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Books > Health, Home & Family > Family & health > Coping with personal problems > Coping with disability
Why is Autism Spectrum Disorder so misunderstood in girls and women
and why do so many go under the radar without the support that they
need? This practical guide explains the unique issues that affect
females with autism and provides tools and strategies that girls,
women and their families can use in day-to-day life. Following the
story of Alison, a girl diagnosed with Asperger Syndrome, through
both childhood and adulthood, we get an inside view of the
challenges that girls and women with autism face. Straightforward
information and advice is provided on key topics including: *
social skills and communication * how to overcome bullying *
sensory issues and food sensitivity * the need for routine *
perceptions of gender * and physiological changes. Essential
reading for parents of daughters on the spectrum, as well as girls
and women who carry the diagnosis themselves.
Meet Mallory Weggemann: a Paralympic gold-medalist, world champion
swimmer, ESPY winner, and NBC Sports commentator whose
extraordinary story will give you the encouragement you need to
rise up to meet any challenge you face in life. On January 21,
2008, a routine medical procedure left Mallory paralyzed from her
waist down. Less than two years later, Mallory had broken eight
world records, and by the 2012 Paralympic Games, she held fifteen
world records and thirty-four American records. Two years after
that, a devastating fall severely damaged her left arm. But despite
all of the hardships that Mallory faced, she was sure about one
thing: she refused to give up. After two reconstructive surgeries
and extended rehab, she won two gold medals and a silver medal at
the 2019 World Para Swimming Championships. And even better, she
found confidence, independence, and persevering love. She even
walked down the aisle on her wedding day against all odds.
Mallory's extraordinary resilience and uncompromising commitment to
excellence are rooted in her resolve, her faith, and her sheer
grit. In Limitless, Mallory shares the lessons she learned by
pushing past every obstacle and expectation that stood in her way,
teaching you how to: redefine your limits remember that healing is
not chronological be willing to fail lean on your community embrace
your comeback write your own ending Mallory's story reminds us that
we can handle whatever challenges, labels, or difficulties we face
in life, and we can do it on our own terms. Because when we refuse
to accept every boundary that hems us in--physical, emotional, or
societal--we become limitless.
Covering principles of therapy dog team training, assessment,
skills, and ongoing monitoring, Canine-Assisted Interventions
provides guidance on the most evidence-based methods for therapy
dog team welfare, training, and assessment. The authors offer a
linear approach to understanding all aspects of the screening,
assessment, and selection of dog-handler teams by exploring the
journey of dog therapy teams from assessment of canines and
handlers to the importance of ongoing monitoring, recredentialing,
and retirement. In addition to reviewing key findings within the
field of human-animal interactions, each chapter emphasizes skills
on both the human and dog ends of the leash and makes
recommendations for research-informed best practices. To support
readers, the book culminates with checklists and training resources
to serve as a quick reference for readers. This book will be of
great interest for practitioners, in-service professionals, and
researchers in the fields of canine-assisted interventions and
counseling.
Adolescence has been known as the "second crisis" for some
families. Successful navigation of this emotionally complex time
can be difficult, and for girls with Autism Spectrum Disorders
(ASDs) the teenage years can be particularly challenging, as there
are issues specific to them that have been very sparsely addressed
in current resources, such as menstruation, puberty, safety and the
complications of girls' friendships due to fears of loneliness and
the lack of group inclusion. This book is the first resource for
families to provide the key information they need to know to help
their daughters
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and the whole family
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through adolescence. It puts topics into the context of typical
development and addresses core issues of ASDs such as cognition,
communication, behavior, sensory sensitivities and social
difficulties, and provides information, practical teaching,
intervention strategies and resources regarding topics specific to
being a teenage girl with ASD.
'I was born on 31 January 1979 - a Wednesday. I know it was a
Wednesday, becasue the date is blue in my mind and Wednesdays are
always blue, like the number nine or the sound of loud voices
arguing.' Like the character Hoffman portrayed, he can perform
extraordinary maths in his head, sees numbers as shapes, colours,
textures and motions, and can learn to speak a language fluently
from scratch in three days. He also has a compulsive need for order
and routine. He eats exactly 45 grams of porridge for breakfast and
cannot leave the house without counting the number of items of
clothing he's wearing. If he gets stressed or unhappy he closes his
eyes and counts. But in some ways Daniel is not all like the Rain
Man. He is virtually unique amongst people who have severe
autisitic disorders in being capable of living a fully-functioning,
independent life. It is this incredible self-awareness and ability
to communicate what it feels like to live in a totally
extraordinary way that makes BORN ON A BLUE DAY so powerful.
Taking Flight provides the essential information students with
disabilities will need to be successful in college. Rather than
just focusing on the academic skills needed in college, Taking
Flight addresses college as a system that needs to be mastered and
the strategies and self-awareness needed to be successful. Thus, it
explores topics including: The concept of disability
Self-expression The college bureaucracy Roommate relationships And
having fun! Perry T. LaRoque explores these topics by using
personal stories, humor, frank advice, and years of expertise.
Taking Flight addresses the truly relevant topics and issues needed
for happiness and success in college and provides readers with not
only how to do well in the system, but how to overcome a system not
designed for today's diverse learners.
Roxy lives in the forest with her three best friends, who she loves
to visit and play games with. Roxy is in a wheelchair, so sometimes
it is harder for her to go to the same places and play the same
games as the other animals. Roxy and her friends realise that by
making a few small changes and working together, they can make the
forest a better place for everyone. Roxy teaches us that there are
bunches of ways to be more inclusive of those who have a disability
so that everyone can join in. Part of the Truth & Tails series,
which aims to eliminate prejudices and encourage acceptance in
young children aged 4-8, the story of Roxy and her friends is
accompanied by hand-drawn, watercolour illustrations.
A beautifully designed book (packed with photos) full of wise words
and encouragement from successful dyslexics working in comedy,
architecture, law, fashion and many other amazing (and achievable!)
careers. Honest about the challenges of dyslexia (like problems or
embarrassment at school), while showing how its strengths can be
used to your advantage (for example how visualising and big picture
thinking can make you shine at work), this is a book of colourful
conversations with creative, motivated and successful people who
are brilliant at what they do, and who achieve incredible things
because of their dyslexia. There is also a section from people
working to support people with dyslexia, who have researched the
subject or work directly helping dyslexics on a day to day basis,
who they share their top tips and advice gleaned from their years
of experience. Read on to gain encouragement and inspiration in
your own careers!
Bringing together a collection of narratives from those who are on
the autism spectrum whilst also identifying as lesbian, gay,
bisexual, transgender, queer, intersex and/or asexual (LGBTQIA),
this book explores the intersection of the two spectrums as well as
the diverse experiences that come with it. By providing knowledge
and advice based on in-depth research and personal accounts, the
narratives will be immensely valuable to teenagers, adults,
partners and families. The authors round these stories with a
discussion of themes across narratives, and implications for the
issues discussed. In the final chapter, the authors reflect on
commonly asked questions from a clinical perspective, bringing in
relevant research, as well as sharing best-practice tips and
considerations that may be helpful for LGBTQIA and ASD teenagers
and adults. These may also be used by family members and clinicians
when counselling teenagers and adults on the dual spectrum. With
each chapter structured around LGBTQIA and autism spectrum
identities, Gender Identity, Sexuality and Autism highlights the
fluidity of gender identity, sexual orientation and neurodiversity
and provides a space for people to share their individual
experiences.
Young, Disabled and LGBT+ brings together the work of an
international team interested in exploring the intersection of
sexuality, gender identity, and disability in the lives of young
people and aims to further develop this area as a distinct area of
study. This volume features original research and writing into
lives that are often misunderstood, marginalised and
under-represented in research. It is framed with artwork, poetry
and writing from young disabled LGBT+ people, and centralises the
voices and lives of young disabled LGBT+ people throughout. Drawing
from disciplines including: sociology, psychology, disability and
youth studies, and with contributions from practitioners, it
examines experiences and research from a number of perspectives,
such as education, personal lives and activism. Featuring work from
the UK, Canada, United States, India and Australia, it is a timely
and topical book which will appeal to scholars particularly
interested in sexuality, gender, disability and youth studies;
professionals within health, education, social work and youth work
who aim to understand and support young disabled LGBT+ people; and
young people themselves.
Wall Street Journal and USA Today Bestseller The Courage to Go
Forward shows that individuals need to think differently about
creating supportive communities to help each other set and achieve
goals, both individually and collectively. Those interested in
making a positive impact on society need to consider how to
complement societal programs designed for the "average" person with
customized approaches tailored to the unique needs and aspirations
of every individual. Focused on the inspirational relationship
between Cigna, a global health service company, and Achilles
International, a nonprofit focused on encouraging disabled people
to participate in mainstream athletics, The Courage to Go Forward
demonstrates the power and triumph of the human spirit and provides
valuable insight into the formation and importance of micro
communities. David Cordani, president and CEO of Cigna, and
Achilles International founder and president Dick Traum come from
very different backgrounds yet share a similar set of passions that
eventually brought them together, forming a relationship that has
positively impacted communities ranging from inspired employees to
thousands of disabled athletes competing at the highest levels.
Filled with wisdom from two impactful leaders, a collection of
inspiring profiles of Achilles athletes, and stunning imagery, The
Courage to Go Forward offers a combination of powerful inspiration
and important business lessons, including the potential power of
partnership between for-profit and nonprofit organizations, and
should be required reading for anyone who wants to drive positive
societal change, and to encourage others-or themselves-to achieve
beyond their perceived limitations.
This book provides a diverse range of basic information and
practical advice for adults with dyspraxia. Colley is able to
describe in detail the impact that coordination and motor learning
difficulties can have on many everyday activities, including
cooking, shopping, sewing, gardening and swallowing medicines. This
book provides a very readable, comprehensive and useful resource
for adults with dyspraxia and their carers. It might also be useful
for clinicians who are new to the field and have limited practical
experience.' - British Journal of Occupational Therapy 'This
concise and interestingly written handbook is aimed at helping
dyspraxic adults to understand their condition and its impact on
work, study, social relationships and leisure activities. It
contains practical tips on everyday living, including voice
control, body language, cooking, study skills, driving and
self-care. Especially fascinating are the accounts by four
dyspraxic adults of their own experiences. I would recommend the
book to teachers and parents, student therapists and clinicians
(especially those working in a multidisciplinary setting) who need
an insight into developmental dyspraxia as experienced by
adolescent and adult clients and an overview of the help
available.' - Speech and Language Therapy in Practice For people
with Developmental Dyspraxia, everyday life can pose a multitude of
problems. Tasks the majority of people would find simple can often
be taxing and fraught with difficulty. Living with Dyspraxia was
written to help all adults with Dyspraxia tackle the everyday
situations that many people take for granted. It is full of
practical advice on everything from getting a diagnosis to learning
how to manage household chores. Important topics are addressed,
such as self-esteem, whether to disclose your condition within the
workplace, how to communicate more effectively and also how
Dyspraxia often interacts with other conditions, such as Dyslexia,
ADHD and Asperger's Syndrome. This practical resource will be of
use to adults with Dyspraxia, the professionals and families
members who come into contact with them as well as those who simply
wish to learn more about Dyspraxia.
This book sets out to understand how students with disabilities
experience higher education and the transition to the workplace. It
foregrounds the voices of students and graduates in order to
explore identity, inclusion, participation and success of youth
with disabilities in higher education, as well as their transition
from university to employment. The author proposes a new
understanding of disability, considered in terms of a continuum of
abilities, balancing empirical data, theory and policy analysis
with specific regard to the interests of youth with disabilities,
making a unique contribution to discussions on access, inclusion
and success in higher education and employment. These discussions
inform social development and educational policy planning and
implementation, not only in South Africa, but also in countries
with a similar context, particularly in terms of remedial courses
of action that bring social justice to people with disabilities.
Students with Disabilities and the Transition to Work will be of
interest to all scholars and students working in the fields of
disability studies, particularly those with a focus on critical
disability studies and disability in the global south, as well as
those working in higher education, sociology, development studies
and social policy.
Jonathan and Polly Tommey's eldest son, Billy, was diagnosed with
severe autism at the age of two. Today, Billy is a high-functioning
teenager - thanks to the determination of his parents to discover
as much as possible about autism, its causes and potential
treatments. They show through their own experience how it is
possible to improve the quality of life for children with autism.
The book will give parents the confidence and knowledge to tackle
the problems they face and find solutions, treatments and
educational options that will work for their child. In his quest to
help his son, Jonathan trained as a nutritional therapist and now
supports many individuals with ASD at his Autism Clinic. His
expertise forms an important part of this book. Contents include:
getting a diagnosis; the gut-brain connection; tests and
treatments; the link with toxins; diet and nutrition; health and
wellbeing; coping as a family; educational approaches; choosing a
school; looking to the future; and a comprehensive resource
section. Practical and positive, this book provides much needed
support, advice and encouragement for parents of children on the
autism spectrum.
From a leading neurologist, neuroscientist and practitioner of
Ayurvedic medicine, comes a rigorous scientific investigation of
the healing power of sound, showing readers how they can use it to
improve their mental and physical wellbeing. Why does a baby's cry
instantaneously flood a mother's body with a myriad of stress
hormones? How can a song on the radio stir up powerful emotions,
from joy to anger, regret to desire? Why does sound itself evoke
such primal and deeply felt emotions? A vibration that travels
through air, water and solids, sound is produced by all matter, and
is a fundamental part of every species' survival. But there is a
hidden power within sound that has only just begun to be
investigated. Sound Medicine takes readers on a journey through the
structure of the mouth, ears, and brain to understand how sound is
translated from acoustic vibrations into meaningful neurological
impulses. Renowned neurologist and Ayurvedic expert Dr. Kulreet
Chaudhary explains how different types of sound impact the human
body and brain uniquely, and explores the physiological effects of
sound vibration, from altering mood to healing disease. Blending
ancient wisdom with modern science, Dr. Chaudhary traces the
history of sound therapy and the use of specific mantras from
previously unknown texts-traced back to the Siddhas, a group of
enlightened yogis who created a healing tradition that served as
the precursor to Ayurvedic medicine-to explain the therapeutic
application of sounds for a wide range of conditions. Sound
Medicine offers practical, step-by-step lessons for using music and
mantras, whether you're a beginner or searching for a more advanced
practice, to improve your health in body, mind, and spirit.
'A hymn to life, love, family, and spirit' DAVID MITCHELL, author
of Cloud Atlas The vividly told, gloriously illustrated memoir of
an artist born with disabilities who searches for freedom and
connection in a society afraid of strange bodies. ***WINNER OF THE
BARBELLION PRIZE*** In 1958, amongst the children born with spina
bifida is Riva Lehrer. She endures endless medical procedures and
is told she will never have a job, a romantic relationship or an
independent life. But everything changes when as an adult Riva is
invited to join a group of artists, writers, and performers who are
building Disability Culture. Their work is daring, edgy, funny, and
dark, and it rejects tropes that define disabled people as
pathetic, frightening or worthless, instead insisting that
disability is an opportunity for creativity and resistance. Riva
begins to paint their portraits - and her art begins to transform
the myths she's been told her whole life about her body, her
sexuality, and other measures of normal. 'A brilliant book, full of
strangeness, beauty, and wonder' Audrey Niffenegger 'Wonderful. An
ode to art and the beauty of disability' Cerrie Burnell 'Stunning'
Alison Bechdel ***SHORTLISTED FOR THE NATIONAL BOOK CRITICS CIRCLE
AWARD***
Get moving on that injury with this humorous guide to
rehabilitation from the comfort of your home! Does it Hurt When I
Do This? is designed to educate readers on the workings of the
human body, how to keep it healthy, and how to prevent and
rehabilitate injuries. In a light, humorous style that has endeared
him to thousands of patients, Mark Salamon presents this "owner's
manual for the human body" in a logical order, starting with very
basic concepts and progressing gradually to more complex ideas. His
continual references back to the basics stem from his observations
over twenty-five years of patients who were frustrated because
their doctors or therapists had never explained them. With a better
understanding of how the body's different parts work together to
protect itself from injury and repair itself if one occurs, readers
learn how to care for all the parts together so injuries become
less frequent and easier to fix. Guiding readers through hows and
whys of rehabilitating injuries to specific body parts, starting
with the feet and working up, Salamon emphasizes that this
knowledge is meant to enhance, not replace, the reader's
relationship with their physical therapist and doctor. When poor
insurance coverage or high co-pays limit the number of office
visits, the knowledge gleaned from this work helps patients better
understand how to enhance and stick with their home programs, and
when to seek help when things are not improving as expected.
Disabled women represent one of the most marginalised minority
groups in the world, hence they are largely silent while their
sexuality is ignored, suppressed, forbidden and buried underneath
the carpet. Until recently, most of the Global Northern published
literature on the subject of the sexuality of disabled women has
predominantly been constructed from hearsay and second-hand
narratives in studies which draw from the perspectives of parents,
service providers and advocates, without much consultation of the
relevant women. By facilitating the voice of disabled women in
Zimbabwe and illuminating their experiences of sexuality, this book
hopes to shift the experiences of sexuality of disabled women from
the periphery of society to the fore. Disability and Sexuality in
Zimbabwe presents original research on an issue that is thus far
not found in local research data. Whilst addressing the paucity of
literature on the subject, the book informs policy and practice and
enhances the existing body of knowledge by making recommendations
towards the development of a disability and sexuality framework
that is rooted in the African context. This book is of interest to
students and scholars of African studies, disability studies,
sociology, psychology, social work, nursing, education studies,
geography, women's and gender studies and interdisciplinary
studies. Additional audiences include a wide range of health,
social care, and educational professionals and practitioners, as
well donors, disabled people's organisations, charities, government
departments, NGOs, supranational organisations, and policy makers
'A beautiful and important book that is both deeply engaging and
usefully practical. I loved it.' CATHY RENTZENBRINK 'An insightful
and well-timed book ... forces us to confront the stereotypes - and
prejudices - we hold.' SUNDAY TIMES 'profoundly important...full of
wisdom and bright insights on what it really means to love someone,
by a fearless and generous writer. ' CLOVER STROUD 'A beautiful and
timely reminder that each and every one of us has the ability to
care, the capacity for empathy, and the potential to grow.' ANDY
PUDDICOMBE, FOUNDER OF HEADSPACE 'A wonderful book: compassionate,
honest, carefully-reasoned and genuinely helpful... This will
benefit many people.' KATHERINE MAY, author of WINTERING 'An
invaluable tool for any invisible carers or anyone who wants to
learn how to better support their loved ones... we ALL have many,
many things to learn from Penny's beautiful, wise, charming,
thoughtful words' SCARLETT CURTIS, Sunday Times bestselling author
'Moving and beautifully written, nuanced and wise, alert to every
paradox at the heart of love. A hugely important book not only for
current or future carers, but anyone learning to accept that life
tends to resist our control.' OLIVIA SUDJIC, author of EXPOSURE
'Tender captures the powerful capacity of people to care for
others, and all the heartbreaking and heartwarming complexity that
this involves. Penny brings the crucial, yet often overlooked, role
of caring into our collective consciousness and, in doing so,
demonstrates what it means to be human.' -DR EMMA HEPBURN, author
of A TOOLKIT FOR MODERN LIFE 'Penny Wincer's TENDER manages to
combine both unromanticised honesty about the realities of care
with a genuine uplifting hopefulness... is a must-read.' RUTH
WHIPPMAN, author of THE PURSUIT OF HAPPINESS We are all likely - at
some point in our lives - to face the prospect of caring for
another, whether it's a parent, child or partner. It is estimated
that there are 7 million people in the UK caring for loved ones.
And yet these are the unpaid, unsung people whose number is rising
all the time. In Tender: the imperfect art of caring, Penny Wincer
combines her own experiences as a carer with the experiences of
others to offer real and transformative tools and insights for
navigating a situation that many of us are either facing or will
face at some time. Penny Wincer has twice been a carer: first to
her mother, and now as a single parent to her autistic son. Tender
shows how looking after oneself is a fundamental part of caring for
another, and describes the qualities that we can look to cultivate
in ourselves through what may otherwise feel to be an exhausting
task. Weaving her lived experience with research into resilience,
perfectionism and self-compassion, Penny combines the stories of
other carers alongside those who receive support - offering an
often surprising and hopeful perspective. Penny hosts a podcast Not
Too Busy To Write.
'Urgent, compelling and lyrically, luminously beautiful . . . a
brilliant, heart-rending read.' Psychologies Magazine Brown
constellates the subjects that define her inside and out: a
disabled and conspicuous body, a religious conversion, a missing
twin, a life in poetry. As she does, she depicts vividly for us not
only her own life but a striking array of sites and topics, among
them Mary Shelley's Frankenstein and the world's oldest anatomical
theater, Eugenics, and Jerry Falwell's Liberty University.
Throughout, Brown offers us the gift of her exquisite sentences,
woven together in consideration, always, of what it means to be
human: flawed, potent, feeling.
If you only buy one book to improve your life this year, make it
this one. Temple Grandin, Liane Holliday Willey, Anita Lesko,
Stephen M. Shore, and many other Aspie mentors, offer their
personal guidance on coping with the daily stressors that Aspies
have identified as being the most significant, in order of urgency
- anxiety, self-esteem, change, meltdowns, depression, friendship,
love, and much, much more. Based on years of personal experience,
this book is packed with advice from Aspie mentors who have all
been there and done that! World expert Dr. Tony Attwood rounds up
each chapter with professional analysis and extensive
recommendations. He includes essential information on destructive
strategies that may look attractive, but that have
counter-productive effects. Including full color artwork from Aspie
artists showing visually how they interpret each stressor, this is
THE inspirational guide to life for young adults, the newly
diagnosed, and as a life-long reference for anyone on the spectrum
- written by Aspies for Aspies.
For people with ASDs, depression is common, and has particular
features and causes. This outstanding book provides a comprehensive
review of these aspects, and an effective self-help guide for
anyone with an autism spectrum disorder (ASD) affected by
depression. Written by the leading experts in the field, the book
explains and describes depression, the forms it can take, and how
it looks and feels for a person on the autism spectrum. The authors
draw on the latest thinking and research to suggest strategies for
coping with the effects of depression and provide a complete
step-by-step CBT self-help programme, designed specifically for
individuals with ASDs. The programme helps increase self-awareness,
including identifying personal triggers, and provides the tools to
combat depression.
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