The authors meticulously provide information gathered from their experiences working with schools, educational agencies, and organizations across the United States and Canada and show how school leaders can:Gain a personal understanding of what cultural proficiency means in practice Use collaborative activities to effect change in a school Lead a learning community toward becoming a culturally proficient organization

    Yet many who travel this path discover rich, unexpected rewards along the way. In this candid and poignant collection of personal stories, sixty-three mothers describe the gifts of respect, strength, delight, perspective, and love, which their child with Down syndrome has brought into their lives. perspectives, and draw from a wide spectrum of ethnicity, world views, and religious beliefs. Some are parenting within a traditional family structure; some are not. Some never considered terminating their pregnancy; some struggled with the decision. Some were calm at the time of diagnosis; some were traumatised. Some write about their pregnancy and the months after giving birth; some reflect on years of experience with their child. Their diverse experiences point to a common truth: the life of a child with Down syndrome is something to celebrate. These women have something to say - not just to other mothers but to all of us.

    But whatever precautions Brenda Serotte was subjected to, they were not enough. Shortly before her eighth birthday, in the fall of 1954, she came down with polio—painfully singled out in a world already marked by differences. Her bout with the dreaded disease is at the heart of this poignant and heartbreakingly hilarious memoir of growing up a Sephardic Jew among Ashkenazi neighbors in the Bronx. This was a world of belly dancers and fortune tellers, shelter drills and vast quantities of Mediterranean food; a world of staunchly joined and endlessly contrary aunts and uncles, all drawn here in loving, merciless detail. The Fortune Teller’s Kiss is a heartfelt tribute to a disappearing culture and a paean to the author’s truly quirky clan, especially her beloved champion, her father. It is also a deft and intimate cultural history of the Bronx fifty years ago and of its middle-class inhabitants, their attitudes toward contagious illness, womanly beauty, poverty, and belonging.

    In the midst of the overwhelming struggles that accompanied autism, he continues to persevere. Her father’s love enabled her to overcome insurmountable obstacles, discovered the power of love and embraced the gift of life.

    His girlfriend’s father hates him and his own parents’ opinion of him isn’t much better.Broke and down on his luck, Sebastien robs a grocery store, making off with nearly $4,000. His image is all over the television within hours, but before Sebastien can be arrested, a drunk driver smashes into his Jeep in the middle of town. Things couldn’t get much worse until a Marine recruiter who witnesses the accident gives Sebastien a ride home…and a way out.Embarking on an unexpected journey, the Marine Corps shows Sebastien another world—of abuse and authority, of war and compassion, of lust and consequences—and by the time he returns home, he’ll be forever changed.

    Arguing that as the elderly lose contact with the outside world, they turn inward and to the past to work through unresolved emotional issues from their lives, Naomi Feil presents her method for therapeutically dealing with patients with Alzheimer's and other dementias.

    Perfect for fans of When Breath Becomes Air.In 1990, Robert K. Brown was an ordinary college student studying abroad in England when a series of unexpected and extraordinary events would change the trajectory of his life forever. Choosing to ignore ominous early symptoms, he was still troubled enough to write in his journal "just for the record ... I am frightened because things are happening to me that I can’t explain away."What follows is a race against time to return home to Seattle for months of chemotherapy, countless complications, and a search for as much normalcy as possible when you're forced to face your mortality at twenty."While memoirs of surviving disease are plenty, Hundred Percent Chance stands apart through its genuine humor and unflinching portrayal of both the physical and psychological struggles that accompany a diagnosis of disease. Brown avoids inspirational platitudes, instead demonstrating the need for perspective and perseverance in the face of illness."Every person Brown introduces, whether their role is significant or small, will leave a memorable impression on readers. This memoir's focus on the tiny moments that ultimately shape and define a life, are particularly poignant and engrossing" (The BookLife Prize).10% of all proceeds will benefit The Leukemia & Lymphoma Society.

    On a spring night in 2010, Noel Holston, a journalist, songwriter, and storyteller, went to bed with reasonably intact hearing. By dawn, it was gone, thus beginning a long process of hearing-restoration that included misdiagnoses, an obstinate health-insurance bureaucracy, failed cochlear-implant surgery, and a second surgery that finally worked. He negotiated the gauntlet with a wry sense of humor and the aid of his supportive wife, Marty. Life After Deaf details his experience with warmth, understanding, and candor. It’s the story not only of his way back to the world of the hearing, but of a great marriage that weathered serious testing. Their determination and resilience serve as a source of inspiration for all.Life After Deaf is not just for the more than forty million people in the United States alone who cope with some form of hearing loss, but is also for their wide circles of friends, family, caregivers, and audiologists. This highly readable book will be an invaluable guide and source of hope for the large number of baby boomers now handling hearing loss.

    But what if the person receiving the diagnosis--young, physically fit, poised for a bright future--is himself a doctor?At thirty-one David biro has just completed his residency and joined his father's successful dermatology practice. Struck with a rare blood disease that eventually necessitates a bone marrow transplant, Biro relates with honesty and courage the story of his most transforming journey. He is forthright about the advantages that his status as a physician may have afforded him; and yet no such advantage can protect him from the anxiety and doubt brought on by his debilitating therapies. The pressures that Biro's wild "one hundred days" brings to bear on his heretofore well-established identity as a caregiver are enormous--as is the power of this riveting story of survival.

    Just a few years later, a doctor refused to believe such a diagnosis could ever have been given to this healthy, happy boy. This is the true story of how Jonah's mother, Christina, seized his limited window of opportunity for recovery. Detailing how she utilized a combination of a special diet and one-on-one tutoring with speech therapists and behavioral psychologists, Christina shares the entire journey she undertook to give her child a second chance at a full life.

    He's out of work, he's been through a breakup, and now his friends are kicking him out of the house. Little does he expect how much his life will change when he answers an ad in the newspaper for a position as a caretaker to a cantankerous, neurotic writer. This book contains sexually explicit content not suited for those under the age of 18. The book is approximately 35,000 words, has a happy ending and does not end in a cliffhanger. There is a free bonus chapter that can be obtained at the end of the book. However, the bonus chapter is not required to finish the book.

    Tortured by the ghost of a fallen Marine, he is faced with the truth, it may be too late for the ones he loves. Hell is cold, and Death stands at the end of his road, the Korean Road.