Showing posts with label Margaret Somerville. Show all posts
Showing posts with label Margaret Somerville. Show all posts

Monday, June 7, 2021

Can we find a vaccine for the euthanasia pandemic?

This article was originally published by Mercatornet on June 7, 2021.

Margaret Somerville
By Margaret Somerville

The Covid-19 virus pandemic is a threat to our physical and mental health and wellbeing, as both individuals and societies.

The euthanasia “virus” pandemic is, likewise, a threat to our physical and mental health and wellbeing, as both individuals and societies. Most seriously, it is a threat to our “human spirit”, the intangible, invisible, immeasurable reality that all of us need to find meaning in life and to make life worth living, that deeply intuitive sense of relatedness or connectedness to all life, especially other people. The “human spirit” does not require a belief in the supernatural. Everyone has a “human spirit”, whether or not they are religious.

Like the Covid-19 virus, euthanasia seems to be contagious, at least in post-modern, Western democracies. (Note: I use the word euthanasia to include medically assisted suicide.) Jurisdiction after jurisdiction has considered or is considering its legalization, although some have expressly rejected it. From one perspective, this spread is not surprising, because we know that suicide is contagious. In fact, general suicide rates — that is, exclusive of euthanasia — have risen in most and possibly all jurisdictions, which have legalised euthanasia.

As well, there is a well-established pattern, as we have seen in Australia, of pro-euthanasia advocates returning to legislatures and courts, time after time, until they achieve their initial goal of the legalization of euthanasia. Subsequently, as can be seen in the Netherlands, Belgium and, most recently, Canada, pro-euthanasia advocates persistently seek reduction of the requirements for its availability, that is, the initial safeguards, and expansion of the people who may have access to it.

In order to stem the Euthanasia pandemic, those of us who view this as a historic disaster and human tragedy must understand how it has arisen and where it is going. To do that we need to ask and seek answers to a multitude of questions. I can only very briefly mention a few of them here. I have spent over four decades researching and writing on them and still have many to address and new ones constantly emerge. We can think of this research as searching for an “anti-euthanasia vaccine”.

Before I do that, however, I want to emphasize that the people on both sides of the euthanasia debate are well intentioned and believe they are fighting for the greater good, it is just that we do not agree on what that is.

None of us on either side wants to see people suffer and the euthanasia debate is not about if we will die – we all will at some point. The debate is about how we will die and whether some ways of dying, namely euthanasia, are unethical and dangerous, especially to vulnerable and fragile people, and destructive of important shared values on which we base our societies.

We need to start our exploration of the euthanasia pandemic by asking the many questions, which could provide us with insights that will lead to understanding why the euthanasia pandemic has erupted and how we might deal with it. In the rest of this essay, I identify some of those questions.

Why now do people support legalizing euthanasia?

People have always become ill, suffered and died and, for millennia, our laws have expressly and clearly prohibited killing them, especially having doctors, who promise in their Hippocratic Oath “to cure where possible, care always and never to intentionally kill”, doing so. So why now, when there is so much more we can do to relieve pain and suffering, is euthanasia thought to be necessary and a good idea?

There is a perfect storm of causes functioning at all the levels of decision-making from that of individuals in relation to their own experience of suffering, to that of governments formulating health, social and public policy.

In post-modern societies, so-called “progressive values” have become ubiquitous. These values favour legalizing euthanasia and dominate the more traditional or conservative values, which oppose that. The progressive values advocates’ mantra is, “control, choice, change”.

Control. In the context of euthanasia, control translates to taking control of death. We cannot avoid death, but euthanasia allows a person to get it before it gets them. This eliminates uncertainty about the time, place and manner of death. It is psychologically difficult to live with uncertainty about outcomes that we dread, including because we do not know which psychological coping mechanisms we need to employ to deal with the fear we experience.

Taking control is what social psychologists call a “terror-reduction” or “terror management” device. Intense fear of death can be linked to a fear of mystery, the latter of which evokes profound free-floating anxiety. People who experience this can deal with their fear and anxiety by converting the mystery to a problem and seeking a technological solution to the problem. The mystery of death becomes the problem of death and the technological solution is a lethal injection – euthanasia.

Choice. Advocates justify euthanasia by claiming a right to choose to end one’s life, an overriding right to individual autonomy. “Intense or radical individualism” means the right to self-determination is given priority over any other considerations, such as what protecting the “common good” requires or the risks and harm to vulnerable people, such as fragile elderly people or those with disabilities. These harms include that euthanasia sends a message to them that they have “lives not worth living”.

Change. To have control and be able to choose death, the law must be changed to permit euthanasia.

Why has the pro-euthanasia case been so successful and the anti-euthanasia case so unsuccessful? *

The case for legalizing euthanasia is easy to make in contemporary post-modern Western democracies, especially those in which moral relativism and utilitarianism are the main philosophies informing the dominant worldview of a society.

Moral relativism takes a stance that nothing is absolutely or inherently wrong, rather what is right or wrong all depends on the circumstances and the individual person’s preferences. Utilitarianism in the context of euthanasia proposes that euthanasia is a means that has an outcome or end goal of reducing suffering and, therefore, can be justified and is ethical. The discussion and analysis of the impact of legalizing euthanasia is limited to only the present time – I call this restriction “presentism” – and its impact on the individual person who seeks it. What we could learn from our “collective human memory” (the past or history) and through employing our “collective human imagination” (the likely future outcomes of legalizing euthanasia) are ignored or rejected as irrelevant or invalid considerations.

The pro-euthanasia case is promoted and buttressed by stories of “bad” natural deaths – those where great suffering is experienced – and “good” euthanasia deaths – those where suffering is promptly and completely eradicated through the intentional extinguishing of life with euthanasia. The media, which overall has a bias towards legalizing euthanasia, are especially prone to presenting euthanasia as a topic for discussion in the public square in this manner, that is, with a focus on an individual suffering person and only taking into account the immediate impact in the present of providing that person with euthanasia.

The case against euthanasia is much more difficult to promote, not because it is weak – it is not – but because it is much more complex.

To convince people who do not believe that euthanasia is inherently wrong to reject it, requires looking, not just to the present, but also to our “collective human memory” for lessons from the past and to our “collective human imagination” to try to anticipate the full, wider and long-term consequences of legalizing euthanasia. Aboriginal and Torres Strait Islander people have much to teach us in these regards.

While the individual person and their wishes and respect for their right to autonomy are always important considerations, they are not alone sufficient, if we are to make wise decisions as a society with respect to the legalization of euthanasia or, if legalized, its governance. That requires, for example, taking into account the immediate and long-term, wider ramifications of authorizing physicians, and in some cases nurses, to end the life of another person through administering lethal medications with a primary intention to cause death.

These ramifications include the effects on healthcare professionals and the healthcare professions; on the institutions in which they practice, such as hospitals and aged care homes; on society and the shared values on which it is based and which create the glue that bonds us as a community; and even on our global reality. There is a dearth of literature in these regards. The 2021 book, The Other Side of Euthanasia, referred to above, recounting stories from frontline healthcare professionals in Belgium where euthanasia has been normalized as a way to die, makes an important contribution to starting to fill these lacunae.

Of particular concern in relation to the wider impact of legalizing euthanasia is the possibility of its being “thrust on” or “seeping into” the lives of fragile and vulnerable people – those who are poor, uneducated, or least vocal. For example, doctors in Belgium have admitted to euthanizing people in a coma on a ventilator, without any family present to defend their best interests. We cannot afford to trivialize or underestimate the dangers of the abuse of legalized euthanasia.

We must also keep in mind that in a secular society, such as Australia, law and medicine carry the value of respect for life for society as a whole. Euthanasia destroys their capacity to do that because the law is changed to allow intentionally taking life and medicine implements that permission in practice. If euthanasia is legal, it should be kept out of medicine and a new profession created to undertake it. Euthanasia is not medical treatment and it should have no role in palliative care. Indeed, the philosophical bases of palliative care – to live as well as possible until we die a natural death – and euthanasia – to choose death, rather than life – are in direct conflict.

It is also essential to recognize that the value of respect for life must be upheld at two levels: for the life of each individual person and for human life, in general, in society. Euthanasia damages respect for life at both these levels.

Good facts are essential for good ethics and good ethics for good law. This means we must ask, what are the correct facts about euthanasia?

Are pro-euthanasia advocates correct that euthanasia will be rarely used and there is no danger of “slippery slopes”?

Euthanasia advocates often propose that euthanasia will be rarely used and only as a last resort. Let us look at some recent Canadian statistics: “As of April 30, 2021 there has been 7549 reported assisted deaths in Ontario since legalization [in June 2016]. 7547 were euthanasia deaths (lethal injection) and 2 were assisted suicide deaths (lethal prescription)”.

This is very important information that cries out for in-depth research. What could this astonishing disparity in numbers between euthanasia and assisted suicide tell us? It is noteworthy that, so far, in the American states, which have legalised physician-assisted suicide, but have not allowed euthanasia, the number of such suicides are orders of magnitude below the Canadian statistics.

Might the explanation for the high Canadian numbers include that euthanasia masquerades as medical treatment and we trust doctors and assume they are acting ethically and only doing good? To wisely judge the acceptability of euthanasia, we must take the medical cloak off it.

Then there are the claims of pro-euthanasia advocates that legalizing euthanasia does not open up “slippery slopes”. Let us look again at Canada’s experience:

“The number of assisted deaths has been continually increasing in Ontario. There was a 33% increase in 2020 with 2378 reported assisted deaths, up from 1789 in 2019, 1499 in 2018, 841 in 2017, and 189 in 2016. Euthanasia was legalized in June 2016. Ontario euthanasia deaths have increased, in spite of COVID lock-down. …[There have been] 24,000 estimated assisted deaths in Canada since legalization”.

Again, these statistics show that euthanasia will not be used only rarely and is very quickly normalized, that is, the number of cases of euthanasia that occur once it is legalized, rapidly increase in a very short time.

This is not surprising. Once we step over the clear line that we must not intentionally inflict death, there is no logical stopping point. Currently around 5 percent of deaths in Belgium are by euthanasia, it is predicted that this number will increase to 25 percent within a few years.

The normalization of euthanasia and its frequent use, also opens up the unavoidable “logical slippery slope”, that is, once euthanasia is legalized the situations in which it is available and the people who may access it rapidly expand. Indeed, there is now discussion in Canada whether all restrictions on access to euthanasia should be abandoned. The argument is that the justification for euthanasia is respect for the individual’s right to autonomy and self-determination and this should not be limited. We can also see this justification being put forward in the Netherlands where the government is considering proposals that being “over 70 years of age and tired of life” or feeling that one has “a completed life” can be sufficient grounds to provide the person with access to euthanasia.

The pattern is that legislators who first approve euthanasia do so with “strict safeguards”, but these are quickly dropped and the people who can have access and in what conditions are greatly expanded.

As is already the case in the Benelux countries, Canada has now deleted from the MAiD (Medical Aid in Dying) legislation a requirement that “death be reasonably foreseeable”, on the grounds that it discriminates against people with serious disabilities, who are not terminally ill and want euthanasia. Canada is also legislating to allow people with early dementia to give advanced directives consenting to euthanasia to be carried out when they are incompetent to consent. In two years’, time, it will also allow people with serious mental illness, but no physical illness, to access euthanasia.

As American psychiatrist Dr Mark Komrad commented, “The proper role of a psychiatrist is to prevent suicide, not to provide it”. Moreover, some children will have access to euthanasia and a group of healthcare professionals at the renowned Toronto “Sick Kids” hospital has already published a protocol, which could govern this.

Examples of the “practical slippery slope”, that is, once euthanasia is legalized it is provided not in accordance with the law, are legion. One study of doctors in the Flanders region of Belgium who had euthanized patients found that, by their own admission, 32 percent had done so on at least one occasion not in accordance with the law. When this evidence is presented in other jurisdictions pro-euthanasia judges and politicians reject its relevance to their jurisdiction, by claiming that “our doctors are not like Belgium doctors”.

In summary, even though we might have lost the battle against legalizing euthanasia, our work is not over. We must now work to prevent its expansion and abuse.

Why is euthanasia euphemized?

In short, I believe it is because people do not want to face the reality of what is being done, intentionally killing a human being. We have natural inhibitions against killing other humans. Advocates of euthanasia even object to the words “assisted suicide”, arguing physician-assisted death is not suicide, and to euthanasia, saying it has harmful connotations and associations. They use terms such as Voluntary Assisted Dying (Victoria) or Medical Assistance in Dying (Canada) and reduce those to acronyms VAD and MAiD respectively, which have even less negative emotional impact. In the same vein of whitewashing what is involved, they speak of euthanasia as “the final act of good palliative care”.

Words, descriptions and labels matter. They activate or suppress many of our “human ways of knowing”, such as examined emotions, moral intuition, experiential knowledge and common sense, that recent research shows play an important role in decisions about ethics. Our choice of words is closely linked to whether we activate, what physician-ethicist Dr Leon Kass called the “wisdom of repugnance” to guide us.

Consequently, to argue, as I have on occasion, that “we cannot afford to have doctors killing their patients”, evokes a storm of outraged protest from pro-euthanasia advocates. However, if that is not what euthanasia involves, what does it involve?

Likewise, any mention of what we might learn from the Nazi doctors and the warnings that history (human memory) can provide triggers furious opposition. This is the case, even when one can show articles in the New York Times in the early 1930s describing the introduction of euthanasia by the Third Reich in Germany, which recount eerily similar justifications of euthanasia to those put forward today by the pro-euthanasia advocates. (See, for example, “Nazis Plan to Incurables to End Pain: German Religious Groups Oppose Move”, NYT 8 October 1933.)

Then the media’s role in promoting euthanasia through its “woke washing” of words and the ubiquitous post-truth reality of the early 21st century must be taken into account.

Recently I published an article hoping it might cause people to think differently about what euthanasia involves. The question I addressed was “Why, if one agrees with euthanasia, would they not support carrying it out by giving the person a general anaesthetic and removing their vital organs – heart, liver, lungs – for transplantation”?

Currently, 25 percent of lung transplants in Belgium are from euthanized donors and Canada uses such donors with their consent. In fact, it is reported that Ontario doctors notify the Ontario transplant authority in advance of planned euthanasias and the authority’s representatives call the patient – or family – to ask for consent to donating their organs.

In these cases, the person is first euthanized and then, after they die, the organs are taken. In my article, I questioned why combining euthanasia and organ donation into the same act, that is, giving the person a general anaesthetic and carrying out the euthanasia by removal of their vital organs, which results in more viable organs, was not employed. Many people, including those who support euthanasia, reacted very negatively to my suggestion and I explored the possible reasons for their reaction. They included that it would make organ donation seem horrific and cause people to reject donating their own organs after death.

I believe it was also that it causes us to we see directly, “unsugar-coated”, what euthanasia involves – doctors killing their patients. 

Why have so many politicians voted in favour of euthanasia?

We hear constantly that polls show that a sizeable majority of the public want euthanasia to be legalized and politicians might be trying to win these people’s votes. Whether the members of the public understand what they are agreeing to in supporting euthanasia is a further question, because surveys have shown that often they hold a mistaken belief that refusing life support treatment or its withdrawal or providing necessary pain or suffering management are euthanasia and, as we all do, they want these to be available. However, they are not euthanasia and are already legal and, appropriately used with no primary intention to cause death, are ethical, indeed, ethically required treatment.

Politicians are often reluctant to have to deal with matters that involve conscience and, for some people, religious belief, and when they must deal with these matters, they want to get rid of them quickly and with the least conflict and publicity possible, especially if an election is looming.

Might they just “read the wind” and, if the polls show voters want legalized euthanasia and its legalization seems highly likely, they just go along with that, whatever their personal values?

All postmodern Western nations are currently in a period of uncertainty about the nature and sustainability of flourishing democracy and, hence, of the ethical basis on which political decisions should be made, especially when they involve fundamental shared values on which these societies are based, such as respect for human life.

In the final section, I will suggest some possibilities regarding what we might be able to do to limit or discourage the use or extension of legalized euthanasia.

If euthanasia is legal, our goal must be to reduce to the minimum the number of people requesting it. In order to achieve that, we need to understand the reasons for their requests and to find ways to make those reasons no longer important to them. We also need to try to prevent extensions of the people who may access euthanasia and the abolition of safeguards, which restrict access.
Why do people ask for euthanasia?

Many people believe that pain is the most common reason that people ask for euthanasia, but pain is well down the list.

The three most common reasons are feelings of loss of dignity, loss of independence and of being a burden on others. Palliative care research shows many ways to change these feelings. For example, Dr Harvey Max Chochinov, a Canadian psychiatrist specializing in the care of terminally ill patients has developed a psychotherapeutic intervention called “dignity therapy”. In a book of that name, he explains how helping the terminally ill person to review and record their life story to leave as a record for future generations of their family gives them back a sense of their own worth and hope, through eliciting a feeling that something of themselves will have a presence in the future.

Hope requires a sense of connection to the future. Hope is the oxygen of the human spirit. Without it our spirit dies, with it we can overcome even seemingly insurmountable obstacles. Dying people cannot have long-term hopes, but they can be given mini-hopes that make life worth living.
How can we help dying people find a ‘why to live’?

Dr Chochinov speaks of a psychological state he calls “hopelessness” as being the trigger for the person seeking medical assistance to end their life. Professor David Kissane, an Australian specialist palliative care psychiatrist, has identified a similar condition he calls “demoralization” with its accompanying loss of the will to live, as having the same effect of triggering requests for euthanasia.

These findings are consistent with the powerful insight of Nazi Concentration Camp survivor, Victor Frankl, who famously said when asked how he helped other inmates to survive, “If you can give people a why to live, they can find a how”.

We all need to have hope and be able to find meaning in life, even when we are dying, indeed, especially when we are dying, if we are to have a “good death”. Euthanasia does not provide this, rather it eliminates the person and with that the possibility of finding hope and meaning. Helping dying people to find hope and meaning can be difficult and requires skilled carers interacting with both the dying person and their loved ones, which is one reason easy access to high quality palliative care is such an important safeguard against people choosing euthanasia.
What is the impact of ‘time compression’ on how we die?

We live in a world in which we expect instantaneous outcomes; we are not prepared to watch and wait. We have moved from primarily seeing ourselves as “human beings”, grateful for being alive, to becoming “human doings”, obsessed with what we can achieve in the shortest possible time. However, some experiences cannot be time compressed without destroying their essence. As the book, Euthanasia: Searching for the Full Story, powerfully demonstrates, dying is such an experience and not just for the dying person, but also for those who love them.
Who suffers when a loved one is dying?

When a loved one is dying, not only the dying person can suffer, but also those close to them. Much of the patient’s suffering can be ameliorated with fully adequate palliative care and even those who have asked for euthanasia may change their minds in that regard, when provided with such care.

It is appalling that a very large percentage of people, who need and could benefit from palliative care, do not have access to it – for example, studies have shown that is true for up to 70 percent of such people in Canada and, likewise, Australia. Especially if we believe that legalizing euthanasia is a terrible mistake, we must work to make high quality palliative care readily available.

Without access to good palliative care, accompanying a dying loved one can be a very traumatic experience, especially if they are in serious pain and there is poor pain management. It is easy to imagine that euthanasia could seem an attractive option in such circumstances. To remedy this situation, in 2010 the Declaration of Montreal was promulgated at a meeting of the International Association for the Study of Pain (IASP). It provides that for a healthcare professional knowingly and unreasonably to leave a patient in serious pain is a breach of fundamental human rights. The World Health Organisation and the World Medical Association have endorsed this approach, as have many national Pain Societies, including Pain Australia.

Despite how it is described by its advocates, euthanasia does not necessarily avoid the problem of the suffering of loved ones of the dying person. Accompanying a person we love who is dying through euthanasia can also be a very traumatic experience as I have witnessed first-hand.

I have a friend in Toronto whose long-term partner, a specialist physician, was diagnosed with inoperable metastasized cancer. He arranged for a physician friend to euthanize him only days after receiving this diagnosis. She and I were having lunch in a busy Bistro and she started to speak of her partner and his death. Suddenly she burst into uncontrollable sobs and kept repeating, “It was horrible, it was horrible! I couldn’t stay with him! I ran out of the room!”. I was shocked, because she is a highly respected professional woman, known for her strong emotional control in difficult circumstances, and is adamantly secular. She was clearly deeply traumatised by witnessing the euthanasia of her partner. The book referred to above, Euthanasia: Searching for the Full Story, recounts many similar narratives.

Why is it important to recognise the potentiality of euthanasia?

The potentiality of legalizing euthanasia requires that we consider what kind of world we will have left for future generations. Might it be one in which no reasonable person would want to live? What message does legalizing euthanasia send to vulnerable people – fragile elderly people and people with disabilities? It is that they have “lives not worth living” or, even more reprehensibly, that they, themselves, do not have any worth?

Paradoxically, euthanasia tells them that they lack dignity, when the pro-euthanasia case is that euthanasia is necessary to respect their dignity.

How will euthanasia affect healthcare institutions and professionals? We already know that many are psychologically traumatised by carrying it out, some developing PTSD. The Dutch Medical Society has recognised this problem and recommended, where possible, the use of assisted suicide, rather than euthanasia.

There has been a massive increase in Belgium in the use of “terminal sedation” (sometimes called “slow euthanasia”), where the patient is permanently deeply sedated until they die. (“Terminal sedation” needs to be distinguished from “palliative sedation” which is justified pain and symptom management, when means other than sedation are not sufficient, and there is no primary intention to shorten life.)

Moreover, what about respect for freedom of conscience of healthcare professionals and institutions, who believe euthanasia is unethical? This is a major field of conflict among a wide variety of people and institutions.
A momentous decision

I have been pondering a great deal lately about what we can do about stopping the “euthanasia virus” pandemic. What would vaccinate us, as both individuals and societies, against it? I have concluded that it is useless saying it is wrong or unethical or even dangerous and that we need a completely different approach, including along the lines of what we have to lose as individuals and societies by legalizing it.

Euthanasia is a very complex issue in terms of the forces that have led to the current situation, including such small yet hugely impactful changes as “time compression” – we expect everything to be instant. Applied to natural dying, which can take an extended period, euthanasia is the “quick fix”. I believe that the overall societal Zeitgeist has activated the push for legalized euthanasia and we have to change that Zeitgeist if we think, as I do, that legalizing euthanasia is a very, very bad idea.

I have written elsewhere that one step we need to take in order to move in that direction is to recover our sense of “amazement, wonder and awe” about both ourselves and our world. I believe that this experience will help to guide us ethically regarding what we should and most importantly should not do and the latter includes legalizing euthanasia.

I predict that History will see the decision whether to legalize euthanasia, as one of the two most momentous values decisions of the first half of the 21st Century. (The other decision is whether to allow the use of new molecular biology and genetic science and technologies to design our children and all their descendants, through alteration of the human germ line.) We need a new iteration of the old virtue of prudence, which can be re-named “wise ethical restraint”.

For all our sakes, both those who are dying and those who are not yet dying, we must kill the pain and suffering of dying people, not the dying people with the pain and suffering.

Note
* This section is an edited version of Margaret Somerville and E Wesley Ely, Forward 2, in Timothy Devos, Editor, Euthanasia: Searching for the Full Story: Experiences and Insights of Belgian Doctors and Nurses, Springer Cham, Switzerland 2020 pp. ix –xv. The online edition is available free of charge.

Monday, May 17, 2021

Normalising euthanasia can be dangerous: A Belgian nurse explains some of his experiences.

This article was published by Mercatornet on May 17, 2021

By François Trufin

Euthanasia: Searching for the Full Story: Experiences and Insights of Belgian Doctors and Nurses would be a bargain at any price, but it is free to download from the website of Springer, the publisher of many medical journals.

Euthanasia, though legal in Belgium, is opposed by some healthcare professionals. This collection of essays contains insights and thought-provoking stories from the authors’ professional experience.

The authors are ten Belgian health care professionals, nurses, university professors and doctors specializing in palliative care and ethicists who fear that euthanasia has become normalised and trivial.

Far from being polemical, the perspectives in this book present another side to the narrative of patient autonomy. As Margaret Somerville, an Australian bioethicist and Wes Ely, an American critical care specialist, observe in their forward, there is a dearth of literature about the societal ramifications of legalising euthanasia. They write that: 

“The case against euthanasia is much more difficult to promote, not because it is weak—it is not—but because it is much more complex. This case requires looking not just to the present but also to our ‘collective human memory’—that is, history—for lessons from the past and to our ‘collective human imagination’ to try to anticipate the full and wider consequences of legalizing euthanasia.”

The following is a selection of reminiscences by François Trufin, a hospital emergency nurse in Belgium.

Euthanasia, a stage in accepting one’s illness

A request for euthanasia is not the end of the road. We need to look at it as a new phase, among the other stages of grief, on the way to acceptance. At the end of this process, we hope that the person, with the help of the palliative care team, will be able to die a natural death, having lived their life to the full till the end. A patient who requests euthanasia is usually in the thralls of dread: fear of suffering, of dying, of being a burden… Euthanising them in that distress deprives them of the time to ease their worries and find answers to their questions. Furthermore, it confirms a failure and denies them the hope to overcome it.  

The health professional who is aware of this possible care pathway will no longer feel apprehensive around a patient requesting euthanasia; they will take them by the hand and walk alongside them to the end of the road.

[Once] a patient arrived in our department accompanied by her husband. She was about 50 and had so far been living at home, taking 32 medications a day. Convinced that she was a burden to her husband and her two children, she repeated day in day out: ‘Let me go, I want to die, please don’t give me any more medication’.

She attempted suicide four times. On the fourth attempt, she pushed herself down the staircase in her wheelchair. Her husband, who loved her deeply, was totally overcome. He was devastated at the thought that he could not prevent her throwing herself down the staircase. To the GP it was clear that she wanted to die and he referred her to the hospital for euthanasia.

When she came in her husband shouted: ‘Don’t let anyone get in our way, she is to be euthanised’. The team started to panic. I went to see the patient and we had a 4-hour conversation with husband and wife. We argued and as I was not agreeing to go ahead with euthanasia, he wanted to take his wife back home and have her referred elsewhere.

I told him: ‘The choice is up to you, but right now, your wife cannot be transported; any movement is extremely painful and we need to take care of her pain first. I guarantee you we will do all we can to make her comfortable. When she is, you can still decide whether you want her to be transferred in order to be euthanised’. Thus, the situation calmed down, the husband decided to leave his wife in our department and we worked together.

Seeing how, with the combined use of painkillers and controlled sedation, his wife rested peacefully in bed, he became convinced that palliative care was effective. A very tactile man, he appreciated the massages with essential oils we gave his wife. We encouraged him to bring the CDs they listened to together.

The two children, both young adults, followed suit, even though they were ill at ease at the start. They feared they might betray their mother’s resolve who had been adamant from the start that she wanted euthanasia. We reassured them saying that she was receiving no more medical treatment and we did nothing to prolong her life, only to make her comfortable.

This lady died peacefully in her husband’s arms, listening to the music they had played at their wedding. After a week, her husband came back, asking to see me. He thanked me with a box of chocolates… and asked whether I could keep a place for him in our palliative care ward when his time came!

The sad thing is that it took 32 medications and four suicide attempts for this woman to be heard and cared for, rather than be the object of therapeutic obstinacy. 

Euthanasia as a wake-up call from indifference 

During the Christmas holiday, a 75-year-old lady, whose convalescence after hip surgery was difficult, suffered several falls at home. Feeling relatively well but no longer able to live alone, she was placed in a nursing home—which happened to be cruelly understaffed—by her overworked children.

In the home for a whole month, she witnessed people being left in bed—even for meals—three or four days running during long weekends, for instance, when the staff was reduced. Sometimes residents’ cry for help to go to the bathroom would go unnoticed, and the like.

Fearing she might end up in a similar situation, she preferred to end her life right away. She stated her wish to the GP, completed the documents in due form, and was given the all clear to be euthanised. The nursing home sent her to the hospital.

Since she was not imminently dying, there needed to be, by law, a month’s delay between acceptance of the request and the actual euthanasia. During this time, she was cared for by our palliative care team, even though her condition did not warrant it. The psychologist saw her regularly.

When I overheard the following sentence, it rang like thunder to my ears: ‘Did you notice? I had to request euthanasia for people to start taking an interest in me’. Indeed, she had several visits a day, received proper care, saw the psychologist, some people would bring chocolates… Even people from the nursing home came to visit the star she had become. And this all came about after she had volunteered for ‘death’s corridor’. It was a very unhealthy situation where it appeared that requesting euthanasia became an ‘open sesame’ to receiving proper care and support.

That patient caused a professional electroshock for me! She made me realise how important those moments at a patient’s bedside are, when we give them our time to talk or even play cards, and simply to be human. Her experience spurred me to call together a group of volunteers who give of their time to go and sit at a patient’s bedside. It also taught me that, whether a euthanasia request comes from the patient or a family member, it is worth checking whether they want to test the medical world. I have been positively surprised to realise that when we say calmly: ‘No, we do not practise euthanasia, but we have something better to offer you’, people are willing to listen. And when we explain that pain will be relieved and that their quality of life is our main concern, the euthanasia request quickly fades away. Relief from pain and being treated as a human being is what most patients and families long for. 

When trust meets professional integrity

But I do not despair. Even if today many are trained for euthanasia, believing it to be a part of patient care, I am convinced that there will always be enough people to look reality in the eye and not run away from life’s tragedy. And I hope that they may discover by themselves what I was brought to understand.

One day I was travelling home after having dealt with a particularly difficult situation. I was in total turmoil, at the end of my tether . Driving home from the hospital takes me about half an hour, across beautiful scenery. That evening, the sun was highlighting the autumnal colours, and suddenly it dawned on me: ‘Fortunately nature does not react like us humans… What if the leaves said at the end of the summer: “I want to die. Soon, there will be no more  tree sap, so better end my life right away”. If this were the case, we would miss out on the autumnal beauty. As early as July many still green leaves would litter the ground and there would be none left to display their colours in fall.

The richness of autumn lies in the time leaves take to let the vital juice dry out and die. In spring and even more in summer, all the leaves are green, but in fall an extraordinary variety of colours is displayed.

Similarly, a human being in the twilight of life lets go of their masks and reveals their true self. In everyday life, running after time, we all have green leaves and, sometimes, it is not until the end of our lives that we realise that, beneath the green, there is a wide array of warm and exquisite colours.

Palliative care is the autumn of our life; it is the time the leaf takes to gradually detach from the tree. Even though the sun is not always shining and there are difficult times of heavy showers and wind storms, the leaf holds on to the tree with all the colours it has left. Could we imagine a year with three seasons only? Could we go from 35 °C in summer to -10 °C winter without any period of transition? No!… However, that is what happens with euthanasia’.

I have met all sorts of people during my career, from the humblest to those who are used to being in the limelight. For each and all of them, masks come down at the end of life. No doubt this is very difficult for the person, but it is also very beautiful to watch. They reveal their deep inner self and remind us that they are unique and irreplaceable. We see a person readying themselves to leave this life. For sure, their body is often falling to pieces, and their mind is slowed down, but what is being said, what is being experienced, is of a beauty and intensity that remind me of the autumn leaves…

François Trufin is a hospital emergency nurse. He is secretary of the palliative care platform of the Belgian German-speaking Community and Vice-President of the Belgian Chamber of German-speaking Nurses.

Friday, October 25, 2019

Canada’s euthanasia philosophy: ‘control, choice and change’

This article was published by Mercatornet on October 25, 2019

After having spent most of your professional life in Canada, you must have a special insight into its cultural tectonics. Why does euthanasia appear to have so much support there amongst doctors and the judiciary?


Margaret Somerville: 

Margaret Somerville
Recently, I read that the beginning of wisdom is to know when one should say “I don’t know”. Certainly, I cannot give you a comprehensive answer to this question.



What we do know is that approval of physician-assisted suicide (PAS) and euthanasia is highest among highly educated, high socioeconomic status persons -- sometimes described as “elites” -- in a society. Doctors and judges belong in this group, although I hasten to point out that far from all doctors and judges support euthanasia.

Those who do support it often adopt so-called “progressive values” on a range of issues including reproductive technology decision-making, abortion, same-sex marriage, and so on. “Progressive values” adherents are characteristically intensely individualistic – they give almost absolute priority to the value of individual autonomy, which can mean that they fail to take into account what is needed to protect the “common good” and, in particular, vulnerable members of the society. They also focus just on the present – they do not take into account warnings from history (“collective human memory”) or probable future consequences that can be recognized through “collective human imagination”. I call this approach to decision-making of excluding what considering the past and the future can teach us, “presentism”.

I’ve often described the mantra which informs progressives’ worldview as “control, choice and change”: They want control over what happens, especially to them personally; choice that accommodates the outcomes they seek; and the changes, for instance, in the law or cultural norms, that will make such control and choice possible.

Is there widespread popular support as well?

Well, there certainly seems to be in Canada, especially when we look at the statistics on how many people are using MAiD (Medical Aid in Dying the euphemism used for PAS and euthanasia in Canadian law). For example, in the Province of Ontario, as of 30th September 2019, 3,822 people accessed “assisted dying”, 3821 in the form of euthanasia, one assisted suicide. (It’s an interesting question as to why, in jurisdictions where both PAS and euthanasia are legal, PAS is very rarely used.) Accurate overall statistics for Canada are not available, but it’s estimated that 1.12% of all deaths now involve MAiD and is known that there have been over 8000 such deaths since its inception.

Initially, when legalizing euthanasia was being proposed and euthanasia advocates were lobbying for its legalization, I believe that many members of the general public – and even a substantial percentage of healthcare professionals - were confused as to what was and was not euthanasia, which inflated the statistics showing the public’s approval of euthanasia. Rights to refuse all medical treatment, including life-support treatment when this would result in death, and rights to fully adequate pain management, even if it ran the risk of shortening life, but was necessary to relieve pain, are not euthanasia, but many people classified them as such. This confusion was not, however, accidental; it was a strategy used by pro-euthanasia advocates to advance their cause through showing strong public support for legalizing euthanasia.

The idea of an end-of-life slippery slope is ridiculed by many politicians and doctors. But in the case of Canada, it seems relevant. What is the next development, do you think?

Canada is already considering whether to allow access to euthanasia to children, to people with serious mental illness but no physical illness, and to people with dementia through their advance directives. In light of the widespread normalization of euthanasia and the large number of people accessing it, I believe all of these expansions are likely to be allowed.

The reason such expansion is unavoidable is that once one steps over the line that says it is never ethically acceptable to inflict death on another human being, the sole exception being where that is the only reasonable way in which to save innocent human life, as in justified self-defense, there is no logical stopping point.

I have mused about the denial of slippery slopes by euthanasia advocates, such as Andrew Denton here in Australia, when it is so well documented that once introduced access to it expands rapidly. I realized that these deniers take an approach that there is no slippery slope if they regard any given expansion of access to euthanasia as a good decision, but only such a slope if they see the expansion as a bad decision, which seems to be a rare classification.

It merits mentioning that there are also doctors who initially supported the legalization of euthanasia who are now publicly speaking out against it. A prominent example, is Dr Yves Robert the registrar of the College of Physicians and Surgeons of Quebec (the medical licensing authority in the Province) who wrote an open letter under the College banner with the headline “Death a la carte” (that is a menu of choices among the options for how one wants to die) withdrawing his support for euthanasia.

Dr Robert was a major proponent of legalizing euthanasia and in 2009 the College was one of the main instigators of the movement to do so in Quebec. At that time, Dr Robert rejected anti-euthanasia proponents' claims that effective safeguards could not be put in place to regulate euthanasia. And, as in the current Australian debate, he accepted the usual claim of pro-euthanasia advocates that it would be rarely used. The estimate given by physician proponents, including the Quebec Minister of Health who was a specialist physician, was about 100 cases a year in the province. As can be seen from the Ontario statistics above that is very far from the reality which has emerged, including in Quebec.

Dr Robert changed his mind about euthanasia when calls were made to have “death on demand” declared a constitutional right. A very recent Quebec case that has struck down as unconstitutional the requirement that “natural death must be reasonably foreseeable” as a condition for access to MAiD is a step towards this possibility.

This claim that there is a right to “death on demand” is consistent with the arguments used to legalize euthanasia: that people have a right to autonomy and self-determination concerning their own bodies and lives.

In his letter, Dr Robert notes that opinion leaders and the media have denounced cases where people who do not fulfil the conditions for access to euthanasia in Quebec have been refused it. He also notes the paradoxical discourse that calls for safeguards to avoid abuse of “medical aid in dying” which are meant to limit its availability, while asking doctors to act as if there were no restrictions. He continues that if euthanasia is an unfettered right, then it’s not within the scope of “medical aid to die”, but simply “assisting dying” and he says the society must consider other options than involving the medical profession in that.

Dr Robert says that the law was a “major opening” to euthanasia and expresses surprise at how quickly public opinion seems to have judged the opening insufficient. In short, euthanasia has become normalized with astonishing rapidity and that has caused calls for access to it to be expanded, indeed, calls to have no restrictions at all on access to it.

The question that this development leaves us with is why so many Canadian doctors and lawyers of goodwill and professional integrity, such as Dr Robert, so adamantly disagreed that such expansion would occur.

Some Canadian doctors have suggested that euthanasia organ donation would be a good idea. Could you explain what’s wrong with that if the patient wants both to end his life and to give his organs? It seems like a good way to make the best of a difficult situation.

I have recently written an article dealing with this issue in The Linacre Quarterly, "Does It Matter How We Die? Ethical and Legal Issues Raised by Combining Euthanasia and Organ Transplantation".

For a variety of reasons I conclude that the ethical dilemmas are such that euthanasia and organ donation should not be connected in any way. These reasons include uncertainty regarding the definition of death which could be more critical in the context of euthanasia. Then there is disagreement about what constitutes conscientiously objecting healthcare professionals’ involvement in euthanasia. Would a transplant surgeon using organs from a euthanized person be complicit in the euthanasia of that person? Similarly, would the recipient of an organ from a euthanized person need to be told that and give informed consent to receiving that organ? And does connecting euthanasia and transplantation makes conflicts of interest for healthcare professionals unavoidable?

The reality is, however, that euthanasia and organ transplantation already are connected in Canada: the Ontario Coroner reported that the organs of 30 of the 3822 people who died by MAiD in the province were donated for transplantation.

Some suggestions are more radical, aren’t they? The patient would be killed by the act of donation, ensuring that the organs are as fresh as possible. Is this ethically worse than other forms of euthanasia?

Yes, there are more radical suggestions. Some people who agree with euthanasia and organ donation after death by euthanasia are arguing that death by donation is ethically acceptable. This would involve giving the person a general anaesthetic and carrying out euthanasia by removing their vital organs, such as the heart, to be used for transplant. Additional ethical issues raised by death by donation include breach of the “dead-donor rule” – that the person must be dead before removal of vital organs and the donation must not be the cause of death. Other considerations include what would constitute informed consent to euthanasia by donation and what impact its acceptance would have on important foundational societal values, especially respect for human dignity and for human life. 

It’s often mentioned that euthanasia patients might feel that their life becomes worthwhile by donating organs. Your thoughts?

That’s a possibility that I discuss in my article referred to above. It’s a sad thought that one is only valuable and has a purpose when one is dead. It’s true, as Ely Wiesel said, that people need a “why” to live, but surely we should not be promoting a “why” to die.

What can put a brake on the rapidly expanding boundaries for euthanasia in Canada?

Once the barn door is open and the horses have escaped shutting the barn door does not confine them, so I’m not at all sure that a brake can be put on the expanding boundaries of euthanasia in Canada. It will take possibly many generations for the full tragedy of the legalization of euthanasia to become obvious, at which time initially small voices will be magnified by others joining them and there could be a ground swell of opposition. Perhaps the reverse of how euthanasia has come to be legalized.
I sometimes think of the outrage of a young woman who made a lasting impression on me. She was born from artificial insemination by an anonymous donor and was searching for her father because she felt that “half of her was missing”. She angrily shouted at a conference panel of which I was a member, “How could society have allowed this? How could they have let this happen to me?” Societies came to see anonymous sperm donation as unethical. The law was changed in many jurisdictions to make anonymous sperm donation illegal. Perhaps the same will happen with euthanasia, except that, unlike that young woman, dead people are no longer able to shout at a society that authorized doctors to intentionally inflict death on them.

Does the Canadian experience hold any lessons for other jurisdictions – like the Australian states – which are debating whether or not to legalise it?

Yes and here are some that I would suggest:

Recognise that we live in a post-truth era, so the first lesson should be get the real facts. Good facts are essential for good ethics and good ethics for good law.

Move beyond making public and social policy decisions -- and there is no more important one than whether to legalize euthanasia -- only on the basis of respect for individual autonomy and its impact in the present.


I believe that if people have the facts on euthanasia and on its alternatives, and look not only to what individuals want, but also to the protection of vulnerable people and the common good, and take into account what human memory can teach us and human imagination tell us about future consequences, we will decide that legalizing euthanasia is a very bad and dangerous idea.

Professor Margaret Somerville taught medical law and ethics for nearly 40 years at McGill University in Canada. Few people are better qualified to comment on Canada’s embrace of euthanasia.

Friday, February 15, 2019

Can doctors be neutral on euthanasia and assisted suicide?

This article was published by Mercatornet on February 14, 2019. 

By Margaret Somerville

Margaret Somerville
The BMJ has recently published two articles, one by Dr Sandy Buchman, a palliative care physician and the incoming president of the Canadian Medical Association (CMA), the other by Dr Jeff Blackmer, a physician and vice president of international health at CMA presenting a very positive and benign picture of the implementation of legalized physician-assisted suicide and euthanasia in Canada, euphemistically called “Medical Aid in Dying” (MAiD).

Canadian Medical Association exaggerates its support for conscience rights.
As an academic medical ethicist at McGill University in Montreal for nearly four decades and now living and working in Australia, I am concerned that Australian legislatures, which are currently considering whether to legalize physician-assisted suicide and euthanasia, might accept the picture presented in these articles, without identifying their deficiencies.

In focusing only on respect for the autonomy and relief of the suffering, of an individual, personally identified, educated, mentally competent patient who requests and gives informed consent to MAiD, Dr Buchman makes the strongest case possible for the ethical acceptability of euthanasia and its legalisation. But, apart from other concerns, generalizing even these justifications beyond Dr Buchman’s patient and his specific characteristics and circumstances raises problems. In reality, how many people requesting euthanasia or assisted suicide (MAiD) will have the intensive attention, medical and family support Dr Buchman describes, or be as informed, articulate and highly educated as this patient, who himself was a doctor?

Respect for individual autonomy is used, as Dr Buchman does, by pro euthanasia advocates as a justification for legalizing MAiD. But it is far from the only consideration which needs to be taken into account, even if one does not object to MAiD on the most fundamental basis that we should not authorise anyone, let alone doctors, to intentionally inflict death on other human beings.

Dr Buchman makes no mention of any such considerations, in particular, risks and harms to the “common good” and society. These include breaches of the value of respect for human life at both the individual and societal levels, and serious physical and existential risks and harms to vulnerable people, especially those who are disabled and fragile elderly people.

Whether we agree or disagree with MAiD, we can all agree with Dr Buchman’s goal of relief of suffering, but we must kill the pain and suffering, not the person with the pain and suffering.

Dr Blackmer’s article raises a wide range of important issues, which he does not identify. They include: Is MAiD medical treatment? It can be argued that it is not. Likewise, MAiD is not, as its promoters argue, just a legitimate incremental extension of “good palliative care”. The informing philosophies of MAiD and palliative care are in conflict. Palliative care is based on a commitment to help people to live as fully as possible until they die a natural death. The informing principle of MAiD is that it is ethical to intentionally inflict death to relieve suffering or even the fear of future suffering.

Whether to legalize MAiD is a societal and political decision, not primarily a medical one and it’s suggested that if a society wants it to be available and legalizes it, for many reasons, it should be kept out of medicine. I call this “taking the white coat off euthanasia”.

By embracing euthanasia and assisted suicide as medical treatment the CMA made physician participation an expectation and refusing to provide them became an exception requiring justification. Despite assurances from the CMA leadership, Canadian doctors who object to participation in “therapeutic homicide” now risk discipline and even expulsion from the medical profession.

Euthanasia has been rapidly normalized and routinized in Canada at a rate that even one of its strongest advocates, Dr Yves Robert, registrar of the College of Physicians of Quebec, has found alarming, in that it has quickly become just another choice of how to die.

Not everything that is legal is ethical. So, the Canadian Medical Association could have maintained its long-established stance -- which reflects almost 2,500 years of medical ethics wisdom -- that it is unethical for physicians to participate in MAiD, even though it is now legal in Canada. When the cloak of medical approval is absent, the public are much more likely to question the wisdom of legalizing it.

Finally, while the CMA might be neutral with respect to who may be a member, in that it accepts as members both physicians who are pro-MAiD and those who are anti-MAiD, there is not, as Dr Blackmer claims, any “neutral stance” on the ethical acceptability of MAiD. In not continuing to oppose physicians’ involvement in it as unethical, the CMA is unavoidably supporting it in some or other form, which is not a neutral position. In fact, we can see precisely that outcome in the use of CMA statements by Canadian courts, legislatures and regulators in promulgating and implementing the law legalizing MAiD in Canada.

In short, there is no neutral stance on the ethics of MAiD but a clear choice to be made as to whether one is for or against it, as the present conflict among Canadian physicians so clearly demonstrates, despite the CMA’s and Dr Blackmer’s desire to whitewash the situation.

Margaret Somerville is professor of bioethics in the school of medicine at the University of Notre Dame Australia. This article was originally published in the BMJ Rapid Responses online.

Monday, August 13, 2018

Bioethics Professor calls on Australian Senate to reject assisted dying

Alex Schadenberg
Executive Director - Euthanasia Prevention Coalition

The Australian Senate was urged by a professor of Bioethics to reject the legalization of euthanasia.

Margaret Somerville
Reporting for the Sydney Morning Herald Dana McCauley wrote about the testimony by Professor Margaret Somerville, an expert on the Canadian euthanasia law, told the Australian Senate that:

the assurance by early proponents of euthanasia that it would not lead to a "slippery slope" had been proven wrong, with research showing that safeguards were being routinely violated. 
"In one study in Belgium, they surveyed doctors and found that 32 per cent had gone outside of the regulations," she said. 
While originally only available to consenting adults, voluntary assisted dying has in some countries been extended to young children, the mentally ill and even newborn babies. 
In January, a 29-year-old physically healthy Dutch woman with mental illness died after drinking poison supplied by a doctor in a medically assisted death.
The Australian federal Senate is debating a private member’s bill brought by Liberal Democratic Party senator David Leyonhjelm, which would enable the ACT and Northern Territory to make their own laws on voluntary assisted dying.

Friday, July 28, 2017

Euthanasia slippery slope: a failure of memory and imagination

This article was published by Mercatornet on July 28, 2017
When the splash of assisted-suicide and euthanasia blinds us to their far-reaching ripples.
Margaret Somerville
By Margaret Somerville

Very recently, two senior physicians who have championed the legalization of euthanasia in their jurisdictions, Dr Boudewijn Chabot in the Netherlands and Dr Guy Robert in Quebec, have rejected current “appalling” developments in euthanasia in their countries. Yet, these developments should have been anticipated. So, why weren’t they?

Pro-euthanasia advocates focus just on individuals and only in the present – a combination of radical autonomy/ intense individualism and “presentism” - which blocks out considering both lessons from the past and likely future developments. In other words, the pro-euthanasia stance rests on a failure of people’s individual and collective human memory and imagination.

Those opposing euthanasia look to human memory – history and what the past can teach us – and imagination – what the future might hold – as well as the present. They also look beyond euthanasia’s impact just on individuals to the wide-ranging and multitudinous major issues and consequences it raises for medicine and law, for practitioners of these two professions, and for all of us as families, communities and a society.

Human memory

Human memory warns us of the “slippery slopes” euthanasia opens up: The “logical slippery slope”, the situations where euthanasia is allowed constantly expands, and the “practical slippery slope”, euthanasia is undertaken not in compliance with the law.

Once euthanasia becomes normalized slippery slopes are unavoidable, because, as British moral philosopher Dame Mary Warnock explains, “You cannot successfully block a slippery slope except by a fixed and invariable obstacle”, in the case of euthanasia, the rule that we must not intentionally kill.

Pro-euthanasia advocates dismiss the nearly 2,500 year history of the Hippocratic Oath’s guidance of medicine – cure where possible, care always, never kill – and, especially, any lessons from the Nazi regime. No one believes euthanasia will lead to a second Holocaust, but as the distinguished Canadian historian, Margaret MacMillan, has said, without knowing the past, we deprive ourselves of an important source of understanding.

Renowned Canadian disability rights advocate Professor Catherine Frazee, who says that what happened to people with disabilities in Nazi Germany is “part of my history as a person with severe disabilities”, explains “that one key to tackling complex problems is to ask the right questions, and history, through its cautionary tales and analogues, is a rich vein of 'right questions'” to ask about euthanasia.

We can also look to indigenous people’s practice of looking to Elders past and present, to argue it is wrong and dangerous to exclude human memory from informing our important societal decisions, and legalizing euthanasia is clearly such a decision.

Psychiatrist Dr Boudewijn Chabot, a very prominent pro PAS-E advocate in the Netherlands, who has been called the “patron saint of euthanasia”, is horrified at what is currently happening in his country.

He’s not anti-euthanasia (he is prepared to accept tens of thousands of euthanasia cases) but aghast at the rapid rise in the number of people with psychiatric illness or dementia who have been euthanized.

Writing in a leading Dutch newspaper, Chabot says that “legal safeguards for euthanasia are slowly eroding away and that the law no longer protects people with psychiatric conditions and dementia.”

He recognizes “we are dealing with a morally problematic act: how do you kill someone who does not understand that he will be killed?”. And he concludes bitterly, “I don’t see how we can get the genie back in the bottle. It would already mean a lot if we’d acknowledge he’s out.”

Why did the Dutch not look to the past for warnings? Why did they fail to use their imaginations to foresee these future consequences?

We need to ask these questions in relation to vulnerable Australians, those who are elderly and fragile, especially those with dementia, people with disabilities, including newborn babies, who can also be euthanized in the Netherlands.

Human imagination


A failure to look to the future is resulting in an extreme example of calls for expansion of euthanasia unfolding in Quebec.

Dr Yves Robert, the registrar of the College of Physicians and Surgeons of Quebec (the provincial medical licensing authority) was a major proponent of legalizing euthanasia and in 2009 the College was one of the main instigators of the movement to do so. Euthanasia was legalized in December 2015.

Robert adamantly rejected claims that effective safeguards were not possible, that euthanasia was not a medical act, and that it should be kept out of medicine. He constantly referred to a “continuum of good end-of-life care”, which included euthanasia as part of palliative care.

As in Australia, the claim it would be rarely used (about 100 cases a year in the province) was made. The first year saw over 400 cases. (In the first 7 months, 21 of 262 cases did not meet legal requirements: in two the patient was not terminally ill and in one not seriously ill – she probably had a urinary infection.)

But none of that seemed to raise any questions for the College, or I assume Robert, about whether legalizing euthanasia had been a good idea.

Here is what has, as he explains in a letter dated 10 May 2017, on College letterhead, entitled “Death a la carte”. That is, instead of food choices, it’s a menu of options for how one wants to die.

There are now calls and possibly the launching of a court case to have “death on demand” declared a constitutional right. The claim is that having to fulfil certain conditions to have access to euthanasia is a breach of the right to control one’s life and body and legally actionable discrimination.

Claiming a right to “death on demand” is consistent with and just an extension of the autonomy arguments used to legalize euthanasia.

The discrimination claim is unusual: It’s discrimination against people who do not have disabilities because those who do have access to euthanasia and those without disabilities cannot.

Robert notes opinion leaders and the media have denounced cases where people who do not fulfil the conditions for access to euthanasia in Quebec have been refused it. Such denunciations and the refusals being characterized as 'cruelty' are familiar pro-euthanasia strategies.

Robert recognizes the “paradoxical discourse” that calls for safeguards to avoid abuse of “medical aid in dying” (euthanasia) which are meant to limit its availability, while asking doctors to act as if there were no such restrictions.

He continues that if euthanasia is an unfettered right, then it’s not within the scope of “medical aid to die”, but simply “assisting dying” and society must consider other options than involving the medical profession in that.

He explains it’s to transform “medical aid in dying” to “legally authorized aid in dying”, a form of assisted suicide which, he says, could be provided by private enterprise as in Switzerland.

Indeed, if society legalizes euthanasia, all euthanasia should be kept out of medicine. Specially trained technicians could provide it.

Robert notes that the Quebec law was “a major opening” to euthanasia and expresses surprise at how quickly public opinion seems to have judged the opening insufficient, when testing the law is still in the “apprenticeship phase and the application and consequences of its provisions are not fully assimilated.”

In short, euthanasia has become normalized with astonishing rapidity and that has caused calls for access to it to be expanded, indeed, calls to have no restrictions at all on access.

Robert concludes: “Let us take the time to reflect deeply before going any further. There is no urgency to die.” I totally agree but, to use a common saying, “it’s too late to lock the barn door after the horse has bolted.”

As for me, after being heavily involved in the euthanasia debate over many years in Quebec, to use another common saying, “you could have knocked me down with a feather” when I read what Robert wrote. That said, I applaud his honesty and integrity.

Why did so many doctors (and likewise lawyers) of goodwill and professional integrity, such as Dr Robert so adamantly disagree that such expansion would occur – although none of us expected a proposed expansion to this degree?

I believe it was a total failure of individual and collective memory and imagination, including professional memory and imagination, resulting in “intense individualism” and “intense presentism” governing the decision making and leading it astray. Let’s avoid that in Australia.

Margaret Somerville is Professor of Bioethics in the School of Medicine at the University of Notre Dame Australia.