Professional Documents
Culture Documents
Ian Dowbiggin
2003
www.oup.com
Ian Dowbiggin.
p. cm.
ISBN 0-19-515443-6
R726.D69 2002
179.7—dc21 2002022458
9 8 7 6 5 4 3 2 1
Printed in the United States of America
on acid-free paper
To Jamie,
Acknowledgments ix
Introduction xi
1. Origins 1
2. Breakthrough, 1920–1940 32
3. Stalemate, 1940–1960 63
Notes 181
Bibliography 229
Index 241
asks another (most often a physician) for help in dying. But by kill-
ing Youk, he very well might have done irreversible harm to his life’s
mission.
Kevorkian’s conviction and the backlash it triggered are among
the most recent in a long series of events stretching back to the
nineteenth century that represent attempts by numerous men and
women to change the nation’s attitudes and laws about euthanasia.
A handful, like Kevorkian, have resorted to sensationalist, open de-
fiance of the law in the effort to gain acceptance of an individual’s
unlimited right to choose the time, manner, and place of his or her
death. Others have tried a quieter approach, but they too have
shared Kevorkian’s conviction that they were engaged in a revolu-
tionary struggle to free Americans from ethical codes of conduct
that date back to classical antiquity. They have been united by their
commitment to fighting for “the right not to suffer,” whether be-
cause of unwanted pregnancy, deferred sexual gratification, or a
lingering, painful death. Still others agree that Americans have every
right to refuse unwanted medical treatment, but believe that such a
right is entirely different from a right to have a physician either
administer or prescribe lethal drugs to a terminally ill patient. To-
day, as in the past, Americans sharply disagree over what constitutes
death with dignity, but very few think that the question of how we
die should be a hidden secret.
This book, thanks to privileged access to confidential records of
the euthanasia movement, is the first to chronicle how America
reached this state of affairs. It tells the story of one of the most
contentious yet neglected chapters in the history of American policy
reform, a cautionary tale of a political, social, and cultural struggle
that since its origins has been firmly embedded in the frequent and
surprising twists and turns of broader history and now shows signs
of raging well into the twenty-first century. We now know a great
deal about Nazi medical killing between 1939 and 1945, a program
that, in the name of euthanasia, ultimately cost the lives of some
100,000 handicapped adults and children. In recent years, there has
also been extensive media coverage and analysis of the Netherlands’
experiment since the 1970s with both physician-assisted suicide and
active voluntary euthanasia, in which doctors or others directly end
a consenting patient’s suffering. But what little we know about eu-
thanasia in modern America chiefly comes from those accounts that,
in their partisan approach to sources, have left out much of its his-
xiii | Introduction
tory and fostered myths that persist to this day. They have tended
to depict euthanasia advocates as engaged in a triumphalist struggle
between virtuous representatives of democratic rights and hide-
bound professional and religious institutions dedicated to defending
their self-interests at the expense of individual freedom.
This book explodes both this myth and the other myth that the
modern euthanasia movement began only in the 1960s and 1970s
with the introduction of life-prolonging medical technology, the de-
cline of the doctor-patient relationship, the rise of the “rights cul-
ture,” medicine’s inept handling of end-of-life care, and the AIDS
epidemic. As important as these factors were, they simply helped to
focus public attention on a century-old discourse, predating World
War I, which affirms a theory of individualism stressing emancipa-
tion, independence, and autonomy. Euthanasia—or “the right to
die,” as the movement is more widely known today—certainly was
popularized by shifts in medical technology or practice and truly
became grassroots after the 1960s, but its ideological strands have
long been entangled in the divisive cultural conflicts in America over
what defines the boundaries between personal autonomy and public
authority, between individual freedom and the notion of a common
good.
Attention to the discourse of autonomy behind the euthanasia
movement reveals, however, some disturbing paternalist tendencies.
While most right-to-die advocates today stress that they seek only the
freedom of competent, terminally ill individuals to choose medical
assistance in dying, up to the end of the twentieth century various
proponents have also expressed a worrying willingness to extend the
legalization of euthanasia to cover persons with disabilities, handi-
capped newborns, and unconscious geriatric patients, or to justify
the right to die for social and economic reasons. This combination
of a fervent quest to maximize human freedom and the reformist
urge to socialize individual identities in the service of utilitarian
goals is as old as the Progressive era of the early twentieth century.
The enduring nature of this current within America’s euthanasia
movement justifies the concerns of some, more recent, interested
parties that legalizing physician-assisted suicide or active euthanasia
will lead to a “reduction of respect for human life,” ultimately af-
fecting the disabled and other vulnerable persons in society. The
right to die can all too easily become “a duty to die.”1
At the same time, however, there is little historical evidence that
Introduction | xiv
nasia programs, but its failure to erase the Nazi taint crippled its
attempts to convince state legislators to enact laws giving consenting
adults the right to a medically administered death. The ESA’s battle
with the Catholic Church, waged within a cultural climate domi-
nated by anticommunism and heightened religiosity, ended in de-
feat, and euthanasia advocates would spend much of the 1960s de-
vising new strategies for winning over popular opinion.
Changes in strategy paid off by the late 1960s. As chapter 4 shows,
during that decade the ESA reinvented itself as a organization ded-
icated to passive rather than active euthanasia, the right to refuse
unwanted treatment rather than the right to a medically adminis-
tered, speedy death. Public interest in death, spurred by the writings
of Elisabeth Kübler-Ross and others, became a virtual “craze” by the
1970s, as Americans celebrated the end of “the conspiracy of silence”
surrounding death. Thanks to the help of the advice columnist “Dear
Abby” and the introduction and distribution of “living wills” (ad-
vance directives written by individuals specifying under what condi-
tions treatment would be withheld), the ESA capitalized on the con-
stitutional recognition of a right to privacy and the sixties’ emphasis
on individual choice. Euthanasia ceased being defined as active
mercy killing, with its disturbing overtones of coercion and social
usefulness, and increasingly became viewed as personal freedom from
unwanted interference in one’s own life. This redefinition of eutha-
nasia benefited enormously from the rise of the women’s movement
in the 1960s, with its celebration of “our bodies, ourselves.” As so-
ciety’s traditional caregivers, women all too often have watched their
spouses, parents, children, and friends die, and thus the notion of
preventing unnecessary suffering has had special meaning for them.
The women’s movement, blossoming in the sixties and seventies,
provided a nurturing environment for the revived euthanasia
movement.
Yet even in a cultural climate stressing personal choice, right-to-
die advocates never totally rejected utilitarian justifications for eu-
thanasia. In the 1960s and 1970s, the ESA attracted wealthy backers
of population control such as the tycoon Hugh Moore and philan-
thropist John D. Rockefeller 3rd, and the idea spread that euthanasia
was the responsible thing to do in an overpopulated world of di-
minishing resources.
Success crowned the ESA’s efforts to redefine euthanasia as a right
to refuse unwanted medical treatment in the 1970s and 1980s, when
xvii | Introduction
state after state legalized living wills and money poured into the
group’s coffers from a sympathetic public. The massive press cover-
age surrounding the tragic story of Karen Ann Quinlan, who lapsed
into an irreversible coma in 1974, put a human face on the right to
die in ways that all the ESA’s official literature could never do. But
just as the movement seemed poised to make the big breakthrough
to the legalization of active euthanasia, its unity began to crumble,
as chapter 5 shows. The ESA itself underwent various name changes
and split into two factions during the 1970s, a sign of the creative
ferment, quiet reflection, and acute disagreements among eutha-
nasia advocates. Tensions abruptly developed between radicals in-
terested only in winning the legal right to active euthanasia and
physician-assisted suicide, and a growing number of moderates who
believed that the issues surrounding death and dying were far more
complex than earlier imagined and warranted further study and
public discussion. These fault lines hardened with the founding of
the World Federation of Right-to-Die Societies and Derek Hum-
phry’s grassroots Hemlock Society in 1980. By then, the center of
gravity for the entire euthanasia movement was shifting from the
East Coast to the West Coast, from the fashionable and affluent Man-
hattan locations where the ESA’s board used to meet to the drafty
and damp church basements where the rank-and-file (“little old
Ohio ladies in running shoes,” as one activist described them) of
the new, populist right-to-die organizations congregated to hammer
out policy.
The momentum of the 1980s led to fierce legal and legislative
battles over the right to die in the 1990s. The poignant fate of Nancy
Cruzan highlighted the plight of families faced with difficult end-of-
life decisions. Ballot initiatives in three states in the early 1990s came
close to winning the right to die with medical assistance, and victory
was finally achieved in 1997 when Oregon became the first American
state to permit physician-assisted suicide. Overseas, as the decade
drew to a close, Belgium and the Netherlands enacted analogous
legislation allowing doctors to help patients die, after the Dutch had
tolerated the practice since the 1980s. Thoughtful individuals such
as the physician Timothy Quill supported assisted suicide as a re-
grettable yet indispensable “last resort” in palliative care. By the end
of the 1990s, international and national trends seemed to indicate
that euthanasia enjoyed public backing as never before.
In the 1990s, however, as interest in palliative care, pain manage-
Introduction | xviii