I'm the Bob and Cathy's Kid: Emotions - Love and Fury

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This is a story about Suzanna Bailey, who at the age of fourteen months began experiencing epileptic seizures. Consequently, these seizures led to countless appointments with medical professionals. Six successive brain surgeries left her with life-changing brain injuries, resulting in physical disabilities and behavioural challenges.
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About the author

As you read our story, you will notice that we reference interviews and articles written by the “Book Team”: Jane, Sylvia, Aga, and BettyAnne.

When the Bailey family requested assistance from our agency, the Langley Association for Community Living, it was decided that a home with a family-like type of environment was to be designed so that care and support for Suzanna and her parents could be offered in a holistic and caring manner.

The staff of the first home (Benz Crescent) were instrumental in these early years of Suzanna’s life, as they attended to her needs with compassion and caring. Over the years, many staff members offered support and guidance for Suzanna, but two ladies (and their families) who have been most influential were Jane and Sylvia. Both were staff supervisors and have known Suzanna and her family since she was ten years old. Their long-term relationship with the Baileys provided valuable insight and recollections as groundwork for this book. Today, both Jane and Sylvia and their families still include Suzie in many social events.

BettyAnne was the Respite and Family Support Coordinator for LACL and offered administrative support until Suzie reached adulthood. BettyAnne continues to applaud Suzie’s successes up to this day. She provided gentle direction to the whirlwind of ideas, often guiding the team to find a solution pleasing to all when differences of opinion occurred.

As Suzanna moved into her own townhouse complex, several key staff along with Sylvia continued to provide guidance to ensure Suzie was reaching her potential. Upon Sylvia’s retirement, Aga became her staff supervisor, and an instant bond developed. Building on the groundwork set by Sylvia and Jane, and with an understanding of Suzie’s challenges and strengths, she supports the staff to ensure that Suzie has a meaningful and full life.
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Additional Information

Publisher
FriesenPress
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Published on
Jun 18, 2018
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Pages
196
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ISBN
9781525517068
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Language
English
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Genres
Biography & Autobiography / Medical
Medical / Caregiving
Medical / Neuroscience
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Content Protection
This content is DRM protected.
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Read Aloud
Available on Android devices
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Eligible for Family Library

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This volume is one in a series of monographs being issued under the general title of "Disorders of Human Communication". Each monograph deals in detail with a particular aspect of vocal communication and its disorders, and is written by internationally distinguished experts. Therefore, the series will provide an authoritative source of up-to-date scientific and clinical informa tion relating to the whole field of normal and abnormal speech communication, and as such will succeed the earlier monumental work "Handbuch der Stimm und Sprachheilkunde" by R. Luchsinger and G. E. Arnold (last issued in 1970). This series will prove invaluable for clinicians, teachers and research workers in phoniatrics and logopaedics, phonetics and linguistics, speech pathology, otolaryngology, neurology and neurosurgery, psychology and psychiatry, paediatrics and audiology. Several of the monographs will also be useful to voice and singing teachers, and to their pupils. G. E. Arnold, Jackson, Miss. F. Winckel, Berlin B. D. Wyke, London Preface Neurologists, neuropsychologists, speech pathologists and other clinicians who care for dysphasic patients have often complained that available books on dysphasia tend to be parochially theoretical, and insufficiently directed towards clinical reality. These books provide the categories, labels, and theoretical speculations of one school or another; but dysphasic patients as often as not do not fit neatly into a specific theoretical category. Clinical patterns of dysphasic syndromes of most patients with dysphasia rarely conform fully to the pictures painted in the textbooks.
The fifth book from bestselling author and specialist foster carer Casey Watson.

A recent census shows that there are at least 175,000 child carers in the UK, 13,000 of whom care for more than 50 hours a week. Many remain invisible to a system that would otherwise help them. Abigail is one of those children. This is her story.

Ten-year-old Abigail has never known her father. Her mother, Sarah, has multiple sclerosis, and Abigail has been her carer since she was a toddler – shopping, cooking, cleaning and attending to her personal needs. When Sarah is rushed to hospital, suddenly this comes to the attention of the social services, and Abigail has nowhere to go.

Though she doesn’t fit the usual profile of a child that specialist foster carers Casey and Mike Watson would take on, they are happy to step in and look after Abigail. It’s an emergency, after all – and all that’s needed is a loving temporary home, while social services look into how to support the family so that they can be reunited.

But it soon becomes clear that this isn’t going to happen. Sarah’s MS is now at a very advanced stage, and the doctors are certain that there will no longer be periods of remission. Abigail’s emotional state starts to spiral out of control as she struggles to let go of the burden of responsibilities she has carried for so long.

Sarah and Abigail insist that they do not need help, but with no other family to contact, social services are left with no choice but to find long-term care for Abigail, against their wishes. But Casey never gives up on a child in need, and she knows there must be another solution...

Includes a sample chapter of Sunday Times bestseller Trafficked.

“An inspiring, intimate memoir about faith, resilience and the tenacity of love.”—People

“In this emotional tale, a young couple see their lives changed in the blink of an eye—and learn to find love again.”—US Weekly

Five months pregnant, on a flight to their “babymoon,” Allison Pataki turned to her husband when he asked if his eye looked strange and watched him suddenly lose consciousness. After an emergency landing, she discovered that Dave—a healthy thirty-year-old athlete and surgical resident—had suffered a rare and life-threatening stroke. Next thing Allison knew, she was sitting alone in the ER in Fargo, North Dakota, waiting to hear if her husband would survive the night.

When Dave woke up, he could not carry memories from hour to hour, much less from one day to the next. Allison had lost the Dave she knew and loved when he lost consciousness on the plane. Within a few months, she found herself caring for both a newborn and a sick husband, struggling with the fear of what was to come.

As a way to make sense of the pain and chaos of their new reality, Allison started to write daily letters to Dave. Not only would she work to make sense of the unfathomable experiences unfolding around her, but her letters would provide Dave with the memories he could not make on his own. She was writing to preserve their past, protect their present, and fight for their future. Those letters became the foundation of this beautiful, intimate memoir. And in the process, she fell in love with her husband all over again.

This is a manifesto for living, an ultimately uplifting story about the transformative power of faith and resilience. It’s a tale of a man’s turbulent road to recovery, the shifting nature of marriage, and the struggle of loving through pain and finding joy in the broken places.

Praise for Beauty in the Broken Places

“Bold and commendable . . . A strength of this memoir is [Allison Pataki’s] scrupulous honesty.”—USA Today

“A memoir about . . . determination and gratitude, and the value of putting one foot in front of another during a crisis.”—The Washington Post

“Heart-wrenching.”—Women’s Health

“Powerful and immersive . . . Pataki delivers an insightful look at how two people faced a life-altering test as a team ‘fighting to make the dreams of our future possible.’”—Publishers Weekly (starred review)
Sunday Times bestselling author and foster carer Casey Watson’s inspiring memoirs Mummy’s Little Helper and Little Prisoners combined in a single volume with her deeply moving latest title Breaking the Silence, about two troubled little boys who both desperately need a loving home, and find comfort and friendship in the most unlikely of places.

Breaking the Silence is the true story of Jenson, a nine-year-old boy who has been left home alone while his mother goes on holiday, and Georgie, who has been living in a children’s home since he was a toddler and is autistic. Both boys are about to become members of the Watson family and test Casey to her limits. Are their differences unreconcilable?

When Casey takes in two innocent and frightened ‘unfosterable’ children who do not know what it means to be loved in Little Prisoners, she is shocked by the levels of neglect that the pair have been subjected to. Casey is desperate to help these poor, lost children, who have been taken away from their family because they were considered at risk, but before she can even start to understand the horrific things that have happened in the past, she has to teach them the most basic of behaviours.

Ten-year-old Abigail is Mummy’s Little Helper, a child left to cope alone since she was 3 with her mother who has progressive multiple sclerosis. She’s suddenly no longer invisible to the care system, and needs support, but the emotional strain of her total change in circumstances starts to show when she arrives at Casey’s home. She doesn’t know how to cope without huge burdening responsibility. Casey is determined to find solution for this brave girl.

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