical linguistic maneuver that flies in the face of ordinary language, expressed over thousands of years. The Latin suicidium—from which the English word suicide is derived—means the act of killing oneself intentionally or voluntarily. To be clear: we do not deny that there are often psychological and motivational differences between those with terminal illnesses who take their own lives and those who do so in the context of severe psychiatric illness, as the AAS statement details. But in both instances, the act is that of suicide.

As philosopher Gerald Dworkin, PhD, has put it

[A] s a philosopher, I feel an obligation to point out that, as a conceptual matter, there is nothing inaccurate or false about stating that a person who takes a drug, knowing that it will cause her death, and takes it because it will cause her death, is committing suicide on any reasonable conceptual analysis of what suicide is.
Dr Mark Komrad
They then discuss the issue of patients with Cognitive Distortions, who are not mandated to accept treatment:

Furthermore, most MAID laws do not require treatment for serious medical conditions, even when it is available to the patient. For example, a patient whose metastatic cancer stands a reasonably good chance of remission with aggressive treatment, but who nevertheless chooses MAID, is not required by state laws to undergo the treatment. Choosing assisted suicide in such a scenario may superficially appear to be a rational choice; but may instead represent a decision grounded in certain cognitive distortions that also characterize so-called conventional suicide. Importantly, this may be so, even in the absence of a diagnosed psychiatric disorder.

For example, Tomer T. Levin, MD, and Allison J. Applebaum, PhD, noted that some cancer patients may make erroneous assumptions, like, “No one can help me” or “No one understands what I am going through.” Such cognitive distortions may respond favorably to cognitive behavioral interventions and potentially avert or abort a request for PAS. Indeed, it has been found that “Requests for physician-assisted suicide are unlikely to persist when compassionate supportive care is provided.”

Unfortunately, in almost every US jurisdiction where PAS is allowed, no attempt to offer treatment by a mental health professional is required by law; and the psychiatrist’s role is typically relegated to ruling out mental illness and certifying competency for PAS.

Dr Cynthia Geppert
They then discuss why the Issue is not about intractable pain and suffering:

As Daniel P. Sulmasy, MD, PhD, noted, “Despite public arguments that PAS is needed to avoid excruciating pain and other symptoms, the reasons attributed to patients who seek PAS are not uncontrolled symptoms but lost autonomy, independence, and control.” These are forms of psychological distress which, in our view, are best managed with supportive and empathic counseling and/or cognitive behavioral interventions, provided to patients and their families—not by prescribing lethal drugs.

They then discuss the often forgotten but essential - Precautionary Principle:
This means erring on the side of caution and treating MAID requests from patients with terminal illnesses with the same degree of psychiatric scrutiny and concern that we would bring to any patient’s expressed wish to die. However, in most states, psychiatric assessment is not mandated in the MAID process and does not occur unless specifically requested by the evaluating physician who has initiated the MAID process.. This rarely happens. For example, in Oregon in 2020, only 0.8% of patients who were prescribed lethal medication were referred for psychiatric evaluation.

Moreover, the fairly subtle cognitive distortions described by Levin and Applebaum are unlikely to be detected in a superficial assessment of mental competence. It is no contradiction or paradox to argue, as we have, that pronouncing a patient qualified or competent for MAID is a violation of psychiatric ethics, since this unethically colludes with the process of aiding a patient’s suicide. Psychiatric involvement in end-of-life care is indeed essential, but it should remain well outside the procedures and processes involved in MAID deliberations.

They then discuss the stigma of suicide and how assisted suicide shifts it to "other" suicides:

Indeed, as numerous suicide prevention websites note: “Most suicidal people do not want to die. They are experiencing severe emotional pain, and are desperate for the pain to go away.” We would suggest that the same may be said of at least some individuals with cancer who seek MAID. Whenever complex ethical dilemmas are formulated as black-and-white categories, the many grey instances are often misclassified, with tragic consequences.

In short, the AAS position may have the perverse effect of merely shifting societal stigma from one group—those with terminal medical conditions—to those whose suicidal behavior occurs in the context of psychiatric disorders. We do not need such a 2-tiered classification, in which there are good and bad methods of taking one’s own life.

...We believe that efforts to promote MAID would be better directed toward destigmatizing the mental illnesses that underlie the majority of suicides and toward bolstering the availability of state-of-the-art palliative care.

Pies et al then conclude their article with the following statement:

Physician-assisted suicide is neither a therapy nor a solution to difficult questions raised at the end of life. On the basis of substantive ethics, clinical practice, policy, and other concerns, the ACP does not support legalization of physician-assisted suicide. … However, through high-quality care, effective communication, compassionate support, and the right resources, physicians can help patients control many aspects of how they live out life's last chapter.

More articles on this topic:

  • Psychiatrists must prevent suicide not provide it (Link).
  • 12 myths about assisted suicide and medical aid in dying (Link). 
  • Psychiatrists prevent assisted suicide not provide it (Link). 
  • Euthanasia and physician-assisted suicide are unethical acts (Link).