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Psychological Therapy for
Paediatric Acquired Brain Injury
Children, young people and families living with an acquired brain injury (ABI),
whether through accident, illness, injury or abuse, are rarely offered psychological
therapy, and yet the benefits of such interventions can be profound. This important
new book, providing a selection of practice examples and insights from frontline
practitioners, will be essential reading for any paediatric therapist or clinician.
Beginning with a “life story” of the brain where emphasis is placed on how
brain development is fundamentally related to its environment, the book offers key
background knowledge before showcasing the core topics of assessment, psychological
formulation and intervention. It features a range of therapeutic models, includes direct
and indirect work, group work and family therapy, with settings varying from inpatient
neurorehabilitation to community work and the transition to education. The long-term
needs of those in the criminal justice system are also addressed. The closing chapters
focus on the debate around effective outcome measurement and outline a vision for
better services.
Elevating the voices of our children, young people and families living with ABI, this
pioneering book will provide practitioners with the confidence to work collaboratively
across a range of children and young people with disorders of consciousness or
communication to those with behaviour that challenges others to manage. It offers
new ways to understand both children’s pasts and their futures, and will be essential
reading for anyone in the field.
Jenny Jim (DClinPsy, MSc, BSc (Hons)) is a Consultant and Principal Clinical
Psychologist with a passion for improving the lives of children, young people and
families affected by acquired brain injury. Dr. Jim is the Deputy Programme Director
(Clinical) of the Professional Doctorate in Clinical Psychology at the University of East
London. She is a clinical academic who works with families, develops and researches
innovations, lectures and trains clinical psychologists for the NHS. Jenny is the recipient
of the British Psychological Society, Division of Neuropsychology’s Early Career
Award (2020).
List of illustrationsx
Editors’ acknowledgementsxii
About the editorsxiv
List of contributorsxv
Prefacexx
Series editors’ forewordxxii
Experts by Experience Reflections – Jackie Solaimanxxiv
Introduction 1
JENNY JIM AND HEATHER LIDDIARD
PART I
Getting started9
PART II
Innovations in psychological therapy91
PART III
What differences can we make?205
Box
3.1 Ten ideas that influence practice of assessment of paediatric
ABI in the community 51
Figures
2.1 Data extracted from Parslow et al. (2005) highlighting the
relationship between age and cause of TBI 29
3.1 Diagram showing the reciprocal interaction between individual
and contextual aspects of development, the disruption of this
interplay arising following ABI, aligned with key principles for
consideration in assessment, formulation and rehabilitation 47
3.2 Developmental trajectories post-childhood ABI 49
3.3 The CCPNR interdisciplinary formulation and planning
framework based upon the ICF-CY, WHO (2007); McDougall
et al. (2008) 56
3.4 Visual presentation of standardised assessment scores 63
3.5 Assessment scores presented with standard deviation curve 64
4.1 The SPECS model 74
4.2 A SPECS profile: strengths and needs 75
4.3 The SNAP model: The Systematic Neuropsychological
Assessment Profile 77
4.4 NIF-TY: The Neuropsychological Integrated Formulation profile 78
4.5 NIF-TY: pre-injury, developmental stage, brain injury and
impact post-injury 81
4.6 NIF-TY: presenting problem, risks, measures and CYP’s view 82
4.7 NIF-TY: intervention and evaluation 83
4.8 Diagram of the clinical process underlying formulation and
goal setting 85
7.1 Provisional developmental model of capacities required to
develop insight 112
Illustrations xi
Tables
7.1 Positive story themes in Theo’s document 117
7.2 Summary of therapy sessions with Grace and Theo 117
7.3 Grace’s ratings of therapy outcome using Likert scale 119
7.4 Theo’s ratings of therapy outcome 120
8.1 Themes and dilemmas families face when their CYP sustains a
profound brain injury 124
9.1 Narrative approach: neuropsychological adaptations 146
13.1 ABI: challenges for transition 196
14.1 CDE recommended outcome measures for children with ABI,
comparison with measures used in different settings 215
Appendix: Theory-practice links in “Narrative-inspired interview with
the brain” 234
Editors’ acknowledgements
We are indebted to all the wonderful and learned contributors who agreed to join
us in this endeavour. To the many people behind the scenes who have given us
words of guidance or encouragement, we have not forgotten you. Special thanks
to Dr. Heather Liddiard, Consultant Clinical Neuropsychologist, for her steadfast
support and to Danielle Pearce, Assistant Psychologist, for helping with proof-
reading and formatting challenges!
This book is a reflection of so many of the seminal influences on one’s life.
For those who inspired and scaffolded, Jenny would like to thank Professor
Peter Fonagy, University College London, UK, for his validation throughout her
early career as faculty on the Doctorate in Clinical Psychology Programme. To
Professor Liam Dorris, University of Glasgow, UK, and Professor Peter Rankin,
Institute for Child Health, University College London, UK, for their unwaver-
ing support and wise words from the start of her professional training in clinical
paediatric neuropsychology. To Professor Piet Hut at the Institute for Advanced
Study, Princeton, US, for his invitation to join his Program for Interdiscipli-
nary Studies to exchange ideas with a multitude of great minds. To Professor
Barry Beyerstein, Simon Fraser University, Vancouver, Canada, who sparked
intrigue and amazement through teaching with endless compassion and excite-
ment, unravelling and explaining mysteries of consciousness with such vim.
To Dr. Ann Miller, Marlborough Family Service, UK, who helped support her
growth as a systemically informed practitioner personally and professionally.
To Professor Alan Parkin, who first inspired her love of neuropsychology during
undergraduate studies.
We would also like to thank Ste Weatherhead for being Esther’s mentor through
the editorial and publication process. He was instrumental in giving her the confi-
dence, as a newly qualified psychologist, to gather a team of editors and contribu-
tors together to pitch a proposal to Karnac Books. We would like to thank all the
children and families who inspired us. It is your life stories that make the book
truly authentic and of value. As your therapists, it is your lives and those of others
affected for whom we want to make the difference. We also thank Ethan Murtagh-
Kelly, Caroline Murtagh and Gary Kelly, who were the inspiration for this book.
Editors’ acknowledgements xiii
and training roles and in private practice. She has worked with children with
acquired and neurodevelopmental disorders over the past 20 years. Her cur-
rent writing and research interests include writing collaboratively with service
users and the processes of therapeutic work.
Isobel Heyman qualified in medicine at University College London and gained
a PhD in developmental neurobiology before training as a child psychiatrist at
the Maudsley Hospital and Institute of Psychiatry, London. Dr. Heyman works
at Great Ormond Street Hospital for Children in London, UK, where she leads
a team specialising in liaison/consultation psychiatry and neuropsychiatry. She
is an Honorary Professor at the Institute of Child Health, University College
London. Her current research programme focusses on integrating physical and
mental health care, particularly in relation to neurological conditions. Com-
mon treatable psychiatric disorders are often undetected in this population –
she aims to improve early evidence-based intervention in these children. She
was awarded UK Psychiatrist of the Year in 2015 by the Royal College of
Psychiatrists.
Liz Ireland is a Specialist Clinical Psychologist who works part time at Great
Ormond Street Hospital in London. Dr. Ireland specialises in working with
children with a diagnosis of cancer, specifically children with brain tumours,
and their families. She also works for Recolo UK Ltd, an independent com-
munity neurorehabilitation service for children and young people with ABI.
Having completed the post-graduate diploma in paediatric and clinical neu-
ropsychology, she combines her knowledge of neuropsychology with systemic
ideas in her clinical work.
Heather Liddiard is a Consultant Clinical Neuropsychologist and Head of Neu-
ropsychology at Blackheath Brain Injury Rehabilitation Services (the Hunt-
ercombe Group). Dr. Liddiard has spent the majority of her career to date
working in the field of intellectual disabilities and ABI in both the NHS and
private sectors. She has particular interests in the assessment, formulation and
intervention around challenging behaviours. As such, she has an additional
qualification in positive behaviour support.
Tara Murphy is a Consultant Paediatric Neuropsychologist and Clinical Psy-
chologist. Dr. Murphy worked at Great Ormond Street Hospital between 2003
and 2017 in neuropsychology and intervention services. She has expertise in
providing and supervising neuropsychological assessment of children with a
range of ABI and neurodevelopmental conditions. She has also been involved
in leading research on quality of life, educational interventions, neuropsycho-
logical assessment and psychological treatment. Dr. Murphy believes in the
importance of supporting families, teachers and other important people in the
system on how to understand a child’s cognitive strengths and weaknesses and
mental health. She volunteered in Uganda during 2018, providing training,
teaching and being involved in child mental health and neuropsychological
xviii Contributors
services. She currently works and is leading research in Saint Helena in the
South Atlantic.
Alison Perkins is a Clinical Psychologist working in paediatric ABI. Dr. Perkins
practises as part of a multidisciplinary team at The Children’s Trust, which
provides neurorehabilitation for children with an ABI and their families. Over
many years of working within the field of paediatric ABI, she has developed
a particular interest on the impact of an ABI on the young person’s develop-
ing identity. She believes that promoting the development of a resilient self-
construct is an essential part of holistic paediatric neurorehabilitation.
Sara Portnoy is a Consultant Clinical Psychologist who works at University Col-
lege Hospital in London working with children who have a chronic illness,
where she developed and runs the “Beads of Life” programme. She also works
for Life Force, a community multidisciplinary paediatric palliative care and
bereavement team, which works in the London boroughs of Camden, Haringey
and Islington. She also volunteers for the Refugee Resilience Collective, which
is a group of systemic and narrative therapists who work with refugees and
long-term volunteers in Northern France. She has over 25 years of experience
working with children with physical illnesses.
Suresh Pujar is working as a Locum Consultant in Paediatric Neurology at Great
Ormond Street Hospital for Children, and his research interest is in under-
standing the long-term effects of neuronal injury in the developing brain. For
his doctoral thesis at Great Ormond Street UCL Institute of Child Health, Dr.
Pujar conducted a prospective population-based study to investigate the long-
term outcomes following prolonged seizures (convulsive status epilepticus) in
childhood.
Elizabeth Roberts is a Specialist Educational Psychologist in Paediatric Neu-
ropsychology. Dr. Roberts has undertaken post-doctoral qualifications in Clini-
cal Paediatric Neuropsychology. She works within a multidisciplinary team at
the Children’s Trust, a residential rehabilitation setting for children with ABI.
She also has several years of experience working as a local authority Educa-
tional Psychologist, providing psychology support to nurseries, schools and
colleges.
Jackie Solaiman is an Occupational Therapist and mother to four children, the
youngest of which is Rafi who experienced a severe acquired brain injury, due
to a bleed in 2012, at the age of 12. Jackie has written from the perspective of
an Expert by Experience for this book. Jackie is passionate about enabling Rafi
to have an interesting and fulfilling life, and is motivated by his positivity to
have a go at anything! Rafi has been selected to represent Team GB in Race-
Running at the 2019 World Para Athletics in Dubai.
Contributors xix
I think it is fair to say that this is a vitally important book. It joins less than a
handful of books worldwide that outline psychological therapy for children and
families affected by paediatric acquired brain injury (ABI). It has a market in this
expanding client population, which is growing with improvements in emergency
medicine, surgery and intensive treatments. Clinicians are facing dilemmas of
addressing such an overwhelming level of need that cuts across all domains of
functioning. We hope this book can provide a resource to help clinicians make
sense of, prioritise and intervene appropriately and realistically within the service
contexts they find themselves.
We use storytelling in a therapeutic capacity within this book. I would like to
open it by telling the story of how the book came to life. It was initiated in an
entirely unconventional way. I first saw Dr. Jenny Jim speak at an event in London
for widening access to the profession of clinical psychology in 2006. During my
final placement as a trainee clinical psychologist in Autumn 2012, I was later for-
tunate enough to meet a young man with an ABI who made me realise the gap in
psychological therapy provision for children and young people affected by brain
injury, and their families.
After giving a well-received talk on “James” (Chapter 9) to the Paediatric Neu-
ropsychology Special Interest Group in 2015, I contacted Ste Weatherhead. He
was the only author of a book on narrative approaches for brain injury, and I asked
him why there was no similar book for children: Narrative Approaches for Child-
hood Brain Injury. It was he who suggested I initiate and edit this book, and he
gave me the confidence, as a newly qualified clinical psychologist, to approach
specialists in the area to write the book proposal with me – serendipitously, one
of whom was Jenny Jim.
So, this is a unique book for many reasons: one of which is that it is edited by
a specialist clinical psychologist who works in paediatric ABI and me, a clinical
psychologist who has worked predominantly in mainstream mental health and
dementia services. However, our hope is that this book will appeal to a much
wider audience of therapists; therapists who, unexpectedly, come across a history
of paediatric brain injury in mainstream child and adult mental health settings,
as I do. I represent the majority of clinicians who will come across adults and
Preface xxi
children with ABI histories in other contexts. They are, poignantly, more likely to
meet a psychologist, therapist or counsellor than a paediatric neuropsychologist,
throughout their lifespans.
With a child sustaining a brain injury through illness, accident, injury or abuse
every 30 minutes in the UK alone (CBIT, 2018), it has been suggested that up to
five children in any given classroom may have sustained a brain injury (HC Deb,
2018). We, therefore, hope that childhood brain injury features on everybody’s
agenda.
It has been a privilege for me to write with a team of experts breaking new
ground in paediatric psychological therapy and neurorehabilitation. As men-
tioned, brain injury can affect all domains of functioning, so the breadth of needs
of the children and young people affected cut across many different services: the
health, social, education and justice sectors, to name a few. I, therefore, also hope
this book will appeal to commissioning bodies, researchers and the government:
the ministries of health, education and justice in the UK and internationally.
There are a range of professionals, stances and theoretical orientations in the
book: clinical and educational psychologists, a psychiatrist, neurologist and a
play therapist. I want to thank everyone who collaborated on this project and had
faith in the process. This enabled me to contribute to the project management, co-
ordination, development and editing of this book from the position of an outsider
looking in on real excellence, expertise and innovation.
Esther Cole
Series editors’ foreword
Our brain injury series takes a bold new step forward in this publication edited
by Drs. Jenny Jim and Esther Cole into therapeutic work with children and young
people who have survived acquired brain injury (ABI) and their families. It is a
privilege to host this innovative work within our book series for several reasons.
Firstly, I (GY) remember looking to the paediatric ABI literature nearly 20 years
ago for inspiration when we were developing our initial perspectives on fam-
ily work in adults with ABI. The paediatric ABI outcome studies led by Keith
Yeates and Stephanie Taylor operationalised non-linear complex path modelling
to explore the interrelationship between injury-related, individual survivor-related
and family/social context–related factors in the evolution of outcomes over time.
This was conceptually leaps ahead of thinking in the adult ABI field at the time.
What has struck me then and since is that this sophistication of thinking in the
outcome literature was not visibly matched by an applied therapeutic engagement
with such ideas in the published paediatric literature. When asking UK colleagues
about this, I was assured that such work was going on, but the innovative clini-
cians concerned were too busy to write up and disseminate their work. There
were disparate moments when the potential of this community’s work did become
visible to the reader, notably Sarah Helps’s (2013) edited special issue of Con-
text (a systemic and family therapy journal) on family work with paediatric ABI.
Alongside this, other psychotherapeutic approaches to child ABI and explicit
presentations of neurorehabilitation models that engage with both injury, child
and contextual factors have become more numerous in the last ten years (refer-
enced throughout this book).
We have been awaiting with interest a more substantial presentation of systemic,
family therapy and narrative ideas in this field that engage with neurology, context
and everything in between to fully realise the applied potential of the conceptual
advancements mentioned earlier. Well, here it is, and we proudly believe that this
book meets such expectations and takes the field on significantly further – once
again inspiring related clinician communities such as adult neurorehabilitation
and paediatric work with other long-term conditions. To our knowledge, this is
the most developed exposition of systemic and social context-oriented therapeu-
tic ideas in the field, but retaining a core innovation in paediatric applied clinical
Series editors’ foreword xxiii
As the old adage goes, once you have seen one child with a brain injury, you
have seen one child with a brain injury.
(Wilde, 2016)
Hearing these words was a Eureka moment for me, (Jenny Jim), as I sat in the
audience of Professor Elisabeth Wilde’s keynote speech at the 2016 Recolo con-
ference. It encapsulated the importance for respecting the centrality of hetero-
geneity when working with our children and young people with brain injuries
when as a clinician, you really do not see the same presentation twice (the same
diagnosis often but, not presentation). Therein lies the uniqueness, but also the
continual challenges, for all those committed to helping our children and young
people living with the aftermath of a brain injury.
Terminology to describe the causes of brain injury such as “RTA”, for road traf-
fic accident, can give us a false sense of uniformity but in reality, it does little to
explain what life is really like for our children and families affected. More of our
children are surviving with serious injuries due to advances in intensive medicine,
and the therapeutic field is challenged to come up to speed to meet the myriad
sequelae. No two injuries are the same, and thus our approach to be of help needs
to dovetail differently to each family we see. Embracing the heterogeneity rather
than disguising it with labels is vitally important for our work as clinicians.
Paediatric neurorehabilitation is a burgeoning field, growing exponentially
in the past few decades. Robust empirical studies from Professor Vicki Ander-
son’s team at the Murdoch Research Institute (Melbourne) have been central in
demonstrating the devastating effects of early and severe childhood brain injury,
challenging common myths around children having a greater ability to “bounce
back”. Theoretical ideas from Professor Faraneh Vargha-Khadem’s team at the
Institute of Child Health (UCL, UK) also contribute greatly to understanding
why greater childhood brain plasticity may not necessarily equal positive brain
recovery not only due to the fundamental negative impact the primary injury
may have but also due to its ability to hinder and derail normative ongoing child-
hood development.
2 Jenny Jim and Heather Liddiard
Concurrent with this dose of “bad news” punctuating our knowledge is the coun-
terweight of an increasing recognition of how the relationships and support around
a child or young person positively affect organic brain recovery and psychologi-
cal resilience (which interact with each other). Dr. Rima Shore’s seminal book
Re-thinking the Brain (1997) eloquently presents the “new news” of seeing the
brain as ever changing, especially in response to nurturing relationships – that it is
simply impossible that our fundamental neural architecture cannot change in rela-
tion to the love and care it receives. The work of Dr. Allan Schore at UCLA makes
vital connections between psychology, attachment and neuroscience – further
breaking through from the myth of mind-body dualism that seems to implicitly
pervade clinical work and organisation of our clinical services to this day.
Systematic reviews of risk and resiliency factors in paediatric TBI provide yet
more evidence for the interplay of social and environmental context on recovery
(Gerring & Wade, 2012; see also Wade, Carey, & Wolfe, 2006; Wade, Michaud, &
Brown, 2006; Wade, Walz, Carey, & Williams, 2008). This is not only behavioural
or emotional recovery but also neuropsychological recovery. For instance, paren-
tal mental health and distress affect emotional outcomes for the child but also
affect cognitive and behavioural outcomes such as verbal IQ, fine motor control,
social competence, adaptive behaviour and levels of behaviour problems (Taylor
et al., 1999). Likewise, positive parenting is predictive of IQ and practical judge-
ment (Gerrard-Morris et al., 2009). Strengthening the capabilities of the family
system around our children is paramount (see the work of Gan, Gargaro, Kreutzer,
Boschen, & Wright, 2010; Gan & Ballantyne, 2016). It is also now widely rec-
ognised that severity of injury does not show a linear relationship to quality of
life and disability (Hurst, 2009). These findings further propel our practice with
children with brain injuries to evolve, embracing both traditional clinical and
neuropsychological practices. Remits of current services can be based on out-
dated ideas about the nature of brain development and recovery, and so can limit
chances for innovation.
Why has it taken so long to recognise that rehabilitation through therapy is
vital for childhood brain injury? If we look to the field of adult neuropsychology,
such brain and behaviour relationships have been widely recognised, certainly
since the world wars and prior to that through the infamous 19th-century “case
study” of Phineas Gage. Perhaps the starkness of the changes in personality and
functioning made it easier for an observable cause-and-effect relationship to be
determined. For children, as they only have a subset of the skills that they will
eventually acquire when they meet with say an accident or neurological illness,
it is much harder to discern that their functioning is compromised. Think about a
3-month-old baby sustaining a brain injury – his or her realm of self-expression
is limited arguably to subtle motor abilities – measuring an impact on those is
extremely hard. It is only later when baby grows up and miss his or her milestones
that one is likely to see the actual effects of injury months earlier.
Such “sleeper effects” are likely to have added to the hiddenness and invisibility
of childhood brain injury and thus why we as a society have not provided nearly
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golden image of the god, gleaming between the open columns in the
morning sun. Further away appeared the mighty and fortified
buildings of the temple of Ashmon or Æsculapius. To the left of the
city the fanes of Neptune, Diana, and Astarte glittered in the sun,
while occupying the absolute centre of the town, and standing apart
in a large and now crowded open space, was clearly visible the huge
circular temple of the awful Sun god—Saturn, Baal Hammon, or
Moloch. The drums and trumpets loudly sounding from the vicinity of
this temple, and the wreaths of smoke winding up between the triple
domes plated with solid gold, told that the terrible sacrifices had
already begun. Indeed, the yells of execration of the myriads of
brightly-robed populace, most of them women, as victim after victim
was dragged forward by the priests and thrown upon the dreadful
sloping arms of the god, a sight Hannibal could easily observe
between the rows of columns, often nearly drowned the blare of the
trumpets and the rolling of the drums.
Well, indeed, might they scream, these women of Carthage, for
owing to the cruelties and massacres of those upon whom they were
now wreaking their vengeance, all who had been their husbands or
lovers were gone. There were now scarcely any men left. Thus they
saw themselves condemned either to a perpetual virginity, with no
hopes of ever knowing the joys of motherhood, or fated at the best to
a share with many other women in the household of some rich and
elderly noble, since polygamy had been recently decreed as a
means of repopulating the State. All the young men remaining alive,
Hamilcar had enrolled in his army, and although a few of the more
luxurious and ease-loving might leave him and remain in Carthage,
that army was, so rumour said, about to start with him and the flower
of Carthaginian manhood for unknown battle-fields, whence it was
improbable that they would ever return. Thus, the older women
screamed and yelled with fury at the loss of husbands or sons, and
the young women screamed with rage at the loss of the once
possible husbands, who never had been and never could be theirs.
Yet, all alike, having put off their mourning for the day, were gaily
attired for joy at the burning alive of their enemies. They had even
adorned their raven locks with the brilliant crimson flowers of the
pomegranate, as red as their own red lips, or the blood which had
been shed in torrents by Spendius and Matho, and which was again
to flow that very day on this joyful occasion of revenge.
Leading from the harbours and the Great Place up through the
town to all these temples were three streets—the Vicus Salutaris, on
the right, leading to the temple of Æsculapius; the Vicus Satyrnis, in
the centre, leading to the great brazen god Moloch; and to the left,
the Vicus Venerea or Venus Street, leading to the temple of the
Carthaginian Venus and Juno in one; Tanais, Tanith, or Astarte, the
Goddess of Love and the Queen of Heaven combined. These last
two streets swept round on either side of the hill of the Byrsa or
Citadel, and it was on this hill that the eye of the youthful Hannibal
chiefly rested, for within and above its walls he could see on the
summit of the hill the temple of Melcareth, the unknown and invisible
god of whom no image had ever been made. Melcareth was the
great Spirit of life and the protector of his father, before whom he
was to register his vow.
Plainly built of white marble, in simple but solemn simplicity, it was
surrounded with plain Doric columns of Numidian marble. This very
plainness made the exterior of the building more impressive; and as
it occupied the highest point in the whole city, the boy could see it
clearly.
At length, with a sigh, he took one last lingering look all round,
from the mountains of the Hermæan Promontory to the Gulf, from
the Gulf to Cape Carthage, and to the city from the hill of the
Catacombs, round and past the triple wall enclosing the Megara,
away to the white buildings of Tunis in the distance, and to the lake
near at hand.
“I have seen it all, my father,” he said at length; “not a headland
nor a house, not a tree nor a temple, will ever fade away again from
my memory. It is all engraven on my heart.”
“It is well,” said Hamilcar; “now go and prepare thyself to
accompany me to the temple of Melcareth; thou shalt accompany
me upon my elephant, for I shall go in state. Here, Maharbal! Imlico!
Hanno! Gisco!”
A crowd of officers rushed in from the ante-chambers, where they
were waiting; the great General gave directions about the ceremony
that was to take place, and orderlies and messengers were soon
galloping in every direction.
CHAPTER III.
HANNIBAL’S VOW.
END OF PART I.
PART II.
CHAPTER I.
ELISSA.
All the lower parts of Spain had been conquered and settled.
Hamilcar had died, as he had lived, fighting nobly, after enjoying
almost regal rank in his new country. Hasdrubal, who had succeeded
him, was also dead, and now Hannibal, Hamilcar’s son, a man in the
young prime of life, held undisputed sway throughout the length and
breadth of the many countries of Iberia that his father’s arms and his
father’s talents had won for Carthage.
In the delightful garden of a stately building reared upon a hill
within the walls of the city of Carthagena or New Carthage, a group
of girls and young matrons were assembled under a spreading tree,
just beyond whose shade was situated a marble fish pond, filled with
graceful gold and silver fishes. The borders of the pond were fringed
with marble slabs, and white marble steps led down into the basin for
bathing purposes. In the centre a fountain threw up in glittering spray
a jet of water which fell back with a tinkling sound into the basin.
Upon the marble steps, apart from the other young women, sat a
maiden listlessly dabbling her fingers and one foot in the water, and
watching the fishes as they darted hither and thither after some
insect, or rose occasionally to the surface to nibble at a piece of
bread which she threw them from time to time. The girl, who was in
her seventeenth year, was in all the height of that youthful beauty
which has not yet quite developed into the fuller charms of
womanhood, and yet is so alluring with all the possibilities of what it
may become.
Of Carthaginian origin on the father’s side, her mother was a
princess of Spain—Camilla, daughter of the King of Gades. She had
inherited from the East the glorious reddish black hair and dark liquid
eyes, and had derived from the Atlantic breezes, which had for
centuries swept her Iberian home, the brilliant peach-like colouring
with its delicate bloom, seeming as though it would perish at a touch,
which is still to be seen in the maidens of the modern Seville. For
this city of Andalusia had been, under the name of Shefelah, a part
of her grandfather’s dominions. Tall she was and graceful; her
bosom, which was exposed in the Greek fashion on one side, might
have formed the model to a Phidias for the young Psyche; her ivory
arms were gently rounded and graceful. Her rosy delicate foot was of
classical symmetry, and the limb above, displayed while dabbling in
the water, was so shapely, with its small ankle and rounded curves,
that, as she sat on the marble there by the fish pond in her white
flowing robes, an onlooker might well have been pardoned had he
imagined that he was looking upon a nymph, a naiad just sprung
from the waters, rather than upon the daughter of man.
But it was in the face that lay the particular charm. Above the
snow-white forehead and the pink, shell-like ear, which it partially
concealed, lay the masses of ruddy black hair bound with a silver
fillet. The delicious eyes, melting and tender, beamed with such
hopes of love and passion that had the observer been, as indeed
were possible, content for ever to linger in their dusky depths of
glowing fire, he might have exclaimed, “a woman of passion, one
made for love only, nothing more!” Yet closer observation disclosed
that above those eyes curved two ebony bows which rivalled Cupid’s
arc in shape, and which, although most captivating, nevertheless
expressed resolution. The chin, although softly rounded, was also
firm; the nose and delicious mouth, both almost straight, betokened
a character not easily to be subdued, although the redness and
slight fulness of the lips seemed almost to proclaim a soft sensuous
side to the nature, as though they were made rather for the kisses of
love than to issue commands to those beneath her in rank and
station.
Such, then, is the portrait of Elissa, Hannibal’s daughter.
The other ladies, including her aunt, the Princess Cœcilia, widow
of Hasdrubal, a buxom, merry-looking woman of thirty, kept aloof,
respecting her reverie. For, notwithstanding her youth, the lady
Elissa was paramount, not only in the palace, but also in the New
Town or City of Carthagena during the absence of her father
Hannibal and her uncles Hasdrubal and Mago at the siege of the
Greek city of Saguntum, and had been invested by Hannibal, on his
departure, with all the powers of a regent. For, being motherless
almost from her birth, Hannibal, a young man himself, had been
accustomed to treat her as a sister, almost as much as a daughter.
He had been married when a mere lad, for political reasons, by his
father Hamilcar, and Elissa had been the sole offspring of the
marriage. Since her mother’s death he had remained single, and
devoted all his fatherly and brotherly love to training his only
daughter to have those same noble aims, worthy of the lion’s brood
of Hamilcar, which inspired all his own actions in life. And these aims
may be summed up in a few words: devotion to country before
everything; self abnegation, ay, self sacrifice in every way, for the
country’s welfare; ambition in its highest sense, not for the sake of
personal aggrandisement, but for the glory of Carthage alone. No
hardships, no personal abasement even—further, not even extreme
personal shame, or humiliation if needful, was to be shrunk from if
thereby the interests of Carthage could be advanced. Self was
absolutely and at all times to be entirely set upon one side and
placed out of the question, as though no such thing as self existed;
the might, glory, and power of the Carthaginian kingdom were to be
the sole rule, the sole object of existence, and with them the undying
hatred of and longing for revenge upon Rome and the Romans, as
the greatest enemies of that kingdom, through whom so many
humiliations, including the loss in war of Sicily, and the loss by fraud
of Sardinia, had been inflicted upon the great nation founded by
Dido, sister of Pygmalion, King of Tyre.
These, then, were the precepts that Hannibal had ever, from her
earliest youth, inculcated in his daughter; and with the object that
she might learn early in life to witness and expect sudden reverses
of fortune, he had hitherto, since her twelfth year, ever taken her with
him upon his campaigns against the Iberian tribes. Thus she might