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Dementia,
Narrative and
Performance
Staging Reality, Reimagining Identities
Janet Gibson
Dementia, Narrative and Performance
Janet Gibson
Dementia, Narrative
and Performance
Staging Reality, Reimagining Identities
Janet Gibson
UTS Insearch
University of Technology
Sydney, NSW, Australia
Cover illustration: FAIRY FLOSS. Photo of Phillip Mills and Katia Molino from Theatre
Kantanka’s production of Missing the Bus to David Jones. Photo by Heidrun Löhr. Used
with permission of Carlos Gomes.
This Palgrave Macmillan imprint is published by the registered company Springer Nature
Switzerland AG.
The registered company address is: Gewerbestrasse 11, 6330 Cham, Switzerland
To Julia, Mary-Jane, and Sandy, with love
Acknowledgements
vii
viii ACKNOWLEDGEMENTS
thinking. From first reading her article “God is a Talking Horse” to shar-
ing ideas over breakfast in Milwaukee, Anne continues to both impress
and surprise me with the depth of her intellect and her unwavering com-
mitment to creativity.
Carlos Gomes, the artistic director of Theatre Kantanka, was the soul of
generosity, answering questions and sending me DVDs and other material
which helped me dig deeper into Missing the Bus to David Jones. This the-
atre piece deserves an unquestionable place in the canon of great (demen-
tia) theatre. Thank you, Kate Denborough, for filling me in so promptly
on certain details to do with Sundowner.
Thanks, Vicki Sanchez, for all the information about The Bucket List.
Vicki is one of those very important dementia care workers who love what
they do and do it so well, despite the appalling pay. I hope this situation
changes for all aged care workers in the not too distant future. My grati-
tude also extends to all the people I worked with in TimeSlips sessions at
Uniting Locke Haven : your creativity and imagination refreshed and
inspired me when I was developing many of the ideas which form the
backbone of this book.
The delightful Maureen Matthews and I have been emailing each other
for quite a few years now. I was very lucky to see a performance of her
community readers’ theatre for people living in the early stages of a
dementia diagnosis—To Whom I May Concern®—when I was in New York
in June 2018, an experience which deepened my enthusiasm for this
modality. Thanks also to performers Therese, Julie, and David for wel-
coming me so warmly to the rehearsal before the performance.
My deliberations on To Whom I May Concern® were recently published
in RiDE, adapted for the special issue ‘On Access’. I would like to thank
the anonymous reviewers for input to that article which also helped me in
fashioning the corresponding book chapter. Collette Conroy, RiDE’s edi-
tor, has been very helpful and encouraging about my work since I first met
her at the Performance and Disability working group at the IFTR/FIRT
Stockholm conference 2016. A lot of other people in that group have
heard out my ideas at various stages and I thank you all but in particular
Yvonne Schmidt and Arseli Dokumaci. Arseli—thanks for your input on
some of the chapters, your willingness to do so, and your extremely per-
ceptive feedback. I am indebted to you for the comment in Chap. 8 on the
proliferation of diseases in this day and age in which there are not many
disease-free bodies left to discipline, in Foucault’s dispensation. Likewise,
thanks to Kate Maguire-Rosier and Catherine Maitland, my ad hoc
ACKNOWLEDGEMENTS ix
3 Narrative Regimes 59
xi
xii Contents
Index 279
Abbreviations
xiii
xiv Abbreviations
Fig. 5.1 ‘Fairy Floss’. Katia Molino and Phillip Mills. Missing the Bus to
David Jones. Theatre Kantanka. Photo by Heidrun Löhr. Used
with permission of Carlos Gomes. (The photo shows a man in
a blue, grey and red cardigan wearing a green party hat and a
woman dressed in a black and white houndstooth jacket and
white hat. They are up very close to each other’s faces and are
eating and feeding each other white fairy floss 143
Fig. 5.2 ‘The Bus Stop’. Katia Molino waiting for the bus. Missing the
Bus to David Jones. Theatre Kantanka. Photo by Joanne Saad.
Used with permission of Carlos Gomes. (The photo shows a
woman dressed in a black and white houndstooth jacket, a white
hat, and white gloves, sitting on a seat clutching a black and
white handbag. She is looking off into the distance as if
expecting a bus to arrive any moment. A Filipino nurse or
care attendant wearing black pants and a white t-shirt is
approaching her) 151
Fig. 6.1 Marcia Bannister, Bucket List Sales Manager, and Jessie
Anderson, Bucket List Assistant Sales Manager. Video still from
Finding the Why. Enabling Active Participation in Life in Aged
Care (Fire Films). Still used with permission of Corrine
Maunder. (The photo shows two old women with short hair
sitting on an orange, red, and yellow striped couch with a very
high back. Marcia is on the left. She is taller than Jessie and has
short white hair. She is wearing a blouse with red, yellow, pink,
and green leaf patterns on it. Jessie is on the right with short
brown hair. She is wearing a white top with white beads. They
both have white mugs in their hands) 199
xv
xvi List of Figures
first heard it, is not the whole story either. In sum, I found myself part of
a story for which no template could be found, at that time, in the existing
repertoire.
Narrative sociologist Arthur Frank (2010) contends that, although
people tell their own stories about their lives, they do not make these sto-
ries up by themselves. There is a limited repertoire of stories to be told
from which we then tell ‘our’ stories, as is very evident in the case of
dementia. I now label this restricted arsenal of narratives the ‘right kind’
of dementia story, in Lyotard’s terms (1984), a ‘grand narrative’\, circu-
lating accounts of loss, despair, failure, and tragedy. This story does not
tell of the extant or emergent abilities of people affected by dementia,
particularly those sixty-five years and older. Instead, it focuses on their
pasts or on futures made grim for us all by the probability of a ‘silver tsu-
nami’ coming to destroy lives and push societies towards catastrophe. It
may also tell of long-suffering carers coping with the demands of aggres-
sive, forgetful, dependent, loved ones who are draining personal or famil-
ial emotional, physical, and financial resources. These dependent humans
are framed as ‘burdens’ to the economy, to society, to us all.
In the twenty-first century, in most Western cultures, these types of
stories fit into an overarching performance ‘framework’, which perfor-
mance scholar Jon McKenzie has labelled a “mode of power” (2001, 25).
This mode determines the ways in which, and the contexts where, people
with dementia ‘perform’ their stories and selves, mainly due to the ascen-
dancy of neoliberal capitalism. Neoliberalism can be defined as:
certain ways for people with dementia and their care partners. I contend
that this mode currently predominates among others, regulating both the
manners in which, and the situations where, people with dementia ‘per-
form’ their stories and selves. In the domain of human care, performance
as a “mode of power” (ibid.) insists on task efficiency over quality time,
results over relationships, and measurement over magnanimity, especially
in care homes and in interpersonal relationships.
My encounter with dementia and the subsequent institutionalisation of
my mother in a care home opened new insights into both performance as
a “mode of power” (ibid.) and the relationship between stories and ethics.
Constantly revolving in my mind at the time of my mother’s diagnosis and
beyond were the words of virtue ethicist Alasdair MacIntyre: “I can only
answer the question ‘What am I to do?’ if I can answer the prior question
‘Of what story or stories do I find myself a part?” (2011, 250)—words
which deepened and complicated the research I was undertaking at the
time into verbatim theatre and ethics. I began to wonder if theatre pieces
that worked verbatim—using the words and stories of people with demen-
tia—existed, and if so, what ethical provocations they would offer.
Verbatim theatre normally relies on the life stories of ‘reliable’ narrators
and, in oral history projects anyway, the assumption of the cognitive
“competency” of the primary teller (Pollock 2005, 3). But people with
dementia are often ‘unreliable narrators’4 who frequently struggle to
remember their life stories or segments of them and who regularly resort
to fabrication in the telling. In part because of this, and because of the
(often gradual) decline in many of their cognitive and physical capabilities,
they are repeatedly stereotyped as the “living dead” (Behuniak 2011) and
not seen as ‘real’ people.5
Over the last twenty years or so, and across the globe, there has been an
‘explosion’ of people’s stories and words deployed in theatre productions
across the above-mentioned performance genres. Performed narratives
have included tales of trauma, victimhood, and crisis giving voice to the
socially, economically, or culturally marginalised. These narratives usually
aim to facilitate sociopolitical change for the participants, and/or the spec-
tators, as well as change at a broader social level. Some of these produc-
tions feature the people themselves; in others, actors perform. The
performances may take place in theatres, community centres, or similar
venues. They raise numerous issues and challenges for the theatre makers
creating them, and to their viewing audiences, which theatre and perfor-
mance studies scholars have been keen to interrogate.6
Apart from the emergence of a growing number of professional and
semi-professional art theatre productions dealing with dementia across
Western stages, “theatre of the real” (Martin 2013) productions about
dementia have also started to surface. Certain productions have been cre-
ated using the textual input of people with dementia (and their families, in
some instances). So, what are the challenges to theatre makers working
with these practices when people can no longer say who they are or tell
8 J. GIBSON
dementia and the people who live with it? In the other chapters, in some
to a greater extent than others, I reverse this question to ask: How might
dementia shift or add to questions, debates, and issues in theatre and per-
formance studies? The case studies analysed relate to ideas drawn from all
the above-mentioned literatures, where pertinent, including reminiscence
and the care home. I will now briefly introduce each of these literatures
and their key theorists.
Dementia studies can be delineated into five main, somewhat diverse
approaches: medical and biomedical, personhood, embodiment, relational
care, and social citizenship. Firstly, medical and biomedical approaches
dominate the existing research into, and treatment of, Alzheimer’s disease
and other dementias.9 They are “situated within a discourse of loss” (Beard
2004, 417) and typically prioritise drug treatments or molecular testing
over attention to the social and ethical complexities that dementia also
entails. They advance the separation of the physical, mental, and cultural
dimensions of illness and ageing, reducing the ageing body (and many
others) to a potential diagnosis, while the sociocultural, emotional, and
phenomenological aspects of illness and ageing for individuals and their
families are quite often ignored (ibid., 416).10 Factors like race, class, gen-
der, religion, sexual orientation, disability, family of origin, and cohort
effects will all contribute to differences in the experiences of both ageing
and dementia, but these factors are beyond what medicine and biomedi-
cine generally offer patients.
Secondly, the ‘personhood’ approach, a challenge to the biomedical
episteme, emanated as a reaction to the single-minded focus on cognition
and neurological changes in the brain that had dominated the dementia
industry until the 1980s (Gilleard 2000). This approach opposes the
mainly negative ideas about the person diagnosed with dementia that
arguably dominate studies in biomedicine (Leibing 2006, 254), recognis-
ing the person, not just the disease. It continues to gather numerous new
practices under its mantle. A person-centred focus in dementia care was
initiated principally through the work of social psychologist Tom Kitwood,
largely through the influence of his groundbreaking text Dementia recon-
sidered: The person comes first (1997), and is steadily becoming a seminal
paradigm. Personhood is conceptualised from the standpoint of interac-
tionist social theory, the belief that selfhood is socially acquired and sus-
tained (Kontos 2012, 330).
1 MY MOTHER’S STORY, MY STORY 11
studies scholars (see Davis 1995, 2002, 2013; McRuer 2006; Siebers
2006, 2008) recognise the category of disability to be intensely problem-
atic and unstable. This is for many reasons, including that it swells and
contracts to encompass so-called normal people as well (Davis 1995, xv);
that is, all people chance stepping on and off the disability continuum,
especially as they get sick, age, or are diagnosed with diseases like demen-
tia. Mike Oliver and Len Barton are exceptions here, arguing that the
current interests pursued by many contemporary disability studies scholars
(postmodernism, representation, and embodiment) are hard to justify in
terms of their “immediate relevance to the struggles of disabled people to
lead a decent life” (2002, 8). Basically, disability studies is useful to the
pursuit of my arguments as it helps to clarify how the notion of ‘normalcy’
has been constructed and its intrinsic relationship to what is commonly
regarded as not ‘normal’, across many cultures, that is, to disability. In this
endeavour, I am principally aided by the work of Lennard Davis (1995)
and Tobin Siebers (2006, 2008, 2010). I also work with research in per-
formance and disability studies.14
As with age studies scholars, some post-structuralist disability scholars
have also drawn on Judith Butler’s theories of performativity to theorise
the discursive construction of disability identity. Both Petra Kuppers
(2003, 2011) and Robert McRuer (2006) argue, following Butler, that as
with gender, cultural scripts about disability can and should be resisted
and disrupted along with the discursive practices that produce both the
disabled and the able body. As old age may be experienced as disabling by
some, and as dementia is ordinarily seen as both a cognitive impairment
and a cognitive disability, representations of (old) people with dementia
must be theorised on a spectrum stretching between the disciplinary loca-
tions of age and those of disability studies.
However, the relationship between age studies and disability studies
holds many tensions. Age studies scholarship tends to undermine assump-
tions that ageing disables; it challenges commonly held generalisations
that all old people are “warm but incompetent” (Basting 2009, 26).15
Margaret Morganroth Gullette (2004, 13) proposes that the “[d]ecline
narrative” runs popular discourses on ageing. On the other hand, some
disability scholarship critiques assumptions that the able, fit, and ‘normal’
body is always free from disability, using old age as the point towards
which all able bodies are heading, a kind of ‘disabling normalcy’. Feminist
disability scholar Susan Wendell maintains that unless we die early “we are
all disabled eventually” (1996, 18).
14 J. GIBSON
In this book, I engage disability studies with age studies to show how
the abilities of people living with age-related dementia are greater than
imagined, while at the same time acknowledging the actuality of their
limits. To further complicate matters, the relationship between dementia
and disability resembles “planets spinning on different axes” (Shakespeare
et al. 2017, 1). In disability sectors, dementia is typically perceived as a
health issue; in dementia sectors, people with dementia do not usually
think of themselves as disabled (ibid.). In this book, I mine both dementia
and disability studies where necessary to support my arguments.
I also take some direction from particular theatre and performance
studies scholars working on refugee theatre, primarily Alison Jeffers (2006,
2008, 2009, 2012) and Caroline Wake (2010a, 2010b, 2011, 2013,
2018). I do this because refugee theatre productions across the globe have
tended to rely on the verbatim genre or other “theatre of the real” (Martin
2013) techniques. Given that there is very little work in theatre and per-
formance studies on “theatre of the real” (ibid.) and dementia, the aca-
demic work that has emanated from scholars working on refugee theatre
provides a useful parallel to concerns that match mine—a point I consis-
tently make in Chap. 2, where I attempt to forge this parallel in more
detail concerning the links between the crisis of dementia and the crisis of
asylum. Consequently, in Chap. 2, I also cite the occasional refugee stud-
ies scholar (e.g. Peter Nyers 2006).
But the primary disciplinary location of this book is in theatre and per-
formance studies. I conflate the two disciplines, as they are “merging and
intermingling in various ways” (Balme 2008, 12), which makes it increas-
ingly difficult to separate theorists into camps. However, disciplinary dif-
ferentiations, which can be tracked historically, do still exist (see Balme
2008.). Today, theatre studies has many fields, with a strong focus on live
art performances, and the study of texts (ibid., 11). Work within perfor-
mance studies has inclined towards Richard Schechner’s “is” or “as” of
performance (2013, 38). The former centres on that which is historically,
socially, culturally, and traditionally accepted to be performance; the latter
refers to the way in which events or practices can be seen to be perfor-
mances, including gender, sexuality, and ethnicity, among many other cat-
egories. In this way, “performance studies grants itself a wider range of
‘objects’ or case studies than theatre studies might” (Wake 2010a, 26).16
In essence, my examination of both “theatre of the real” (Martin 2013)
and applied theatre and performance falls under the broad moniker of
1 MY MOTHER’S STORY, MY STORY 15
theatre and performance. The works discussed in this book dialogue with
the notion that we perform ourselves on a continuum that ranges from
daily acts of the self to systemised stage performances and rituals both
sacred and secular (ibid.).
This book also references theories of narrativity, including the work of
Arthur Frank (2010) and Paul John Eakin (1999, 2001, 2006, 2008), as
well as that of narrative philosopher Galen Strawson (2004). Additionally,
input comes from medical anthropology (Leibing and Cohen 2006; Lock
2013) and medical history (Ballenger 2006; Beach 1987; Whitehouse and
George 2008). Other material is drawn on at various stages: for example,
the work of philosophers Jacques Rancière (2004, 2007) and Ian Hacking
(1995, 1999).
My methodological approach is varied. Adopting “performance analy-
sis” (Pavis 2003) for my examination of both art theatre and applied the-
atre productions, I draw on notes taken visiting live performances,
watching videos of the performances (Balme 2008, 136), and referencing
“supplementary documents” (Pavis 2003, 40), including theatre reviews,
photographs, programmes, and other outreach materials like education
packs and websites. As well, I opt for (post-structuralist) discourse analysis
due to my sustained interest in how discourses shape reality and power-
fully influence what gets ‘storied’. ‘Discourse’ is used here in the
Foucauldian sense, to do with how knowledge is composed alongside the
social practices, subjectivities, and power relations built into such knowl-
edges, as well as into the relations between them. More than just ways of
thinking and producing meaning, discourses constitute the body, mind,
and emotional lives of the subjects they seek to govern (Weedon 1987,
108). I temper my acknowledgement of the power of discourses to consti-
tute bodies and minds by recognising that biological, material, and
embodied elements also play a role in the construction of dementia sub-
jectivities. Both post-structuralist and phenomenological insights are use-
ful for theorising dementia personhood. For people diagnosed with
dementia, the body speaks, conveying meaning, even if the world in which
they live is created, in large part, linguistically (Vasterling 2003, 212).
Given the material force of discourses in forming and reforming the
normal, the natural, and the true, I am primarily concerned with excavat-
ing the values and politics underlying these discourses in twenty-first-
century Western cultures, both to make them visible and to disturb their
facile endorsement. In view of my interest in the discourses circulating
about age-related dementia in the mass media and on the internet, I
16 J. GIBSON
practices do have specific charters, along with separate literatures and his-
tories that map them, I incorporate both of these in this section under the
moniker of ‘performance’. I do this because, when the seemingly incon-
gruent practices and products of select applied theatre interventions (often
shown to known audiences with a focus on health, well-being, and process
over product) are situated side by side with professionally devised ‘art’
theatre products for public stages, what emerges is their commonalities
and the way they ‘speak’ to each other. For example, although innovation
and experimentation may be more to the fore with art pieces, and drama-
turgical, aesthetic, and reception issues likely to surface, “theatre of the
real” (ibid.) productions may also intend to educate, inform, and change
political and ethical landscapes as well as the views of its spectators; these
productions may also deploy a stripped back aesthetic consonant with
some theatres of social change (applied theatre). Playwright Robin Soans
contends that “the quintessence of verbatim theatre is a group of actors
sitting on chairs, or cardboard boxes or a sofa, talking to the audience,
simply telling stories” (2008, 21).
Furthermore, the concerns of many “theatre of the real” (Martin 2013)
and applied theatre practices are not always discrete. For example, an
applied theatre intervention may also use “theatre of the real” (ibid.) tech-
niques, like verbatim or documentary materials, be devised in a commu-
nity setting, and principally be constructed from the autobiographical
stories of its participants, as is To Whom I May Concern® (TWIMC), my
autobiographical case study. In fact, certain applied theatre products may
be framed as art pieces with a strong aesthetic focus, even if applied theatre
has conventionally focused on social efficacy over aesthetics (Prentki 1998;
Thompson 2009).
In Chap. 4, I navigate the complex terrain of ‘the real’ and ‘reality’. I
argue that any reality being framed on stage will inevitably cite the frames
of reference underpinning and bolstering this reality, which is a reality
always already mediated, making it almost impossible to avoid replaying
the ‘right kind’ of dementia story. These stories include discourses and
cultural narratives about ageing and specifically about old people living
with dementia, which summon what I call ‘normative age-and-dementia-
effects’ (following Moore 2014), that is, the naturalised effects of discur-
sive representations of ‘old’ people living with dementia and the biases and
assumptions underpinning and sustaining these representations.
Chapter 4 also provides extended definitions of the similarities and dif-
ferences between the terms “theatre of the real” (Martin 2013), “Theatre
18 J. GIBSON
of Real People” (Garde and Mumford 2016), and “reality theatre” (Wake
2010b, 6–8). Additionally, it begins an examination into the connection
between words, stories, identity, and the materialisation of reality in “the-
atre of the real” (Martin 2013), taking a particular interest in verbatim
theatre and its history, as well as considering what provocations dementia
offers verbatim theatre and its scholarship, as dementia draws attention to
the nature of the ‘truth’ of any story. Building on these underpinnings,
Chap. 5 examines two very different Australian experimental art theatre
productions with postdramatic leanings as optics through which ethical,
political, and aesthetic problems to do with dementia and age representa-
tion are exposed. The extent to which they tell the ‘right kind’ of demen-
tia story is also assessed.
In Chap. 6, the focus shifts to applied theatre practices, as well as para-
theatrical modes. This chapter critiques chronological life story narrative
when conceived as a universal ethical and political act of healing for people
with dementia, or as an unfailing practice of late life therapy, by extending
James Thompson’s (2009) challenges to narrative hegemony in applied
theatre contexts. This allows entry to the claim that the pressure to pro-
duce a life story, in the context of dementia, might in fact be oppressive
rather than therapeutic. I then analyse TimeSlips, a storytelling interven-
tion increasingly being used in aged care facilities around the world, com-
paring it with the popular Reminiscence Therapy covered in Chap. 3. I
also explore what I term ‘narra[tive]-theatrical spaces’: alternative ways of
reconfiguring performance in care homes which take seriously the oppor-
tunities offered by the location itself in transforming the lives of people
living in care homes.
Chapter 7 moves on to public autobiographical performances by peo-
ple living with dementia and probes one specific performance modality To
Whom I May Concern® (TWIMC), both a play and a therapy, operating
virtually and as live theatre. TWIMC reframes well-worn issues in the
autobiographical literature as complex and fresh, especially the construc-
tion of the self and its relationship to narrative, identity, and representa-
tion. Not widely taken up by people living with dementia, the shortage of
public autobiographical performance is undoubtedly connected to, and
limited by, taken-for-granted understandings of dementia and by dis-
courses about the capabilities of (old) people living with dementia, which
both create and control the situations, perceptions, and worlds in which
these people can perform their narratives and audiences can listen to them.
1 MY MOTHER’S STORY, MY STORY 19
Notes
1. I prefer the term ‘care partner’ to ‘caregiver’ because I wish to challenge
the notion implicit in the tag ‘giver’ that people living with dementia are
‘takers’. The relational dynamics between the two parties are far more
complex than that. In fact, (old) people living with dementia may often
give a lot to those caring for them, if the latter can learn to open up to the
possibilities of the relationship.
2. Using ‘our’ highlights that all ‘personal’ stories are born out of interrela-
tionship, co-created with and through the stories of significant others in
our lives. However, in claiming that this story is ‘ours’, I am ‘speaking for’
my mother, given the non-normative features of our communication.
Although ‘my’ story is inextricably bound up with my mother’s, I am not
her. I cannot know what it is like to live with AD, as I have not (yet) expe-
rienced it.
3. Regarding terminology: throughout the book, I generally use the terms
‘people with dementia’ or ‘people living with dementia’ not to suggest that
all people with dementia form a homogeneous group or that dementia is a
1 MY MOTHER’S STORY, MY STORY 21
stable disease category; rather, these terms are preferred over the more
reductive ‘victim’, ‘sufferer’, or biomedically oriented ‘patient’.
4. The term ‘unreliable narrator’ was first coined in 1961 by Wayne Booth in
The Rhetoric of Fiction (158–159). It refers to a narrator, most often in
literature, but sometimes in film or theatre, whose credibility has been seri-
ously compromised.
5. I have placed the word ‘real’ in inverted commas to highlight the many
debates between certain philosophers and disability studies scholars over
the personhood of the cognitively disabled and who counts or not as a
bona fide person (Kittay 2009; Kittay and Carlson 2010). However, the
real is not only a philosophically contentious idea but, especially within
theatre and performance studies, a more problematic and ambiguous term
than the mere application of inverted commas could underscore. These
ideas are taken up in Chap. 4.
6. Widely discussed to date have been, among other issues, its “paradoxical
pairings” (Wake 2011, 1) including, for example, the personal and the
political (Heddon 2008); replication (reiteration and re-enactment) and
addition (formerly excluded stories) (Wake 2010a); the archive and the
repertoire (Wake 2011); and reality and representation (Tigner 2002;
Reinelt 2006, 2009; Bottoms 2006; Heddon 2008; Martin 2006, 2010,
2013). Interest has also been shown in trauma, telling, and witnessing
(Salverson 1996, 1997, 1999, 2001; Stuart Fisher 2011; Jeffers 2006,
2008, 2009, 2012; Wake 2010a; Thompson 2004, 2005, 2009); the
appropriation of life stories by theatre makers (Couser 2004; Dolan 2005;
Baglia and Foster 2005; Heddon 2008; Casey 2009; Jeffers 2012); and the
ethical and political challenges of dealing with people’s stories and the aes-
thetic challenges of creating interesting theatre from them (Patraka 1996;
Peterson 1997; Salverson 1994, 1996, 1997, 1999; Lathem 2005; Jeffers
2006, 2008, 2009, 2012; Stuart Fisher 2011).
7. Publications on drama therapy interventions with old people living with
dementia are available, but they do not specifically look at the nexus
between narrative and identity (Jaaniste 2011; Reinstein 2004). Innovative
work is emerging in the applied theatre literature on care homes (Nicholson
2011; Hatton 2014) but not in regard to performed narratives in particular.
8. In The presentation of the self in everyday life, Erving Goffman posits that
the “self itself does not derive from its possessor, but from the whole scene
of his [sic] action” (1959, 252). Using these ideas as a basis, Anne Basting
argues that selves with dementia are more dependent on others than some
other selves may be, but that this is not necessarily a problem if we picture
selfhood to be on a continuum from a state of mythical independence to
that of extreme dependence (2001, 79). Basting further argues that people
22 J. GIBSON
with dementia will usually rely heavily on others for their sense of selfhood
but that, to some extent, we all do.
9. These terms are often used interchangeably to refer to conventional medi-
cine. Biomedicine is the application of the principles of the natural sci-
ences, especially biology, physiology, and biochemistry, to clinical medicine
or research (MacIntosh 1999; OED Online 2014/2015). Medicine is “the
science or practice of the diagnosis, treatment, and prevention of disease”
(OED Online 2014/2015).
10. The word ‘illness’ refers here to an individual’s experience of ‘disease’
(pathology), or of poor health, although ‘disease’ and ‘illness’ are com-
monly used interchangeably (Dokumaci 2013, 107).
11. Care ethics is most often defined as a practice or virtue rather than a theory
as such. It is based on the idea of the importance of caring for the depen-
dent and vulnerable in society and is inspired by the mother–child relation-
ship. Rooted in the sentimentalist tradition of moral theory, care ethics
upholds the importance of care as an incentive in ethical thought, along
with recognising the significance of emotion, the body, and reasoning from
particulars over abstract ideas such as justice and agency which are
enshrined in liberal human rights theory. It emerged in the mid-1980s
from work done by psychologist Carol Gilligan and philosopher Nel
Noddings who critiqued traditional moral approaches accusing them of
male bias. Most care theorists argue that care involves maintaining rela-
tionships by focusing on the well-being of care-givers and care-receivers in
a network of social relations (https://www.iep.utm.edu/care-eth/).
12. Age studies is interdisciplinary and collaborative, drawing on research
efforts from both the humanities and the social sciences, despite their very
different research approaches. This is to be expected, given that age is a
phenomenon that affects so many areas of life. However, some scholars are
surprised at how long it has taken for interest in this field to burgeon, as it
is a relatively new area of inquiry. These same academics have been arguing
about the importance of its presence in the academy for decades where it
should take “its rightful place with other intersectional classifications, such
as gender, race, class, and ability” (Lipscomb and Marshall 2010, 4).
13. ‘The term “normative age-effects” is used by Bridie Moore (2014, 2), fol-
lowing Judith Butler, to underscore that age is produced as an effect gener-
ated by “cultural apparatus” (Butler 1990, 199) through media images,
performances on stage, and so forth. “Temporal depth” is a model of age-
ing that embraces change across the life span (Basting 1998, 22). For
Basting, the ageing body on stage is valuable exactly because it can repre-
sent the spread of difference and variety of age across time (1998, 141).
Cristofici’s (1999) “significant form” is a term moved over from Cristofici’s
analysis of Jeff Wall’s photography to performance by Bridie Moore
1 MY MOTHER’S STORY, MY STORY 23
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Occasionally the plant tissues have assumed a black and
somewhat ragged appearance, giving the impression of charred
wood. A section of a recent burnt piece of wood resembles very
closely some of the fossil twigs from the coal seam nodules. It is
possible that in such cases we have portions of mineralised tissues
which were first burnt in a forest fire or by lightning and then
infiltrated with a petrifying solution. An example of one of these black
petrified plants is shown in fig. 74 B. Chap. x. In many of the fossil
plants there are distinct traces of fungus or bacterial ravages, and
occasionally the section of a piece of mineralised wood shows
circular spaces or canals which have the appearance of being the
work of some wood-eating animal, and small oval bodies sometimes
occur in such spaces which may be the coprolites of the
xylophagous intruder. (Fig. 24, p. 107.)
FOSSIL PLANTS IN VOLCANIC ASH.
“Robinson Crusoe did not feel bound to conclude, from the single human footprint
which he saw in the sand, that the maker of the impression had only one leg.”
Huxley’s Hume, p. 105, 1879.
The fact that plants usually occur in detached fragments, and that
they have often been sorted by water, and that portions of the same
plant have been embedded in sediment considerable distances
apart, is a constant source of difficulty. Deciduous leaves, cones, or
angiospermous flowers, and other portions of a plant which become
naturally separated from the parent tree, are met with as detached
specimens, and it is comparatively seldom that we have the
necessary data for reuniting the isolated members. As the result of
the partial decay and separation of portions of the same stem or
branch, the wood and bark may be separately preserved. Darwin[143]
describes how the bark often falls from Eucalyptus trees, and hangs
in long shreds, which swing about in the wind, and give to the woods
a desolate and untidy appearance. In the passage already quoted
from the narrative of the voyage of the Challenger, illustrations are
afforded of the manner in which detached portions of plants are likely
to be preserved in a fossil state. The epidermal layer of a leaf or the
surface tissues of a twig may be detached from the underlying
tissues and separately preserved[144]. It is exceedingly common for a
stem to be partially decorticated before preservation, and the
appearance presented by a cast or impression of the surface of a
woody cylinder, and by the same stem with a part or the whole of its
cortex intact is strikingly different. The late Prof. Balfour[145] draws
attention to this source of error in his text-book of palaeobotany, and
gives figures illustrating the different appearance presented by a
branch of Araucaria imbricata Pav. when seen with its bark intact
and more or less decorticated. Specimens that are now recognised
as casts of stems from which the cortex had been more or less
completely removed before preservation, were originally described
under distinct generic names, such as Bergeria, Knorria and others.
These are now known to be imperfect examples of Sigillarian or
Lepidodendroid plants. Grand’Eury[146] quotes the bark of
Lepidodendron Veltheimianum Presl. as a fossil which has been
described under twenty-eight specific names, and placed in several
genera.
Since the microscopical examination of fossil plant-anatomy was
rendered possible, a more correct interpretation of decorticated and
incomplete specimens has been considerably facilitated. The
examination of tangential sections taken at different levels in the
cortex of such a plant as Lepidodendron brings out the distribution of
thin and thick-walled tissue. Regularly placed prominences on such
a stem as the Knorria shown in fig. 23 are due to the existence in the
original stem of spirally disposed areas of thin-walled and less
resistant tissue; as decay proceeded, the thinner cells would be the
first to disappear, and depressions would thus be formed in the
surrounding thicker walled and stronger tissue. If the stem became
embedded in mud or sand before the more resistant tissue had time
to decay, but after the removal of the thin-walled cells, the
surrounding sediment would fill up the depressions and finally, after
the complete decay of the stem, the impression on the mould or on
the cast, formed by the filling up of the space left by the stem, would
have the form of regularly disposed projections marking the position
of the more delicate tissues. The specimen represented in the figure
is an exceedingly interesting and well preserved example of a Coal-
Measure stem combining in itself representatives of what were
formerly spoken of as distinct genera.
Fig. 23. A dichotomously branched Lepidodendroid stem (Knorria
mirabilis Ren. and Zeill.). After Renault and Zeiller[147]. (¼ nat. size.) The
original specimen is in the Natural History Museum, Paris.
The surface of the fossil as seen at e affords a typical example of
the Knorria type of stem; the spirally disposed peg-like projections
are the casts of cavities formed by the decay of the delicate cells
surrounding each leaf-trace bundle on its way through the cortex of
the stem. The surface g exhibits a somewhat different appearance,
owing to the fact that we have the cast of the stem taken at a slightly
different level. The surface of the thick layer of coal at a shows very
clearly the outlines of the leaf-cushions; on the somewhat deeper
surfaces b, c and d the leaf-cushions are but faintly indicated, and
the long narrow lines on the coal at c represent the leaf-traces in the
immediate neighbourhood of the leaf-cushions.
IMPERFECT CASTS.