Layers of Dying and Death PDF
Layers of Dying and Death PDF
Layers of Dying and Death PDF
Kate Woodthorpe
Layers of Dying and Death
Edited by
Kate Woodthorpe
Advisory Board
Volume 40
A volume in the Probing the Boundaries project
>Making Sense Of: Dying and Death=
Published by the Inter-Disciplinary Press
Oxford, United Kingdom
All rights reserved. No part of this book may be reprinted or reproduced or utilised in any
form or by any electronic, mechanical, or other means, now known or hereafter invented,
including photocopying and recording, or in any information storage or retrieval system,
without permission in writing from the publishers.
ISBN: 978-1-904710-39-5
EAN: 9781904710395
Contents
Introduction ................................................................................................ 3
Complicated Grief
Sandra Jones .................................................................................. 31
“Of Death I Try to Think like This”: Emily Dickinson’s ‘Play’ with Death
Lucia Aiello ................................................................................. 139
Notes
1
Zygmunt Bauman, Mortality, Immortality and other life strategies
(Cambridge, Polity Press, 1992).
Family Assisted Suicide in the British Media
Daphna Birenbaum-Carmeli
Abstract
The paper tackles the subject of family assisted suicide through its
presentation in the British press during the 1990s. Looking for basic
characteristics of the coverage, the paper reveals a consistently supportive
stance towards family assisted suicide that is produced by depictions of
the dying persons and the perpetrators as autonomous and conscientious
individuals; by idyllic portrayals of family relations; and by praising
judges for their lenient verdicts. Presentations of the law as a dated State
system, as well as marginalization of opposing voices, further enhanced
the supportive message. The argument of the paper is that this presentation
may carry implicit political implications: in commending actors’ self-
reliance and in calling for decreased State interference in personal affairs,
the press augments the neo-liberal spirit that has come into prominence in
Britain since the 1980s. Within this context, we raise some ethical
questions regarding the broader political significance of such media
representations.
The image of moral integrity and the purity of motive was given
official validation through quotes from judges’ parallel evaluations: “the
circumstances … showed plainly that she was a caring and loving
daughter.” The prosecution’s sharing of this positive evaluation provided
still further evidence.
Formative in the justification of the perpetrators’ actions was the
explicit absence of any hesitation or regret: “I [Jennison] don't regret what
I have done. I'd never have forgiven myself for letting her be in this living
death.” The law makes Paul [Brady] a guilty man, but the family’s only
regret is that they let Jim suffer for so long.
The brief, scarce allusions almost trivialised the moral debate
surrounding FAS. Indeed, the marginalisation of the case against FAS was
consistent, with criticism relegated to one or two sentences at the end of
the piece that were not followed by any engagement with the arguments:
C. Families
Family dynamic was virtually written off by the press. Through
‘normalised’ descriptions, family relations were made to appear as purely
loving and harmonious, suggesting a lifelong closeness. Jim Brady’s death
was located in a family Christmas gathering. Mrs. Wilks’ end was framed
within a cosy weekend scene:
These scenes of warmth paved the way for the act that was about to
follow, which could then be framed as the culmination of harmonious
family togetherness:
In each other’s arms they lay, the loving daughter and her
suicidal mother, talking about old times. Annie swallowed
her pills - two at a time - sipped her sherry and slipped
slowly into the big sleep.
2. Discussion
The one-sided, supportive coverage that we identified relied heavily
on the notion of the ‘normal’ family. Suggesting similarity of actors’
sentiments across the cases, this narrative replaced the idiosyncrasy and
complexity that one would expect in a real life consideration of FAS with
descriptions of wholesome harmony. As such, the articles advanced a
moral discourse on living and dying, effectively “reducing the traumatic
event to a set of standardized narratives… turning it from a frightening
and uncontrollable event into a contained and predictable narrative.” 3
From this perspective, the normal family discourse helped deny the very
trauma by toning down complexity and anxiety, and emphasising
individual heroism and beatific acts.
Another constituent of the one-sided supportive coverage was the
episodic framing of FAS, namely, reading the problem at a micro level, as
10 Family-Assisted Suicide in the British Media
___________________________________________________________
a difficult decision made between two individuals. As the arguments
against euthanasia address broader socio-ethical issues, they are harder to
contain within an episodic framework. The concept of dignity can
illustrate the difference. Opposition to euthanasia revolves around a form
of dignity that is neither negotiable nor reducible. 4 In contrast, arguments
in favour of euthanasia turn on a concept of dignity that is personal and
can be diminished or lost. 5 Episodic framing, with its focus on the
individual, ultimately privileges personal conceptions of dignity and is
therefore structurally biased against the major claims of euthanasia
opponents.
Located in the context of late 1990s Britain, the courageous
individual narrative dove-tailed with a neo-liberal discourse of autonomy,
and a move towards a State withdrawal from caring labour. Since the
1980s, the neo-liberal rationalities that came into prominence in Britain
accorded a vital value to a self that is to aspire to autonomy, it is to strive
for personal fulfilment in its earthly life, it is to interpret its reality and
destiny as a matter of individual responsibility, it is to find meaning in
existence by shaping its life through acts of choice. 6
The decisions made by the deceased and the perpetrators could be
said to ally with this notion of the individual, as suicide became an act of
self-determination. The emphasis on self-reliance and the near
glorification of suicide further reinforced the neo-liberal accent on
individualism and, possibly, the justification of cuts in State services.
During the 1990s, neo-liberal reforms had legitimated the shrinking of
health services, reducing the number of nurses, and hospitals as well as
long term care facilities. While we are not suggesting that journalists were
intentionally promoting a neo-liberal agenda, we suggest that the British
press of the late 1990s constituted FAS in accordance with this vision. By
framing particular types of suicide within a self-assured harmonious
family narrative, family-assisted suicide emerged as commensurate with
neo-liberal ideals in terms of care, family and societal morality at large.
If our analysis is acceptable, then it raises several questions: How
do such media presentations impact on circulating views regarding FAS?
What do they imply regarding the role of relatives and the State in caring
for the terminally ill? Is the coverage in fact advancing the privatization of
death? More generally, could the glorifying of one's courage to die, in the
sensitive context of FAS, contribute - if inadvertently - to a social climate
in which people would be encouraged to ‘courageously’ end their lives?
Further enquiries into this emerging territory would hopefully help
elucidate these issues.
Daphna Birenbaum-Carmeli 11
___________________________________________________________
3. Epilogue
On January 14, 2005, the BBC featured on its front website news-
page the story of Brian Blackburn, a 62 year old policeman who pleaded
guilty to manslaughter after having killed his wife who was dying of
cancer. The journalist quoted the husband citing his deceased wife saying
that this was the “last loving thing you could do for [me].” The judge was
quoted stating that Blackburn “had acted as a ‘loving husband’,” and then,
noting that the circumstances were exceptional, gave him a suspended
nine month sentence. The couple’s two sons emerged from the piece as
fully supportive, pledging for mercy. A description of Blackburn being
“greeted by friends and family as he left the court” sealed the report. No
opposing voices were included.
Notes
1
S.D. Reese, O.H. Gandy, & A.E. Grant (eds.). Framing public life:
Perspectives on media and our understanding of the social world.
(Mahwah, NJ: Lawrence Erlbaum, 2001).
2
M. Baum, Sex lies and war: How soft news brings foreign policy to the
inattentive public. American Political Science Review, 96 (2002), 91-109.
3
K. Tal, Worlds of hurt. (Cambridge: Cambridge University Press, 1996).
4
L. Gormally, Euthanasia and assisted suicide: Seven reasons why they
should not be legalized <http://www.euthanasia.com/sevenreasons.html>
(1997).
5
D. Pullman, Death, dignity, and moral nonsense. Journal of Palliative
Care, 20 (2004), 171-78.
6
N. Rose, Inventing ourselves: psychology, power, and personhood.
(Cambridge: Cambridge University Press, 1988).
Irina Novikova
Abstract
The article focuses on how death and dying as an insistent
discursive and emotional agenda of ‘post-Soviet-Hamlets’ have been
represented in the post-Soviet Russian films of the 1990s-early 2000s.
Post-Soviet cinematic ‘hauntology’ was marked by an emancipatory
inventiveness to unsettle and re-imagine future uncertainties beyond the
spectres of the past. Gendered imageries of death and dying plotted mainly
in the father-son relationship have been central to the ‘real’ of the visual
and political re-imagination of the nation, history, borders, and boundaries
of post socialist ‘rebirth’. For my argument I will address particular
instances of filmed death in the cine-texts by Russian ‘necrorealism’,
Pavel Chukhrai, Sergei Bodrov, Aleksandr Sokurov, Andrei Zvyagintsev.
The death of a hero has been among the most favourite plot
elements in cinematic storylines as it
Notes
1
Felicitas Becker, Knowing the Limits. Kinoeye. New Perspectives on
European Film, 10 November 2003, (5 May 2006).
< http://www.kinoeye.org/03/13/becker13.php>.
2
Boris Groys, Utopiia i obmen. (Tr. Utopia and Exchange). (Moskva:
Znak, 1993), 354.
3
Ibid., 64.
4
Jacques Derrida, The Specters of Marx. Tr. Peggy Kamuf. New York:
Routledge, 1994, 91, 97.
5
Ibid., 10.
6
Metanarrative “is a global or totalizing cultural narrative schema which
orders and explains knowledge and experience”. In John Stephens.
Retelling Stories, Framing Culture: Traditional Story and Metanarratives
in Children's Literature (1998)
7
Christina Stojanova, The New Russian Cinema, Fall 1998, (9 May 2006).
<http://www.kinema.uwaterloo.ca/sto982.htm>.
8
Thomas H. Campbell, The Bioeasthetics of Evgenii Jufit, 26 January
2006, (16 May 2006).
<http://www.kinokultura.com/2006/11-campbell.shtml>.
9
Alexei Yurchak, The Politics of Indistinction. Bioaesthetic utopias at the
end of Soviet history, 5 April, (2 June 2006).
Irina Novikova 21
___________________________________________________________
<http://cas.uchicago.edu/workshops/pcs/yurchak-politics-
indistinction.pdf>.
10
A Soviet communal flat was inhabited by several tenant families sharing
a kitchen, toilet and bathroom.
11
R.W Connell, Masculinities. (Berkeley: University of California Press,
1995).
12
The title of the film refers to the second circle of hell depicted in The
Divine Comedy, Volume I: Inferno by Dante Alighieri.
13
Phallogocentrism, by Jacques Derrida, refers to locating the centre of
text/discourse within the logos and the phallus and privileging of the
signified over the signifier.
Outi Hakola
Abstract
Death is an open area for beliefs, fears and fictions. The
cinematic living dead, as vampires, mummies and zombies, represent and
visualize death in a corporeal way. These creatures are familiar from the
horror genre where they threat humanity because of physical and mental
transformation through death. The living dead are uncanny other and they
create abjection. They highlight the fear of death and otherness, unknown
existence and marginal phenomena. In the living dead film the undead
characters symbolize contradictions of race, class, sexuality or nationality.
In my presentation I will consider the nature of the living dead
character between life and death and those fears and imaginative
possibilities these creatures open to us. At the same time I will consider
the narrative tradition of these films and how the narration marks these
creatures as monsters. I use as an example Francis Ford Coppola’s film
Bram Stoker’s Dracula. In this film the un-dead character is both evil and
empathetic and victims are both sinful and innocent at the same. In this
film love and sexuality become the driving forces for the unnatural
extension of life beyond death.
3. Narration of dying
As figures of death the living dead can be feared and admired at
the same time. They image the post-mortem to be both rewarding and
punitive experience. Their unnatural corpses are appalling, but their
freedom from social limitations is envied. However the narration of the
horror films puts these monsters in their places. For horror fiction, as
Yvonne Leffler states, the antagonist is a central narrative and structural
element. 8
The narrative structure with beginning, middle and end brings
forward a narrative progress were a monster is born, then its existence is
accepted and finally the monster is destroyed and the order regained. In
this progress the beginning is the introduction of the main antagonist,
Dracula. Then the threat is materialized with human victims, like Lucy.
The victim is contaminated and he/she returns as a representative of the
undead. The body is alive, but the personality has replaced with
monstrousness. In the end, both main antagonist and other reborn
monsters must be destroyed.
The narration does not only picture a transformation process into
a monster, but also describes beautifully and horrifyingly the processes of
loss, grieve and rejection. One needs to accept the death of a loved one in
order to survive. These films make a viewer to concentrate more on the
cultural and personal meanings of death than on the medical definitions of
it.
Notes
1
Yvonne Leffler, Horror as Pleasure (Stockholm: Almqvist & Wiksell
International, 2000), 156.
2
Gregory A. Waller, The Living and the Undead. From Stoker´s Dracula
to Romero’s Dawn of the Dead (Urbana, Chicago: University of Illinois
Press, 1986), 16.
3
Harto Hänninen, and Marko Latvanen, Verikekkerit. Kauhun käsikirja
(Helsinki: Otava, 1992), 58-59.
4
Vesa Sisättö, ’Hirviö on tuhottava! Vampyyrimagian rajoituksista ja
kehityksestä’, in Kirjallisuus, tunteet ja keskipäivän demoni.
Outi Hakola 29
___________________________________________________________
Sandra Jones
Abstract
The families of death row inmates experience unique grief and
loss issues that have largely been neglected by scholars and clinicians
alike. This study uncovers the meaning that lies within the specific forms
of grief and loss experienced by family members who currently have a
loved one on death row or have already lost their loved one to an
execution. The concepts of disenfranchised grief 1 and non-finite loss 2 are
utilized to bring attention to the ways in which the circumstances
surrounding an execution complicate the grieving process for the family
members of those condemned to death. Obstacles to effective grief therapy
for these family members are further examined and addressed within this
study. Qualitative interviews were conducted with 50 family members of
Delaware death row inmates. The reactions of family members to having a
loved one on death row are varied and complex, yet they include the
following common responses: social isolation; loss of the assumptive
world; intensified family conflict; diminished self-esteem; fragmented
sense of security, trust, and meaning; guilt and shame; and a chronic state
of despair. These symptoms create numerous barriers to these family
members receiving effective grief therapy.
1. Introduction
Anyone who has experienced the death of a loved one is likely to
feel that their life has been complicated by their loss. Even under the best
conditions, grieving is a complex and an individual process, yet there are
particular types of deaths that make the grieving process even more
complicated due to the circumstances surrounding the death. 3 Research
aimed at determining the prevalence of complicated grief has led to an
estimation that 14-30% of grieving people develop some form of
complicated grief. 4 Although the mental health profession lacks a formal
diagnostic category for complicated grief, a significant amount of
literature has emerged in recent years aimed at defining and treating those
who suffer from this intensified form of grief. 5
Examples of particular types of deaths that are likely to lead to
complicated grief among the survivors of the deceased include those that
carry a social stigma and those that occur through violent means.6 The
sources of stigmatized deaths are many, yet perhaps no greater stigma
32 Complicated Grief
___________________________________________________________
exists than that which accompanies the death of a loved one due to
execution. While much of society may not see an execution as a violent
death, the family members of death row inmates certainly view it as
violent.7
While much has been written about the effects of incarceration on
family members of the offender8 and there is an important body of
literature on grief and bereavement,9 there has been little research into the
grieving process associated with a death sentence and execution. This
paper explores the effects of a death sentence and execution on family
members of the accused, and their unique bereavement. The obstacles that
interfere with these family members receiving effective grief therapy are
further examined. This article not only provides insight into the
complicated grief experienced by this population, but it also yields
information that should prove crucial to mental health professionals who
strive to address the clinical needs of these families.
3. Methods
The primary source of data collection was qualitative interviews
conducted with the family members of capital offenders. The family
members participated in a 45-minute to several hour interview, which
included questions that explored the nature of their grief as they have
moved from the time of the arrest of their loved one throughout the
various stages of the death penalty process. Topics that were explored
include their relationship with the accused, changes in their family
structure, and their interactions with the criminal justice system, the
media, and their community. Their mental health status was assessed as
they were asked to discuss whether or not they have sought any mental
health services to assist them through the grieving process. When they
indicated that they have received mental heath services were asked to
evaluate the effectiveness of such services. More often than not, the family
members indicated that they have not received such services, thus these
family members were asked a series of questions to assess the obstacles
that prevented them from receiving mental health treatment.
Participation observation served as a secondary source of data
collection, as I visited the prison on numerous occasions to meet with the
men on death row. The time I spent in the prison visiting area provided me
with opportunities to observe the grief of the families. The moments
leading up to, during, and immediately after the time that the families
spend with their loved one on death row allowed me to observe the ways
in which they cope with the realization of their loss and the intensity of
their response
4. Sample
The state of Delaware has a very small death row population, yet
when the small size of the state is taken into account, the rate of
executions is alarming. For nearly a decade following the first execution
in 1992, after the death penalty was re-enacted within this state in 1974,
Delaware held the distinction of executing more people per capita than
any other state in the United States.15 The current Delaware death row
population includes 16 men and 14 others have been executed over the last
14 years since the death penalty was reinstated. My sample includes 37
family members who are related to eleven of the sixteen men currently
sitting on death row and 13 family members who are related to four of the
fourteen men who have been executed since Delaware resumed executions
in 1992.
34 Complicated Grief
___________________________________________________________
5. Non-finite loss
The theory of non-finite loss contributes to our understanding of
the ways in which factors associated with particular types of deaths
complicate the grieving process. Non-finite loss refers to those situations
in which losses are slowly manifested over time, and often do not have an
impending ending. It is loss that is continuous, and exacerbated by such
things as milestones, which are not met by the affected individual. The
continuous nature of the loss eludes the family member’s ability to go
through the stages of grief to a point of recovery.16 Authors Bruce and
Schultz, who coined the term, state that the grieving person is lost between
two worlds, one that is known and one that is dreaded.
There are three conditions for non-finite loss. The first is that the
loss must be continuous and often follows a major event. The second
involves developmental expectations that cannot be met. This is well
illustrated by examining the grief felt by parents of developmentally or
physically disabled individuals. These parents grieve when their children
reach an age that carries significant milestones that cannot be obtained.
The last condition described by Bruce and Shultz is the loss of one’s own
hopes and ideals. Those who experience a non-finite loss question who
they could/should/might have been. An examination of these conditions
that must be met in order for a loss to be considered ‘non-finite’ suggests
that such a loss is very likely to lead to complicated grief on the part of
those who are grief-stricken. Many of the factors associated with the
specific deaths that complicate the grieving process of the mourners can
also be found with non-finite losses. These factors include death from an
overly lengthy illness, the unique nature of the loss, the mourner’s
perception of the deceased’s fulfilment in life, the secondary losses that
come with such loss, and the anticipatory grief that accompanies such a
loss.
6. Disenfranchised grief
The theory of disenfranchised grief contributes to our
understanding of the ways in which particular antecedent and subsequent
variables complicate the grieving process. Disenfranchised grief is a term
that was developed by Kenneth Doka,17 and refers to instances when the
bereaved are denied the ‘right to grieve’ by the larger society.
Disenfranchised grief occurs when a loss cannot be openly acknowledged,
publicly mourned, or socially supported. Doka and others have found that
when disenfranchised grief occurs, the emotions of the bereaved are
intensified and healing becomes more difficult. In addition, the bereaved
often experience high levels of distress, disorganization, and prolonged
grieving. The concept of disenfranchised grief becomes more profound
Sandra Jones 35
___________________________________________________________
when it is combined with Romanoff’s finding18 that grief is most
effectively addressed when there is community support for the bereaved,
and the relationship between the dead and his or her mourners is
acknowledged.
The mourner who is disenfranchised from his or her grief is
likely to face many of the same antecedent and subsequent variables that
have been noted to occur with complicated grief. These variables include
anger, ambivalence, or marked dependence directed toward the deceased,
‘mourner liabilities’ such as prior or concurrent unaccommodated losses
or mental health problems, and the mourner’s perceived lack of social
support.19 The most obvious variable operating prior to, during, and after
the death of their loved one for those mourners whose grief is both
‘complicated’ and ‘disenfranchised’ is a lack of social support within the
community. As a result of the social isolation that typically ensues from
their loss, it is not uncommon for disenfranchised mourners to feel anger
or ambivalence toward their deceased loved one. Their grief is further
complicated by the assaults waged against their notion of the “assumptive
world,”20 as they are often disillusioned by the lack of social support that
they receive from others during their time of sorrow. Other antecedent and
subsequent variables that complicate grief, including mental health
problems and such social factors as the mourner’s educational, economic,
occupational, or legal status, are frequently found to occur among
disenfranchised grievers.
7. Findings
A. Non-finite loss
When the grief experienced by those families directly affected by
the death penalty is examined, it becomes apparent that many aspects of
their mourning are indicative of a ‘non-finite loss’. In all cases, the pain
started after a specific event, the crime and subsequent arrest. Rebecca’s
description of her family’s reaction to her husband’s arrest was typical
among the families interviewed.
B. Disenfranchised grief
The concept of ‘disenfranchised grief’ sheds light on another
dimension of the unique grieving process experienced by the families of
death row inmates. The stigma associated with having a loved one on
death row is so enormous that the families who were interviewed for this
research frequently indicated that they do not feel comfortable
acknowledging their loss with anyone outside of their family. Stated by
one mother of a death row inmate, “I don’t tell anybody. They will never
know it from me.” Of course, it is not so easy to keep this information
from people within the community, due to the high level of publicity that
typically surrounds the case of their loved one. When people within the
community note the associations that family members have with death
row inmates, the reaction is typically negative. As a result, the families of
these men on death row are essentially disenfranchised from their grief.
Elizabeth is the mother of a man who was executed for the
murder of four people, including three children. She recalled the harsh
treatment that she received by strangers in her community during the early
period of her son’s incarceration, when she entered public places like
grocery stores and heard people yell out “There’s the mother of the baby
killer!” The taunting that Elizabeth was exposed to throughout her son’s
death row sentence continued through to his execution. She insisted on
being a witness to her son’s execution, yet was not prepared for the taunts
that she would hear from the victim’s family in the execution chamber as
she watched her son being put to death.
The families of death row inmates are further disenfranchised
from their grief in that their loss is never acknowledged. Even if their
relationship with an inmate were to be recognized as a legitimate and
significant one, many people would not consider the unfortunate
experience of having a loved one on death row to be a real ‘loss.’ To the
extent that the feelings of the family members are even taken into
consideration, it is not usual for outsiders to dismiss any thoughts that
families are suffering a loss because they are considered to be better off
without a murderer in their family.
38 Complicated Grief
___________________________________________________________
Perhaps the time when the families of death row inmates are most
often left feeling as though their loss is not recognized occurs soon after
their loved one is arrested and convicted, when the community’s memory
of the horrific murder is still fresh. Several family members who were
interviewed recalled exchanges that they had early on with the family
members of the murder victim or others who were intimately familiar with
the case against their loved one. These exchanges often left the death row
families feeling not only as though their loss had gone unrecognized, but
also that they were being scoffed at for the mere suggestion that they
might be in pain. Particularly when the loss suffered by the family of the
murder victim was contrasted to their loss, the families of death row
inmates were made to feel as though they did not have a right to their
grief. They received remarks like “at least you can still see your son; mine
is dead.”
9. Discussion
Given the current discussion taking place in the United States
about whether the death penalty should continue to occupy a place within
our criminal justice system, it is crucial to consider the impact of this form
of punishment on the family members of the accused. These family
members have often said they feel like they have been given a death
sentence along with their loved one. The unique experience of having a
loved one sentenced to death row has set them upon a long, complicated
grieving process. Their grief has been made complicated by the interaction
of two circumstances associated with their grief: non-finite loss and
disenfranchised grief. They grieve what may have become of their loved
one before he was accused of murder. They grieve numerous other
secondary losses, including the loss of their assumptive world, the loss of
community support, and for some, and the loss of their own identity.
The mental health needs of this population are great. A majority
of the family members in my sample suffer from some form of a
depressive and/or anxiety disorder. Symptoms of post-traumatic stress in
particular are prevalent among these families at points throughout their
grieving process. This is most often the case among those family members
I interviewed who have survived the execution of their loved one, such as
the mother who witnessed the execution of her son on her birthday.
Unfortunately, the social isolation and stigmatization that is associated
with having a loved one on death row makes it extremely difficult for
these families to feel comfortable enough to reach out for help from a
stranger. They frequently worry that a prospective counsellor may support
the death penalty and, if so; many confided in me that they could not
possibly bear their grief to someone who supports the institution that is
likely to lead to the death of their loved one. Some of them commented
that their loved one had received mental health treatment at numerous
facilities before they committed the crime that landed them on death row.
These family members remarked that they are not inclined to seek
counselling because they are disillusioned by the mental health
community that they see as having failed their loved one.
Sandra Jones 41
___________________________________________________________
The pain of having a loved one on death row becomes so great,
however, that some family members eventually find their way into a
mental health facility. Their entry into treatment is not typically via the
traditional route of mourners who seek grief counselling. They are more
often compelled to seek treatment by the complications arising from their
grief, such as drug addiction, legal problems, or parenting concerns. When
mental health professionals find an occasion to work with the family
members of death row inmates, there are several implications from my
research that they can use to assist them toward their aim of effective
treatment outcomes for these individuals. They need to have an
understanding of the complexities related to a capital crime. Therapists
also need to be willing to disclose their position toward the death penalty
in order to determine if it is an obstacle for their client. Therapists must
work toward enfranchising the family members by validating their grief.
The secondary losses of the family members must also be identified and
addressed.
Notes
1
Kenneth Doka ed., Disenfranchised Grief: New Directions, Challenges,
and Strategies for Practice. (Illinois: Research Press, 2002).
2
Elizabeth Bruce & Cynthia Schultz, Nonfinite Loss and Grief: A
Psychoeducational Approach. (Baltimore, Md.: Brookes Publishing Co.,
2001).
3
John Bowlby, Attachment and Loss, Vol. III. (New York: Basic Books,
1980); Colin Murray Parkes. Bereavement: Studies of Grief in Adult Life.
(New York: International University Press, 1972); P. Marris, Loss and
Change, 2nd ed. (London: Routledge & Kegan Paul, 1986).
4
Linda Schupp, Grief: Normal, Complicated, Traumatic. (Eau Claire, WI:
PESI Healthcare, 2004).
5
It has been identified with different terms, such as ‘traumatic grief’ by
Selby Jacobs, Traumatic Grief: Diagnosis, Treatment, and Prevention.
(Castleton, N.Y.: Hamilton Printing Co., 1999); ‘pathological grief’ by
John Bowlby ‘Pathological mourning and childhood mourning’, Journal
of the American Psycholoanalytic Association, 11 (1963), 500-541; or
‘unresolved grief’ by A. Lazare, ‘Unresolved Grief’ in Outpatient
Psychiatry: Diagnosis and Treatment, ed. A. Lazare (Baltimore: Williams
& Wilkins, 1979); S. Zisook, & L. Lyons, ‘Bereavement and Unresolved
Grief in Psychiatric Patients’, Omega, 20 (1988-1989), 43-58. Regardless
of the terminology utilized, increasingly more attention has been given to
complicated grief in an effort to equip clinicians with the diagnostic tools
42 Complicated Grief
___________________________________________________________
and treatment strategies that will allow them to respond in the most
effective manner possible to those suffering from this form of grief.
6
Edward Rynearson, Retelling Violent Death. (Philadelphia, Pa.: Brunner-
Routledge, 2001); E.K. Rynearson, & J.M. McCreery, ‘Bereavement after
Homicide: A Synergism of Trauma and Loss’, American Journal of
Psychiatry, 150 (1993), 258-261.
7
Susan Sharp, Hidden Victims: The Effects of the Death Penalty on
Families of the Accused. (New Brunswick: Rutgers University Press,
2005); Recent research indicates that the process of lethal injection may be
far more brutal than it appears. Research suggests that some individuals
may feel enormous pain from the lethal injection, yet are unable to express
it, as the protocol requires three injections and the second one is a
paralyzing agent. L. Konaris, T. Zimmers, D. Lubarsky, & J. Sheldon,
‘Inadequate Anaesthesia in Lethal Injection in Lethal Injection for
Execution’, Lancet 365 (2005), 1412-1414. Professional medical groups,
such as the American Medical Association, have deemed it unethical for
their members to participate in executions. As a result, numerous lawsuits
have recently been filed in the U.S., challenging the constitutionality of
lethal injection as a mode of execution, and a recent U.S. Supreme Court
ruling has made it easier for death row inmates to file such a claim. Death
Penalty Information Center (DPIC) <http://www.deathpenaltyinfo.org>
8
Donald Braman, Doing Time on the Outside. (Ann Arbor: University of
Michigan Press, 2004); Katherine Gabel & Denise Johnston, Children of
Incarcerated Parents. (Lanham, Md.: Lexington Books, 1995); Jeremy
Travis & Michelle Waul, eds. Prisoners Once Removed: The Impact of
Incarceration and Re-entry on Children, Families, and Communities.
(Washington, D.C.: The Urban Institute Press, 2003).
9
John Bowlby, 1980; Colin Murray Parkes, Bereavement: Studies of Grief
in Adult Life. (New York: International University Press, 1972); T.A
Rando, Grief, Dying, and Death: Clinical Interventions for Caregivers.
(Champaign, Il.: Research Press, 1984); W. Worden, Grief Counseling
and Grief Therapy, 2nd. ed. (New York: Springer, 1991).
10
E. Beck, S. Britto, and A. Andrews, In the Shadow of Death:
Restorative Justice and Capital Offenders’ Family Members. (New York:
Oxford University Press, forthcoming); E. Beck, B. Sims-Blackwell, P.
Leonard, & M. Mears, ‘Seeking Sanctuary: Interviews with Family
Members of Capital Defendants’, The Cornell Law Review, 88 (2003),
382-418; R. King & K. Norgard, ‘What about our Families? Using Impact
on Death Row Defendants’ Family Members as a Mitigating Factor in
Death Penalty Sentencing Hearings’. Florida State University Law Review,
26 (2003), 119-1174.
Sandra Jones 43
___________________________________________________________
11
J.O. Smykla, ‘The Human Impact of Capital Punishment: Interviews
with Families of Persons on Death Row’, Journal of Criminal Justice, 15
(1987), 331-347.
12
Margaret Vandiver, ‘The Impact of the Death Penalty on Families of
Homicide Victims and of Condemned Prisoners’, p. 477-505 in America’s
Experiment with Capital Punishment: Reflections on the Past, Present and
Future of the Ultimate Penal Sanction, eds. by James R. Acker, Robert M.
Bohn, and Charles S. Lanier. Durham, (N.C.: Carolina Academic Press,
1998).
13
Susan Sharp, Hidden Victims: The Effects of the Death Penalty on
Families of the Accused. (New Brunswick: Rutgers University Press,
2005).
14
Ibid.
15
Oklahoma recently rose to the position of the state that executes more
people per capita than any other state in the country, bumping Delaware to
second in line for this dubious distinction Death Penalty Information
Center (DPIC) <http://www.deathpenaltyinfo.org>
16
Bruce & Schultz, 2001.
17
Doka, 2002.
18
B.D.Romanoff & M. Terenzio, ‘Rituals and the grieving process’,
Death Studies, 22, 697-711.
19
T.A. Rando, Treatment of Complicated Mourning. (Champaign, Il.:
Research Press, 1993).
20
Colin Murray Parkes, ‘Bereavement as a psychosocial transition:
Processes of adaptation to change’, Journal of Social Issues, 44, 3, 53-65.
Britain’s ‘Punk’ Mourning Culture
Gerri Excell
Abstract
In 1977 the British music industry was rocked when the Sex
Pistols catapulted into the music world with their anti establishment
assault on the industry. Now it’s the turn of the British mourning culture,
out with established rules of mourning and, in with the new anti
establishment mourning culture of the roadside memorial. There are no
prescribed rules of what constitutes a roadside memorial and, this is
exactly the characteristic that appeals to the bereft, the personalisation of a
memorial site. A content analysis of 50 roadside memorials in the UK
reveals that it is the individuality of the symbolism that is important for
those bereft in today’s society. The roadside is a public space and is the
perfect space to incorporate a memorial that can draw attention to the end
of a life; the roadside can be used as a place to celebrate the life whilst at
the same time protest the untimely death. Religious iconography does not
focus heavily in the roadside memorial culture of the UK, is this because
the roadside is not perceived as the place for a religious icon? Could it be
that the death itself has questioned their faith? This paper will chronicle
the development of the roadside memorial in the UK and, discuss how the
proliferation of memorials is challenging established rules of mourning.
The new ‘punk’ movement of mourning will not go away but may
possibly evolve as policy is fashioned and attempts are made at
standardising the memorials. However, more can be learnt from the
individualised memorials; what are societal values today? What makes a
statement about this life, and maybe more importantly what might have
been missed about this life if a memorial had not been placed? The
roadside memorial provides a voice for a life that may only have a brief
eulogy in a crematorium by an officiant who never knew that individual,
this voice encourages freedom of speech.
1. Introduction
In this world nothing can be said to be certain except death and
taxes Benjamin Franklin, 1 death is the greatest leveller for all, besides
being born death is the only other certainty we have. However, how our
deaths are memorialised remains one of the great uncertainties, unless of
course plans have been made in this age of the buy now die later pre-
payment funerals. The mode of your death, however, may have a
qualifying effect on how you are memorialised. Since the 1980s there has
46 Britain’s ‘Punk’ Mourning Culture
___________________________________________________________
been a substantial growth in the number of spontaneous and roadside
memorials in the UK. 2 This paper will examine the phenomenon of the
roadside memorial and compare their emergence on British mourning
culture to that of the onslaught of punk music on the British music scene
of the 1970s. I will argue that Britain’s mourning culture has been subject
to the same processes that the music industry suffered at the hands of the
punk music genre. What was once a bottom up movement moves into the
mainstream. Whilst at first being feared by the established music world
and society, punk music quickly became part of the mainstream and lost
some of its original power. The same argument will be levied at the
roadside memorial phenomenon, what once courted controversy, has once
again joined the mainstream. This paper draws heavily on a previous
research project carried out in 2004 as part of my Masters degree. The
focus was roadside memorials in the UK, in which interviews were
conducted with those who have placed and maintained memorials at the
roadside.
3. The study
Having previously established the rationale for the placing of a
spontaneous memorial in an earlier research project 8 , focus was placed on
the material culture of the roadside memorials. Cataloguing over 100
memorials from the UK, 50 random memorials were selected and their
material culture recorded. Cataloguing the unique features of each
memorial in the sample revealed some fascinating insights into our
memorial culture of the UK. Drawing from previous published research
into roadside memorials from the USA and Australia 9 , it was evident that
the UK was unique in its spontaneous memorial culture. Most noticeable
was the dearth of “crosses” in our roadside memorials, In Australia Clark
& Cheshire 10 report that 80% of the memorials in their sample had a small
white cross in the material culture. Similarly in the USA white crosses are
the most common form of memorialisation in the roadside memorial
culture, many states in the US provide formal white crosses to be placed
on the roadside, and only these official white crosses may be placed. 11 The
top ten totems found in British roadside memorials were (1) Flowers; (2)
Names; (3) Footballing items (flags, shirts, tickets); (4) Candles; (5)
Messages; (6) Photographs; (7) Soft toys; (8) Alcohol; (9) Clothing; and
(10) Automobile wreckage. 12
This post-modern mourning culture surrounds itself in personal
representations of the individual, the individual is the focus, what football
team they supported, who they have left behind and what their loss means
to society. The study supported the assumption that roadside/spontaneous
48 Britain’s ‘Punk’ Mourning Culture
___________________________________________________________
memorialisation is a bottom up movement, where there are no rules of
what makes a good memorial it is entirely personal and organic.
6. Inclusive mourning
British mourning culture has embraced this new form of
memorialisation and added it to the repertoire and acknowledged that this
form of memorialisation encompasses disenfranchised grievers into the
fold. The sample of fifty UK spontaneous memorials used in this study
revealed that the usually absent group of young individuals 16-25 19 are
heavily involved in this form of memorialisation. Youth culture has
embraced a way in which they can actively participate in the
Gerri Excell 51
___________________________________________________________
memorialisation process and infuse their own values and beliefs into this
practice. Although, this form of memorialisation has allowed a more
inclusive mourning practice here in the UK it is sad to see that what was
once a powerful individualistic way of expressing private grief publicly
has been diluted by its very popularity.
7. Conclusion
The premise for this paper was that Britain’s memorial culture
has been transformed by the same processes and sub cultural
undercurrents that transformed the music world in the late 1970s. In the
USA purpose made memorial crosses and plaques can be purchased from
websites eager entrepreneurs finding a lucrative business. The
spontaneous memorial has become the ‘darling’ of the mass media,
poignant images of a spontaneous memorial site being used as the
backdrop of the new report of the incident. The once spontaneously hastily
placed bunch of flowers in its supermarket cellophane wrapping with
attached price tag, has become a stage-managed prop. Recently on British
television a favourite character was ‘killed off’, the character was stabbed
and died in the street. The next episode began with a panoramic shot of the
gates of the square decked with floral tributes to the dead character 20 .
Most of this episode focused on the memorial and characters central to the
show were seen placing their tributes and talking about who actually had
the right to place tributes there. This can be cited as evidence of how the
spontaneous memorial has become part of the norm when it comes to
memorialising a tragic death. The soap opera in question claims to
represent modern living in London and by using a spontaneous memorial
it is enforcing what would be expected to happen in that locality in real
life .Real life is reflected in the totems found at these post modern
memorial sites . Each memorial is unique, previous research 21 has
highlighted the importance to the bereft of the site of death itself a site that
is made sacred by the bereft and a place in which reflections of a lost
individual can be used in a way to regain control of the tragic
circumstances surrounding the death.
Cemeteries throughout the UK have introduced wide ranging
rules and regulations regarding the decorations and adornments allowed
on the graves. Not surprisingly then that the bereft may attempt to find
another avenue for displaying their grief. The roadside provides this
freedom, the freedom of expression, and the spontaneous memorial is
valuable as it is spontaneous. It provides society with an immediate
response ho the death, whether this response is an angry protest or a
touching human personal response to the death providing a valuable
resource for researchers into death, bereavement and post modern
52 Britain’s ‘Punk’ Mourning Culture
___________________________________________________________
mourning practices. In the formalized memorial world it may take weeks
often months before a permanent memorial is in place, in the events of
homicide it may be months of bureaucratic demands before the bodies are
released for cremation or burial.
Post war British memorial culture has been dominated by the
denial of death paradigm, Tony Walter 22 has written extensively on the
‘revival of death’ and a Modernist approach to the rationalization of death;
however this rationalization of death only serves to distance death once
again from the bereaved. The spontaneous memorial provides a new fresh
avenue for active involvement in memorial practices, and holistic
approach that was inclusive for all. Lessons can be learnt from the eclectic
array of totems so representative of a post – modern world
I fear that the once innovative spontaneous memorial has lost
some of its initial power and influence on society as a whole. Evidence
has been provided where the cultural image of a spontaneous memorial
has become part of the TV and music video repertoire, this is a double
edges sword it may bring the genre to the masses but, some how reduces
the whole aspect and meaning of a memorial of this type. The law of
diminishing returns, where once a powerful icon of sudden death now the
return has lessened and will we see familiarity breeding contempt?
Notes
1
Benjamin Franklin, Letter to Jean Baptiste Le Roy (1789) US author
diplomat, inventor, physicist, politician & printer (1706-1790).
2
Gerri Excell, Roadside Memorials in the UK: Private Grief made Public.
Unpublished MA thesis, The University of Reading, UK (2004).
3
Geoffrey Gorer, Death, grief and mourning in contemporary Britain
(London: Cresset, 1965), 41.
4
Peter Griffiths, ‘Words cannot say what she is’, in Planet Diana Cultural
studies and Global Mourning, ed. Public (Kingswood: University of
Western Australia, 1997), 47-48.
5
George Monger, ‘Modern Wayside shrines’, Folklore 108 (1997), 113-
114.
6
Anne Eyre, ‘Post-Disaster Rituals’, in Grief, Mourning and Death
Rituals, ed. Jenny Hockey, Jeanne Katz & Neil Small (Buckingham: Open
University Press, 2001), 104-111.
7
RoadPeace actively campaign in the UK for the rights of road crash
victims to ensure the trauma they suffer is acknowledged. Since 31st
August 2003, over 3,000 A4 plaques have been placed nationally,
resulting in over 400 articles in local and national press.
Gerri Excell 53
___________________________________________________________
8
Excell, 2004, 68.
9
Roadside memorials have been subjected to academic debate in the USA
and Australia for some years. The first International symposium on
Roadside Memorials was held in Australia in 2004.
10
Jennifer Clark and Ashley Cheshire. ‘RIP by the roadside: A
comparative Study of roadside memorials in New South Wales, Australia
and Texas, United States’, Omega 48 (2004), 229-248.
11
MADD, Mothers against Drunk Drivers in the USA have campaigned
since the 1980s and are a tour de force in the US. MADD sanctioned the
White Crosses to be placed at the scene of a fatality where alcohol was
involved.
12
Gerri Excell, ‘Contemporary deathscapes’ paper given at 7th Annual
International Conference on Death, Dying & Disposal, The University of
Bath, September 15th-18th (2005).
13
Situationist International (SI) a political movement formed in 1957 in
Italy. It grew out of a number of avant-garde artistic and political
movements. Its main aim was to challenge conformity and overthrow
capitalism.
14
Sarah Thornton, ‘General introduction’, in The Subcultures Reader, ed.
Ken Gelder and Sarah Thornton (London: Routledge, 1997), 1.
15
Stanley Cohen, Folk Devils and Moral Panics: The creation of Mods
and Rockers (London: Mac Gibbon & Kee, 1972), 57.
16
Bill Grundy presented the Thames Television news show ‘Today’ the
show was aired only in the London area. On December 1st 1976 the Sex
Pistols were a last minute stand in the band Queen who cancelled at the
last minute. The band were all intoxicated and were goaded and patronised
by Grundy throughout the interview. Grundy succeeded in getting the
band to swear live on air, the next day the tabloids were outraged, Grundy
was sacked from the show and ‘Today’ was taken off the air for two
months.
17
Erving Goffman, The Presentation of Self in Everyday Life
(Harmondsworth: Penguin, 1971), 70.
18
Sophie Kummer. ‘Road Fatality Signs are Morbid and Un-English’,
Edgware Times, sec3, p.4., 12 July (2003).
19
In my local neighborhood a sixteen year old boy tragically drowned. His
peer group held nightly vigils until his funeral. T-shirts were produced by
the group and worn throughout the period prior to his funeral and at the
funeral. Walls were ‘tagged’ with RIP Tyson and signs defaced with text
speak messages. The group received press coverage throughout the
mourning period those interviewed were in the age range was 14-25.
54 Britain’s ‘Punk’ Mourning Culture
___________________________________________________________
20
Eastenders is a BBC 1 soap opera shown three times a week in the UK,
first aired in 1985 it portrays the fictional London town of Walford. The
episode in question was shown over the Christmas/New Year period 2005.
21
Excell, 2004, 40.
22
Tony Walter, The Revival of Death (London: Routledge, 1994), 51.
Bibliography
Hartig, Katie & Kevin Dunn. ‘Roadside Memorials: Interpreting New
Deathscapes in Newcastle, New South Wales’. Australian Geographical
Studies 36 (1998), 5-20.
RoadPeace, ‘About RoadPeace’ Available online at
<http://www.roadpeace.org/> [accessed 17 August 2006].
Kate Woodthorpe
Abstract
Studying death is by no means a new adventure in sociology.
However, making connections between the different areas of research that
largely follow the chronological pattern of dying, moment of death, and
after death practices, have to date not been systematically made. Thus, this
paper is going to make some preliminary associations between pre-death
and post-death literature, via the concept of the ‘good death’. Specifically,
it will use Bradbury’s 1 conceptualisation of the good death in order to
make sense of how practice in the cemetery is becoming increasingly
subjected to norms of behaviour, and constructions of what conforms to/is
defined as ‘good’ mourning practice. Using this valuable concept I wish to
suggest that, similar to the arguments proposed by Field and James 2 -
whereby the hospice is becoming increasingly institutionalised - that the
contemporary cemetery could now be understood as an institution that
dictates memorialisation behaviour and activity, creating powerful norms
of ‘good’ memorialisation that in turn are utilised to signify how
individuals are ‘coping’ with their bereavement.
1. Introduction
Social research into death and dying is by no means a recent
endeavour. However, the sociality of death and dying remains on the
periphery of sociology, with a lot of the literature being produced in this
area coming from more anthropological perspectives. The origins of these
anthropological perspectives owe much to Hertz, 3 who is commonly
regarded as one of the first, and most significant, anthropologists
exploring the social meaning of death rituals. In terms of Western death
practices, sociological interpretation has tended to reflect the growth of the
death work industry, which recently has been dominated by the
monumental developments in health care.
The 1960s can lay claim to being one of the most progressive
decades in the development of a ‘death movement’, with the establishment
of the Hospice Movement by Dame Cicely Saunders, and the publication
of Jessica Mitford’s ‘American Way of Death.’ 4 Importantly however,
whilst these two isolated occurrences reflect the progress of intellectual
endeavours on death and dying, whereby they did not act to establish a
link between the periods before and after death. This separation between
work on before and after death has prevailed since then, with a huge
56 The Making of ‘Good’ Memorialisation
___________________________________________________________
growth in dying and palliative care study, and less attention paid to issues
surrounding disposal and after-death practices. Evidence for the current
state of affairs in England today includes many academic departments
devoted specifically to researching hospices. Cemeteries, on the other
hand, remain on the periphery of academics’ remits, although there have
been important developments with the establishment of the Cemetery
Research Group at the University of York and the Death Centre at the
University of Bath within the last decade. In addition, whilst there have
been individual academic authors who have attempted to bridge the gap
between dying and death 5, 6 , 7 these works have not fully entered the
contemporary cemetery landscape, tending to focus on exploring wider
ritual activity and frameworks of understanding. This paper therefore
intends to expand on these tentative bridges between disciplines, and
incorporate ‘dying’ literature into an ethnographic study of the
contemporary cemetery and memorialisation practice, underpinned by “a
dawning realisation that contemporary attitudes to death and dying are
unsatisfactory and that society has somehow lost touch with the meaning
of life.” 8
As sites of remembrance, cemeteries have a lot to offer us in
terms of how people understand and remember the dead, both individually
and collectively, locating the activity of bereaved people in the social
world; something which, to date, has been neglected in the positivist
climate of bereavement research. 9 Thus, I wish to create a dialogue
between accounts of those experiences of dying and contemporary
mourning behaviour, using the model of the good death 10 to describe and
suggest there is scope for utilising concepts from the dying experience
when exploring post-death experience, specifically memorialisation. This
will then be extended to suggest that there are similarities between the
institutionalisation of hospice activity 11 and an institutionalisation of
‘good’ memorialisation activity.
The data for this paper comes from an ESRC funded
ethnographic study of the contemporary cemetery landscape, co-funded by
the City of London and Institute of Cemetery and Crematorium
Management. All fieldwork took placed at the City of London Cemetery
and Crematorium in Newham, East London. This 220-acre site is
celebrating its 150 year anniversary this year. It is run by the Corporation
of London, employs approximately 90 staff, and is in the process of
establishing itself as a ‘Centre of Excellence for Best Practice’. In addition
the cemetery prides itself in offering a range of choices for the burial of
dead individuals, including lawn burial, traditional burial and woodland
burial. In this vein, the cemetery attempts to cater for everyone, placing
accessibility and individuality at its core. The purpose of this project has
Kate Woodthorpe 57
___________________________________________________________
been to explore conservation and how different groups of people (visitors,
staff and the local community) perceive this dynamic and complex
landscape. In turn, this has developed into a wider exploration of
meanings and values attributed to the dead and conceptualisations of life,
as “the issue of death throws into relief the most important cultural values
by which people live their lives and evaluate their experiences.” 12
D. Modern memorialisation
As in the case of modern dying, this type of memorialisation is
about control and limitations placed upon visitors by ‘the experts’ - who in
Kate Woodthorpe 59
___________________________________________________________
this instance are the cemetery staff. Emphasis is placed on controlling of
expressions of grief through particular forms of memorialisation, and a
practical regulation of any expressions that breach the limits of
acceptability constructed by the cemetery management and enacted
through the cemetery regulations. For example, the City of London
Cemetery and Crematorium Regulation 27 number 86 states that: ‘We do
not allow curbs, posts or vases in the lawn section’. Regulation 94 further
states: ‘We do not allow crosses made of wood, bell glasses, shells, grass
wreaths or other moveable or fragile items in the cemetery.’ Thus
memorialisation activity is perceived as either abiding by or breaking
those rules. The wider meaning or purpose behind it is implied by the
enforcement of memorial directives and the need to maintain a controlled
landscape overall. Much like Lawton’s 28 assertion that patients were
sedated or moved due to the collective nature of wards in the hospice and
the distress dying could cause for others, cemetery staff clear graves of
prohibited memorialisation in order to ensure that the collective space
fulfils their ideal of good memorialisation practice, based on their reading
of the public’s reaction – and then incorporated into the regulations.
F. Natural memorialisation
Similar to the ambiguous nature of other items within Bradbury’s
typology, this form of memorialisation can simultaneously be seen as
about being ‘in’ nature and/or being ‘natural’. Burial could take place in a
woodland area or a more conventional municipal lawn section;
importantly, the focus is not where the body is buried, but rather it is this
theme of intervention that is key here. In natural memorialisation there is
an emphasis on the normality of death, an acceptance, and a sentiment
towards the individuality of the person, rather than expert technical
knowledge. Thus, there may be elements of the sacred and modern in this
type of memorialisation, but the focus is on the individual rather than
wider frameworks of shared beliefs and values. In this way, it is the
60 The Making of ‘Good’ Memorialisation
___________________________________________________________
ultimate late modern act of memorialisation, ‘done my way.’ 30 Inevitably,
in a collective landscape, this individuality can cause conflict, as one staff
member told me:
6. Conclusion
Through exploring these conceptualisations of good
memorialisation practice, I have shown how the cemetery shapes
mourning behaviour and practice, similar to ways in which activity is
shaped within a hospice. There is much scope for a greater integration of
the cemetery into local communities, in the way that hospices have been,
yet they continue to remain on the periphery of local communities and
policy makers’ agendas. This low status has been reflected in research into
death-related spaces, with only a few notable exceptions in recent years 43,
44
. However, it is my hope that this will begin to change, as
interdisciplinary conferences such as Making Sense of: Dying and Death
promote a dialogue between the different researchers and audiences
working with death and dying. If we - as individuals, academics, policy
markers and practitioners - can begin to develop a constructive across-
discipline conversation about our understandings of how people deal with
dying, death and disposal, there is a greater potential for providing the best
64 The Making of ‘Good’ Memorialisation
___________________________________________________________
and most appropriate space, landscape and service for the dying, the dead,
and the bereaved, both now and in the future.
Notes
1
Mary Bradbury, Representations of death: a social psychological
perspective (London: Routledge, 1999).
2
David Field, & Neil James, ‘Where and how people die’, in D. Clark,
(ed) The Future for Palliative Care: Issues of Policy and Practice
(Buckingham: Open University Press, 1993), 6-29.
3
Robert Hertz, Death and the Right Hand, Tr. R. and C. Needham
(London: Cohen West, 1960 [1907]).
4
Richard Huntington & Peter Metcalf, Celebrations of Death: the
anthropology of mortuary ritual, 2nd ed. (Cambridge: Cambridge
University Press, 1991).
5
Tony Walter, The Revival of Death (London: Routledge, 1994).
6
Jenny Hockey ‘Encountering the ‘reality of death’ through professional
discourses: the matter of materiality’, Mortality, 1, 1 (1996), 45-60.
7
S.M. O’Gorman ‘Death and Dying in contemporary society: an
evaluation of current attitudes and the rituals associated with death and
dying and their relevance to recent understandings of health and healing’,
Journal of Advanced Nursing, 27 (1998), 1127-1135.
8
Ibid, 1133.
9
Christine Valentine, ‘Academic constructions of bereavement’,
Mortality, 11, 1 (2006), 57-78.
10
Maurice Bloch & Jonathan Parry (ed.s) Death and the Regeneration of
Life (Cambridge: Cambridge University Press, 1982).
11
Field and James.
12
Huntington and Metcalf, 25.
13
Barney Glaser & Anselm Strauss, Awareness of Dying (New York:
Aldine, 1965).
14
Phillipe Ariès, Western Attitudes towards death: from the middle ages to
the present, tr. P.R. Ranum (London: John Hopkins University Press,
1974).
15
Bloch and Parry.
16
Jonathan Parry, ‘Sacrificial death and the necrophagous ascetic’, in
Death and the Regeneration of Life, ed. M. Bloch and J. Parry
(Cambridge: Cambridge University Press, 1982), 74-110.
17
J. Watson, ‘Of flesh and bones: the management of death pollution in
Cantonese Society’, in Death and the Regeneration of Life, ed. M. Bloch
and J. Parry (Cambridge: Cambridge University Press, 1982), 155-186.
Kate Woodthorpe 65
___________________________________________________________
18
Maria Càtedra, ‘Kinds of Death and the House’, in Death, Mourning,
and Burial: a cross-cultural reader, ed A.C.G.M. Robben (Oxford:
Blackwell Publishing, 2004), 77.
19
Norbert Elias, The Loneliness of the Dying, tr. E. Jephcott (Oxford:
Blackwell, 1985).
20
B. Hart, P. Sainsbury. & S. Short ‘Whose dying? A sociological critique
of the ‘good death’’, Mortality, 3, 1 (1998), 65-77.
21
Beverley McNamara, C. Waddell & M. Colvin, ‘Threats to the good
death: the cultural context of stress and coping among hospice workers’,
Sociology of Health and Illness, 17, 2 (1995) 222-244, 237.
22
Hart et al, 65.
23
Bradbury.
24
Beverley McNamara, C. Waddell, & M. Colvin, ‘The
Institutionalization of the Good Death’, Social Science and Medicine, 39,
11 (1994), 1501-1508.
25
Julia Lawton, The Dying Process: patients’ experiences of palliative
care (London: Routledge, 2000).
26
McNamara et al, 1994.
27
City of London Cemetery Regulations, 2000 (30th May 2006)
<http://www.cityoflondon.gov.uk/Corporation/our_services/health_safety/
cemetery_crematorium/>.
28
Lawton.
29
Bradbury, 152.
30
Walter, 1994.
31
Beverley McNamara, Fragile Lives: death, dying and care
(Buckingham: Open University Press, 2001).
32
Tony Walter, On Bereavement: the culture of grief (Buckingham: Open
University Press, 1999).
33
Simon Williams, Medicine and the Body (London: Sage, 2003).
34
see E.K. Abel, ‘The Hospice Movement: institutionalizing innovation’,
International Journal of Health Services, 16, 1 (1986).
35
McNamara et al, 1994.
36
Hart et al.
37
Field and James.
38
McNamara et al, 1995.
39
Lawton.
40
see Carol Komaromy, ‘The performance of the hour of death’, in
Palliative Care for Older People in Care Homes, ed J. Hockley and D.
Clark (Buckingham: Open University Press, 2002), 138-150.
41
Hart et al.
66 The Making of ‘Good’ Memorialisation
___________________________________________________________
42
Ian Hussein, Paper given at Memorial Awareness Board session, Houses
of Parliament, (3rd May 2006).
43
Phillip Bachelor Sorrow and Solace: the social world of the cemetery
(Amityville, NY: Baywood Publishers, 2004).
44
Doris Francis, Leonie Kellaher, & Georgina Neophytou, The Secret
Cemetery (Oxford: Berg, 2005).
Melanie K. Finney
Abstract
Multiple deaths occurring at academic institutions present
interesting challenges for those trying to help others adjust and cope with
such losses. This article addresses the characteristics of higher educational
institutions that make them vulnerable to extreme forms of grieving, and
that may complicate coping with major traumas. In particular, these
factors serve to emphasize the dialectical tensions involved in coping with
major loss that are present when multiple deaths occur in university
communities. Drawing on the dialogism of social theorist Bahktin, five
particular dialectical tensions are outlined: (1) tensions between
individuals’ needs to remember and institutions' need to move on; (2)
tensions regarding the demonstration of private grief and public mourning;
(3) tensions between performance of public and private rituals; (4)
tensions as individuals move between roles as mourners and consolers;
and (5) tensions as individuals struggle to accept pain and move towards
growth. This essay considers how institutions must be aware of, and
address, the frequently competing needs of the various parties as they
encounter these types of losses.
Notes
1
Melanie K. Barnes, et al., ‘The Relativity of Grief: Differential
Adaptation Reactions of Younger and Older Persons’, Journal of Personal
and Interpersonal Loss, 1 (1998), 375-392.
2
Ronnie Janoff-Bulman & Michael Berg, ‘Disillusionment and the
Creation of Values: From Traumatic Losses to Existential Gains’, in
Perspectives on Loss: A Sourcebook, ed. John H. Harvey (Philadelphia:
Brunner Mazel, 1998), 35-47.
3
Harold S. Kushner, When Bad Things Happen to Good People. (New
York: Avon Books, 1981).
4
Melanie K. Barnes, ‘A case study approach to support needs following
the death of a loved one’, Journal of Personal and Interpersonal Loss, 1
(1996), 275-298.
5
Mikhail M. Bakhtin, The Dialogic Imagination: Four Essays by M. M.
Bakhtin, ed. Michael Holquist, trans. Caryl Emerson & Michael Holquist
(Austin: University of Texas Press, 1981).
6
Leslie A. Baxter & Barbara M. Montgomery, Relating: Dialogues and
Dialectics (New York: Guilford, 1996).
7
Ibid, 9.
8
Melanie K. Finney, ‘Accommodating Dialectical Tensions in Academic
Institutions Following Traumatic Events’ (in prep).
9
Margaret Strobes, Hank Schut, & Wolfgang Stroebe, ‘Trauma and Grief:
A Comparative Analysis’, in Perspectives on Loss: A Sourcebook, ed.
John H. Harvey, (Philadelphia: Brunner Mazel, 1998), 91.
10
Ibid, 92.
11
Terry L. Martin & Kenneth J. Doka, Men Don’t Cry… Women Do:
Transcending Gender Stereotypes of Grief (Philadelphia: Brunner Mazel,
1999).
12
John H. Harvey, Give Sorrow Words: Perspectives on Loss and Trauma
(Philadelphia: Brunner Mazel, 2000), 208.
Melanie K. Finney received her Ph.D. from The University of Iowa and is
Associate Professor of Communication and Theatre at DePauw
University, Greencastle, Indiana, United States.
Traumatic Bereavement and Coping:
Implications for a Contextual Approach
Abstract
Bereavement responses and outcomes depend on multiple factors,
such as circumstances of the death, the relationship with the deceased,
individual characteristics, social context, and cultural factors. Responses
to natural death differ from those following traumatic death. Death of a
child or spouse is most difficult, while age mitigates coping. Social
support is important and cultural differences affect funeral rites and coping
patterns.
Using Northern Ireland as a case in point, this paper explores
implications of violent death over time. Northern Ireland lived in civil
unrest and political violence, commonly known as the Troubles, since
1969. Over 3,600 people have been killed as a result. In 1994/05,
ceasefires were negotiated and since then, violent incidents have decreased
dramatically, although they have not completely stopped.
In the early years of the Troubles, the impact of the violence on
people’s mental health was underestimated and there was a lack of
structured support. Since the ceasefires, more attention has been paid to
those affected and community support groups have grown rapidly.
In this paper, we report data from pre-ceasefire studies and
contrast these with newly emerging post- ceasefire research in regard to
psychological health, depression, and PTSD in individuals who
experienced traumatic bereavement. Quantitative as well as qualitative
data will be reported and implications for a contextual analysis outlined.
1. Introduction
Bereavement is an inevitable and universal experience, although
how each individual reacts to the death of a loved one depends on multiple
factors. Dillenburger and Keenan 1 suggested that bereavement outcomes
and coping are shaped by at least four different yet intertwined contexts:
(1) the Death itself, including the circumstances surrounding the death,
and how the death was communicated; (2) Individual factors, such as age,
gender, relationship with the deceased, and health prior to bereavement;
(3) Social circumstances, such as the extent of social support and quality
of social network; and (4) Cultural context, including cultural norms and
rites, historical circumstances and political situations. In this paper, we use
76 Traumatic Bereavement and Coping
___________________________________________________________
their D.I.S.C model to look at traumatic bereavement and, we compare
data of the PAVE Project (People Affected by Violence) 2 with data of the
first study on violent bereavement in Northern Ireland in the mid-
eighties. 3
Bereavement caused by violence is clearly more traumatic than other types
of bereavement. 4 Since 1969, over 3,600 people were killed as a direct
result of violent conflict in Northern Ireland. This means that thousands
have lost immediate family members, relatives, and close friends in
shootings, beatings and bombings. Mass violence is not unique to
Northern Ireland, and there are many other examples where people have
suffered mass-scale bereavement through war, genocide or natural
disasters. The question is, how do people cope in the long-term?
Ten years after the ceasefires, one could expect that people have
learned to live with their loss, however, recent research shows that many
are still suffering twenty, thirty or even thirty-five years after their loss 5 ,
“for many, the hurt of thirty years ago is just as strong as it was then and
remains undiminished by the passage of time.” 6 In 1985/6, a violently
bereaved widow said:
Twenty years later, these widows cannot stop thinking about their loss:
These data are similar to findings from the mid 1980s when the
GHQ-30 mean score for violently bereaved widows was 10.69 (SD 9.4). 18
3. The death
It is widely believed that the circumstances of the death are one
of the crucial factors that affect bereavement outcome. Certain
circumstances, such as sudden death and lack of anticipation, violence, or
multiple deaths, are more likely to lead to more problematic bereavement
or to so-called ‘complicated grief’. 19 For example, Kaltman and
Bonnano 20 found that bereavement following violent death (accidental
death, suicide or homicide) is likely to result in PTSD symptoms and
enduring depression.
In Northern Ireland, a widow in 1985/6 revealed how her
husband was killed and how his violent death affected her:
The gunmen had shot him straight into the face. His face
was so bad that they just put a plastic bag over it. All I
can see when I close my eyes now is that white plastic
bag. I cannot even remember his face. 21
78 Traumatic Bereavement and Coping
___________________________________________________________
In 2006, a widow explains how seventeen years after the violent death of
her husband, the way he was killed still has an impact on her:
If there was a door here, we were sitting, I would have
to go over and open the door. I can’t bare the door
closed. Probably because of the way they came in
through my back door and murdered my husband. 22
5. Social context
The social context, in particular the level of social support, is an
important factor in terms of bereavement outcome. Twenty years ago,
bereaved widows relied almost exclusively on support from family and
friends, as very little structured support was available:
Most bereaved PAVE project participants (40 out of 59) had received
some support from support groups (n=19), family (n=14), and friends
(n=5). Being able to talk clearly mitigates poor psychological health,
depression, and PTSD (Table 3).
6. Cultural context
The effect of cultural and political contexts on the bereavement
process is difficult to assess. Because of dramatic political changes over
recent years, Northern Ireland supplies an intriguing example. During the
early phase of the Troubles, shootings and bombings were nearly daily
occurrences. The effect on people’s coping is reflected in this quote from a
widow:
82 Traumatic Bereavement and Coping
___________________________________________________________
Whenever I listen to the television and another terrorist
attack happened I feel most under stress. I switch the
television off. I just cannot stand any more murders. 36
7. Summary
Traumatic bereavement amalgamates the effects of trauma and
grief. 41 Data reported here opens an extensive range of questions for
trauma and bereavement researchers and practitioners. How do those who
have lost a loved one in violent circumstances cope over the years? What
needs to happen for them to move on? Why do some people cope better
than others do? Why do some bereaved individuals still suffer twenty or
thirty years after their loss? In this paper, we argue that a holistic approach
is needed in order to address these questions. Coping with traumatic
bereavement does not happen in isolation and we explored Death-related,
Individual, Social, and Cultural (D.I.S.C.) contexts in order to illustrate
this process.
Notes
1
Karola Dillenburger and Mickey Keenan, ‘Bereavement: A D.I.S.C
Analysis’, Behavior and Social Issues, 14 (2005), 92-112.
2
Karola Dillenburger et al., ‘The PAVE Project’, Victims and Survivors
Newsletter 2nd Edition, (Belfast: Victims Unit, OFMDFM, 2005).
3
Karola Dillenburger, Violent Bereavement: Widows in Northern Ireland
(Aldershot: Avebury, 1992).
4
See: Janice L. Genevro, Report on Bereavement and Grief Research
[report on line] (Washington DC: Center for the Advancement of Health,
2003, accessed 15 July 2005); available from the Center for the
Advancement of Health: http://www.cfah.org/pdfs/griefreport.pdf/; and
Colleen Murray et al, ‘Death, Dying, and Grief in Families’, in Families
and Change. Coping with Stressful Events and Transitions, ed. Patrick C.
McKenry and Sharon J. Price (Thousand Oaks, CA: Sage Publications,
2005, 3rd Ed.), 75-102.
5
see Karola Dillenburger, 1992; Peter S. Curran et al., ‘Psychological
Consequences of the Enniskillen Bombing’, The British Journal of
Psychiatry 156 (1990), 479-482; Patrick Hayes and Jim Campbell,
‘Dealing with Post-Traumatic Stress Disorder: The Psychological Sequel
of Bloody Sunday and the Response of State Services’, Research on
Social Work Practice 10, 6 (2000), 705-721; Dermot O’Reilly and Mike
Stevenson, ‘Mental health in Northern Ireland: have “the Troubles” made
it worse?’, Journal of Epidemiology and Community Health, 57 (2003),
84 Traumatic Bereavement and Coping
___________________________________________________________
488-492; Ed Cairns and John Mallet, Who are the Victims? Self-assessed
Victimhood and the Northern Irish Conflict; NIO Research and Statistical
Series, Report No.7 (Belfast: NIO Statistics and Research Branch, June
2003); and PAVE Project, 2005/6.
6
Michael Potter, In Their Own Words: A Research Report into the Victims
Sector in Northern Ireland (Belfast: Training for Women Network, April
2004), 4.
7
Widow in Dillenburger, p. 91.
8
A., widow, January 06. PAVE project.
9
M., widow, February 06. PAVE project.
10
Morris Fraser, Children in conflict (Norwich: Norfolk Pelican Book,
1973).
11
Alf McCreary, Survivors (Belfast: Century Books, 1976); and Ed Cairns
and Ronnie Wilson, ‘The impact of political violence on mild psychiatric
morbidity in Northern Ireland’, The British Journal of Psychiatry 145
(1984), 631-635.
12
Curran et al., 479; and Dillenburger, 1992.
13
John Darby and Arthur Williamson, eds, Violence and the Social
Services in Northern Ireland (London: Heinemann, 1978).
14
see Marie Therese Fay et al , The Cost of the Troubles Study. Report on
the Northern Ireland Survey: the experience and impact of the Troubles
(Belfast: INCORE, 1999); Hayes & Campbell, 705; Karola Dillenburger
and Mickey Keenan, ‘Islands of Pain in a Sea of Change: Behavior
Analysis and Bereavement’, European Journal of Behaviour Analysis 2
(2001), 187-207; Cairns and Mallet, Who are the Victims?; O’Reilly and
Stevenson, 488.
15
David Goldberg, Manual of the General Health Questionnaire
(Windsor: NFER-Nelson, 1978).
16
Aaron T. Beck et al., ‘Psychometric properties of the Beck Depression
Inventory: Twenty-five years of evaluation’, Clinical Psychology Review
8, 1 (1988), 77-100.
17
Edna B. Foa et al., ‘The validation of a self-report measure of
posttraumatic stress disorder: The Posttraumatic Diagnostic Scale’,
Psychological Assessment 9, 4 (1997), 445–451.
18
Dillenburger, 1992.
19
Therese A. Rando, The treatment of complicated mourning (Champaign,
IL: Research Press, 1993).
20
Stacey Kaltman and George A. Bonnano, ‘Trauma and bereavement:
Examining the impact of sudden and violent deaths’, Journal of Anxiety
Disorders 17, 2 (2003), 131-147.
21
Widows in Dillenburger, pp.91-92.
Karola Dillenburger et al. 85
___________________________________________________________
22
M., widow, February 06. PAVE Project.
23
E. Kirschner, ‘Data on bereavement and rehabilitation of war widows’,
Series in Clinical & Community Psychology: Stress & Anxiety, 8 (1982),
219-224.
24
Karola Dillenburger and Mickey Keenan, Some suggestions for a
behaviour analysis of bereavement and loss. Behaviour Analysis in
Ireland, 25 years Anniversary Conference, Maynooth, Ireland, 5 May
(2002).
25
Dillenburger and Keenan, 92.
26
C., bereaved daughter, March 06. PAVE Project.
27
D., bereaved brother, March 06. PAVE Project.
28
Widow in Dillenburger, p. 71.
29
M., widow, February 06. PAVE Project.
30
Widows in Dillenburger, p. 89.
31
M., widow, February 06. PAVE Project..
32
S., bereaved daughter, March 06. PAVE Project.
33
M., widow. February 06. PAVE Project.
34
S., bereaved daughter, March 06. PAVE Project..
35
Paddy Hillyard et al., Bare Necessities: Poverty and Social Exclusion in
Northern Ireland (Belfast, Democratic Dialogue, 2003).
36
Widow in Dillenburger, p. 71.
37
D., bereaved brother, March 06. PAVE Project.
38
Hayes and Campbell, 705.
39
A., bereaved widow, February 06. PAVE Project.
40
M., bereaved widow, January 06. PAVE Project.
41
Kaltman and Bonnano, 131.
Can the Dying Mourn?
Kate Powis
Abstract
Seale, in identifying the late modern patient-centred ‘scripts’
adopted by the hospice movement, has declared that the dying themselves
can now play the role of chief mourner. For the aware dying, it is
proposed that some of their grief is anticipatory and the manner in which
they mourn their prospective death will offer guidance and even hope to
those who will have to negotiate their own bereavement after the death of
their loved one.
This paper will examine the psychoanalytic roots of mourning
theories to be found in Freud’s ‘Mourning and Melancholia’ in order to
determine how appropriate it might be to apply psychological models of
bereavement to the dying. While there can be no doubt loss is a major
feature in the experiences of the dying, meaning that elements of such
models may have relevance, I will propose that a key feature of Freud’s
foundational theory cannot be available to the aware dying, thereby
rendering the notion that the dying can ‘successfully’ mourn untenable. I
go on to suggest an alternative account of what may be intermingled with
the experiences of loss for the dying: the fear of annihilation.
1. Introduction
Constructivist theorists studying this topic have proposed that the
‘aware dying’ have recourse to social scripts that allow them to negotiate
their way through the dying trajectory. One such script has been
transplanted from psychological theories of bereavement and mourning.
Such accounts have been developed into stage theories, identifying a path
through the mourning process, and in turn allowing those accompanying
the bereaved, and indeed the bereaved themselves, to assess how
successful they are in working through this process. The efficacy of these
theories in the area of bereavement, based as they are on profound
psychoanalytic insights and an understanding of infant experiences of loss
and separation, has meant that attempts have been made to transpose the
model to the dying themselves; the most well-known, indeed some would
say notorious, being that of Kübler Ross.
The purpose of this paper however is not to launch yet another
broadside against Kübler-Ross’s ‘Five Stages’, 1 or propose an alternative
modelling for the dying process. Instead I will examine the psycho-
analytic roots of mourning theories to be found in Freud’s ‘Mourning and
88 Can the Dying Mourn?
___________________________________________________________
Melancholia’ 2 in order to determine how appropriate it might be to apply
psychological models of bereavement to the dying in the first place. While
there can be no doubt loss is a major feature in the experiences of the
dying, meaning that elements of such models may have relevance, I will
propose that a key feature of Freud’s foundational theory cannot be
available to the ‘aware dying’, thereby rendering the notion that the dying
can ‘successfully’ mourn untenable. I go on to suggest an alternative
account of what may be intermingled with the experiences of loss for the
dying drawn from the work of Freud again, and two contemporary
psychoanalysts: Hurvich and Grotstein and their analysis of trauma and
the fear of annihilation and the trinity of powerlessness, meaninglessness
and nothingness.
8. Conclusion
My starting point in this paper has been a doubt around the
efficacy of a wholesale transposition of mourning theories to the
predicament of the aware dying, albeit that this inevitably involves a range
of losses. With this doubt came a suspicion that what prompted us to rely
on these theories was an unwillingness to examine the ultimate source of
anxiety in dying, the fear of annihilation. This may be seen as
defensiveness on both an individual and a social and cultural scale. Even
psychoanalysts have recognised that their discipline may be prey to this;
Hurvich acknowledges that it is a relatively undeveloped concept in the
literature, with no comprehensive definition. 36 He cites Langs who
suggests “classical psychoanalytic theory and technique has been designed
to some extent as a defence against such primitive anxieties.” 37 I believe
that Grotstein’s discussion of powerlessness as the dialectic of power
offers one answer as to why this might be. In a culture that is driven to
Kate Powis 95
___________________________________________________________
holding and maintaining power on an individual, social and global scale,
the ultimate relinquishing of it that all humans must face is a terrible threat
indeed.
And finally, to return to Ivan Ilyich: I wish that there had been
time and space to do more justice to this work, but I will end with a brief
glimpse of the predicament of Ivan himself. He faces terrible despair that
racks up the pain and suffering he must endure as he realises that all he
has valued in his life is meaningless. His powerfully connected friends,
status hungry wife and self-regarding doctor can offer him no way out of
his agony. The only person who can bring temporary ease is his serf who
cheerfully stays with him and supports his legs to make him more
comfortable. Finally, an hour before his death, Ilyich is shrieking
desperately. His young son comes to him and kisses his hand and bursts
into tears. It as at this point that Ilyich finds relief, can turn away from
bitterness and looks with compassion on his family, and at last
relinquishes fear. The two least powerful figures in the story are finally the
ones to help.
Notes
1
Elisabeth Kübler-Ross, On Death and Dying (London and New York:
Routledge, 1973).
2
Sigmund Freud, ‘Mourning and Melancholia’ (1917) from On
Metapsychology: The Theory of Psychoanalysis, Volume 11 of The
Penguin Freud Library, Standard Edition edited by James Strachey,
present volume compiled and edited by Angela Richards (London,
Penguin, 1984), 251-268.
3
Clive Seale, Constructing Death (Cambridge: Cambridge University
Press, 1998), 118.
4
Seale, 118 -119.
5
John Bowlby, Attachment and Loss. Vol. III: Loss: Sadness and
Depression (London: Penguin, 1980).
6
C.B. Wortman and R.C. Silver, ‘The myths of coping with loss’, Journal
of Consulting and Clinical Psychology: 57, 3 (1989) 349-57.
7
Tony Walter, ‘A new model of grief: bereavement and biography’,
Mortality 1, 1 (1996), 7-25.
8
Kübler-Ross, 34-121.
9
Seale, 107.
10
Joy Schaverien. The Dying Patient in Psychotherapy: Desire, Dreams
and Individuation (Basingstoke: Palgrave, 2002), 125.
11
Freud, 1917, 252.
96 Can the Dying Mourn?
___________________________________________________________
12
Ibid.
13
Ibid., 254.
14
Ibid., 253.
15
Ibid., 265.
16
Ibid.
17
Leo Tolstoy, The Death of Ivan Ilyich, tr. Rosemary Edmonds (London:
Penguin [1886]1960).
18
Ibid., 102.
19
Ibid., 103.
20
Ibid., 104.
21
Ibid., 107.
22
Sigmund Freud (1926) ‘Inhibitions, symptoms and anxieties’ from The
Standard Edition 20, edited by James Strachey (London: Hogarth, 1959),
77 -175.
23
Sigmund Freud (1933) ‘Anxiety and instinctual life’ from New
introductory lectures on psychoanalysis (Lecture 32), Standard Edition 22
edited by James Strachey (London: Hogarth, 1933), 81-111.
24
Freud, 1926, 162.
25
Freud, 1933, 94 -95.
26
Freud, 1926, 166.
27
Hurvich, 312.
28
Wilfred Bion Learning form Experience (London: Karnac, 1984).
29
James Grotstein, ‘The psychology of powerlessness: Disorders of self-
regulation and interactional regulation as a newer paradigm for
psychopathology’, Psychoanalytic Inquiry, 6 (1986) 93 -118.
30
James Grotstein, ‘Nothingness, Meaninglessness, Chaos, and the ‘Black
Hole’’, Contemporary Psychoanalysis, 26 (1990), 257- 290.
31
Grotstein, 1990, 257.
32
Bion, 1962b.
33
Grotstein, 1990, 267.
34
Ibid., 264.
35
Bion, 1962b.
36
Hurvich, 1989.
37
Langs, 1981, cited by Hurvich, 1989, 318.
Lloyd Steffen
Abstract
This paper argues that one of the reasons the abortion issue is so
intractable is that a metaphysical notion of ‘innocence’ has attached to the
foetus, thus subverting our ordinary, morally framed understanding of how
and why abortion can be justified. Attention is focused on the refusal of
some anti-abortion advocates, including the moral teaching of the Roman
Catholic Church, to accept that a pregnant woman can justifiably abort a
foetus if that foetus poses a threat to her life or health. The just war notion
of ‘non-combatant immunity’ is offered as a non-absolutist point of
contrast with absolutized notions of innocence that would value the foetus
over the pregnant woman.
Key Words: abortion, just abortion, just war theory, religious innocence,
non-combatant immunity, foetal death.
1. Introduction
Why has the abortion debate been so intractable? I suggest in this
paper that the reason may involve people talking past one another over
issues that have not been fully presented for reflection and critique. One
such issue is that of foetal innocence
My argument is that invocations of foetal innocence have
elevated the foetus to a peculiar metaphysical status even beyond the
moral category of person; and to expose this development I shall contrast
this metaphysical claim with more accessible moral notions of innocence
as they arise in non-sectarian moral thinking. The just war idea of ‘non-
combatant’ immunity will serve to expose this moral notion of innocence.
The contrast between metaphysical and moral ideas of innocence will
illumine the meaning of foetal death as it arises in the debate over
abortion.
2. Moral innocence
In our ordinary moral discourse, we make reference to ‘innocent’
persons. We acknowledge in the moral life the threat to innocent lives
posed by a terrorist or armed bank robber who may be panicking; and
what we mean innocence in such situations is that persons so threatened,
all of whom possess a right to life, have been positioned by unwanted life
circumstances, to be in harms way. These persons are agents and capable
of action; their right to life is protected by their inclusion in the moral
category of personhood; and it would be morally wrong to intentionally
98 The Death of Innocents
___________________________________________________________
kill one of these innocent persons. The duty to protect them may lead
others, say, the police, to use deadly force to protect them.
This idea of protecting innocent persons because they are persons
and possessed of a right to life which it is a moral duty to protect has been
enshrined in what we know as just war theory. Just war has always made
appeal to the idea of restraint of force, and underwriting just war as a
policy tool is a moral framework - a structure for moral thinking - that is, I
believe, enormously practical and helpful for thinking through moral
issues and dilemmas. Just war, as a moral perspective, presumes
reasonably that force ordinarily ought not to be used to settle conflicts,
then imposes various tests of justice that must be satisfied if that
presumption against using force is to be lifted so that a use of force then
could make a reasonable claim to being morally justified. The tests of
justice - he jus ad bellum criteria so familiar to us - deal with such matters
as competent authority, just cause, announcement of intention, last resort
and so on; and in the classic jus in bello requirements for the actual use of
force once a use of force has been justified and is underway, two other
constraints, a proportionality requirement that the use of force must be
proportionate to the end of peace (this deals with weapons that are
disproportionate and ought not be used); and a ‘non-combatant immunity’
provision. What this provision says is that the actual use of force requires
that persons not engaged in the conflict must be protected - they are not to
be directly attacked. Non-combatant immunity makes reference to what
we typically call ‘innocent persons.’
What do we mean by this? Combatant and non-combatants are all
persons and all possess a right to life; but non-combatants are immune
from the use of force and it is presumptively wrong to directly use force,
especially lethal force, against them. They are innocent. They are by-
standers in the bank that is being robbed, they are in the line of fire when
warring parties unleash urban mop-up operations; they are in office
buildings and subways when terrorists strike. Directly intending to harm
and kill non-combatants, those not party to a conflict where lethal force is
being used, is, according to just war ethics, morally wrong. Targeting
civilians to achieve some end is wrong; using terrorist tactics, which by
definition are directed at civilian non-combatants, at innocent persons, is
wrong; and every effort must be made, just war wants to say, to prevent
harming these ‘innocent persons.’ The only thing that would make the
killing of an innocent person permissible is if every conceivable effort was
made to prevent such killing and when such killing did take place it
happened as a regrettable and foreseen - but always unintended conse-
quence of a morally legitimized use of force. The doctrine of double-effect
has been devised in the natural law tradition to take note of the messiness
Lloyd Steffen 99
___________________________________________________________
of moral life and the possibility that even innocent persons may be put in
harm’s way and killed as an unwanted and regretted consequence of a
conflict where force is being used.
I suggest that immunity from harm identifies a reasonable notion
of innocence. The use of force always poses some threat of harm, even
non-violent force. Martin Luther King used to worry enormously about
starting non-violent boycotts, because they would harm innocent persons
not directly involved in the conflict. King, like Gandhi, understood non-
violent force to be a use of force and followed a non-combatant immunity
provision by seeking to avoid inflicting harm on innocent persons in
conflict situations where even the force of non-violent resistance was to be
used.
In summary: In the moral life, we acknowledge that persons not
party to a conflict should be immune from direct action that would cause
them harm. No mantle of absolute protection can be thrown over the
innocent bystander or innocent civilian, however, and in the application of
justified uses of force the death of an ‘innocent’ may be ‘justifiable’ if
every reasonable effort has been made to avoid inflicting such harm. In the
moral life, then, the idea of innocence is attached a duty that falls on the
parties in conflict to respect the lives and well-being of non-combatant,
innocent persons. The innocence is not absolute and can even be rendered
justifiable, even if always regrettably so.
5. Conclusion
Invoking a sectarian notion of foetal innocence is socially
dangerous especially in a pluralistic society where different religious
views are held about such matters as abortion rights and no one religious
view should receive official sanction as privileged and commanding and
authoritative over all. Furthermore, to hold that the foetus is absolutely
innocent is to create a divine foetus that is also, for purposes of religious
valuation, also interpretable as an idol, and idol making for some religious
people violates clear prohibitions on such activity. The injection of a
sectarian metaphysics has the effect of devaluing the pregnant woman as
agent and decision–maker because the god within her subverts her
Lloyd Steffen 105
___________________________________________________________
autonomy as person, as agent, as decider. She is the Nara family member
who must pay a terrible fine for killing a divine deer. The meaning of that
killing reaches beyond moral meaning and is superseded by religion.
The abortion debate is intractable because the terms of the debate
are not commensurate - it is a debate over moral apples and theological
oranges. . The debate over abortion ought to be a moral debate conducted
by reasonable people respectful of women as persons, as fully endowed
members of the moral community. The problem is that a sectarian
viewpoint, represented by the idea of ‘absolute innocence’ has skewed the
terms of the debate and made rational conversation difficult and in some
contexts impossible. Those who want to affirm an absolutely innocent
foetus should be free to do so. The moral community situated in a
pluralistic society condones this absolutizing tendency to its peril. The
moral point of view centres on the imperfections of existence and the
conflicts that arise over goods and values. It advances the view that even
life itself ought not be considered ‘an absolute good’ that trumps every
other value. Such a viewpoint reflects a commitment to a religious purity
the moral life cannot sustain and ought not to accept as normative; for the
religious viewpoint is powerful and dangerous enough to create moral
chaos.
Notes
1
Mary Anne Warren, ‘On the Moral and Legal Status of Abortion’, The
Monist, 57, 1 (1973).
2
John T. Noonan, Jr., ‘An Almost Absolute Value in History’, reprinted in
Christina Sommers & Fred Sommers, eds., Vice and Virtue in Everyday
Life, 7th edition, (Belmont, CA: Wadsworth, 2006), 391.
3
John Paul II, ‘The Unspeakable Crime of Abortion’, from Evangelium
Vitae, March 25, 1995; reprinted in Thomas Mappes and David DeGrazia,
Biomedical Ethics, 6th Edition (New York: McGraw-Hill, 2006), 458.
Liz McKinnell
Abstract
Much has been written about moral obligations to future people. 1
In this piece I look at the related area of our obligations to past people (the
dead). Past people have some morally relevant similarities to future
people. Neither group of people exists at the present time. There are also
some interesting differences: We can do things that affect the identities of
future people, not with dead people; and we can do things which affect the
experiences of future people; but again this is not the case with the dead. I
address the question of whether there can be a wrong done against
someone when we cannot affect his experiences. I conclude that this does
not present us with a major obstacle to having obligations to the dead, and
identify the biggest problem as lying in the fact (if it is a fact) that the
dead do not presently exist, and therefore do not meet the ‘existence
condition’ for harm. 2 After exploring a number of responses to this, I
conclude that we can wrong the dead, but by a process of ‘backward
signification’ (distinct from backward causation) we wrong them while
they are alive.
1. Introduction
The intuition that we have obligations to the dead is at once a
very strong one and a very old one. There have always been moral beliefs
about what we owe to our ancestors, just as there always have been about
what we owe to our descendents. Our culture’s respect for these traditions
is no exception. For example, institutions such as wills are held as very
important, and on a more personal level, we often feel we owe something
to those who are no longer around. However, as we shall see, the notion of
having an obligation to someone who has died can be metaphysically
puzzling.
Notes
1
The prime example being Derek Parfit, Reasons and Persons (Oxford:
Clarendon, 1984).
2
Fred Feldman. ‘Some Puzzles about the Evil of Death’, The
Philosophical Review (1991), 205-227.
3
Parfit 351-381.
4
Feldman, 205.
5
Ruben, David-Hillel. ‘A Puzzle about Posthumous Predication’, The
Philosophical Review (1988), 213.
6
Oxford Dictionary of Quotations 4th ed., (1996).
7
Ruben, 224.
Liz McKinnell 115
___________________________________________________________
8
Geoffrey Scarre. ‘On Caring about One’s Posthumous Reputation’,
American Philosophical Quarterly (2001).
9
George Pitcher. ‘The Misfortunes of the Dead’, American Philosophical
Quarterly (1984), 188.
Simon Cushing
Abstract
I begin by sketching the Epicurean position on death - that it
cannot be bad for the one who dies because she no longer exists - which
has struck many people as specious. However, alternative views must
specify who is wronged by death (the dead person?), what is the harm
(suffering?), and when does the harm take place (before death, when
you’re not dead yet, or after death, when you’re not around any more?). In
the second section I outline the most sophisticated anti-Epicurean view,
the deprivation account, according to which someone who dies is harmed
to the extent that the death has deprived her of goods she would otherwise
have had. In the third section I argue that deprivation accounts that use the
philosophical tool of possible worlds have the counterintuitive implication
that we are harmed in the actual world because counterfactual versions of
us lead fantastic lives in other possible worlds. In the final section I
outline a neo-Epicurean position that explains how one can be wronged by
being killed without being harmed by death and how it is possible to
defend intuitions about injustice without problematic appeal to possible
worlds.
1. Introduction
First, let me clarify that when I talk about death in this paper, I
mean the state of being dead. None of what I say should be taken to apply
to dying (which Epicureans can certainly concede to be harmful) or death
as a moment, whereby one can debate whose death is better, Joan of Arc’s
or Elvis’s (Joan of Arc’s was painful but heroic, while Elvis’s was quick,
but, all things being equal, one wants to avoid any chance of the phrase
“straining at stool” appearing on one’s death certificate).
Next, a disclaimer: I am not an Epicurus scholar. When I talk
about the Epicurean position, I will not attempt to argue that this is
precisely what Epicurus said or even what he meant. With that in mind, as
I take it, the Epicurean position on death is essentially as follows:
That is, Aunt Ethel’s being dead is a harm to her while alive
because she is potentially aware of the comparative brevity of her life in
comparison to “alternative possible life-wholes” in which she lives longer.
It seems we are to picture Aunt Ethel as a disembodied self in something
like Rawls’s Original Position (minus the veil of ignorance) asked to
choose which among the various possible lives she would prefer. If there
is one that is better (which, for now, simply means longer) than the actual
one, then her death is a misfortune for her.
However, what exactly are we to understand by alternative
‘possible life-wholes’ (henceforth PLWs)? The most philosophically
familiar way to spell out this idea is using possible worlds, as Fred
Feldman (among others) makes explicit.
Assuming, purely for the sake of engaging Epicurus on common
ground, a crude form of hedonic calculus, Feldman suggests the following
analysis to explain the harm of dying in a ‘plane crash:
Shane McCorristine
Abstract
The spread of spiritualism in the second half of the nineteenth
century led to the establishment of the Society for Psychical Research
(SPR) in London in 1882 as a scientific society dedicated to investigating
the phenomena emanating from the spiritualist séances. In the landmark
quasi-sociological study, ‘Phantasms of the Living’ (1886), the SPR
published some 700 cases which pointed away from the traditional
concept of the ghost as a disembodied spirit, in favour of a new theory
based upon the telepathic awareness of (living) loved ones in a state of
crisis, or in a dying situation – in essence a percipience of an embodied
ghost, a ‘phantasm of the living’.
The SPR reformatted the popular ghost story through the
language of psychical research by positing a modernist death-ritual that
invested the bodies of both the agent and percipient in the ghost story with
a telepathic apparatus that extensively mirrored the developments in
contemporary tele-technologies. With the telepathic hypothesis entrenched
in interpretations of ghost-seeing, psychical research suggested a salient
feature of modernity – the idea that the spectres of the self expressed a
disturbing psychical reality more marvellous by far than the sensational
accounts of ghosts so prevalent in Victorian and Edwardian fiction.
Notes
1
The author wishes to acknowledge the funding and support provided to
him by the Humanities Institute of Ireland.
2
William F. Barrett, On the Threshold of the Unseen: An Examination of
the Phenomena of Spiritualism and the Evidence for Survival after Death
(London and New York: Kegan Paul, Trench, Trübner &Co, 1917), 197-
198.
3
William F. Barrett, A.P. Percival Keep, Charles C. Massey, Hensleigh
Wedgwood, Frank Podmore, and E.R. Pease, ‘First Report of the
Committee on Haunted Houses’, PSPR, Vol. I (1882-1883), 101-115.
4
Barrett et al, ‘Literary Committee’, 117.
5
Ibid, ff.
6
William F. Barrett, Charles C. Massey, Stainton Moses, Frank Podmore,
Edmund Gurney, and Frederic W. H. Myers, ‘Second Report of the
Literary Committee’, PSPR, Vol. II (1884), 43-55.
7
Barrett et al, ‘Haunted Houses’, 117-118.
Shane McCorristine 137
___________________________________________________________
8
William F. Barrett, Charles C. Massey, Stainton Moses, Frank Podmore,
Edmund Gurney, and Frederic W. H. Myers, ‘Third Report of the Literary
Committee’, PSPR, Vol. II (1884), 109-136.
9
Ibid, 112.
10
See John Peregrine Williams, The Making of Victorian Psychical
Research: an Intellectual Elite’s Approach to the Spiritual World,
unpublished Ph.D. Thesis, (University of Cambridge, 1984).
11
Edmund Gurney et al, Phantasms of the Living, 2 vols. (Gainesville,
Florida: Scholars’ Facsims & Reprints, 1970).
12
Ibid, 188, 192, 196-198.
13
See Frederic W.H. Myers, Human Personality and Its Survival of Bodily
Death (New York: Longmans Green, 1909).
14
Gurney et al, 316.
15
Ibid, 271.
16
Nicolas Abraham, ‘Notes on the Phantom: A Complement to Freud’s
Metapsychology’, Critical Inquiry, vol.13, no.2, (Winter, 1987), 287-292.
17
See for instance Steven Connor, “Voice, Technology and the Victorian
Ear”, Roger Luckhurst and Josephine MacDonagh eds, Transactions and
Encounters: Science and Culture in the Nineteenth Century (Manchester:
Manchester University Press, 2002), 16-29.
18
On the influence that psychical research had upon probability theory see
Ian Hacking, ‘Telepathy: Origins of Randomization in Experimental
Design’, Isis, Vol.79, no.3, (September, 1988), 427-451.
1919
See Hans Vaihinger, The Philosophy of ‘As If’: A System of the
Theoretical, Practical and Religious Fictions of Mankind. tr. C.K. Ogden
(London: Routledge & Kegan Paul, 1965).
Bibliography
Brandon, Ruth. The Spiritualists: the Passion for the Occult in the
Nineteenth and Twentieth Centuries. (London: Weidenfeld and Nicolson,
1983).
Cerullo, John J. The Secularization of the Soul: Psychical Research in
Modern Britain. (Philadelphia: Institute for the Study of Human Issues,
1982).
Gauld, Alan. The Founders of Psychical Research. (London: Routledge &
Kegan Paul, 1968).
Haynes, Renée. The Society for Psychical Research 1882-1982: A History.
(London and Sydney: MacDonald & Co, 1982).
138 Tele-visions of the Dying: Ghost-Seeing in the Society for
Psychical Research in the 1880s
___________________________________________________________
Lucia Aiello
Abstract
This paper explains Emily Dickinson’s use of the concept of
‘Death’. The paper argues that in her poetry Dickinson divests death of
traditional metaphysical connotations and turns it into a signifier shedding
light on the composite nature of human experience. Within her poetry the
concept of death is divested of its intimidating power, without falling into
the cliché of becoming replete with ‘positive’ meaning. ‘Death’ in
Dickinson is a figure of the poetic form that, together with other figures
such as ‘Life’, ‘Poet’, ‘I’, ‘Immortality’, ‘Grief’, etc., assumes a
conceptual dignity beyond the role allocated to it by traditional semantic
definitions. New combinations become workable, innovative associations
emerge as a result of the expansion of perception and prefigure
possibilities of new meanings. The paper explores some of these
possibilities using Dickinson’s poems as examples.
The paper concludes by advancing the hypothesis that
Dickinson’s playful engagement with death at the level of the conceptual
covers in fact a deeper ontological need, namely the need to make sense,
not of death, but of human experience as a whole. The paper argues that a
fear of a loss of sense is an anxiety concerned with the ineffable, the
unspeakable, and therefore the meaningless.
1. Kenosis
In poem 1052, Emily Dickinson writes:
2. The experiment
Interestingly, when Heidegger seeks to give an ontological
definition of Dasein, it is to the German lyric poet Friedrich Hölderlin that
he turns. Heidegger’s interest in Hollering has been commented upon both
by Theodor Adorno and by Paul de Man.
In ‘Parataxis’, one of the most remarkable essays of his ‘Notes to
Literature’, Adorno thus comments on Hölderlin’s use of ‘abstractions’ in
his late hymns: “In his poetic usage they [the abstractions] acknowledge
themselves as something historical rather than pictorial representations of
something beyond history.” 12 One could hardly find a better and more
appropriate definition of the non-metaphysical use of names in
Dickinson’s poetry. Dickinson’s poetic universe is made of a
‘constellation of abstractions’, stemming from a self-reflective
consciousness, aware of the illusory character of the correspondence
between name and meaning. Perhaps the fact that originally Adorno refers
this comment to Hölderlin gives us an insight into unexplored affiliations
of Dickinson with the poetic continental tradition including poets such as
Hölderlin, Rainer Maria Rilke, and Paul Celan, the translator of Dickinson
into German. All these poets’ works, and Dickinson’s with them, address
the question of the impossibility of the subject to speak for itself. In this
sense their poetry stands in contrast with the poetry of experience. As
Adorno writes: “Only by virtue of the fact that the abstractions put an end
to the illusion that they can be reconciled with the pure concrete entity are
they granted this second life.” 13 This ‘second life’, in which the concept is
abstracted into and mediated via the poetic form, does not turn words into
“living organisms,” as some critics have inferred in regard to Dickinson, 14
Lucia Aiello 143
___________________________________________________________
but into simulacra through which the whole of human experience is
rethought in completely different terms.
Heidegger’s rhetoric of the presence of Being, which he sees
enacted in Hölderlin’s poetic language, neglects what Adorno calls “the
agency of form” and turns concrete experience into an ultimately inward
circuit of Being. 15 Heidegger places Being-towards-death right at the core
of Dasein’s Being and accredits Hölderlin’s poetic language with a
foundational quality that, as Paul De Man demonstrates, language simply
does not have. In a crucial passage of his essay called ‘Heidegger’s
Exegeses of Hölderlin’, Paul De Man writes:
Notes
1
The poems are numbered according Thomas Johnson’s arrangement in
The Complete Poems of Emily Dickinson, ed. Thomas Johnson (Little,
Brown and Company, 1957), which reproduces the 1955 Harvard edition
but gives only one version of each poem. “Of Death I try to think like
this” is the first line of poem J 1558.
2
Respectively poem J280 and J465.
3
Poem J 455.
4
Poem J 7.
5
Poem J 71.
6
Poem J 172.
7
Poem J 194.
8
Poem J 822.
9
Poem J 548.
10
Martin Heidegger, Being and Time, trans. John Macquarrie and Edward
Robinson (Oxford: Blackwell Publishing, 1962), 295.
11
Heidegger, 303.
12
Theodor W. Adorno, ‘Parataxis’, in Notes to Literature Volume Two,
trans. Shierry Weber Nicholsen (New York: Columbia University Press,
1974), 124.
13
Adorno, 125.
14
See Joseph Raab, ‘The Metapoetic Element in Dickinson’, in The Emily
Dickinson Handbook, ed. Gudrun Grabher, Roland Hegenbüchle and
Cristanne Miller (Amherst and Boston: University of Massachusetts Press,
1998), 273-295.
15
Adorno, 114.
16
Paul de Man, ‘Heidegger’s Exegeses of Hölderlin’, in Blindness and
Insight: Essays in the Rhetoric of Contemporary Criticism, 2nd ed.
(London: Routledge, 1989), 259.
17
Poem J907.
Lucia Aiello 147
___________________________________________________________
18
Poem J1112.
19
Cristanne Miller, ‘Dickinson’s Experiments in Language’, in The Emily
Dickinson Handbook, 249.
Phil Fitzsimmons
Abstract
This paper details how Jenny Wagner’s best selling children’s
picture book ‘John Brown, Rose and the Midnight Cat’, explores the
onset of death and coping with death. Although this text was the
Australian picture book of the year in 1978 and has continued to be a
children’s favourite for almost three decades, the description of the book
on the Healthy Books website as “a strange little fable, but quite
beautiful in both words and pictures” 1 reveals just how widely
misinterpreted and misunderstood this text continues to be. An overlay
of archetypal analysis discloses a deeper subtext where the concept of
death becomes a para-textual sliding signifier revealing the current First
World’s fear of death.
With the notion of death at the fore, this text then moves into a
continuing pattern of illustrations above the text. However, despite the
simple and often single sentence descriptions, the notion of death is
152 Coming to Grips with Death
___________________________________________________________
subtly carried forward in nearly every illustration or linked illustrations.
However, one has to look beyond the text, as this text is deceptive
because of its elegance. As copyright and limited editorial space does
not allow me to reproduce the book in tact, the following summary is
provided so that you the reader can begin to understand the paratextual
interplay in this narrative.
Rose and John Brown live alone in a small farmhouse. The are
seemingly comfortable in their existence, feeding the animals and sitting
reading under a tree until Rose, looks out the window one night and
thinks she sees a cat. Refusing to accept she sees a cat, John Brown in
subsequent frames refuses to even look in the direction that Rose is
gazing, stating that he doesn’t see any cat. It is in the next frame that a
pivotal confrontation occurs. In one of the two most focussed pages in
the entire book, John Brown is seen aggressively facing the cat as it
quietly sits:
But that night when Rose was safe in bed, John Brown
went outside. He drew a line around the house… and
told the midnight cat to stay away. “We don’t need you,
cat,” he said. “We are alright, Rose and I.” 9
In the following pages Rose is seen again peering out the window
and winding back her clock as she debates with John Brown about being
able to see the cat. John Brown moves into total denial, finally closing
his eyes. In the next six pages there is an ebb and flow of denial and
acceptance of the cat. Rose puts out milk for the cat, John Brown tips it
out and is shown facing in the opposite direction to Rose. The last page
of this section, the two are facing each other and John Brown exclaims,
It is at this point that the midnight cat appears at the window, and
Rose wants to let him in but John Brown again refuses. Rose then goes
to bed. John Brown waits for his breakfast but nothing happens. When
he visits Rose in her room she states that she is staying in bed;
In one the last of the two largest and most focussed frames, John
Brown thinks things through, and after waking Rose asks if letting the
cat in would make her better. “Yes”, she replies. “That’s just what I
Phil Fitzsimmons 153
___________________________________________________________
want.” The cat is let in and Rose gets out of bed to join her animals
companions, and the book ends with the cat purring.
While cast as being happy in these opening two pages, Rose does
not smile again in this text until the final frame. This is a carefully
constructed signal because despite the appearance of contentment, Rose
does not look directly John Brown again until he allows the midnight cat
154 Coming to Grips with Death
___________________________________________________________
into the house. While the text tends to indicate otherwise, the pictures
reveal that Rose is living an inauthentic life. With the written narrative
purporting an apparently comfortable existence within the four walls of
her house with her pet as her only companion her downcast face gives
off the sense that she is otherwise absorbed. Her house is in fact her
prison. Typically, the house is emblematic of the universe and its
inhabitants with the points of architecture representing the intervention
of light into darkness. However, in this case instead of a microcosm of
transcendence, Rose’s immediate world is the opposite in focus and
direction. With her eyes down cast or peering outside, she is both
physically and symbolically unable to see the truth that is all around her.
The initial symbolism of the brevity of summer quickly passing into
winter in conjunction with her gaze gives metaphoric voice to her
ignoring of the passing of time. In tandem with this the blazing fire in
the opening scenes is seen to die down in subsequent frames. With the
chimney presenting the universal passageway from this world to another,
in the very opening scenes the text may frame a life of ease, the visual
elements reveal a life in denial.
In harmony with the symbols of transformation and change, Rose
is also framed by archetypal elements representing a further series of
polarities. The wallpaper in her house is a patterned with roses. In
mythic terms, and a corresponding “life as art view” 17 this flower is a
more modern version of the lotus, representing both spiritual direction
and universality. In this text the central character’s name and immediate
surroundings reveal her need but her actions, reveal that Rose’s
existential view was becoming “…hardened,… fixed,… and
irreparable.” 18
That is until she sees the midnight cat and realises that the life
she has been living in denial. Life without death is role-playing one’s
entire existence, and having accepted this she is then seen at doors and
windows, the universal symbols of the gateway to the genuine soul.
Notes
1
Healthy Books, ‘On-line sales’ 3 June 2005, (14 February 2006).
<http://www.healthybooks.org.uk/cgibin/get.pl?name=bookInfo&se=03.3
>.
2
Jacqueline Rose, The Case of Peter Pan or the Impossibility of
Children’s Fiction. (Philadelphia: University of Philadelphia Press, 1984),
15.
3
Carol F. Feldman, ‘The Construction of Mind in an Interpretive
Community’. In Literacy, Narrative and Culture, edited by Jens
Brockmeier, Min Wing and David R Olson, 52-66. (Surrey: Curzen Press,
2002), 58.
4
Michael Hilton, Potent Fictions. Children’s literature and the challenge
of popular culture. (London: Routledge, 1996), 25.
5
Steven .A. Galipeau, The Journey of Luke Skywalker: An analysis of
modern myth and symbol. (Chicago: Open Court, 2001), 3.
6
Maire Messenger-Davies, ‘The Child Audience - Pre-School
Programming’. In The Television Genre Book, edited by Glen Creeber, 97-
102 (London: British Film Institute, 2002), 99.
7
Susan Wallis, Portents of the Real: A primer for post 9/11 America.
(New York: Verso, 2006), xiv.
8
James Park, Our Existential Predicament: Loneliness, Depression,
Anxiety and Death, 5th Edition. (New York: Existential Books, 2000), 183
9
Jenny Wagner and Ron Brooks. John Brown, Rose and the Midnight Cat.
(Camberwell: Puffin), 1.
10
Wagner and Brooks, 5.
11
Wagner and Brooks, 15.
12
Wagner and Brooks, 31.
13
Wayne C. Booth, The Rhetoric of Fiction. (Chicago: University of
Chicago Press, 1961), 24.
14
Patrick Conty, The Genesis and Geometry of the Labyrinth:
Architecture, Hidden Language, Myths and Rituals. (Rochester, Vermont:
Inner Traditions, 2002), 53.
15
Conty, 53.
16
Alfred Adler, Problems of Neurosis. (New York: Harper), 145.
156 Coming to Grips with Death
___________________________________________________________
17
Jeffrey Kaufman, ‘Disassociative Functions in the Normal Mourning
Process’. Omega, 28, (1994), 31-38, 38.
18
Richard Rorty, Contingency, Irony and Solidarity. (Cambridge:
Cambridge University Press, 1989), 45.
19
Charles Pierce, ‘The Fixation of Belief’, in Buchler, J. (ed.),
Philosophical Writings of Charles Sanders Pierce. (New York: Dover
Press, 1955), 12.
20
Ernest Becker, The Denial of Death. (New York: Free Press, 1997), xiii
21
Becker, viii.
22
Fritz Perls, Gestalt Theory Verbatim. (Lafeytette, Cal.: Real People
Press, 1969), 260.
Abstract
This paper presents evidence from a review of 60 studies looking
at older people’s preferences at the end of life published between 1995 and
2005, and highlights the potential for future research in this area. The
review revealed three main areas of focus: treatment decisions, place of
care/death and good death. However, there is some evidence of a cultural
variation in research focus. Whilst much of the research on treatment
preferences originates from the US, where advanced care statements are
more popular, research on place of care mostly originates from the UK.
Studies present conflicting evidence on the impact of socio-demographic
variables such as age, gender, religiosity and ethnicity on treatment
preferences and preferred place of care/death, and there are indications
that patient choice may be service-led and tempered by personal
circumstances such as the availability of informal care, the existence of
local service provision, and awareness of this provision. Although it is
difficult to disentangle the relationship between age, health status and the
dying experience, it would appear that there may be certain features of a
good death that remain constant.
Key words: older people, death and dying, end-of-life, end of life,
preferences.
1. Introduction
The proportion of older people in the United Kingdom population
is growing. In 1961, just 0.7% of the population were aged 85 and over,
but by 2002 this rose to 1.9%. Projections for 2031 indicate that this will
rise to 3.8%. 1 This growing ageing population has implications for health
and social care service provision. The UK National Health Service already
spends around 40% of its total budget on people over the age of 65, and
approximately 50% of Social Services expenditure is also allocated to this
age group. The Government has declared its commitment to providing
high quality person-centred care for older people, as well as dignity in care
at the end-of-life 2 and it is important that resources are carefully targeted
to meet older people’s needs. Death is now most likely to occur at the end
of a long life 3 and the recent growth in hospice and palliative care services
has drawn attention to the importance of quality of death and dying, in
addition to quality of life, in old age. However, research has found that the
modern way of death does not always meet people’s hopes and desires. 4
Questions around how to separate, or measure quality of death, rather than
158 Older People’s Preferences at the End-of-Life:
A Review of the Literature
___________________________________________________________
quality of life, have been raised. Is there a particular point in time when
people can be regarded as being “actively dying”, 5 and is this dependent
upon the “dying trajectory” 6 or perceived course of a particular disease or
condition? Organizations such as the Help the Aged and Age Concern
have produced guidelines or definitions and principles of a good death, 7, 8
but we do not know if goals to improve the dying experience of older
people are being achieved in practice. Some evidence exists that their
choices concerning place of death are not being met, with the majority still
dying in hospital, despite saying they would prefer to die at home. 9, 10
However, whilst statistics are available on life expectancy, mortality and
cause and place of death, we still know relatively little about older
people’s personal experience of the dying process.9 This review, therefore,
aims to examine the existing literature on older people’s preferences for
care at the end-of-life and indicate areas for future research.
3. Treatment decisions
These studies focus on advanced care statements/planning, living
wills, health care power of attorney and medical decision-making (issues
around life-sustaining or prolonging treatments/technologies and their
continuation or withdrawal). Several papers seek respondent’s preferences
for life-sustaining treatments (LST’s) in various illness/disability scenarios
presented. Studies looking at the stability of people’s preferences and
gender and cultural variations in end-of-life decision-making are also
included. Eight studies present data on the number of respondents with
some type of advanced care directive, or living will, although it should be
noted that the terminology is used somewhat interchangeably. Four of the
papers originate from the US, but interestingly, the study from the
Eileen Sutton & Joanna Coast 159
___________________________________________________________
Netherlands, where euthanasia was legalised in 2001, revealed the lowest
numbers of written advance directives. 11 Figures range widely from 9% 12
to 64%. 13 Schiff et al’s 14 UK study found that 82% of participants hadn’t
heard of a living will, advance directives or advanced care statements, and
of those who had, only four could describe them correctly, most believing
they were concerned with financial arrangements. Some studies also
present figures for those who have a designated power of attorney or
surrogate decision-maker, ranging from 27% 15 to 49%. 16 Three studies
report that the majority of respondents had discussed end-of-life
treatments with either doctors or relatives, 17, 18 but conversely Matsumura
et al 19 found that few had discussed these issues with a doctor, but many
would like to do so. Gender differences may be apparent, with more
women than men in one study possessing a living will (28% compared to
19%). 20 Hawkins et al 21 report that 55% of older people in their study felt
that it is “definitely necessary” to record patients’ wishes in an advance
directive, although the study does not give figures for the number of
people who had executed such a document. Qualitative research from the
UK emphasises the interdependency between dying people and their
families and concludes that advanced care statements can be helpful with
the burden of decision-making at the end-of-life, but that this process
should involve ongoing discussion and review, to take account of
changing preferences. 22, 23 , 24
A substantial number of papers are concerned with the expressed
preferences of older people for treatment, or its withdrawal, in various
illness/disability scenarios. There is some evidence that people value
cognitive ability more than physical functioning 25,26 with advanced
dementia the most feared condition in one study, becoming even more
unacceptable when combined with other disabilities. 27 Some studies 28, 29
look at the effect of treatment outcomes on people’s preferences, with
varying conclusions. In a study by Fried et al 30 almost all participants
preferred a low-burden therapy that would restore their current health
status, if the alternative without treatment was death, but if the low-burden
therapy resulted in an outcome of severe cognitive impairment almost
90% would not choose to receive the therapy. In contrast, other studies
found that in illness scenarios presented there were many instances when
participants rated the outcomes of treatments as a heath state worse than
death, but still wanted treatment 31 or rejected a recommendation for
palliative care, requesting active treatments. 32 A study of bereaved
relatives has shown that patients’ preferences are often ignored, revealing
that 56% of patients had received at least one LST in the last three days of
life, despite requesting “comfort only” care. 33 Other studies, however,
show that doctors and caregivers have varying perceptions of the patient’s
160 Older People’s Preferences at the End-of-Life:
A Review of the Literature
___________________________________________________________
preferred type of treatment 34, 35 , 36 , 37 with one revealing that 50% of
patient-caregiver pairings disagreed concerning mechanical ventilation. 38
A further study reporting on patient’s chosen surrogate decision-maker’s
lack of knowledge of end-of-life treatment preferences found that 91% of
patients were, nevertheless, willing to let these surrogates have some
leeway to override their written decisions. 39
Results from studies are, in some cases, further analysed for the
impact of personal and socio-demographic characteristics, including
religiosity, gender, and ethnicity. Five papers look specifically at the
attitudes and preferences of different ethnic groups to end-of-life care
40, 41 , 42 , 43 , 44
and ethnicity is one of the variables noted in many of the other
papers reviewed, although much of the research reported here involves
white respondents. African-Americans were found more likely than
European-Americans, Korean-Americans and Mexican-Americans to want
to be kept alive on life support in one study 45 and similarly African-
American patients with terminal cancer desired the use of LSTs more than
their white counterparts in both their current health state, and in a near-
death condition. 46 African-Americans were found to be less likely than
whites to have executed advanced care statements, 47 but there is some
evidence that attitudes towards end-of-life care change with acculturation,
with increasingly positive attitudes towards foregoing care and advance
care statements. 48
Significant gender differences in treatment preferences are
reported in some studies 49,50 with men reporting a stronger preference
overall for LSTs. 51 However, the significance of gender on treatment
preferences is disputed by other authors. 52, 53 The impact of marital status
appears to be less contested, with unmarried individuals more likely to
have discussed their preferences with others 54 or present an “activist”
position towards end-of-life decision-making. 55 In this study “activists”
were seen to prefer a voice in the decision-making process, in contrast to
“delegators” who prefer to delegate decision-making to their doctors, to
God or to fate. “Activists” were more likely to be better educated, held
more professional and managerial jobs and tended to be middle class. 56
Age may also be a relevant consideration, with some participants in a
study by Rosenfeld et al believing that at an advanced age they had lived a
natural life span placing more importance on maintaining function, rather
than living on, and being less willing to tolerate the risks of pain and
uncertain outcomes of some treatment options. 57 The impact of age on
preferences, however, is disputed in another study. 58
The literature presents conflicting information on the impact of
religiosity on older people’s treatment preferences, with Cicirelli et al 59
Eileen Sutton & Joanna Coast 161
___________________________________________________________
reporting that respondents with a greater preference for refusing treatment
and in favour of assisted suicide were less religious, this conclusion is
supported by Klinkenberg et al 60 who found that more religious people
were less likely to have expressed preferences in advance. However, other
studies found no significant association between religiosity and treatment
preferences 61 and only small differences in position on control of dying. 62
A study of male veterans found that, for treatment preferences, only tube
feeding showed a significant relationship with religious affiliation, with
Catholics less willing to undergo this type of treatment than other
Christians. 63
Two studies, one from the US and the other from Israel, report
specifically on the stability of older people’s treatment preferences over
time. In one US study, preferences were reported as moderately stable
over a two-year period, with those concerning the most invasive
treatments showing the greatest stability. 64 The second study found that
preferences were relatively alike and quite stable over a similar time
period, with around 70% of respondents showing no change in
preferences, but with a slightly stronger trend towards wanting less
treatment. 65 Declining health status could also impact on preferences over
time. A study examining the relationship between worsening physical
function and depression and preferences for LST in older doctors found
that those who experienced clinically significant physical functioning
decline were more likely to prefer high-burden treatment options rather
than no treatment, thus posing a challenge to written advance care
statements which do not take account of declining health status. 66
B. Symptoms/physical care
Many of the papers mention the physical symptoms of terminal
illness and their treatment, and in particular pain control,
85, 86 , 87 , 88 , 89 , 90 , 91 , 92 , 93 , 94 , 95
with broad agreement that patients should have
access to appropriate medication and therapies. Nevertheless, research by
Steinhauser et al with terminally ill patients, bereaved family members,
doctors and other care providers, found that the most highly ranked
attribute by all groups was being kept clean. 96 Interestingly, although
freedom from pain was universally highly rated in this study, patients
themselves judged this attribute to be slightly less important than did the
three other groups. Being able to participate in activities of daily living
such as eating, sleeping, and walking was also rated as significant by
respondents in some studies, 97, 98 , 99 and this is closely connected to the
theme of independence and control (discussed below).
D. Psychological well-being
Closely linked to the above are issues surrounding the
psychological well-being of older people. Authors report the need to be
treated with dignity and respect 114,115 and to receive emotional support
from both professional and family caregivers 116 to help alleviate feelings
of fear, anxiety and depression, which are often experienced at the end-of-
life. 117 Older people’s fears included being a burden, loss of dignity or
“being a vegetable” 118 and having a doctor with whom one could discuss
fears was regarded as significant by 90% of patients in Steinhauser’s 119
study. Similarly, discussing fears was integral to affective communication
in Gautier’s model of end-of-life care. 120
E. Time/place of death
Uncertainty around the dying trajectory of individual diseases
and conditions means that it is difficult to establish at what point people
can be defined as “actively dying.” 121 Some authors viewed death as a
sequential process occurring over a prolonged period of time and
extending beyond the moment of death, to take account of the impact of
death on loved ones. 122 Contradictions existed between some study
respondents’ descriptions of a good death, which envisaged dying quickly,
quietly, unconsciously, in a desired location and free of pain, avoiding
inappropriately prolonged dying, 123, 124 , 125 , 126 with a desire to complete
preparations and having time to say goodbye, possibly surrounded by
family and friends. 127, 128 Age of death was noted as having an impact in
one UK study, which found that in practice older people experienced
better deaths than their younger counterparts. This may have been partly
due to older people feeling that they had lived a full life, that some of their
closest companions had already died and that they might possibly be
reunited with them, if they believed in an afterlife. 129
F. Preparation
Being prepared for death was recorded as an important attribute
of a good death by several authors, this theme covering personal, medical,
practical and financial preparations. As previously mentioned, having the
164 Older People’s Preferences at the End-of-Life:
A Review of the Literature
___________________________________________________________
opportunity to say goodbye to loved ones, and resolving unfinished
business or achieving a sense of closure 130, 131 were all viewed as
significant. Other concerns such as having funeral arrangements in
place 132 and making appropriate financial preparations, including those
concerning care costs, were also regarded as important. 133 Appointing
surrogate decision-makers and deciding on treatment preferences, or
writing advanced care directives, were other aspects of
preparation. 134, 135 , 136 Much of the motivation for making preparations in
these areas was to remove burden from loved ones. 137
G. Independence/control
Several authors mentioned the significance of allowing dying
people to retain some control over their care. 138, 139 , 140 , 141 This might
involve participating in everyday activities for as long as possible, or
permitting them to feel that, even at this time, they had something to
contribute to others. 142 Young and Cullen described the way some study
participants with terminal illness attempted to exercise control by taking
less than their prescribed dose of pain medication, perhaps to reassure
themselves that death was not imminent, as pain and death were closely
associated for some respondents, so managing without pain relief
signalled progress. 143
H. Policy/service provision
The need for co-ordinated health care and related services which
are focused on the requirements and values of the dying, including
specific provision for those suffering from dementia, is highlighted
throughout the studies. 144, 145 , 146 A lack of hospice care provision within
some areas in the UK has resulted in unmet need. 147 The UK Debate of
the Age Heath and Care Study Group recommend that palliative and
terminal care services should be based on the principles of a good death
presented within their report, in order to ensure that older people can
achieve maximum individual autonomy and control over their deaths. 148
5. Place of care/death
Preferences for place of death vary across studies, with figures
for home as preferred place of death ranging from 43% 149 to 94%. 150
There is conflicting evidence on the impact of health status upon
preference, as in one study recently hospitalized patients were more likely
to opt for hospital care, 151 whereas in other studies, respondents with life
limiting or terminal illness preferred either home or hospice care. 152,153
Eileen Sutton & Joanna Coast 165
___________________________________________________________
Age and gender may both impact upon choice, with preference
for home care falling, and hospice care rising, with advancing age. More
women than men opt for hospice care 154 and also express more practical
concerns over care in the home. 155 However, other authors dispute the
impact of gender. 156, 157 There is some evidence that unmarried people are
less likely to opt for home care, 158 this being related to the availability of
informal carers potentially restricting their choice. Dependency when
dying 159 and fears of being a burden to relatives 160 are also important
factors which need to be understood when analysing patient preferences.
Only one of the studies considers the impact of ethnicity upon
preferences and this revealed that a higher number of deceased black
Caribbean than native-born white patients living in the UK had expressed
a preference for location of death, and that, of those patients that had,
slightly more of the former group wanted to die at home. 161 However, the
study also shows that only just over half had this preference met, with
similar figures for both groups. Similarly, only one study published results
by employment status, revealing that those from a professional and
management background were more likely to opt for hospice care and
those from semi-skilled backgrounds had the highest preference for care at
home. 162 One study conducted in a deprived area of London comments on
the potential impact of social disadvantage in shaping patient choice. 163
Two studies mention the impact of religion, with contradictory results,
being either influential 164 or insignificant. 165
6. Conclusions
A review of the literature on older people’s preferences for care
at the end-of-life has revealed three main areas of focus: treatment
decisions, place of care/death and good death (quality of care/dying). The
majority of studies originate from the US and there is some evidence of a
cultural variation in focus. Whilst much of the research on treatment
preferences originates from the US, where advanced care statements are
more popular, research on place of care tends to have been carried out in
the UK, so further research in other geographical areas would be useful to
help to establish the existence of cultural differences in these preferences.
Although many of the studies in this review involve research with white
respondents, there is some evidence that ethnicity has an impact on
preferences for care at end-of-life. Studies present conflicting evidence on
the impact of socio-demographic variables such as age, gender and
religiosity on treatment preferences, but there are indications that patient
choice may be service-led, with older people’s preferences tempered by
personal circumstances such as the availability of informal care, the
existence of local service provision, and awareness of this provision.
166 Older People’s Preferences at the End-of-Life:
A Review of the Literature
___________________________________________________________
Although some evidence exists on the impact of health status,
further research involving direct comparisons between healthy older
people’s preferences with those of older people with terminal illness,
would be helpful to inform health care commissioners targeting end-of-life
service provision and to improve patient choice.
The second section of the review attempted to elaborate on the
many and complex components of a good death. Although it is difficult to
disentangle the relationship between age, health status and the dying
experience, it would appear that there might be certain features that are
constant, such as the importance of family and friends, and the adequacy
of symptom relief and physical care. Other important issues noted
included those surrounding holistic, culturally sensitive care;
psychological well-being; preparation; and retention of
independence/control. As previously observed, much of the research in
this section originated in the US. Further research investigating the
relationship between health status and preferences, which takes account of
different cultural perspectives, would be helpful to inform future policy
provision within the UK.
Studies on preferred place of death/care reveal that older people
have a range of preferences for care at the end-of-life, but, in general there
is a strong preference for home death/care, and that this preference
remains fairly constant across national boundaries, although it should be
noted that the majority of studies in this section of the review originated
from the UK. There is also some evidence of the impact of socio-
economic factors, personal circumstances, health status, age, gender,
religiosity and ethnicity upon choice, although the extent or importance of
such factors remains a matter for debate and requires further clarification.
However, there is evidence to suggest that preference for place of death is
influenced by patients’ knowledge of available services and variances of
service provision, such as hospice care, in different geographical areas.
Further qualitative work investigating older peoples’ preferences at
different stages on the dying trajectory, possibly comparing the
preferences of healthy older people, those living in residential care and
those receiving palliative care in a contemporary UK setting, would also
be useful to establish the relative importance of different attributes of care
at the end-of-life and aid the targeting of resources.
Eileen Sutton & Joanna Coast 167
___________________________________________________________
Notes
1
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<http://www.statistics.gov.uk/cci/nugget.asp?id=874>
2
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(London: The Stationery Office, 2001).
3
Clive Seale, ‘Demographic change and the experience of dying’, in
Death, Dying and Bereavement, ed. D Dickenson, M Johnson, and J
Samson Katz (London: Sage, 2000), 35-43.
4
Liz Lloyd, ‘Dying in old age: promoting well-being at the end of life’,
Mortality 5, 2 (2000), 171-188.
5
Anita L Stewart, Joan Teno, Donald L Patrick and Joanne Lynn, ‘The
Concept of Quality of Life of Dying Persons in the Context of Health
Care’, Journal of Pain and Symptom Management, 17, 2 (1999), 93-108.
6
Anselm L Strauss and Barney G Glaser, Anguish: the case history of a
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7
Help the Aged, End-of-Life: making decisions around the end-of-life, (20
July 2005).
<http://www.helptheaged.org.uk/NR/rdonlyres/evmneb3k63ooalcmc3lcy2
xrkqdzjpr2r5xk3w75xxcc2vnrnusw6odxkblwnxdpcpbm7gpk7udat4vicljdi
wg2j6f/endoflife.pdf>
8
Melanie Henwood and Debate of the Age Health and Care Study Group,
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9
Richard Smith, ‘A good death’. British Medical Journal, 320, 129
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10
Irene J. Higginson, Priorities and Preferences for end of life care in
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11
Marianne Klinkenberg, Dick L. Willems, Bregje D. Onwuteaka-
Philipsen, Dorly J.H. Deeg and Gerrit van der Wal, ‘Preferences in End-
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12
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13
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14
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15
Klinkenberg et al.
16
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17
Etienne Phipps, Gala True, Diana Harris, Umi Chong, William Tester,
Stephen I. Chavin, and Leonard E. Braitman, ‘Approaching the End of
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18
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19
Shinji Matsumura, Seiji Bito, Honghu Lui, Katherine Kahn, Shunichi
Fukuhara, Marjorie Kagawa-Singer and Neil Wenger, ‘Acculturation of
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20
Phipps et al.
21
Nikki A. Hawkins, Peter H. Ditto, Joseph H. Danks and William D.
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107-117.
22
Jane Seymour, Gary Bellamy, Merryn Gott, Sam H. Ahmedzai and
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23
Jane Seymour, ‘Technology and Natural Death: A Study of Older
People’, Z Gerontol Geriat, 36, 5 (2003), 339-346.
24
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about Advance Care Statements’, Social Science & Medicine 59, 1 (2004),
57-68.
25
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‘End-of-Life Decision Making - A Qualitative Study of Elderly
Individuals’, Journal of General Internal Medicine 15, 9 (2000), 620-625.
26
Terri R. Fried, Elizabeth H. Bradley, Virginia R. Towle and Heather
Allore, ‘Understanding the Treatment Preferences of Seriously Ill
Eileen Sutton & Joanna Coast 169
___________________________________________________________
44
A.M. Fairrow, T.J. McCallum and B.J. Messinger-Rapport, ‘Preferences
of Older African-Americans for Long-Term Tube Feeding at the End of
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45
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46
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47
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48
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49
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50
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51
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52
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53
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54
Kahana et al.
55
Kelner et al.
56
Kelner, 1995.
57
Rosenfeld et al.
58
Kelner, 1995.
59
Victor G. Cicirelli, Peter MacLean, and Lisa S. Cox, ‘Hastening Death:
A Comparison of Two End-of-Life Decisions’, Death Studies 24, 5
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60
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61
Gramelspacher et al.
62
Kelner et al, 1995.
63
Oscar Heeren, A. Srikumar Menon, Allen Raskin and Paul Ruskin,
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208.
64
Peter H. Ditto, Joseph H. Danks, Renate M. Houts, Kristen M. Coppola,
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65
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Eileen Sutton & Joanna Coast 171
___________________________________________________________
66
Joseph B. Straton, Nae-Yuh Wang, Lucy A. Meoni, Daniel E. Ford,
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67
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68
Karen E. Steinhauser, Nicholas A. Christakis, Elizabeth C. Clipp, Maya
McNeilly, Lauren McIntyre and James A. Tulsky, ‘Factors Considered
Important at the End of Life by Patients, Family, Physicians, and Other
Care Providers’, JAMA 284, 19 (2000), 2476-2482.
69
Elizabeth K. Vig and Robert A. Pearlman, ‘Quality of Life While
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70
Elizabeth K. Vig and Robert A. Pearlman, ‘Good Deaths, Bad Deaths,
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71
Ezekiel J. Emanuel and Linda L. Emanuel, ‘The Promise of a Good
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72
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73
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74
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75
Vig and Pearlman.
76
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77
Emanuel and Emanuel.
78
Donna M Gauthier and Robin D. Froman, ‘Preferences for Care near the
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79
Patrick et al.
80
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81
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82
Singer et al.
83
Michael Young and Lesley Cullen, A Good Death: conversations with
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84
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172 Older People’s Preferences at the End-of-Life:
A Review of the Literature
___________________________________________________________
85
Karen E. Steinhauser, Nicholas A. Christakis, Elizabeth C. Clipp, Maya
McNeilly, Lauren McIntyre and James A. Tulsky, ‘Factors Considered
Important at the End of Life by Patients, Family, Physicians, and Other
Care Providers’, JAMA 284, 19 (2000), 2476-2482.
86
Vig and Pearlman.
87
Elizabeth K. Vig and Robert A. Pearlman, ‘Good Deaths, Bad Deaths,
and Preferences for the End of Life: A Qualitative Study of Geriatric
Outpatients’, Journal of the American Geriatrics Society 50, 9 (2002),
1541-1548.
88
Williams.
89
Singer et al.
90
Young and Cullen.
91
Steinhauser et al, 2001.
92
Patrick et al.
93
Robin Yurk, David Morgan, Steve Franey, Jennifer Burk Stebner and
David Lansky. Understanding the Continuum of Palliative Care for
Patients and Their Caregivers
94
J. Randall Curtis, Donald L. Patrick, Ruth A. Engelberg, Kaye Norris,
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Members’, Journal of Pain & Symptom Management 24, 1 (2002), 17-31.
95
Joan M. Teno, ‘Patient-Focused, Family-Centered End-of-Life Medical
Care: Views of the Guidelines and Bereaved Family Members’, Journal of
Pain and Symptom Management 22, 3 (2001), 738-751.
96
Karen E. Steinhauser, Nicholas A. Christakis, Elizabeth C. Clipp, Maya
McNeilly, Lauren McIntyre and James A. Tulsky, ‘Factors Considered
Important at the End of Life by Patients, Family, Physicians, and Other
Care Providers’, JAMA 284, 19 (2000), 2476-2482.
97
Vig and Pearlman.
98
Patrick et al.
99
Yurk et al.
100
Patrick et al.
101
Steinhauser et al, 2000.
102
Leichtentritt and Rettig.
103
Stewart et al.
104
Steinhauser et al, 2000.
105
Emanuel and Emanuel.
106
Gauthier and Froman.
107
Yurk et al.
108
Leichtentritt and Rettig.
Eileen Sutton & Joanna Coast 173
___________________________________________________________
109
Ann C. Hurley, Ladislav Volicer, and Zuzka V. Blasi, ‘End-of-Life
Care for Patients with Advanced Dementia’, JAMA: The Journal of the
American Medical Association 284, 19 (2000), 2449-244a.
110
Melanie Henwood and Debate of the Age Health and Care Study
Group, The future of health and care of older people: the best is yet to
come. (London, Age Concern. The Millennium Papers, 1999).
111
Patrick et al.
112
Leichtentritt and Rettig.
113
Steinhauser et al, 2001.
114
Stewart et al.
115
Teno et al.
116
Henwood.
117
Stewart et al.
118
Williams.
119
Steinhauser et al, 2000.
120
Gauthier and Froman.
121
Matsumura et al.
122
Leichtentritt and Rettig.
123
Henwood.
124
Patrick et al.
125
Singer et al.
126
Curtis et al.
127
Patrick et al.
128
Steinhauser et al, 2001.
129
Young and Cullen.
130
Patrick et al.
131
Steinhauser et al, 2000.
132
Steinhauser et al, 2001.
133
Yurk et al.
134
Henwood.
135
Williams.
136
Yurk et al.
137
Steinhauser et al, 2001.
138
Stewart et al.
139
Henwood.
140
Singer et al.
141
Young and Cullen.
142
Steinhauser et al, 2000.
143
Young and Cullen.
144
Henwood.
145
Yurk et al.
174 Older People’s Preferences at the End-of-Life:
A Review of the Literature
___________________________________________________________
146
Hurley et al.
147
Williams.
148
Henwood.
149
Terri R. Fried, John R O'Leary and Margaret A. Drickamer ‘Older
Persons' Preferences for Site of Terminal Care’, Annals of Internal
Medicine 131, 2 (1999), 109-112.
150
Donna M. Wilson, ‘End-of-Life Care Preferences of Canadian Senior
Citizens With Caregiving Experience’, Journal of Advanced Nursing 31, 6
(2000), 1416-1421.
151
Fried et al, 1999.
152
C. Thomas, S.M. Morris and D. Clark, ‘Place of Death: Preferences
Among Cancer Patients and Their Carers’, Social Science & Medicine 58,
12 (2004), 2431-2444.
153
Edward Ratner, Linda Norlander, and Kerstin McSteen, ‘Death at
Home Following a Targeted Advance-Care Planning Process at Home: the
Kitchen Table Discussion’, Journal of the American Geriatrics Society 49,
6 (2001), 778-781.
154
Irene J. Higginson, Priorities and Preferences for end of life care in
England, Wales and Scotland. (London, National Council for Hospice
and Specialist Palliative Care Services, 2003).
155
Merryn Gott, Jane Seymour, Gary Bellamy, David Clark and Sam
Ahmedzai. ‘Older People's Views about Home as a Place of Care at the
End of Life’, Palliative Medicine 18 (2004), 460-467.
156
Fried et al, 1999.
157
Judith C. Hays, Anthony N. Galanos, Tahira A. Palmer, Douglas R.
McQuoid and Elisabeth P. Flint, ‘Preference for Place of Death in a
Continuing Care Retirement Community’, Gerontologist 41, 1 (2001),
123-128.
158
Wilson.
159
Wilson.
160
Thomas et al.
161
Jonathan Koffman and Irene J. Higginson, ‘Dying to Be Home?
Preferred Location of Death of First-Generation Black Caribbean and
Native-Born White Patients in the United Kingdom’, Journal of Palliative
Medicine 7, 5 (2004), 628-636.
162
Higginson.
163
Koffman and Higginson.
164
Thomas et al.
165
Hays et al.
Eileen Sutton & Joanna Coast 175
___________________________________________________________
Leeat Granek
Abstract
Contemporary western psychology teaches that an ‘autonomous’
ontology is the only healthy kind. This view holds that ‘normal’, ‘healthy’
development is towards separation, most especially from the mother in
childhood and adolescence, growing towards individuation, or the total
separation of one’s being from others in adulthood. This ontological view
of humanity, with it’s assumptions of essential separate selves leads quite
naturally into the Western understanding of mourning when there is a loss.
The idea is that when someone you love dies, you grieve for them for a
prescribed period and then you ‘move on’ with your life, perhaps a little
sadder then you were before, but mostly intact. Mourning my mother has
taught me otherwise; this has not been my experience.
Whereas Holub writes of mourning as the process in which we
‘heal and repair the bond between our bodies and souls’, I contend that
grieving is not about mending or repairing, but about learning how to live
with the painful split. Whereas western psychology and the culture in
which its housed insists on putting the pieces together’ in order ‘move on’
and ‘move forward’ as quickly as possible, I believe that mourning is a
process in which we must stand still in the chaos of our shattered pieces
and feel the pain of our brokenness in order to truly heal.
1. Introduction
To create is to reveal the parts from the whole.
4. August 2006
That’s how I felt just after she died, since then, ten months have
passed. The physical pain I describe in this last excerpt is no longer a daily
occurrence but still grips me often and always at unexpected times. While
I was writing this paper, I experienced a wave of such grief that I decided I
needed help. I sent the abstract for this paper to a colleague asking for
some direction with readings on the subject. She sent me back a short note
with a question instead of an answer. She asked, “Do you really want to
theorize your own grief?” This is a good question. After much reflection
on it, I realized that yes, indeed I did want to theorize, or at the very least
think about my grief. I have learned more about life from this year of
mourning than I have from all of my other life experiences combined. And
if I am able to learn, then maybe I am also able to say something
meaningful about death, about dying and about mourning that other people
might be able to relate too.
Out of all these lessons, the one alluded to in the introduction
about brokenness and mending is the one I’m most interested in. I quoted
182 The Wholeness of a Broken Heart
___________________________________________________________
Holub who said that when a person dies, their body and soul separate and
that each person who has been close to that person also experiences a
break or a weakening of the bond between their own body and soul.
Mourning and grieving, according to Holub, is what happens when we try
to mend that split. The interesting part of this idea for me is not that we
break, but why we break when another dies?
Contemporary western psychology teaches that an ‘autonomous’
ontology is the only healthy kind. This view holds that ‘normal’, ‘healthy’
development is towards separation, most especially from the mother in
childhood and adolescence, growing towards individuation, or the total
separation of one’s being from others in adulthood. This ontological view
of humanity, with it’s assumptions of essential separate selves leads quite
naturally into the Western understanding of mourning when there is a loss.
The idea is that when someone you love dies, you grieve for them for a
prescribed period - no longer than three months according to the DSM or
it becomes pathological! - and then you ‘move on’ with your life, perhaps
a little sadder then you were before, but mostly intact. Mourning my
mother has taught me otherwise; this has not been my experience.
Adrienne Rich has written, “The loss of the daughter to the
mother, the mother to the daughter, is the essential female tragedy.” 4 And
it’s true. Losing my mother was a tragedy of epic proportions. More
painful, more shattering, more devastating than I could have ever
imagined. Losing her is about more than love; it’s about more than
missing the familiarity and comfort that only a mother can bring; it is
about more than mourning these terrible incomprehensible losses, it is
about mourning my own death with her passing. It is about mourning the
person that I used to be that died when she died. It is about recognizing
that contrary to the Western insistence on individuation, I was indeed,
undoubtedly part of her and she of me. Our boundaries were blurred, fluid,
osmotic. We are all closer to each other than we think, fluidly connected,
dependant on one another to exist.
I recognize that my mother and I were unusual in our closeness.
She was my best friend, we could intuit each others’ thoughts, we spoke
several times a day and could always make each other laugh. Because I
recognized the finitude of this relationship in my life from a very young
age, I also knew it had to be an accelerated one. There was a time urgency,
we had to live out what should have been a life long mother-daughter
trajectory in just two and a half decades. This awareness of her mortality
intensified our bond to a degree of closeness in my youth that many
people never experience in their entire lifetimes. It is from this place that I
present these observations on mourning and it is ALSO from this place
that I recognize their limitations; they cannot be generalized to everyone.
Leeat Granek 183
___________________________________________________________
While recognizing that the intensity of mourning my mother
comes out of the symbiotic relationship I had with her, I also assert that
the deaths of those we love change us irreparably. Whereas Holub writes
of mourning as the process in which we ‘heal and repair the bond between
our bodies and souls’, I contend that grieving is not about mending or
repairing, but about learning how to live with the painful split. Whereas
western psychology and the culture in which its housed insists on ‘putting
the pieces together’ in order ‘move on’ and ‘move forward’ as quickly as
possible, I believe that mourning is a process in which we must stand still
in the chaos of our shattered pieces and feel the pain of our brokenness in
order to truly heal. In a culture that insists on the total separation of human
beings, this is a radical prescription for mourning. It acknowledges that in
addition to grieving for the person who has died, we are also mourning the
loss of our selves that will never be entirely whole or unscarred again.
In Judaism there are two kinds of prayers for health; the first is a
prayer for ‘re’fuat haguf’, translated to mean the ‘healing of the body’.
The second kind is called ‘re’fuat h’nepshesh’, which calls for the healing
of the whole human being - this includes the body, the mind, psyche, the
soul and every other aspect that makes up each individual person. Healing
in turn comes form the word ‘wholeness’ and has been associated with
‘holiness’. I believe that healing from grief comes when we sit with our
brokenness and acknowledge the fissures as part of ourselves. It is as the
Rabbi I quoted in the introduction says, to heal is to ‘discover the whole
from the shattered parts’.
Notes
1
Org Chabad. A Daily Dose of Wisdom from the Rebbe. (words and
condensation by Tzvi Freeman). Retrieved in an email, April 10, 2006.
2
Joan Didion. The year of magical thinking. (New York: Knof, 2005), 26.
3
Margaret Holub. ‘A cosmology of mourning’, in, Lifecycles: Jewish
women on life passages and personal milestones, ed. Deborah Orenstein
(Woodstock, Vermont: Jewish Lights Publishing, 1994), 341-351.
4
Adrienne Rich. Of woman born: Motherhood as experience and
institution. (New York: Norton, 1986), 237.
Malgorzata Zawila
Abstract
Religion and medicine are both very meaningful phenomena
when considering death and dying. They can be understood as important
elements constructing social attitudes toward death and dying as well as
factors helpful in the process of managing the individual with death and
dying. The question of place and role of religion and medicine in the
context of attitudes toward death and dying is important especially in the
conditions of medicalization and secularization on one hand and the New
Age movement and growth of spirituality on the other. In the context of
the processes mentioned above (medicalization, secularization) religion
and medicine are often understood as opposite to each other. According to
some sociologists and historians in the twentieth century the place and role
of religion in handling the death and dying takes medicine. In my opinion
it is worth to raise the question of this process once more nowadays, in the
twenty first century. The paper focuses mainly on the results of the
research conducted, in three Polish hospices, on the patients, their relatives
and the staff. The main research goal was to study attitudes toward death
and dying among the hospice circle. The method chosen for analysis was
Grounded Theory. Initial analysis of the empirical material gathered
during the research allows treating medicine and religion as
complementary and not opposite to each other, when attitudes toward
death and dying are considered.
1. Introduction
Over the centuries many social institutions were involved in
peoples’ managing with death and dying on an individual and a social
level as well. Magic, religion, medicine and family all are the phenomena,
to some extent, concerning the problem of death and the process of dying.
They all influence social attitudes toward death and dying and help people
to cope with death of their own and grief. There are many different views
on the changes in using those factors like religion, medicine and family in
handling with death and dying on macro and micro level as well. In this
paper I am looking at some ways of understanding of the changes in the
culture of death, as we may call all the human acts, attitudes, and works
concerning the subject of death. I’m focusing especially on the changing
role of religion and medicine in the historical context of death and dying.
186 Religion and Medicine in the Process of Managing
Death and Dying: The Case of Hospice Circle in Poland
___________________________________________________________
In the first part of the paper there are some theoretical
considerations on changes, which took place on a macro scale. In the
second part, there is a presentation of a research project that was run in
three Polish hospices, which shows using religion and medicine in coping
with death and dying on a micro level.
4. Research results
This diagram shows a part of the result of first three mentioned
processes of coding.
Death:
• “Then, the new life starts, about which we don’t know much.”
(P5)
• “I don’t know, for me person comes into another stage of life and
that is normal, that someday body will be dust.” (S2)
• “After the death? Soul will go somewhere and body will stay in a
grave.” (P4)
• “According to what everybody says, what I read in this book
about life after death, that’s exactly what I imagine. Meeting a
lightning creature, first there is a tunnel and then the light and
you go into a different life.” (S5)
• “I think, well I don’t know how to call it; spirit or human
conscious or some kind of energy. I think it comes back to the
source, which is God’s energy, God’s mind, some kind of
wisdom, something like this. It unites. Body is physically
changed.” (S9)
• “I don’t know, I don’t know. If I had known, I’d have easier in
my life. That is a puzzle.” (F1)
Prayer:
• “It can be that grandma suffers a lot, he will thank God that He
took her with Him. Because it will relieve her pain.” (P4)
• “A prayer for peace and averting wars and conflicts.” (F1)
• “He will pray a lot and through it, he will join her.” (S8)
190 Religion and Medicine in the Process of Managing
Death and Dying: The Case of Hospice Circle in Poland
___________________________________________________________
In the category of religion another very meaningful subcategory
is God or higher power. And as the analysis showed it’s also very
important and connected with death, and here are examples of
understanding God and its role in death and dying:
God:
• “Grief he may feel or that they didn’t care for him and hence
their child is dying, or that God punished him.” (P5)
• “Blaming God for taking his child.” (S5)
• "He has already agreed with God’s will.” (F1)
MEDICINE RELIGION
RELATIVES /FAMILY /FRIENDS
In the first stage of the process of dying; started with the diagnosis,
patients’ major role in coping with the disease is a medicine accompanied
by family, then in the second stage (after the redefining the situation) in
Malgorzata Zawila 191
___________________________________________________________
the place of medicine – religion is being used. Here are some sample
citations taken from interviews:
5. Conclusion
On the basis of the analysis of the data some general conclusions
may have been drawn. First of all, religion and medicine are
complementary factors in the individual process of coping death and dying
- that is on a micro level. Then - medicine and religion are equally
important in the process of coping with death and dying for the researched
hospice circle. Another conclusion is that individuals use
medicine/religion according to their subjective estimation of the situation
and the estimation of the effectiveness of used factor. And the last is that
using the specific factor is related with the redefining of the person's role
192 Religion and Medicine in the Process of Managing
Death and Dying: The Case of Hospice Circle in Poland
___________________________________________________________
(from the patient to the dying), that includes the expectations, the plans,
the goals and the estimated perspective, relations and ways of
communicating with others.
Notes
1
Peter Berger, The Sacred Canopy, (Anchor Books, New York, 1967),
107.
2
Ibid, 108.
3
Philippe Aries, Western Attitudes toward Death. From the Middle Ages
to the Present, (London: The John's Hopkins University Press, 1975), 88.
4
Steven Miles, ‘The Role of the Physician in Sacred End-of-life Rituals in
the ICU’, in Managing Death in the ICU, ed. J. Randall Curtis, Gordon D.
Rubenfeld (Oxford: Oxford University Press, 2001), 207-211.
5
Jon Prosser and Donna Schwartz, ‘Photographs within the sociological
research process’, in Image Based Research: a Sourcebook for Qualitative
Researchers, ed. Jon Posser (Falmer Press, 1998), 123.
6
Barney G. Glaser and Anselm L. Strauss, Awareness of Dying, (London:
Aldine Transaction, 1965), 204.
Bibliography
Posser, J. Image Based Research: a Sourcebook for Qualitative
Researchers, (Falmer Press, 1998).
Randall, J.C. and Rubenfeld G. D, Managing Death in the ICU (Oxford
University Press: Oxford, 2001).
Florence Ollivier
Abstract
How does (or does not) a doctor accept to bring death to a
patient? How is the medical staff confronted with this moral problem? We
have studied these questions from the angle of deviance, in order to
understand how a doctor could practice ‘euthanasia’ even if there is an
absence of law, traditional medical ethics, or a request from a patient.
This paper is the result of a sociological study based on
interviews with twenty French doctors. Our study has focused on the
attitudes of doctors confronted with difficult decisions in the context of the
end-of-life. In our choice, we have tried to vary doctor’s specialities in
order to obtain a multiple context of the end-of-life situation (urban
environment, rural environment, hospital/ home). We have examined how
the question of ‘euthanasia’ is understood in accordance with the
speciality of doctors.
We have defined three stereotypes of doctor’s attitudes towards
the end-of-life situation, which are more or less well appreciated. A
distinction is obvious by the use of the drug treatment. Our results
demonstrate that euthanasia is practiced as much in hospital as at home,
but with different drugs and in different situations. These practices are
revealed to young doctors during their hospital training. However it is
quite perceived as a negative point for both doctors and the medical
profession, or it is tolerated as an extreme response to a limit of life.
To minimize deviance, doctors are brought to produce an
arrangement with this ‘secret’ practice within the medical staff. This
practice is tolerated in silence, by all in the profession. Furthermore,
doctors are led to a second arrangement that is a linguistic strategy.
Doctors rename deviant practices under a neutral label. The last
arrangement is the request of a consensus between all actors. Families
rarely denounce euthanasia, because it is often a result of consensus. A
denunciation of euthanasia is more likely to arise from a conflictual
situation within the medical staff.
1. Introduction
In 2003, we were witnesses to the prosecution of a nurse who
was found guilty of killing six patients, and on the opposite side, Vincent
Humbert, 1 a 21-year-old man, was announcing his death to the Public. A
few months later, a couple of caregivers were arrested for having stopped
194 Convenient Arrangements with Death
___________________________________________________________
a patient’s life in a hospice. Death was coming into the open through the
media. A public sphere was created to speak about death in our society:
movies, prosecution and debates in media 2 were promoting these
questions of end-of-life 3 acts. For this reason, my present request to speak
about euthanasia with the doctors I had solicited was less of a surprise. 4
On the contrary, some of them were very talkative on this question of
legalisation. They were less forthcoming in revealing their practice in the
end-of-life. Our questions were how a doctor accepts (or does not) to put a
patient to death and how the medical staff is confronted with this moral
problem.
We have studied these questions from the angle of deviance, in
order to understand how a doctor could practice ‘euthanasia’ even if there
is an absence of law, traditional medical ethics, or a request from a patient.
As society knows deviance and tends to stigmatize this kind of
attitude to reaffirm the order of society. 5 Deviance is related to an
interactive relation. According to Becker’s approach, “We must see
deviance as a consequence of a process of interaction between people,
some of whom in the service of their own interests make and enforce rules
which catch others who, in the service of their own interests, have
committed acts which are labelled deviant.” 6
This paper is the result of a sociological study based on
interviews with twenty French doctors. Our study has focused on the
attitudes of doctors confronted with difficult decisions in the end-of-life
context. In our choice, we have tried to vary doctor’s specialities 7 in order
to obtain a multiple context of the end-of-life situation (urban
environment, rural environment, hospital/ home). We have examined how
the question of ‘euthanasia’ is understood in accordance with the
speciality of doctors.
This study presents a double interest. Firstly, there is still a lack
of knowledge on the medical practice of euthanasia and its conditions in
France. Secondly, studies on deviance in sociology are often about
minorities 8 . It is rare to have qualitative surveys on deviants’ attitudes in
entire professions (and in the dominant class). Therefore, our starting
question is about how a doctor is brought to put a patient to death in spite
of the law and official medical ethics?
B. A Deviant’s Career
Becker‘s analysis helps us to understand social conditions for
pursuing a deviant activity. Becker demonstrates that a deviant practice is
not the result of a deviant actor, but an actor who is brought to practice a
deviant act. During his ‘career’, the deviant will develop a ‘culture’
coherent to his attitude.
According to this theory, a doctor will continue to practice
euthanasia on the condition that he has translated his attitude into a belief,
which brings coherence to his attitude. However, the system of
justification, or the ideology could be different to other deviant doctors.
Thus, deviant actors do not share the same value, or the same beliefs.
To neutralize the bad label (i.e. to consider euthanasia as a
murder), the doctor will use an ideology, or a system of auto-justification
and pass out his deviant position to qualify others as deviant. He stops
feeling guilty after having constructed a meaning of his activity. His
ideology gives him a ‘good’ reason to pursue. Some of deviants keep their
beliefs and no longer trust the official conventions. Good reasons are
supported by the feeling of satisfaction. It could come from the family. 11
Often, this group of doctors is far from the official organization called
Conseil de l’Ordre des médecins.
B. Role of hospital
Death is not taught at school, or even officially at the university.
More than death, it is the dying process which is taboo in our society. I
mean that death is less hidden than the process of dying. The moment of
death is hidden as an impure moment or as a ‘private’ moment for the
individual.
Scientists know the birth process, and even teenagers learn this in
detail at school. They even learn how humans reproduce. It is not the same
for the dying process. That means that dying is still a mysterious event for
people and they more lack knowledge about it, especially since death is
professionalized. 16 Further, our contemporaries have lost their popular
knowledge of the signs of death. They no longer know how to detect signs
of approaching death, as they did when people died at home. They have
become dependant on professional’s experience and expertise. It is quite
the last “knowledge” resistant to the disillusion of the world 17 , and so, it
leaves a place for other interpretations and beliefs around this ‘natural’
event. In this way, even some GPs don’t know how people die, or how to
practice euthanasia. This group of GPs comes more from urban areas.
Anaesthetists are known to be experts in the dosage of
neuroleptics. This medical figure controls techniques in order to put
patients to sleep, to resuscitate and also has the power to save or kill them
with their chemical drugs. In addition, this speciality dominates others
specialities in the medical hierarchy. They should be well placed to give
an advice on the procedures to perform euthanasia. For instance, Dr. M., a
198 Convenient Arrangements with Death
___________________________________________________________
GP in Belgium, had never been socialized to euthanasia in hospital, and
she had never been involved in it before the law allowed it.
5. Conclusion
So what are convenient arrangements with death in an end-of-life
situation? Firstly, doctors make an arrangement “between themselves” and
with nurses to keep this practice secret. This practice is tolerated in silence
by all in the profession. Secondly, there is a convenient arrangement
around a linguistic strategy. Doctors tend to avoid a practice being
labelled as a deviant one by renaming it with a neutral label. Thirdly,
consensus seems to be required as a magic solution to a deviant practice in
medicine.
Further studies can explain more fully how consensus comes up
in the triangle of dependence around the dying patient. ‘Consensus’ is
beginning to be a new obligation for professional caregivers, even if they
had already been constrained to have it before the law was passed.
However, by consulting families and patient’s wishes, it remains to be
seen what doctors will hear, or what families and patients could say.
Notes
1
After a car injury, Vincent Humbert became quadriplegic, blind and
dumb for four years in a hospital. He was the co-author of Je demande le
droit de mourir, (Paris: Michel Lafon, 2004).
2
Between the end of 2003 and 2004, there was a surge of debates on
euthanasia and palliative care which opposed Marie Humbert and Dr.
Chaussoy to medical ethics, added to journalistic comments, a series of
movies (C’est la vie, J-P. Ameris, 2002; The Barbarian invasions, D.
Arcand, 2003 ; Mar adentro, A. Amenabar, 2004; Million dollars baby, C.
Eastwood, 2005) came out the same year. It was public incitement to a
‘reflection’ on end-of-life with a normative background.
3
In this article, we will use the concept of end-of-life in a large meaning.
This concept will include all situations in that patients are, conscious or
not, suffering from a chronic disease or suddenly dying. For instance, few
patients are rapidly confronted with death in case of bleeding.(throat
cancer, patient with an insufficient heart condition.) or in instability
cardiac condition.
Florence Ollivier 201
___________________________________________________________
4
This paper is the result of an investigation led between 2003 and 2004 in
France.
5
Marc Augé, Le sens des Autres. Actualité de l’anthropologie. (Paris:
Fayard, 1994), 95.
6
Howard Saul Becker, Outsiders: Studies in the Sociology of Deviance.
(New York: The Free Press, 1973), 163.
7
Our sample is composed of eight country GPs, five anaesthetists in
intensive care units, three doctors in emergency rooms, two doctors in
palliative care, one cardiologist, and one doctor in geriatrics.
8
H.S. Becker’s studies were focused on marijuana smokers, and the
community of jazz musicians.
9
See Law 22 April 2005 ‘Loi relative aux droits des malades et à la fin de
vie’.
10
Interruption volontaire de la vie (termination of life). This acronym is
deliberately close to IVG (abortion, termination of pregnancy).
11
Care-giver could be thanked, or receive flowers.
12
See E. Ferrand. ‘Withholding and withdrawal of life support in
intensive-care units in France: a prospective survey’, Lancet, 357, (2001)
9249. According to this study, 88% of ‘stopping care’ results from a
unique medical decision.
13
See A. Paillet, ‘Consciences professionnelles, approches sociologiques
de la morale au travail à partir des cas des décisions d’arrêt ou de
poursuite en réanimation néo-natale’, thèse de doctorat de sociologie à
l’EHESS ss dir. Cl. Herzlich, 2003.
14
Jean Jamin, Les lois du silence, essai sur la fonction sociale du secret.
(Paris: Maspéro, Dossiers africains, 1977), 43.
15
Although the interviews were anonymous, only a half of sample
declared to me that they have been personally confronted to euthanasia by
having performed it. That characterizes the importance of secret around
this practice in end-of-life.
16
Annick Barrau, Humaniser la mort: est-ce ainsi que les hommes
meurent? (Paris: L’Harmattan, logiques sociales, 1993), 9.
17
Max Weber, Le savant et le politique. (Paris: 10/18), 63.
18
Claude Got, Les autopsies remis au secrétaire d’Etat à la santé et à la
sécurité sociale, (Sicom, 1997), 68.
19
Laure Patrick, Caroline Binsinger, Les médicaments détournés. (Paris:
Masson, 2003), 111.
20
1996: accused J-M. Préfaut to have poisoned her autistic-girl, a two-
year suspended sentence.
1998: Dr. Duffault is released
202 Convenient Arrangements with Death
___________________________________________________________
Bibliography
Arborio, Anny-Marie, Un personnel invisible : les aides-soignantes à
l’hôpital. (Paris: Anthropos, 2001).
Baudry, Patrick, ‘De la mort à la disparition’, in Savoir mourir , ed.
Christiane Montandon-Binet (Paris: L’Harmattan, Nouvelles études
anthropologiques, 1993), 211- 217.
Douglas, Mary, De la souillure. Essai sur les notions de pollution et de
tabou. (Paris: La découverte et Syros, 2001).
Memmi, Dominique, Faire vivre et laisser mourir. Gouvernement
contemporain de la naissance et de la mort. (Paris: La découverte, Textes
à l’appui, Politique et sociétés, 2003).
Abstract
This study discusses the perception of death and funerals in Sunni
Moslem communities of Turkey whilst evaluating Islamic culture and
urbanised society. The main theme is to understand the attitudes of the
urbanised Islamic Sunni society toward the death phenomenon in
metropolitan cities provincial towns particularly in Ankara and Marmaris.
Emphasis is placed on changes in attitudes over time, in the light of
comparisons between Ottoman and modern Turkish culture. Graves,
tombs, tombstones, epitaphs and cemeteries are also discussed from the
viewpoint of Islamic culture. With these objectives, the study begins with
the analysis of the concept of death. In order to carry out the study, a
method approaching the subject from four disparate points has been
employed. First, literature was surveyed to gain an understanding of the
meaning of death in present-day society. Second, the Islamic canon was
reviewed with regard to the death phenomenon. Third, reflexive narratives
originating from personal observations as a participant in the funerals of
my family members’ were employed in this study. The fourth and last
field of research includes field observations and photographs from
Karşıyaka Cemetery in Ankara, and copies of photographs from several
other sources in order to identify the divergence of the modern from
traditional. The major verdict of this study is that in modern Islamic
culture, in contrast to its earlier traditional evaluation, death is
sequestrated from social communal life and assigned to the status of an
institutional event.
1. Introduction
The aim of this study is to analyse the perception of death, and
the actions performed for the deceased in urban communities considering
themselves Sunni Moslems living in Ankara and Marmaris.
Through visits to the Karşıyaka Cemetery, affiliated with the
Ankara Metropolitan Municipality, I have attempted to observe attitudes
of members of the present-day Turkish urban community regarding death,
the procedures followed death, burial procedures, graves and gravestones.
As interview with the relatives of the deceased might be deemed
offensive, frequent use of participant observation has made use of. In a
manner not common in academic literature, my personal experiences of
the decease and funerals of parents and brother are inevitably reflected in
204 Death and Funerals in Sunni Communities of Turkey
___________________________________________________________
this study. In addition, perception of death in hospitals and death at home
will be included in this study.
5. Cemeteries as a space
In Ottoman cemeteries, until the nineteenth century, practices
similar to western practices of graves and cemeteries may be observed.
The shift in the cemetery culture of Ottoman Empire took place after the
nineteenth century. In the present day, cemeteries are situated far from
cities either because of economical necessities or ‘city planning’
principles. But in big cities like Ankara, or even in small towns like
Marmaris, cemeteries, which were initially intended to be far outside the
city are again becoming situated inside cities because of the haphazard and
rapid growth of these cities.
As is the case with almost all municipally-owned cemeteries, in
Ankara Karşıyaka Cemetery there are wash rooms, mosques or ‘mescit’s,
a large area for funeral praying, and ‘musalla taşı' - a stone used as a table
on which the coffin is temporarily placed - kept ready for the funeral
prayer.
B. Cemetery visits
Before visiting the cemeteries Sunni Moslems still have a wash
‘boy abdesti/ablution’ according to Islamic practices and women cover
their heads with headscarves. Cemeteries may be visited on any day of the
year, but in Islam, it is especially day before the religious bairams. People
take flowers, or as in Marmaris branches of myrtle, believed to be holy, to
put in the vases at the foot of graves. It is also common to take flowers to
funerals. Wreaths prepared for this purpose are readily available in flower
shops, or indeed may be ordered online. The aim of cemetery visits before
bairams is to symbolically celebrate the bairam with those who have
passed away to the ‘other world’. Due to the sacredness of the day, people
read either the prayer of their ‘hatim’- a previous complete read of Qur’an-
or the Sura of Yasin from the Qur’an. Also in compliance with the request
written on the gravestones ‘RUHUNA FATİHA/FATIHA FOR THE
SOUL’, they read the Sura of Fatiha. Writings on gravestones requesting
for a prayer reflect a tradition extending back to Ottoman grave culture. 26
Traditionally, it is suggested that one should not walk or stand on
the graves and complete the visit standing-up. Nowadays, children are not
seen in burial rituals and even at cemetery visits. In 1970s, during my
childhood, children were taken on cemetery visits at least on the day
before bairams. Particularly my grandmother used to take all her
grandchildren to the cemetery to help her in cleaning and watering of the
graves. In complete silence, somewhat bored, but excited by doing
something different and happy that, according to my grandmother, we had
gained some ‘sevap’—credit awarded by God for good deeds—we would
complete the visit.
6. Conclusion
To make an interpretation on how Sunni Moslem society
especially those who live in cities view death and the subsequent funeral
arrangements in today’s Turkey; it may be stated that there change has
occurred since Ottoman Times. Some people, despite their lessening faith
ensure a religious funeral for their relatives and friends. Perhaps the
refrain from funeral rites outside those sanctioned by the Islamic tradition
to preserve the esteem their nearest are held in, on their final journey.
Even people without faith, are left in a position of being the organizer of
an ‘Islamic Funeral Ritual’ as their deceased relative is a Moslem and
would want to be buried in accordance with the Islamic tradition.
Reyhan Varlı Görk 213
___________________________________________________________
To conclude; it seems true to say that these changes point to an
accelerating trend in the social institutionalization of death. Through this
transformation, both death itself and funeral rituals are producing a
services sector within organizations and establishments. In view of all this,
it may be observed that funerals, the last social rituals in which people
participate, will evolve into mechanistic, ever-rationalized and
commercialized procedures participating in the societal division of labour.
Notes
1
‘Cenaze İle İlgili Bazı Uygulamalar’ (Some Practices about Funerals),
22 September 2000, (03 June 2002).
<http:// www.diyanet.gov.tr/makaleler/cenaze.html >
2
(06.06.2006), <http://www.mevlana.net/>
“Mevlana who is also known as Rumi, was a philosopher and mystic of
Islam, but not a Muslim of the orthodox type. His doctrine advocates
unlimited tolerance, positive reasoning, goodness, charity and awareness
through love. To him and to his disciples all religions are more or less
truth. Looking with the same eye on Muslim, Jew and Christian alike, his
peaceful and tolerant teaching has appealed to men of all sects and
creeds.”
3
Yaşar Çubuklu, ‘Ölüm Üzerine Spekülatif Düşünceler’, Defter, 1, 2
(1987), 72-77, 75.
4
Çubuklu, 76.
5
Phlippe Ariés, ‘Yasak Ölüm’, Defter, 1,2 (1987), 78-94. p. 80. [‘Yasak
Ölüm’ The last chapter of ‘Batı'nın Ölüm Karşısındaki Tutumları’ by
Philippe Ariés, Western Attitudes Toward Death (London, Baltimore: The
John Hopkins University Press, 1974)].
6
Ariés, 80.
7
According to traditions burial should not be left after mid afternoon time.
8
Ana Britannica, Volume 7, s.v. ‘cenaze yıkama’ (İstanbul: Ana
Yayıncılık A.Ş., 1994) p. 377.
9
Münif Çelebi, Kuran Dili ve Alfabesi ve Okuma Kaideleri, Tecvit ve
Namaz, (Ankara: Balkanoğlu Matbaacılık Ltd. 1974), 57.
10
Diyanet İşleri Başkanlığı, (Religous Affairs) 03 June 2002,
<http://www.diyanet.gov.tr/dinibilgiler/nampage.html> "... Be it Friday,
Religious Festival or funeral prayer, if women are going to participate in
the group of prayers, they should be situated in a suitable place separated
from that of men. Indeed, Prophet Mohammed organized the prayer group
as the men standing in the front part followed my boys and then women.
214 Death and Funerals in Sunni Communities of Turkey
___________________________________________________________
deeds of the all living and deceased. This is why a religious Moslem,
when enters a cemetery, reads Fatiha not for someone particular, but for
all deceased to be forgiven by God.”
Leila Jylhänkangas
Abstract
The purpose of this study is to examine the different ways in
which people discuss euthanasia in contemporary Finnish society. The
data in this study consist of letters in which ordinary Finns discuss
euthanasia. Arguments today often focus on the question of whether a
terminally ill individual should be allowed to die with active death
assistance. Although active euthanasia has not been legalised in Finland,
the issue occasionally arises in the Finnish media. Unsurprisingly, the data
reflect people’s interest in discussing euthanasia. Representations of
suffering, pain and despair often arise in arguments supporting euthanasia.
Considering this, it is interesting to note that psychological distress
(especially depression) is one of the main factors behind requests for
euthanasia. In Finnish euthanasia discourse, however, the fear of pain, and
the possibility of falling into the care of other people in particular, are the
principal motivators. The data compel one to pose the following questions:
What kinds of cultural representations do people construct concerning
dying and suffering in end-of-life situations? How are representations of
euthanasia related to them?
Key words: euthanasia, death and dying, cultural categories, human body.
1. Introduction
The purpose of this study is to examine some of the different
ways in which people discuss euthanasia 1 in contemporary Finnish society
as well as to shed light on representations of a dying human body in
euthanasia discourse. The data in this paper consist of letters 2 in which
ordinary Finns discuss euthanasia. Arguments today often focus on the
question of whether a terminally ill individual should be allowed to die
with active death assistance. In euthanasia letters, images of the last stages
of one’s life are often associated with despair and worry about pain.
Cultural constructions of the body serve to sustain views of social
relations. Human beings relate to each other through their visible body, a
body that sees and can be seen. Euthanasia discourse represents different
kinds of bodies. One of them is the body of necessities, a human body
dependent on the help of other people to maintain basic, necessary vital
functions and everyday hygiene 3 . I define the body of necessities as
something that is crucially related to dying, the last stages of human life.
The body of necessities is a construct closely and concretely related to
data, in this case Finnish euthanasia discourse, on pain and suffering
218 The Body of Necessities in Finnish Discourse on Euthanasia
___________________________________________________________
related to dying. In euthanasia discourse, dying is considered an
unwelcome intrusion into the midst of a happy life. Representations of
suffering, pain and despair often arise in arguments supporting euthanasia.
Considering this, it is interesting to note that psychological distress
(especially depression) is one of the main factors behind requests for
euthanasia 4 . In this paper I’ll also examine hopelessness and rejection.
Hopelessness at the end of life is not simply ‘the absence of hope’, but
attachment to a kind of hope that is lost 5 . Rejections, on the other hand,
are consequences of hopelessness. Rejection of medical technology
toward the end of life is one example of this.
In this study, the analysis of the data will include category-
theoretical orientations which presume that cultural categories play a
significant role in euthanasia discourse. Following Mark Johnson, I
consider reasoning and experience to be closely linked to one’s
understanding of the human body. 6 Also, the ideas of Mary Douglas are
useful in the analysis of euthanasia discourse, for according to Douglas,
the body is a model standing for any bounded system 7 . We can see in the
body a symbol of society, for the powers and dangers credited to social
structure are manifested on a smaller scale to the human body 8 .
Consequently, the social and cultural categories of the human body are
considered strong influencers of euthanasia discourse. The body is also
central to the construction of metaphors 9 concerning the body of
necessities.
A dying person may consider death the only way to escape from
dying and the concrete physical pain and emotional distress. For example,
the following writers are worried about the pain and suffering various
incurable illnesses cause. The latter person writes about such suffering
‘that only death can end’.
The previous writer is worried about the pain in cancer and notes
that ‘in the last stages of lung cancer, a person experiences terrible pain’.
People want to escape the pain cancer causes, and very often death is
considered the only way to end the pain. Considering this, it is worth
noting that cancer is a risk factor for suicide, and the risk increases with
disease severity 14 . According to Émile Durkheim, melancholia and
depression have ‘a long history’ in the individual who commits suicide.
Although an individual may be driven to suicide by what appears to be an
immediate cause, no such sudden stimulus alone would result in such self-
murder 15 . This notion is analogous to the notion according to which
cancer is a risk factor for suicide (or any other life-threatening illness).
There is a sufficient ‘time to be anxious and depressed’ before death
comes. The following excerpt comes from a letter belonging to a 40-year-
old woman who describes the serious illness and suffering of her own
husband. Her husband had attempted suicide twice:
Technological advances over the past decades are vast, and they
have enabled us to overcome many diseases and have extended life. At
times, however, the result has been an unfortunate prolongation of the
dying process. 18 Due to technological advances made during the past
decades, death has changed radically, having passed largely from the
home to the hospital. According to Ariès, “the hospital is the only place
where death is sure of escaping a visibility - or what remains of it - that is
hereafter regarded as suitable and morbid”. 19 When death has been
222 The Body of Necessities in Finnish Discourse on Euthanasia
___________________________________________________________
removed from the home and taken to the hospital, it has been rendered
invisible.
David W. Meyers writes that “the natural tendency of many
doctors has been to use any available technology, in the hope it may
improve the patient’s condition or extend his life, even if the patient is
suffering from a terminal and incurable malady.” 20 The following writers
are worried about a situation in which an unconscious person is
‘connected to machines’:
Mark Johnson has argued that metaphors are more than just
‘isolated beliefs’. For example, for a physician whose understanding of a
human body is structured by the ‘body as machine’ metaphor,
representations such as ‘breakdowns occur at specific point of injuries in
the mechanism’, influence his or her perception, diagnosis, treatment,
theorising and other practices. Such representations constitute the
physician’s grasp of medical situations. 21 In the same way, the ‘body as a
Leila Jylhänkangas 223
___________________________________________________________
vegetable’ metaphor is a kind of ‘chief metaphor’ that systematically
structures the dying process in a very definite manner. It seems easier to
give up and let a person die when he or she is no longer considered a
human, but rather a vegetable.
In this study, not all of the writers supporting euthanasia use
strong metaphors such as ‘a vegetable’ or ‘a living corpse’. As already
mentioned, some writers worry about ‘the intense physical pain’ and life
being ‘all but distress’. In such a worry, euthanasia can be represented as
‘a salvation’, and as a means ‘to end the suffering’ justifiably, ‘especially
when the physical pain is intense’:
The following writer stresses the value of human life. This excerpt
compels us to remember that death can also be ‘dignified’:
5. Conclusion
The theoretical orientation of this paper combines ideas of Mary
Douglas, George Lakoff and Mark Johnson. Structures of human
understanding have their origin in the body, and human life has always
been a concept confined to the body. 25 George Lakoff and Mark Johnson
have argued that our conceptions of reality should not be separated from
what we experience in our embodied interactions. The movements of our
bodies and their placement in space generate knowledge structures and
modes of reasoning evident in linguistic usage. 26
The socially constructed world of euthanasia discourse sees the
crossing of the line between life and death as a matter of individual
autonomy and as a matter for the whole community. More than death,
which itself is an experience not easily shared with others, dying is an
observable and sometimes lengthy process whose contemplation shapes
peoples’ perceptions of their own lives and forthcoming modes of dying.
226 The Body of Necessities in Finnish Discourse on Euthanasia
___________________________________________________________
In Finnish discourse on euthanasia, people talk about hopelessness and
rejection in end-of-life circumstances.
Hopelessness arises from situations in which life is considered to
hold no greater value than death. Rejections, on the other hand, are
consequences of hopelessness. These rejections are directed at life-
sustaining treatment (especially machine-based) and a life of all but pain,
distress and ‘torture’. The body of necessities appears differently in these
situations. In this paper, I have offered examples in which the body of
necessities is viewed as a suffering person totally dependant upon
machines and the care of others. Finnish discourse on euthanasia
represents the culturally constructed dying human body and its treatment
in the community. The body is also central to the construction of
metaphors concerning the body of necessities.
Notes
1
Definitions of euthanasia are, of course, cultural constructions.
Originally, the Greek word euthanasia meant ‘easy death’, but the
definition of the word has evolved throughout the years depending on the
cultural environment in which it has been defined. In the data of this
study, the concept ‘euthanasia’ usually refers to its active form: a doctor
intentionally ends the life of a terminally ill patient who is in intense pain
and who voluntarily chooses to end his or her own life to stop the
prolonged suffering. Hence, in this article, ‘euthanasia’ refers to its active
form even though the word ‘active’ does not appear in every context.
Passive euthanasia is to allow the patient to die by succumbing to his or
her illness.
2
I obtained the 132 letters (coded KE 2-133) by publishing in several
Finnish newspapers a request in which I invited people to discuss
euthanasia. This article contains excerpts from the data translated from
Finnish into English.
3
Silva Tedre, Välttämättömyyksien ruumis vanhusten hoivassa, (The
Body of Necessities in Old People’s Care), Naistutkimus 9, 4 (1996), 2-14.
4
Ezekiel J. Emanuel, ‘Depression, Euthanasia, and Improving End-of-Life
Care’, Journal of Clinical Oncology, 23, 27 (2005), 6456-6458.
5
Mark D. Sullivan, ‘Hope and Hopelessness at the End of Life’, American
Journal of Geriatric Psychiatry, 11 (2003), 393-405.
6
Mark Johnson, The Body in the Mind. The Bodily Basis of Meaning,
Imagination, and Reason (Chicago: University of Chicago Press, 1987).
7
Mary Douglas, Purity and Danger. An Analysis of the Concepts of
Pollution and Taboo (London and New York: Routledge, [1966] 1996).
Leila Jylhänkangas 227
___________________________________________________________
8
Ibid.
9
According to George Lakoff and Mark Johnson, human thought
processes are metaphorical, and metaphors are part of our everyday
language. George Lakoff and Mark Johnson, Metaphors We Live By
(Chicago and London: The University of Chicago Press, 1981); Mark
Johnson, 1987.
10
David W. Meyers, Human Body and the Law (Edinburgh: Edinburgh
University Press, 1990); Hazel Biggs, Euthanasia. Death with Dignity and
the Law (Oxford: Hart, 2001).
11
Presently, no specific law on euthanasia exists in Finland, and no
legislative enactment mentions the concept of euthanasia. Elise Kosunen
et al., ‘Finland’, in Euthanasia in Europe. National Laws, Medical
Guidelines, Ethical Aspects, eds. Wolfgang Sohn & Michael Zenz
(Stuttgart: Schattauer, 2001), 43-57. Consequently, I define euthanasia as
an ‘imagined ritual’.
12
Sullivan.
13
Ibid.
14
Erlend Hem et al., ‘Suicide Risk in Cancer Patients from 1960 to 1999’,
Journal of Clinical Oncology, 22, 20 (2004): 4209-4216.
15
Émile Durkheim, Suicide. A Study in Sociology (New York: The Free
Press, 1966).
16
Terhi Utriainen, Läsnä, riisuttu, puhdas. Uskontoantropologinen
tutkimus naisista kuolevan vierellä (“Present, Naked, Pure: Study in the
Anthropology of Religion on Women by the Side of the Dying”)
(Helsinki: SKS, 1999), 61-63.
17
Tedre, 2-7.
18
David W. Meyers, Human Body and the Law (Edinburgh: Edinburgh
University Press, 1990); Philippe Ariès, The Hour of Our Death (New
York: Alfred A. Knopf, 1991).
19
Ariès, 571.
20
Meyers, 277.
21
Johnson, 129-130. Susan Greenhalgh has analysed the various ways in
which “the ritualised practices of the initial consultation works to turn
doctor and patient into subject and object, knower and known, mind and
body of medical science”. This is not to suggest, however, that doctors are
cynically manipulative or deliberately exploit the patient’s emotional
vulnerability. Susan Greenhalgh, Under the Medical Gaze. Facts and
Fictions of Chronic Pain (Berkeley: University of California Press, 2001),
77-81.
22
Hazel Biggs, Euthanasia. Death with Dignity and the Law (Oxford:
Hart, 2001).
228 The Body of Necessities in Finnish Discourse on Euthanasia
___________________________________________________________
23
Julia Lawton, ‘Contemporary Hospice Care: the Sequestration of the
Unbounded Body and ‘dirty dying’’, Sociology of Health & Illness 20, 2
(1998), 121-143.
24
Janice M. Morse and Joy L. Johnson. ‘Understanding the Illness
Experience’, in The Illness Experience. Dimensions of Suffering, eds. J. M
Morse and J. L. Johnson, (Newbury Park: Sage, 1991), 1-12
25
Douglas.
26
Lakoff and Johnson.
Emilie Jaworski
Abstract
The globalization may be described as the expansion of the
capitalist system and its ideals. This phenomenon implies deep structural
transformations inside societies and reorganization of worldwide
population, because of the intensification of the migratory movements. It
is then obvious that each society must redefine all their social and cultural
practices, in order to give sense to the new social reality.
The mechanism of those reshapenings obviously appears in
funeral rituals. Those events, which combine economical, social and
cultural dimensions of a society, are interesting to get a better
understanding of a population. The part of participators for funeral is to
establish the dead among the ancestors - references for the identity of a
group - and fix his memory. Then, during this action, they solicit all the
values and ideals of the society. So funerals are a total social fact, 1 which
can be considered as a mirror of the society.
This problematic which involves social change and funerary
rituals, can be applied to the case of Poland and polish community in the
North of France. Since the fall of communism in 1989, the social and
cultural environment of Poland had deeply changed and the population
must adapt itself to a new reality. The polish community also had to
reconfigure its practices but in a foreign environment. A comparative
study of those two common original populations, facing the social change,
can help to understand the mechanisms which drive the social and cultural
reshapenings. According to this aim, I especially focus on a practice which
was common to both of the concerned populations: the post-mortem
pictures, consisting in taking pictures of dead relatives in the coffin before
the funerary mess. By working on social uses and functions of those
pictures and by re-establishing them in the whole of funerary practices, it
is possible to understand how works a society and how a population adapt
itself to changes.
C. The functions
The first function we can attribute to those pictures concerns the
required process of creating ancestors. This concept of ancestor refers to
all the dead who stay alive in the memory of the family. This means a
232 Images of Death, Images of Society
___________________________________________________________
descent is necessary to reach this status. Children, as they are pure
according to Catholicism and do not have descent, become angels, if they
are baptized of course. So the pictures of adults and children belong to
different processes, but actually the most interesting for us is the case of
adults. The first element which drives us to this conclusion appears when
we consider the post-mortem pictures as a part of a more general practice,
which consists in taking pictures of all the great events of a the social life
as for example baptisms, weddings and funerals. All those events are
finally some rites de passage, which confirm a change of status and of
identity. Then post-mortem pictures are an expression of a specific
moment of the life’s cycle: the death. For Catholics, this event is not the
End, but the beginning of a new way of life. The funeral, according to this
point of view, is the first step consisting in raising the soul of the dead and
establishing him among the other ancestors. Here the fact that the post-
mortem pictures work as a pair, which shows the dead alone and with the
family, makes sense. This can be interpreted as an expression of the
individuality of the dead on one hand, and as the expression of his position
in a social network on another hand. In fact, this way of taking pictures
would illustrate the rupture between the dead and his relatives, as
Sakalavas in Madagascar expresses this rupture by the symbolic cut of a
string which fastens the dead husband to his live wife for example. In
general, the funeral is the occasion to create a legend about the dead, to
create a hagiographic speech which consists in deleting his bad sides and
insisting on his good sides and his good actions corresponding to the
values of the society. In fact the aim of this process is to create a local
hero, which will allow the group and the family to recognize themselves in
him and use him as a social and cultural reference.
The ultimate step which ends the process of making an ancestor
occurs the first birthday of the death. Usually the family celebrates this
birthday by cleaning and then adorning the grave of flowers and candles.
This birthday is also connected with the setting up of the real grave. In
Poland a family can choose between a gróbowiec and a nagróbek. This
choice is determined in general by the standard of living of the family. A
gróbowiec is made of a vault, when a nagróbek just includes the funeral
monument. In this last configuration the dead and its coffin are buried
directly in the ground. For this kind of grave the monumental mason must
wait one year before installing the definitive grave. According to them one
year corresponds to the time necessary to get the ground stable. By setting
up this definitive grave starts the ancestor’s cult.
The post-mortem pictures, which illustrate parts of the process of
making ancestors, can be considered as the support of the memory; so do
the graves. They show the last moments of the dead on earth and his
Emilie Jaworski 233
___________________________________________________________
transformation in ancestor with all its implications. Those pictures will fix
this process in the memories and also the values of the society represented
by the ancestor. The post-mortem pictures here work as a metonymy of the
entire life, and do not only refer to the values implied in a particular
moment of the life as weddings for example which are especially focused
on fecundity.
In Poland in general, and probably in the first generation of
Polish immigrants, the family pictures, including post-mortem portraits,
are or have been watched during family meetings. Relatives, by watching
them together, refresh and strengthen the family history, identity and links.
The members of a family recognize themselves in a common ancestor and
in the values funding their culture and which belong to different levels of
the society - it can be national values like the respect of catholic tradition
or patriotism, regional, local, familial and individual values which refer to
the specific history and traditions of the region, the village, the family and
the individual. Those pictures refer also to the social status of the ancestor.
The way the dead is dressed, the quality of the coffin and grave, the kind
of flowers exhibited are all signs revealing and fixing it. So by taking such
pictures, and watching them in special circumstances, a family reactivates
what is meaningful for itself and reaffirms its social position among a
group. Globally those pictures can be considered as non-verbal texts,
which help a family to perpetuate its indoor cohesion, its outdoor position
within a larger group. The comparison between post-mortem pictures and
graves can be made. The grave is a monument which is connected to the
values, to the identity and the social level of a family thanks to its
architecture, its symbols and its quality, but the main difference is that a
grave is fixed when a picture can be given or sent and infinitely
reproduced. This point is really important in a context of immigration. The
families which had been separated can symbolically gather by sending
post-mortem pictures to the part who could not attend the ceremony. So
the entire family is aware with the family history. But the interest of those
pictures is lost without the speech. As they are metonymies of the family
history, they have to be supplemented by the oral evocation of the
ancestors. So their memory is continuously updated, insuring the
perpetuation and cohesion of family identity.
Here the post-mortem pictures and the graves have the same
purpose: to let a track of the stay of somebody on earth. This track works
as a transitional object 3 , which support the psychological process of
mourning. It is a kind of compromise which enable the transition between
the presence and absence of the deceased and which is a proof of the
reality of death. So, post-mortem pictures are also very interesting to help
people who could not participate to funeral by showing them the
234 Images of Death, Images of Society
___________________________________________________________
indisputable reality of death and allowing them to launch the process of
mourning.
3. Conclusion
Post-mortem pictures were involved in practices which were
corresponding to the expectations and the needs of a society and a group.
In such case it’s analyze is really interesting to understand the functioning
of a population. The disappearing of this element is a witness of deep
transformations of a society, which is, in the case of Poland and Polish
community, linked with the phenomenon of globalization. The new
economical configuration requires a population to change its behaviors
and its system of perception of the reality. Here we see clearly how the
capitalist rationality works in the two populations studied. The traditional
knowledge is transferred to specialists who create a funeral market, and
the family is not anymore really concerned by the care of the deceased. So
taking a picture of them does not make sense anymore if they belong in
another dimension of the society more and more autonomous from its
origin, and do not belong anymore in the family surroundings. The same
logical is observable in cemeteries, which are areas submitted to the
knowledge of urbanists and architects. In this new social configuration the
practice of cremation become an alternative which corresponds to the new
rationality and social structure of the society. It implies a gain of space
and time, and then of money, but also a reinventing of funerary rituals
correlatively to the new plurality of lives trajectories and to the
individualism.
The specialization of the funeral knowledge and the diversity of
funeral rituals generally drive people to think the death became a taboo
and the funerals are debased. This conclusion is maybe not totally false,
but could not we appreciate those evolutions of funerals practices as
adaptations which correspond to the new social structures and needs? Are
the funerals debased or do we assist to everyday micro-reinventing
connected with the new realities, more and more diverse, and the personal
needs?
Notes
1. Marcel Mauss, Sociologie et anthropologie (Paris: PUF, 1950).
2. Picture 1 and Picture 2, p.3.
236 Images of Death, Images of Society
___________________________________________________________
Bibliography
8. Results
Question 1: Rank of attachment traumas. Chamorro responses to
two attachment traumas resulted in their being ranked as more stressful
when compared to western perspectives. These included (6), a terminal
illness and (2) a developmental conflict in a family member. Further
comparisons revealed the ranking of divorce, threat of dissolution of the
family, job loss and a move, not all family, as less stressful. Chamorros
ranked sudden death, threatening illness and a move, all family, equally
with western perspectives. The Chamorro Family Crisis Scale, to be found
in appendix B, is portrayed and compared with the western Family Crisis
Scale.
Questions 2 and 3: What are the differences between threatening,
anticipatory and sudden death of a family member? Twenty five percent of
respondents indicated there was no emotional difference between the
situations of threatening, anticipatory and sudden loss of a family member.
Question 4: The occurrence of sudden death. While analysis
revealed 12 subjects had experienced a sudden death in the family in the
previous year, 7 of the 12 likewise indicated the occurrence of a divorce.
244 Attachment Trauma, Sudden Death and Anticipatory Grief:
the Chamorro Sample
___________________________________________________________
Question 5: Frequencies of stressors. The three most frequent
attachment traumas included threat of dissolution of the family tied with
loss of job by a family member. A family member leaves temporarily
ranked second in terms of frequency and a move, all family included, was
third most frequent.
A corollary observation was made to discover that sixty two
percent of respondents ranked most stressful more than once to FCS items.
An understanding of these results are addressed in the next section of this
study.
Attachment traumas affect all human beings throughout their life-
spans. The ability to cope and handle the stress within a family varies
from person to person and family to family. Results from the Family
Crisis Scale reveal several thoughts that allow an understanding of the
psychological demography of the Chamorro people. An analysis of their
responses to the questions generated in this study is presented below.
11. Conclusion
The stress generated losses examined in this study, experienced
by subjects within their families/extended family/clan occur in many cases
without a calibrated, differentiated pattern of emotional response(s)
deemed necessary for coping. It is broadly hypothesized that
psychotherapeutic interventions for Chamorros contain emotion based
models to process the varying types of unavoidable losses, and supportive
cognitive models to enhance cognitive complexity, vis-à-vis, the
coordinated calibrated appraisal of conflict management at home, work
and at school.
Appendix A
The Family Crisis Scale
1. A geographical move. All primary kin, however move together.
Any move, relocation where family remains intact.
2. A family member experiences a developmental obstacle; anxiety,
depression, identity conflict; developmental issues, psychological
distress.
3. A move has occurred but not all primary kin members are
included. Some temporary form of agreed upon separation.
Extended periods of time spent away from family due to work,
travel obligations; a college student.
4. A family member experiences some form of loss of status. A
change in socio-economic standing; loss of job, demotion, a
threat to family well being due to loss of financial stability.
Stephen W. Kane and Vera de Oro 247
___________________________________________________________
5. A threatening illness, accident or harmful physical threat to life
of family member. A loss of anatomical or physiological
functioning; a recoverable form of trauma.
6. A terminal illness or accident/injury of primary kin member.
Eventual loss is perceived; a state of preparedness for loss,
anticipatory grief. Typically the first experience of dying family
member dying from terminal illness is grandparent.
7. A threatened dissolution of the family. Individuals perceive a
break due to separation or divorce. Also indicates warring
factions amongst family members. Inharmonious atmosphere,
chronic conflict, aggression, violence.
8. A separation, divorce, abandonment; a break occurs. Separation
of family members, geographically and emotionally.
9. Death, sudden death of family member due to illness, injury,
accident
Appendix B
1. A geographical move. All primary kin however move together.
Any move or relocation where primary kin unit remains intact.
2. A move has occurred, but not all primary kin members are
included. Some temporary form of agreed upon separation of
family members. Extended periods of time spent away from
family due to work, travel obligations; a college student.
3. A family member experiences some form of loss of status. A
change in socio-economic standing; loss of job, demotion, a
threat to family well being due to loss of financial stability.
4. A family member experiences a developmental obstacle; anxiety,
depression, identity conflict, developmental issues, psychological
distress.
5. A threatening illness, accident or harmful physical threat to life
of family member. A loss of anatomical or physiological
functioning; a recoverable form of trauma.
6. A threatened dissolution of the family. Individuals perceive a
break due to separation or divorce. Also indicates warring
factions amongst family members. Unharmonious atmosphere,
chronic conflict, aggression, violence.
7. A separation, divorce, abandonment; a break occurs. Separation
of family members, geographically and emotionally.
8. A terminal illness or accident/injury of primary kin member.
Eventual loss is perceived; a state of preparedness for loss,
anticipatory grief. Typically the first experience of a family
member dying from a terminal illness is a grandparent.
248 Attachment Trauma, Sudden Death and Anticipatory Grief:
the Chamorro Sample
___________________________________________________________
9. Death, sudden death of family member due to illness, injury,
accident.
Notes
1
Monica McGoldrick et al. Ethnicity and Family Therapy, 3rd ed. (The
Guilford Press, 2005), 4.
2
Ibid, xv-xix.
3
Don A. Farrell, History of the Northern Marianas Islands, (The Public
School System, Commonwealth of the Northern Marianas Islands, 1991),
60.
4
Ibid.
5
Ibid.
6
Ibid.
7
George Vaillant. ‘Natural History of Male Psychological Health’,
American Journal of Psychiatry, 145 (1990), 31-37.
8
Vaillant, 35.
99
T. Holmes and R. Rahe. ‘The Social Readjustment Scale’, Journal of
Psychosomatic Research, 147 (1967), 215-218.
10
Stephen Kane, ‘Family Crisis: An Attachment Perspective’, The 11th
International Conference for Counselling”, Bangkok, Thailand, December
28th -January 2nd 2005/6
Kriss A. Kevorkian
Abstract
Earthquakes, hurricanes, tornadoes, landslides, killer storms and
a recent tsunami illustrate the awesome power of Mother Nature. We
pollute, destroy, and reshape our planet, eliminating animal habitats and
ecosystems to fit human needs. People conscious of the plight of these
events react to this decline by experiencing environmental grief®, the
grief reaction stemming from the environmental loss of ecosystems caused
by natural or man-made events. This is a unique form of disenfranchised
grief; grief that is not openly accepted or acknowledged in society. The
foundation for environmental grief lies in the Gaia Theory, which supports
the concept of interconnectedness, and the considerations found in deep
ecology and the ecology of grief. Despite what some theorists believe
about the plight of our environment, grief issues should and can be
acknowledged. Once a name is put to any type of symptom or feeling,
people are generally able to move forward and begin the healing process.
1. Introduction
Grief is the reaction to loss. When we speak of grief, it is usually
in regard to the death of a loved one. Grief can also be a reaction to many
other losses that occur in life. The losses of a job, a house, or even the
experience of having a friend move away are also associated with grief;
however, these kinds of losses are not often considered in discussions of
grief. Grief is very individual: How one person reacts could be very
different from how another might react.
Grief manifests itself in many ways, including the following:
feelings such as sadness, anger, guilt, anxiety, fatigue, and shock; physical
sensations, such as tightness in the throat or chest, dry mouth, lack of
energy, and shortness of breath; cognitive responses, such as disbelief,
confusion, and sometimes a sense of the presence of the deceased; and
behaviours such as disruptions in sleep or appetite, crying, dreaming of the
deceased, loss of interest, and social withdrawal.
Grief can also express itself in social and spiritual manifestations:
problems functioning in an organization or family and difficulties with
interpersonal relationships; and spiritual issues, such as searching for
meaning, anger, or hostility toward a religious figure.
There are many forms of grief, including anticipatory grief - the
reaction to losses associated with an impending death, which may include
250 Environmental Grief: Hope and Healing
___________________________________________________________
past, present, or future losses during the dying process; complicated grief -
“A significant minority of bereaved persons will experience substantial
impairment in their social and occupational functioning for many months
following the loss, accompanied by marked symptoms of emotional
numbness, disbelief, purposelessness, futility, insecurity, and a sense that
a part of the self has died”; 1 uncomplicated grief - a healthy, normal
response to loss; and disenfranchised grief - grief that a person
experiences for a loss that is not acknowledged by society.
2. Environmental grief
‘Environmental grief’ is the grief reaction stemming from the
environmental loss of ecosystems caused by natural or man-made events.
For purposes of this study, we conclude that environmental grief builds on
the research of Dr. Ken Doka 2 regarding disenfranchised grief, including
the following elements: The relationship is not recognized. In our society,
most support is given to people who have lost family members, such as
parents or children, people to whom they are closely related. The many
losses that occur but are not acknowledged are those in which the
relationship to the deceased is that of friend, life partner, or homosexual
life partner or lover. The loss is not acknowledged. Perinatal deaths,
abortion, or placing a child for adoption are all examples of losses not
acknowledged by society. Another loss is pet loss, which is now becoming
more recognized as society becomes increasingly aware of the roles that
animals can and do play in our lives. Other losses include the loss of a job,
which can also contribute to the loss of self-worth, self-esteem, and self-
respect. Doka also mentions infertility as a loss in adulthood causing a
sense of loss not only that one’s body has failed but also that dreams of
having a child are shattered, which can also lead to the loss of a
relationship. The griever is excluded. In some cases, a person may
disenfranchise herself or himself from the grief. In these cases, the person
is not seen socially as being capable of grief. For example, parents may
exclude children from learning about the grieving process or experiencing
the grieving process because the parents don’t believe the child capable of
grief. Children may then disenfranchise from their own grief because that
is what they believe is right, given their role in the family. The
circumstance of the death is questionable in some way. If there is a suicide
in the family or a death from AIDS, for example, there is often a stigma
involved that precludes the survivors from feeling support for their grief.
These circumstances influence the very nature of the grief reaction and at
times cause the griever to inhibit her or his grief responses.
Doka also mentions that many losses might have occurred in the
past, such as a divorce or the end of a relationship, but when someone
Kriss A. Kevorkian 251
___________________________________________________________
learns that an ex-spouse or an ex-friend has died, that loss may still cause
a grief reaction because there is now an end to that given relationship.
“Even though loss is experienced, society as a whole may not perceive
that the loss of a past relationship could or should cause grief reactions” 3
Oftentimes, when an experience is labelled or named, a certain
validity is acknowledged. The term disenfranchised grief has brought
great validation to people who have felt as though they were ostracized by
society for having an abnormal grieving process. Similarly, the guilt and
shame many women faced after having an abortion was increased by the
lack of support they had from society. The idea of disenfranchised grief
offered validation to these women and opened up support groups for
people dealing with this type of grief.
The term environmental grief was developed to put a name to the
grief that many environmentalists and others who are concerned about the
plight of our environment are experiencing. Jane Goodall has expressed
her feelings eloquently:
3. Gaia theory
In 1961, Dr. James Lovelock, a British atmospheric chemist, was
invited to be an experimenter with the National Aeronautics and Space
Administration on its first lunar instrument mission. At that time, NASA
was investigating the possibility of life on Mars. NASA had difficulty
finding experts in the field regarding life on Mars, so they had to settle for
people who were experts regarding life on Earth. Soon after Lovelock
began work on a lunar probe, he was promoted to designing instruments to
analyze the surface and atmospheres of planets.
In 1972, Lovelock published a paper suggesting that life on a
planet would have to use the atmosphere and oceans to produce raw
materials for the products of its metabolism. The gases in Earth’s
atmosphere are in a persistent state of disequilibrium, but a look at Mars
through infrared telescopes revealed that the atmosphere was dominated
252 Environmental Grief: Hope and Healing
___________________________________________________________
by carbon dioxide and was not far from the state of chemical equilibrium,
strongly suggesting that Mars was lifeless. NASA scientists continued to
investigate in hopes that they would find life on Mars or on our other
neighbour planet, Venus. 5
Lovelock created quite a stir with conclusions that ultimately led
to his development of the Gaia hypothesis. 6 Gaia comes from the Greek
word meaning earth or Earth Goddess. The Gaia hypothesis states that the
Earth is a self-regulating living organism. Lovelock realized that science
in the 1960s looked at our world from a reductionist point of view,
meaning that it was seen from the bottom up, which did not take into
account the chemical compositions of the climate of the earth. When he
had the opportunity to view Earth from the top down, he realized that the
atmosphere of the Earth was a living part of the whole organism, that
Earth itself was a living organism. Looking at the planet from the top
down was not a new approach. Lovelock writes that physiologists,
engineers, and inventors have investigated from the top down for some
time. 7
Lovelock has written extensively regarding the fact that the Gaia
theory has not been accepted by all sciences as yet, but it has become
more mainstream. 8
Although Lovelock developed the Gaia theory and he found that
many environmentalists agreed with it; he did not always agree with the
direction environmentalists were taking in regard to protecting the planet.
Environmentalists at the time appeared to be more concerned with human
rights. “If, in caring for people, we fail to care for other forms of life on
Earth then our civilization and we will suffer.” 9 Environmentalists, it
seems, have to find a balance between the needs of humans and the need
to protect our planet without excluding one from the other.
According to Lovelock, once more than 70% to 80% of the
tropical forest is destroyed, the remaining forest will no longer sustain its
climate, meaning that the whole ecosystem will collapse. 10 If that is the
case, and we continue to destroy the tropical forest, it will not be long
before the tropical forests vanish and the people in those regions find
themselves living in a desert. Lovelock expressed it this way in 1999:
4. Interconnectedness
Rory Spowers, freelance writer and broadcaster, writes that the
common thread that unites much of science today is the recognition of the
254 Environmental Grief: Hope and Healing
___________________________________________________________
interconnectedness in nature of all life. 15 This new paradigm in science
“shares the same vision as the ancient mystics, suggesting that there are no
boundaries between the individual and the rest of the universe.” 16
Knowing that we are connected to the earth and all its
inhabitants, we must now learn to be conscious of our actions toward our
environments. Field biologists, ecologists, botanists, and biologists appear
to have been conscious of their actions on the planet. Most often, people in
the fields of biological sciences are drawn to that field because of a love
for the environment.
Ecologist Phyllis Windle wrote about her connectedness to nature
not only as an ecologist but also on an emotional level.17 In 1990, she read
an article regarding the dogwood trees that were dying due to a fungus that
had been killing dogwood trees since the 1970s. Dr. Windle did not realize
that her reaction to the demise of the dogwoods would be so strong. She
related her reactions to those of grief, but added,
5. Deep ecology
Bill Devall and George Sessions credit Arne Naess, a Norwegian
philosopher and mountain climber, with coining the terms shallow ecology
and deep ecology in the 1970s. 19 Shallow ecology describes the more
human-centred version of ecology that was mainstream at the time; it
placed the needs of humans over the needs of nonhuman species. Shallow
ecology had more to do with economic well-being, with what the
environment could do to make humans more comfortable. Deep ecology,
Kriss A. Kevorkian 255
___________________________________________________________
on the other hand, involves looking out for the welfare of the whole
system of life, including nonhuman species. The philosophy behind deep
ecology is that it is a long-term process of change for most people,
awakening an environmental ethic, a land ethic, taking into account that
humans are equal to the rocks and rivers, for example, that we are not
better than other species or things on this planet. As Aldo Leopold has
written,
6. Hope
Thankfully, many people believe there is still hope for saving our
planet. For example, despite all the destruction that she sees, Dr. Jane
Goodall remains hopeful that humans will soon learn that we must nurture
nature and no longer continue to destroy it. 21 In this respect, our
environmental grief can turn to a state of healing. It is interesting that
when people share their grief with one another, it seems to allow others to
open up and share as well. In that case, they are also sharing their hope
because they have just educated another person about the effects humans
are having on our environment.
Dr. Jane Goodall began her research of wild chimpanzees on the
shore of Lake Tanganyika in 1960. Her study has become the longest field
study of any animal species in its natural surroundings. Dr. Goodall has
seen firsthand the destruction of our environment as she returns to Gombe
National Park where she began all those years ago. Gombe has changed a
great deal, yet Dr. Goodall remains hopeful that our world will be
preserved:
256 Environmental Grief: Hope and Healing
___________________________________________________________
There are many signs of hope. Along a lakeshore in
Tanzania, for example, villagers are planting trees where
all the trees had disappeared. Women are taking more
control over their lives, and, once they become better
educated, then the birth rate begins to drop. And the
children are being taught about the dire effects of habitat
destruction. There is the terrible pollution around the
world, the balance of nature is disturbed, and we are
destroying our beautiful planet…But in spite of all this I
do have hope. 22
7. Healing
As stated earlier, environmental grief is the term that validates all
the emotions of despair, hopelessness, and anger. Joanna Macy discusses
the “despair work” she has created. It is similar to grief work, but she
states that one does not have to accept the loss, given that the loss has not
yet occurred and is “hardly to be accepted.” She does write, however, that
Notes
1
Robert Neimeyer and Louis A. Gamino, ‘The Experience of Grief and
Bereavement’, In Handbook of Death and Dying, Volume 2, ed. Clifton D.
Bryant (Thousand Oaks, CA: Sage, 2003), 849.
2
Ken J. Doka, ed., Disenfranchised Grief: New Directions, Challenges,
and Strategies for Practice (Champaign, Illinois: Research Books, 2002).
3
Ibid, 11.
4
Jane Goodall, ‘Digging Up the Roots’, Orion 13 (1994), 21.
5
James E. Lovelock, ‘Gaia as Seen Through the Atmosphere’,
Atmospheric Environment, 6 (1972), 579.
6
James E. Lovelock and E. Margulis, ‘Atmospheric Homeostasis by and
for the Biosphere: The Gaia Hypothesis’, Tellus, 26 (1973), 2.
7
James E. Lovelock, ‘The Environment Now and the Gaian Perspective’,
in The Spirit of Science from Experiment to Experience, ed. D. Lorimer,
(New York: Continuum, 1999), 129-148.
8
James E. Lovelock, Homage to Gaia: The Life of an Independent
Scientist (Oxford: Oxford University Press, 2000).
9
Ibid, 4.
258 Environmental Grief: Hope and Healing
___________________________________________________________
10
Ibid.
11
Lovelock, 1999, 148.
12
Steven Fenwick, The Dreaming Earth: Foundations for a Process-
Oriented Approach to Ecopsychology (Ann Arbor, Michigan: UMI, 1998),
88.
13
Richard Leakey and Roger Lewin, The Sixth Extinction: Patterns of Life
and the Future of Humankind (New York: Anchor Books, 1995).
14
Ibid, 139.
15
Rory Spowers, Rising tides: A History of the Environmental Revolution
and Visions for an Ecological Age (Edinburgh: Canongate Books, 2002).
16
Ibid, 232.
17
Phyllis Windle, ‘The Ecology of Grief’, BioScience, 42 (1992).
18
Ibid, 363, 366.
19
Bill Devall and George Sessions, Deep Ecology: Living as if Nature
Mattered (Salt Lake City, Utah: Peregrine Smith Books, 1985).
20
Aldo Leopold, A Sand County Almanac: With Essays on Conservation
(New York: Oxford University Press, 1949), 171.
21
Jane Goodall, ‘My Three Reasons for Hope’, 2001 [article available
online] (accessed 17 November 2003)
<http://www.janegoodall.org/jane/essay.html>
22
Ibid, para. 2.
23
Joanna Macy, World as Lover, World as Self (Berkeley, California:
Parallax Press, 1991), 16.
24
Leigh Calvez, in interview with author, October 2002, quoted in Kriss
Kevorkian, Environmental Grief: Hope and Healing, Ph.D. diss., Union
Institute and University, Cincinatti, Ohio, (2004), 64.
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