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The Right to Physician-Assisted Suicide “The Montana Supreme Court ruled on Thursday that state law
protects doctors in Montana from prosecution for helping terminally ill
patients die. But the court, ruling with a narrow majority, sidestepped the
larger landmark question of whether physician-assisted suicide
is a right guaranteed under the state’s Constitution.” – The New
York Times By Kirk Johnson; Published: December 31, 2009 In
this paper I wish to examine what kind of general right a right to an available
medical service is, and what specific kinds of obligations it bestows on others
(i.e., physicians, nurses, pharmacists, and other health care providers), if
any. In particular, I will discuss the
right to physician assisted suicide[1]
because it engenders serious objection by those who believe it is a morally
wrong act which should not be done at all and which they believe therefore does
not bestow an obligation on health care providers to perform. In essence, I want to address the two
questions I believe are presented by the Montana case: 1) Does a dying person
have a moral right to hasten his/her own death? And 2) does a physician or
other health care provider have a moral right or a moral obligation to assist a
dying person who makes the request for medical assistance to hasten his/her
death? First,
the right to do an act does not necessarily mean the act is right to do. Nor does having the right to do something
necessarily mean others are obligated to help you exercise that right. There are rights that bestow obligations on
others, but not all do. E.g., the right
to certain liberties means that others have at least a prima facie obligation[2]
not to restrict your liberty; but the right to squander your talent and waste
your opportunities does not mean it is right to do that or that others should
help you do it. One might have the right
to stay in a hotel that has vacancies – thus bestowing a prima facie obligation
on the hotel to rent the room to you.
But a hotel corporation has no obligation to build hotels or extra rooms
in a town where you might wish to stay.
On the other hand, a right to a public education does bestow an
obligation on communities, not only to provide access to available facilities,
but to provide the resources and make certain there are such facilities
available for everyone who is entitled to the right. Second,
rights are not necessarily absolute in a simplistic way. Freedom of speech does not make it right to
say just anything any time one wants to no matter what the consequences. Freedom to travel does not necessarily mean
free tickets on trains or airplanes; nor does it mean freedom to drive drunk. Freedom in general does not mean serious
crime, such as murder of innocent people, is allowed or that imprisonment or
capital punishment is necessarily wrong for those who commit it. Liberty is not
an unrestricted, “absolute” right. I
will try to make the case here that the right to specific medical treatment is
right to exercise under and only under particular kinds of circumstances, and
that it bestows obligations on health care providers under, and only under,
particular kinds of circumstances. Thus,
even if the right to physician assisted suicide were to be a constitutional
right, I will try to show that does not mean it is either right in all kinds of
circumstances or that others are obliged to provide it in all kinds of
circumstances, though it may be right and obligatory in some kinds of
circumstances. Third,
medical necessities, like any other necessities, are not always possible or
feasible to meet. So no matter how
desirable or important medical care is, it is not always available, and thus
the right cannot always be exercised. Clearly
one does not have a right to medical treatment that is not available or
possible or reasonable to receive. One
cannot expect a liver transplant if there are no voluntary donors available, if
there are no surgeons available to perform it, or no adequate facilities
available in order to perform it. To
the extent it is a political/governmental matter of how much resource to devote
to providing medical training, equipment, and labor for any particular area,
medical necessities will compete with other necessities for finite resources. I do not wish to try to argue here for some
order of economic prioritizing of necessities.
I do think an interdependent[3] society
of relatively affluent means should rank making medical treatment (and other
necessities) available for all above making available luxuries and
conveniences, but in a free society, the social/governmental means for doing
that should normally be ones of motivation and incentive (whether through moral/emotional/psychological
exhortation and/or financial means) rather than through legal demands or
requirements. The main point though is
that medical treatment is not normally necessarily the kind of right that takes
resource and labor priority over all other rights in the way, say, that a war
for self-defense against annihilation might.
The only time it might have such an economic or labor and resource
allocation priority would be in the case of a seriously debilitating,
disabling, or deadly, widespread epidemic or pandemic that puts everyone at
risk.[4] But
the sociopolitical, economic issue of what services ought to be readily
available is beyond the scope of this essay, and that is why I am limiting the
major portion of it to the rights and obligations involved in readily or feasibly
available medical services which could readily be performed if allowed, and if
available health care providers are willing to perform them; services for which
there are no economic or practical impediments, but at most only moral or
personal ones. Fourth,
even if an act is wrong, people might still have a moral right to be the ones
to determine whether to do it or not in those cases where autonomy is more
important than consequences. E.g., while
one should not let a three year old determine whether it is safe to play near a
busy street or best to go on a total ice cream diet, it may be preferable to
let him/her wear his/her choice of outfits to preschool even if they may be
somewhat embarrassing or foolish rather than to demand s/he wear what you want. It may be better to allow children and others
to make harmless errors than to control their every action. It may be better for a society to be relatively
free rather than to be a police state, even if a free society has a possibility
of serious crime that a police state would prevent. Furthermore,
governmental decisions are not always better than personal ones, and in some
cases it might be better to allow any errors to be made by the person most
directly related and/or affected by the decision, rather than by someone else,
particularly someone in government or a hospital board who may not sufficiently
appreciate the patient’s feelings and beliefs.
E.g., while it might be wrong or a mistake for a particular person to be
removed from life-saving medical technology, it might be a morally preferable
to allow the patient to decide in consultation with the physician rather than
to require a court or legislature to decide such cases, particularly if the
latter are as likely to make errors as the individual. It is perhaps better that a person be a victim
of his own mistakes than a victim of someone else’s. The government might want to make sure that
the physician, or a patient advocate, has some training to make, and to help
patients make, morally reasonable decisions, or the government might require a reasonable
methodology to try to insure truly knowledgeable and informed (not just formal)
consent by the patient that includes all the relevant considerations s/he
should take into account. But beyond
something like that, it is reasonable to believe that combined
patient/physician autonomy is better than government regulation or control,
unless it turns out to allow for a kind of abuse of patients that would be
important for government to prevent. If
such an abuse were uncovered, government’s role would be to eliminate it
without thereby taking control of the decision-making process itself. I will say more about a reasonable
decision-making process later. The
real questions are 1) what circumstances, if any, make it right for a patient
to receive voluntary assistance from a health care provider in dying – whether
it is a) the passive help of dying from the condition by removal of medical
treatment or b) active assistance in dying from the application of a treatment
that will hasten death, and 2) what circumstances, if any make it obligatory
for an available health care provider to honor a patient’s request for such
assistance. Resources for this sort of
thing are not usually a problem, since non-treatment requires relatively little
cost or medical skill, and since actively assisting dying also requires relatively
minimal cost or medical skill. There
are bad rationales given on both sides of these issues, and I wish to consider
them first: 1)
One is “playing God” when one helps someone die. That is true, but irrelevant, since one is
“playing God” by thwarting death or illness also, and in particular, one is
“playing God” in the kind of cases under consideration by not helping someone
die when they want to and instead forcing them to stay alive and have to suffer. There is a great line in the movie Something the Lord Made, where a priest
is arguing with the surgeon who is going to attempt the first open heart
surgery, in this case on an infant. The
priest says the surgeon should leave the baby’s life in God’s hands and not
tamper with it. The surgeon, certain
that the baby will die without medical intervention, says that although God may
want to kill this child, he would prefer to save it. In terms of being responsible for the
outcome, one is playing God either way, since the option of what to do is
within the power of the people making the choice. The issue is not whether one should take the
responsibility, since one has the responsibility already either way. The issue is which option should one choose, not
whether one should choose an option. One
does not eliminate a choice or responsibility by ignoring it or pretending it
does not exist. 2)
One should not hasten death because one should not intervene in the dying
process. That “begs the question” which
is whether intervention is right or not in particular cases. It doesn’t help to say “there should be no
intervention because there should be no intervention”; that is just circular
reasoning. Moreover, it seems false or
there would be no point in the practice of medicine at all. Medicine is
an intervention. The idea is to intervene, though normally it is to keep the
patient alive. But that is because it is
normally considered that life is a good thing, if not only in itself, but as a
means of being able to experience other good things such as joys and pleasure
or insight and knowledge. Unfortunately,
medicine has reached a point where it seems there can be life without its being
any good. If so, medicine’s role in
preserving life may have only been a special case of the general case of
preserving the benefits of being alive. When there are no such benefits, and when only
harms exist, then the obligation to preserve life would no longer be in effect.
Also, medicine has ostensibly always had
two roles: a) prolonging life and b) preventing suffering. Unfortunately, in some cases those two roles
conflict with each other because only death can alleviate certain kinds of
suffering. One must then decide which
role has priority, and there is no obvious reason preserving life should be
more important than alleviating suffering in all cases. Clearly, under normal circumstances,
alleviating suffering trumps hastening death; one doesn’t euthanize a patient
for a case of intestinal flu that makes him wish he were dead. But in certain end of life cases, the
priority is not obvious. 3)
Life is a miracle and an unqualified good.
Life does seem to be special and miraculous just in its complexity alone,
but not to be an unqualified good.
Certainly we try to eradicate some viruses and bacteria or living things
(e.g., cockroaches, rats, and rabid animals) that endanger human life. But even human life is not an unqualified
good, whether miraculous and special or not.
We do not create all the humans we could, particularly if we do not
think we can give them and us an adequate quality of life. If people could be indefinitely kept alive
only by a means that allowed them to experience incessant pain and suffering
and nothing else, I doubt many people would knowingly opt for that. A permanent
living hell is not much better than hell in death. Life is good as a means, not an end in
itself. 4) A
health care provider should not be forced to violate his/her conscience. That is only true when one’s conscience is
either correct or where the right act is not able to be adequately determined,
and one of the possibly right options remaining is the one the health care
provider’s conscience holds. We are trying to determine here what the
conscientious decision ought to be, in order not to follow a “mistaken”
conscience. 5)
The patient should be able to decide what is best for him/her. People do not always do what is in their own
best interest. They are not always right
about what is in their own best interest.
They do not always act either rationally, wisely, or with full
understanding of the consequences – even when they are able to state the
consequences. Sometimes temporary
despondency creates mistaken priorities and choices, that one would realize and
regret if given the opportunity to experience both options. Unfortunately death is not a reversible
option. There are times that one should
not make permanent choices to solve temporary problems. Clearly teen suicide over a romance breakup
is not legitimate grounds for suicide.
Neither is refusal of necessary treatment while in despair and pain from
a bad automobile accident an autonomous choice that should be honored. The decision to drive drunk should not be
honored by those who can prevent it. In
many cases, “mental competence” is the determining factor for honoring patient
autonomy, but “mental competence” in general is not the right criterion; a
mentally competent person can make a terrible decision in any particular case. The question is whether the particular
decision is fully informed and made rationally and without undue influence by
temporary or blinding circumstances. And
the follow-up question is whether there can be a moral and practical feasible
way to determine that. 6)
The right to die with dignity. Supposedly
somehow dying by choice of time and method allows one to die with dignity, as
exemplified in the comment by Justice James C. Nelson in a partly concurring
opinion in the Montana Supreme Court in the above case (quoted in the same NY Times article): “This right to
physician aid in dying quintessentially involves the inviolable right to human
dignity — our most fragile right.” I am
presuming that the impetus behind this claim is the desire to avoid needing a
significant amount of help in performing normal functions, particularly messy bodily
functions, as the body (and sometimes the mind) deteriorates in a prolonged
dying process. I take this to be a form
of emotional or mental suffering that is part of what one wants to avoid by
dying, since it cannot be avoided otherwise at this stage of medical
science. Many people don’t want to be
helpless (“don’t want to be a burden” as it is often put) or to be embarrassed
by uncontrollable and/or unsightly physical symptoms and effects of their
deterioration. They don’t want to endure
help with pressure sores, with breathing, with uncontrollable
eliminations. They don’t want to be
poked and jammed with needles or tubes.
They don’t want to be dependent on machines to which they are hooked
up. They don’t want to be seen or
“remembered” by loved ones in that state. There
are two replies to this, however: a) the acute sense of embarrassment and fear
about that sort of death perhaps can be overcome without having to resort to
death as the only remedy. The dignity argument
is not about the deterioration itself but about the fear and embarrassment or
seemingly shameful loss of independence the deterioration and physical
treatments for it causes. So even if
current medical practice cannot prevent the deterioration, there is no reason
to believe the fear and embarrassment cannot be minimized or avoided. And more importantly b) as a type of
suffering that is desired to be avoided, the rebuttal I will give shortly to “the
quality of life” argument will apply to this
argument as well. 7)
The quality of life argument. This is
the claim that when life becomes painful or unhappy past a certain point, it is
better to end it than to continue to suffer or to have to face and endure even
worse suffering. The suffering involved may
be either physical pain or emotional pain, as in the embarrassment and distaste
for being a burden in the above “death with dignity” argument. This argument needs clarification, however,
and it will not stand up as it is normally conceived upon such clarification. There
is a difference between pain and suffering, in that pain may cause suffering
but need not. One can ignore pain or at
least not be so focused on it that it prevents one from doing things which are
enjoyable in spite of the pain. One can
have pain without “suffering” from it other than in the sense of just having
it. “Yes, Mary is in a lot of pain but
she doesn’t let it hold her back or get her down” is a typical way of
expressing the difference between having pain and suffering from it. As to suffering from indignity, many mothers
have said after the experience of having babies that “once you’ve had a baby
and experienced all the doctors, nurses, medical students, residents, etc. that
see you and examine you you quit being embarrassed by some sort of sense of
modesty about being seen naked that you had before.” This is just one example of how embarrassment
can disappear. Another kind of case is
where one gleefully tells others later about their most embarrassing moments –
telling the stories with humor and without any embarrassment. Many of these stories are about medical
moments that were terribly embarrassing or scary at the time, sometimes even
physically painful. Sometimes the right
word by a health care provider can even avoid the embarrassment and minimize
the fear and to some extent even the pain.
When I went for a barium enema once, a young nurse or physician
assistant or tech was in charge of my preparation. Upon introducing herself, she said to me “For
the next half hour, I am going to be your best, and most intimate friend.” That immediately reduced all my anxiety
because she defused the embarrassment and showed compassionate
understanding. One does not have to lose
dignity just because one is in what seems like it will have to be a most
undignified situation. Furthermore,
embarrassment and disdain are often arbitrary, culturally induced
phenomena. If a society venerated age in
the way ours worships youth, it would not think any more badly of the
infirmities of age than it does of the infirmities of infancy. If we respected the accomplishments and
wisdom in older people’s pasts as much as we anticipate the potential
accomplishments in babies’ and toddlers’ futures, there would be no
embarrassment or disdain for again needing help to live. So
rather than expressing the “quality of life” argument in terms of pain or loss
of dignity or emotional/psychological embarrassment or discomfort, it should be
stated in terms of suffering, since suffering is what we really want to avoid
when possible. But then the problem is
that suffering by itself is hardly grounds for dying. We suffer all the time without seeing the
need to be euthanized or to commit suicide over it. And most likely for most people, even people
of significant financial means (some of whom commit suicide), if they had to
add up the amount of time they spent suffering (or being unhappy or
dissatisfied) versus the amount of time they spent happy, the balance would be
staggering on the side of unhappiness and dissatisfaction. Yet most people don’t want to kill themselves
over that. They don’t want to die
because they have to fill out their taxes or pay them. They don’t want to die because they have to
go to some boring event with a spouse.
They don’t want to die because they have a cold or a backache. They don’t want to die because they played a
lousy round of golf and lost a bet. They
don’t want to die because their favorite team lost an important game. They don’t seriously want to die (even if
they are very depressed or sad) because they went through a bad divorce or
breakup. They don’t want to die because
they have a long day at work that will be boring and then have to come home to
do family chores that are not particularly interesting or exciting. Even in mourning the loss of a dearly loved
one, most people don’t seriously want to die immediately even though they may
feel the loss very sadly and deeply. There
is, of course, a point at which suffering becomes so burdensome and so
unbearable that death would be better, but it is not a matter of “quality” of
life in the sense of relative quantity of happiness over misery or sorrow, or
of having any unalloyed joy or happiness at all. Life can be most hard and difficult and yet
people can and usually do want to live in spite of that. They may welcome death as a way of finally
achieving peace, but yet not seek to hasten it – not just as the philosopher
David Hume pointed out in his Dialogues
Concerning Natural Religion because people fear death, but because they find
that in spite of all their suffering, their lives are worthwhile to them. There are things and moments they want to
experience and find some sort of joy in anticipating and experiencing, even
though temporary and not devoid of their other suffering. It might be anything from wanting to live to
see a grandchild born while one is dying a terrible death to wanting to figure
out some problem that one has become focused on and perplexed by. It
could be something as “trivial” as wanting to see whether one’s team wins a big
game or as important as seeing one’s life work come to a kind of fruition or
recognition one had always hoped for and sought. It might be wanting to hold or to be embraced
by a loved one or to have some meaningful conversation. Even the end of life can have hopes and dreams
and moments that make it worthwhile in spite of all the suffering one has to
endure. It is only when all that is finally lost and impossible
to have restored or replaced or to achieve again, that life becomes not worth
living, and dying may be a reasonable remedy for the suffering one would
otherwise endure, but only if also one chooses to die under such circumstances.[5] It
is, of course, murder to kill someone innocent who wants to live, even if s/he
has nothing for which to live. There are
two criteria, on my view, for making it morally right to assist someone in
hastening their death: 1) there must be nothing possible for which they would
want to continue to live in the condition they will be (i.e., nothing that makes
their living and suffering worthwhile), and 2) they want to hasten their death
in the way and time the physician is to assist. But
that circumstance is far rarer than the ones usually described as lack of
quality of life, which are normally those end of life circumstances where there
is pain one is so focused on that despondency and hopelessness make one forget
or ignore the possibility of looking forward to something worthwhile in a way
that is not just verbally or conceptually understood but is felt in the
emotions with anticipation and attention.
Many times we try to talk dying patients into having hope or telling
them there are things yet for which to live, rather than fostering the desire
for something that they can look forward to experiencing or concentrating their
attention. Arguing people into wanting
to continue to live seldom works. There
are more emotional, psychological, and educational ways one has to foster
attitudinal changes and give one something to anticipate[6].
There can be reason and desire to live for another day or a few more hours,
just as there can be reason to live for fifty more years. Yet we somehow feel that it is okay for a
terminally ill person to hasten their death (with physician assistance) but
know it is wrong for a teenager to commit suicide while despondent. I think that is because we believe the
teenager will still have time to find something that makes life worthwhile, but
we mistakenly think that a despondent terminally ill person who is suffering
cannot be helped to find something for which to live in the little time s/he
has remaining. In states and countries
that allow physician assisted suicide, the patient’s condition must not only be
terminal, but their natural death must be somewhat “reasonably” immediate. That is, having only two years to live is not
normally grounds for immediate physician assisted suicide. Much of value can occur in those two years,
even if a cure or treatment that will extend the time before death is not
found. But it seems to me that “time
remaining” is not the relevant factor.
The relevant factor is whether it is possible or likely for the person
to find (or be helped to find) something worth living for that makes up for all
the suffering they have to endure – that somehow redeems their suffering. That is what makes life valuable in general,
and I see no reason it should be any different in the last few days than it is
when one seemingly has all the time in the world. With
all the above as background, I now turn to the two questions: 1) Does a dying
person have a moral right to hasten his/her own death? And 2) does a physician
or other health care provider have a moral right or a moral obligation to
assist a dying person who makes the request for medical assistance to hasten
his/her death? The
first answer to the first question is that whether one should have the right or
not is not as important as whether it is right for the person to exercise it in
a particular case. There are specific
senses in which it might seem one does not have a right to suicide; for
example, if one takes out an insurance policy that excludes payment of the
death benefit for suicide (in the first year of the policy, for example), then
one has no right to commit suicide in order to collect the death benefit. But more precisely that means one does not
have a right to have the death benefit paid if one commits suicide; and so one
may still have the right to suicide. Or
if one wishes to commit suicide to abrogate some sort of legal agreement, there
may legally and morally be no such right.
But again, more precisely put that just means one does not have the
right to abrogate the agreement that way, not that one does not have the right
to commit suicide. But
I think a case can be made that if suicide is wrong in a particular case, then
one does not have the right to commit it.
For example, if one is merely temporarily despondent, then others have a
right to try to prevent it, and are not culpable for doing so. Thus one does not have a right to commit
suicide in such a case, for actual rights (as opposed to merely prima facie
rights) cannot justifiably be
violated by others. If suicide were a
right, it would be immoral for anyone to prevent a wrongful or mistaken suicide
– which might be considered, for example, to be one that if not committed, the
person was later glad s/he had not done.
I
believe the question of the right to commit suicide only arises in certain
kinds of cases: those in which the suicide may be right because (if I am
correct about all the above) 1) there is no possible way to make the suffering
one has to face for the remainder of one’s life in any way worth having to
experience; i.e., the suffering is not
in any way redeemable, and 2) the patient wants to, and chooses to, hasten
their death in the time and manner that is to be provided. The
practical question then is whether and when the patient has the right to make that determination and thus to commit
suicide. I think the patient should have the prima facie right, meaning that
without some reason to the contrary that would either change the patient’s mind
or clearly convince reasonable, compassionate, sensitive, knowledgeable, and
understanding people the patient is mistaken and will feel differently later,
the patient’s wishes should stand. That
means it cannot be a bureaucratic matter decided by either government or some
sort of formal board somewhat removed from the patient and his/her condition
and feelings. And it cannot be a panel
made up of people who do not understand that suffering can be endured for a
greater purpose even in this earthly existence and who are thus, unfortunately,
willing to terminate the life of anyone who is in pain or poor conditions. Surveys show, for example, that even health
care providers rank the quality of life of disabled patients far lower than the
patients will eventually rank their
own quality of life, and so even health care providers may sometimes be willing
to discontinue life-saving treatment prematurely at the time of the injury when
the patient is distraught and despondent.
Hastening death is a decision that requires knowledgeable, sensitive,
impartial, unbiased judgment, and is not likely subject to formula or to panels
or judges who simply have good intentions. Suppose
then there is a particular patient who has a right to hasten his/her death, and
that has been duly and properly determined.
The question then is “does a physician or other health care provider
have a moral right or a moral obligation to assist a dying person who makes the
request for medical assistance to hasten his/her death?” It
seems to me that if the health care provider can hasten the death in the
compassionate and relatively non-suffering way the patient desires, that s/he
should have every right to do so, as should anyone who is asked to help do
something that is right, in a manner that is right. I believe that normally it
is wrong to restrict people from doing what is right. But that is only true if the person assisting
does not have a real prior, or overriding, obligation that would preclude
him/her from assisting. For example, I
believe it is policy in the United States not to draft into military service a
sole surviving child of parents who have lost their other children in military
action. I could be mistaken about that
being a policy, but it is easy to imagine there could well be such a policy if
there isn’t. The reasons for it would be
not to add further to the grief of parents who have already sacrificed (more
than) their share of the conflict being waged, and also the utilitarian benefit
of the surviving child’s being available to contribute to the parents’
financial and practical well-being and care.
If service in the military in this particular conflict is right, then it
would still be wrong for the last child to be allowed to serve, if s/he has
obligations to his/her family. Or
consider a much more trivial example of the same principle. There are occasions in driving or in standing
in a line where it might be right for another driver to seek to “cut in” without
waiting his turn. If you have time and
can let him/her in front of you, that would typically be a right you would
have. However, it is not your right to
do so if there are people behind you who have not consented to let the person
cut into the line. What
I don’t think should count as a prior obligation is a mistaken or unreasonable
agreement not to provide help in a case where someone needs assistance to do
the right thing. For example, suppose
you promise to take your children to the zoo on a given day, and that it is
right for them to go to the zoo. But on
the way there, the car in front of you gets into a horrific accident, and you
are needed to help in a way that will be time-consuming (perhaps looking after
children of the injured driver, or going with the injured person to the
hospital, etc.) and prevent you from keeping the promise to take your children
to the zoo. I would argue that it is
right for you to break the promise. The
promise was a prima facie obligation, and circumstances arose that overrode it. If physicians took an oath not to hasten
death, that should be regarded as merely a prima facie obligation that can be
overridden by circumstances where death should be hastened, that may not have
been recognized or considered at the time the oath was written or taken. Now,
some argue that if physicians take part in the activity of hastening death, it
would undermine patient trust, and cause more harm overall than the amount of
good that might be caused in a particular case of assisting a patient’s
suicide. I see no reason to think that
particular reason will stand up because I think people understand that there
are safeguards in place for it, and that they would have to request having
their death hastened. Moreover, people
today do make out “living wills” stating their preferences – often asking not
to be put/kept on extraordinary life-saving measures. People also ask for DNR (do not resuscitate)
orders. And none of these people then
fears being euthanized by their physician for a sore throat. And in another instance that is somewhat
similar, people trust veterinarians with their pets without fearing that the
pet will be euthanized on the whim of the veterinarian, even though
veterinarians do euthanize animals. I do
not believe this particular objection will stand scrutiny. It
is also held that doctors should do no harm, but that is not true for surgeons
or for those who give injections of any sort that cause pain or medications
that have unpleasant side-effects. Some
chemotherapy causes a great deal of harm, for example. True, they are not doing (or they are at least
trying to prevent) overall harm, but
they are still doing harm, though for a good reason. If hastening death is the
only way to alleviate non-redeemable suffering, and if alleviating such
suffering is a right of the physician, then it is a case of utilitarianism
where the means can justify the end in the same way that amputation or
disfiguring surgery can be justified by the fact it saves or potentially saves
the patient’s life. Only in this case,
this saves the patient from pointless terrible suffering rather than from dying. If
the above is correct, then health care providers will have a moral right to
hasten the death of patients when such a death itself is right, unless there is
some particular obligation a particular physician may have to the contrary,
that will stand scrutiny. But having the
right to do something that is right does not mean one is obligated to do
it. For example, one has the right, if
one is at the end of a long line, to let as many people as one wants cut in
front of him or her. But one has no
obligation to let any of them in; and certainly one has no obligation to let
all of them cut in, even if one has a full basket of groceries, and each of the
people asking to cut in front of you only has one item. One might be obligated to let in one or two
people, if that, but not a large number. Now
it is my current view that if a health care provider is emotionally and/or
morally disposed not to hasten any patient’s rightfully hastened death, s/he is
under no obligation to assist in doing so, as
long as, and only as long as, there are other means or persons
available who are willing to assist the patient in the endeavor, and whose
doing so will not abrogate other obligations they have to other patients or
other people. What I mean by that is
that if Adamson is unwilling to assist patient suicide, but Smith is, Adamson
is not obligated to help the patient hasten death as long as Smith can do it in
a way that does not overburden Smith and does not detract from his other
obligations, say to his other patients in terms of time spent on their cases or
tending to their care. But
if no one else is available to help the patient hasten his/her death, then as
long as Adamson is free to do it, Adamson has an obligation to the patient to
help relieve his/her suffering in this way.
The reason for that is a population can support only so many health care
providers, and one person’s being in a community first prevents others from
being able to be there under normal circumstances. This is true, for example of hospitals where
communities grant what is essentially an area monopoly to a hospital in order
to prevent competition that will divide up patients so thinly that all of the
hospitals fail. If a case can be made
that patients have a legitimate expectation of medical care that is available
and right for them to have, and one hospital’s or doctor’s being there at the
time the patient needs that care means those who would have provided the care
cannot be there, then that doctor or hospital, it seems to me, has an
obligation to provide that care which their presence otherwise prevents being
available to the patient. In essence, it
is wrong to refuse service one could provide if one is the reason the community
does not have anyone else to perform the service. Some careers are so important that it would
be wrong for a professional to refuse service s/he could easily provide if
his/her success is what is keeping others from being available to provide the
service to the community.
[1]
I use the term “suicide” because it is the termination of a life that would
otherwise last longer, even if only a little while longer; it is the hastening
of death in some sense, and, as in the article quoted at the beginning,
“physician assisted suicide” is the common phrase for this now. Euthanasia would be another term, but the
medical community that is opposed to hastening death does not consider that
term any more neutral than suicide. It is not clear there is a neutral term for
this. And many physicians still cling to the AMA distinction between passively
allowing a patient to die by discontinuing extensive treatment and actively
helping induce death by use of a treatment, even though that distinction cannot
withstand scrutiny, and is like saying that letting a child run out onto a
freeway by purposely letting go of his hand when you know he is headed that way
is morally different from pushing him out onto the freeway. Also, many health care providers argue,
futilely, that giving drugs to alleviate pain, drugs which one knows will also
hasten death, is somehow different morally from giving those same drugs in
order to hasten death. That would be
like allowing as a justified defense in a murder trial the defendant did not intend the victim to
die when he threw him off the skyscraper roof, but just wanted him to have the
thrill of freefall as in skydiving, even though it was known he would die
because of it. Whether a known effect of
an act is “intended” or not, one is responsible for causing it. “I didn’t mean to” is never a justification,
and it is not even an excuse when you knew the consequence was inevitable.
[2]
“Prima facie obligations” are ones that can be overridden, but only with good
reason. Without such a reason, the
obligation is in force. E.g., liberties do not grant
license, and they can be justifiably socially, morally, or legally restricted
when there is good reason to override the right – such as falsely yelling
“fire” in a crowded theater, publicly slandering innocent people, or being rude
and offensive, in the guise of “freedom of speech”.
[3]
By “interdependent” society I mean one where each person’s work contributes to
and depends on the work of others in a complex way that tends to be taken for
granted but which shows up when economic or natural disasters occur that keep
some people from being able to contribute to the economic system. An interdependent society is different from
something like a pioneer society where each person or family is relatively
self-sufficient even if they trade with each other for convenience. I think a
case can be made that we owe much more to others with whom we are
interdependent or on whose labor we have depended and prospered than we owe to
those with whom we do very little or nothing that affects each other.
[4]
Whether rightly or wrongly, behaviorally preventable epidemics are not as
universally accepted as requiring resource allocations to find cures or
preventions for those who will not control their own behaviors and who thus put
themselves at risk for the illness.
[5]
This essay is about patient-requested, physician-assisted suicide, not medical
mercy killing of a patient who has not previously, and cannot currently, make
(known) the choice to die.
[6]
Typically psychiatrists, psychologists, clergy, survivors (in case of serious
disabling, injuries), and/or social workers are called in to try to get a
patient to see they have more to live for.
While that may sometimes be effective, I think what is more likely
needed is anyone who can understand how to see what might give that particular
patient something to live for. What one
might find worthwhile to live for could be anything from a past love to a child
to a pet to a whole new interest in some subject there would be reason to
believe the patient would find stimulating.
It might be a challenging problem for the patient to think about and
want to solve. It could be a book or
videos the patient might find interesting enough to want to read or watch and
that might even be interesting enough to take notice off the pain or
suffering. It might be simply more
understanding care-givers who just make the patient feel happier to be around.
It might be pleasant music. If nothing of any of that sort of thing is
successful, then perhaps there really is no reason for the person to continue
to be forced to live.
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