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Victoria's day
By Maria de Fatima Campos. 2007
Follows a day in the life of a child who has Down's syndrome, showing her with family and friends in…
day-to-day situations, including eating breakfast, going to school, and cooking. Grades K-3. 2007.My mom's having a baby!
By Dori Hillestad Butler, Carol Thompson. 2005
Elizabeth's mom is having a baby, and the whole family is involved. Elizabeth learns all about the baby's development, and…
she traces his growth, month by month. She learns how the baby got inside Mom, too. Finally the big day comes - Mom and Dad head off to the hospital, and soon there's a brand-new little person in the family! Grades 2-4 and older readers. 2005.Tout savoir sur la préménopause
By John R Lee. 2007
"Le docteur John R. Lee a révolutionné l'approche des problèmes de santé de la femme en décrivant l'importance de l'équilibre…
hormonal, notamment entre oestrogènes et progestérone. Il a également été l'un des premiers à mettre en garde contre les effets secondaires des progestatifs de synthèse, à souligner l'influence de l'environnement et du mode de vie sur cet équilibre, et à proposer des solutions naturelles pour remédier à ces problèmes. Dans ce nouvel ouvrage destiné au grand public, il s'est assuré la collaboration du Dr Jesse Hanley, une spécialiste de la médecine holistique (nutrition, plantes, psychosomatique), et de Virginia Hopkins, une journaliste spécialisée dans la santé. S'adressant à toutes les femmes de trente à cinquante ans, il explique clairement le mécanisme hormonal et son implication dans un ensemble de troubles, bénins ou graves, qui surviennent bien avant la période de la ménopause : troubles gynécologiques, syndrome prémenstruel, fatigue, prise de poids, perte de la libido, maux de têtes, cancer du sein... [...]" -- 4e de couvUn cri obscur: l'énigme des enfants autistes
By Denys Ribas. 1992
Les troubles d'apprentissage: comprendre et intervenir (Parents. Éducation et société)
By Denise Destrempes-Marquez. 1999
Les troubles dapprentissage touchent 10 % à 15% de la population. Ils ne sont pas dus à un déficit de…
lintelligence, mais plutôt à des difficultés dans lacquisition et le traitement de linformation. Peut-on imaginer la frustration de lenfant qui narrive pas à faire ses apprentissages au même rythme que ses camarades de classe? Peut-on concevoir linquiétude des parents qui ne comprennent pas la situation et qui ne savent pas comment intervenir? Ce guide fournira aux parents des moyens concrets et réalistes pour mieux jouer leur rôle. -- 4e de couvMénopause, nutrition et santé
By Louise Lambert-Lagacé. 2004
Enfin un livre destiné à toutes les femmes qui font confiance à la vie et qui désirent mieux vivre leur…
ménopause grâce à une alimentation bien adaptée. Certains aliments aident en effet à contrer les bouffées de chaleur, les ballonnements, les pertes d'énergie et les problèmes de poids. En outre, plusieurs aliments et suppléments peuvent diminuer les risques d'ostéoporose, de maladies cardio-vasculaires ou de cancer du sein.Still: A Memoir of Love, Loss, and Motherhood
By Emma Hansen. 2020
“Still is one of those rare books that catches you up and does not let you go. With grace, courage,…
and honesty, Emma Hansen adds an important voice to this tragic and too-often silenced subject. I loved this book.” —Beth Powning, author of Shadow Child: An Apprenticeship in Love and Loss A moving, candid account of one woman’s experience with stillbirth.Emma Hansen is 39 weeks and 6 days pregnant when she feels her baby go quiet inside of her. At the hospital, her worst fears are confirmed: doctors explain that her baby has died, and she will need to deliver him, still.Hansen gives birth to her son, Reid, amidst an avalanche of grief. Nine days later, she publishes a candid essay on her website sharing photos from the delivery room. Much to her surprise, her essay goes viral, sparking positive reactions around the world. Still shares what comes next: a struggle with grief and confusion alongside a desire to better understand stillbirth, which is experienced by more than two million women annually, but rarely talked about in public.At once honest, brave, and uplifting, Still is about one woman’s search for her own definition of motherhood, even as she faces one of life’s greatest challenges: learning to live after loss.Sitting Pretty: The View from My Ordinary Resilient Disabled Body
By Rebekah Taussig. 2020
A memoir-in-essays from disability advocate and creator of the Instagram account @sitting_pretty Rebekah Taussig, processing a lifetime of memories to…
paint a beautiful, nuanced portrait of a body that looks and moves differently than most.Growing up as a paralyzed girl during the 90s and early 2000s, Rebekah Taussig only saw disability depicted as something monstrous (The Hunchback of Notre Dame), inspirational (Helen Keller), or angelic (Forrest Gump). None of this felt right; and as she got older, she longed for more stories that allowed disability to be complex and ordinary, uncomfortable and fine, painful and fulfilling.Writing about the rhythms and textures of what it means to live in a body that doesn’t fit, Rebekah reflects on everything from the complications of kindness and charity, living both independently and dependently, experiencing intimacy, and how the pervasiveness of ableism in our everyday media directly translates to everyday life. Disability affects all of us, directly or indirectly, at one point or another. By exploring this truth in poignant and lyrical essays, Taussig illustrates the need for more stories and more voices to understand the diversity of humanity. Sitting Pretty challenges us as a society to be patient and vigilant, practical and imaginative, kind and relentless, as we set to work to write an entirely different story.This is an inclusive, nonjudgmental, and empowering guide to pregnancy, childbirth, and postpartum life that puts mothers first, offering straightforward…
guidance on all the options and issues that matter most to them and their partners when preparing for a babyUn espace entre les mains: récit
By Émilie Choquet. 2020
Frondeuse et brillante, une jeune femme se prépare à ajouter un élément à la liste de ses réalisations : avoir…
un enfant. Tout au long de la grossesse, la maternité a fait lobjet d'une préparation minutieuse. Les projets ne manquent pas pour remplir de moments magiques le temps avec le bébé. Mais dès l'accouchement, où le scénario prévu ne se réalise pas, le savoir accumulé pendant des mois se retourne contre la mère. Le corps et lesprit, apprend-elle, n'agissent pas toujours de concert. De retour à la maison, la nouvelle mère fait face à la fatigue qui s'accumule et à des journées où s'enchaînent séances d'allaitement, bercements, changements de couche. Malgré ses efforts pour éviter que la situation ne lui échappe, des failles apparaissent partout. Dans l'espace qui se creuse entre sa perception du monde et le réel, sa raison s'égare peu à peu. L'hospitalisation devient nécessaire. On ne sait ni quand ni comment elle parviendra à sortir de la boucle temporelle dont elle est prisonnière. Ce sera à elle de trouver à tâtons la voie hors du labyrintheStill: A memoir of love, loss, and motherhood
By Emma Hansen. 2020
A moving, candid account of one woman's experience with stillbirth. Emma Hansen is 39 weeks and six days pregnant when…
she feels her baby go quiet inside of her. At the hospital, her worst fears are confirmed: doctors explain that her baby has died, and she will need to deliver him, still. Hansen gives birth to her son, Reid, amidst an avalanche of grief. Nine days later, she publishes a candid essay on her website sharing photos from the delivery room. Much to her surprise, her essay goes viral, sparking positive reactions around the world. Still shares what comes next: a struggle with grief and confusion alongside a desire to better understand stillbirth, which is experienced by more than two million women annually, but rarely talked about in public. At once honest, brave, and uplifting, Still is about one woman's search for her own definition of motherhood, even as she faces one of life's greatest challenges: learning to live after lossOne in five people in the United States lives with a disability. Some disabilities are visible, others less apparent—but all…
are underrepresented in media and popular culture. Now, just in time for the thirtieth anniversary of the Americans with Disabilities Act, activist Alice Wong brings together this urgent, galvanizing collection of contemporary essays by disabled people. From original pieces by up-and-coming authors like Keah Brown and Haben Girma, to blog posts, manifestos, eulogies, Congressional testimonies, and beyond: this anthology gives a glimpse into the rich complexity of the disabled experience, highlighting the passions, talents, and everyday lives of this community. It invites listeners to question their own understandings. It celebrates and documents disability culture in the now. It looks to the future and the past with hope and lovePrecious Cargo: My Year of Driving the Kids on School Bus 3077
By Craig Davidson. 2018
NATIONAL BESTSELLERFor readers of Kristine Barnett's The Spark, Andrew Solomon's Far From the Tree and Ian Brown's The Boy in…
the Moon, here is a heartfelt, funny and surprising memoir about one year spent driving a bus full of children with special needs.With his last novel, Cataract City, Craig Davidson established himself as one of our most talented novelists. But before writing that novel and before his previous work, Rust and Bone, was made into a Golden Globe-nominated film, Davidson experienced a period of poverty, apparent failure and despair. In this new work of riveting and timely non-fiction, Davidson tells the unvarnished story of one transformative year in his life and of his unlikely relationships with a handful of unique and vibrant children who were, to his initial astonishment and bewilderment, and eventual delight, placed in his care for a couple of hours each day--the kids on school bus 3077. One morning in 2008, desperate and impoverished while trying unsuccessfully to write, Davidson plucked a flyer out of his mailbox that read, "Bus Drivers Wanted." That was the first step towards an unlikely new career: driving a school bus full of special-needs kids for a year. Armed only with a sense of humour akin to that of his charges, a creative approach to the challenge of driving a large, awkward vehicle while corralling a rowdy gang of kids, and unexpected reserves of empathy, Davidson takes us along for the ride. He shows us how his evolving relationship with the kids on that bus, each of them struggling physically as well as emotionally and socially, slowly but surely changed his life along with the lives of the "precious cargo" in his care. This is the extraordinary story of that year and those relationships. It is also a moving, important and universal story about how we see and treat people with special needs in our society.An inspiring story of beating the odds and learning to overcome--no matter what life hands you.After starting a family and…
flourishing in his career, Tim Hague was struck by misfortune. The irritating tremor in his foot turned out to be early onset Parkinson's disease. He was only 46 years old. But what seemed to be an end became a new beginning. Just three years later, Hague won the inaugural The Amazing Race Canada (with his son, Tim Jr., as his teammate). His remarkable life story shows that perseverance is not just a matter of willpower: it is a skill that can be learned and honed. And perseverance is the theme of his life. From the day he was born, Hague has gone from one struggle to another. Yet, remarkably, he doesn't have a trace of self-pity. In fact, he feels blessed. From his tough start in life as an unwanted mixed-race baby born in Texas in 1964, to his eventual move to the unforgiving climate of Winnipeg, Canada, to start a family under difficult circumstances, and his continuing battle with Parkinson's--Hague's life is a roadmap of perseverance. Parkinson's has forced him to retire early from the work he loves as a registered nurse. But as a healthcare professional, and now suffering from a challenging disease himself, Hague discusses living with Parkinson's like no one else could. He now works with charities to help promote Parkinson's awareness and his "Live Your Best" message. Drawing on his experience winning The Amazing Race, and referencing cutting-edge research and studies, Hague weaves a moving story of failure and success, outlining the elements of his philosophy that anyone can apply to their own lives, including: * The nature of luck: Luck comes to those who keep trying until the end--never stop until the race is over. * Find community: As a nurse, a husband and father, and a man living with Parkinson's, Hague knows better than most that we all need to ask for help sometimes, and that's a good thing. * Accept limits: By focusing on what we can do, we accomplish more than we ever thought possible. * Cease striving: We think of striving as a positive attribute, but all we end up doing is banging our heads against the wall. Have goals, but have fun. Do not create anxiety out of nothing and maintain perspective. * Live Your Best: No such thing as giving 110%--can only do your best. Inspirational and entertaining, Hague's message is both simple and profound: perseverance isn't just something a person has, or a trait we admire in others. Hague's book, like his life, is a guide to how we can all learn to persevere in the face of daily struggles--or even life-changing illness.Haben: The deafblind woman who conquered harvard law
By Haben Girma. 2019
This is the incredible life story of Haben Girma, the first deafblind graduate of Harvard Law School, and her amazing…
journey from isolation to the world stage. Haben grew up spending summers with her family in the enchanting Eritrean city of Asmara. There, she discovered courage as she faced off against a bull she couldn't see, and found in herself an abiding strength as she absorbed her parents' harrowing experiences during Eritrea's thirty-year war with Ethiopia. Their refugee story inspired her to embark on a quest for knowledge, traveling the world in search of the secret to belonging. She explored numerous fascinating places, including Mali, where she helped build a school under the scorching Saharan sun. Her many adventures over the years range from the hair-raising to the hilarious. Haben defines disability as an opportunity for innovation. She learned nonvisual techniques for everything from dancing salsa to handling an electric saw. She developed a text-to-braille communication system that created an exciting new way to connect with people. Haben pioneered her way through obstacles, graduated from Harvard Law School, and now uses her talents to advocate for people with disabilities. Haben takes listeners through a thrilling game of blind hide-and-seek in Louisiana, a treacherous climb up an iceberg in Alaska, and a magical moment with President Obama at the White House. Warm, funny, thoughtful, and uplifting, this captivating memoir is a testament to one woman's determination to find the keys to connectionTout est possible!: André Leclerc, fondateur de Kéroul
By René Kirouac. 2020
À la suite d’une erreur médicale, André Leclerc naît avec une paralysie cérébrale. Jeune adulte, André ambitionne de travailler «…
comme tout le monde », de se marier et de fonder une famille, mais on le traite de rêveur et on s’efforce de le convaincre que ce n’est pas pour lui. Pourtant, il réussira! Il aura deux enfants et, contre vents et marées, il fondera Kéroul, une organisation aujourd’hui reconnue au Québec et ailleurs dans le monde. Son but : rendre le tourisme et la culture accessibles aux personnes à capacité physique restreinte. Découvrez comment, grâce à sa détermination hors du commun, André Leclerc a transformé son combat individuel en service collectif, et comment il a su s’entourer de gens formidables pour mener à bien ses projets.The new rules of pregnancy: what to eat, do, think about, and let go of while your body is making
By Danielle Claro, Adrienne L. Simone, Jaqueline Worth. 2020
Finally, a calming pregnancy book that cuts through the noise to tell expectant mothers exactly what they need to know-and…
what they can stop obsessing about and over-researching. In The New Rules of Pregnancy, two leading OB-GYNs guide you, the modern pregnant woman, through all aspects of pregnant life in an easy-to-digest, compassionate, and motivating way. Instead of a detailed week-by-week look at your baby's development, it's all about you and how to help your pregnancy go as smoothly as possible. It assumes an intelligent, busy listener (who, somewhere inside, is shouting, "Just tell me what to do!"). Every aspect of pregnant life is covered-from the practical details (how to fly pregnant) to the complex issues ("What makes it postpartum depression?"). The book also covers that critical "fourth trimester"-"Nursing" and "How to Feel Like Yourself Again"-because once the baby is born, self-care typically goes out the window, and you really need someone to have your back. Its strong point of view and expertise come from gynecologist Adrienne Simone and obstetrician Jaqueline Worth-two renowned New York doctors dedicated to bringing patients the safest, calmest, least invasive pregnancies possible. The book's voice-motivating, supportive, real-comes from Danielle Claro, coauthor of The New Health RulesA sporting chance: how Ludwig Guttmann created the paralympic games
By Lori Alexander. 2020
Telling the inspiring human story behind the creation of the Paralympics, this young listener's biography showcases a riveting narrative to…
honor the life of Ludwig Guttmann, whose work profoundly changed so many lives. Dedicating his life to helping patients labeled incurables, Ludwig Guttmann fought for the rights of paraplegics to live a full life. The young doctor believed-and eventually proved-that physical movement is key to healing, a discovery that led him to create the first Paralympic Games. Told with moving text, and featuring the life stories of athletes from the Paralympic Games Ludwig helped create, this story of the man who saved lives through sports will inspire listeners of all backgroundsSuch a pretty girl: a story of struggle, empowerment, and disability pride
By Nadina LaSpina. 2020
This is Nadina LaSpina's story-from her early years in her native Sicily, where she contracts polio as a baby, a…
fact that makes her the object of well-meaning pity and the target of messages of hopelessness, to her adolescence and youth in America, spent almost entirely in hospitals where she is tortured in the quest for a cure and made to feel that her body no longer belongs to her and to her rebellion and her activism in the disability-rights movement. LaSpina's personal growth parallels the movement's political development-from coming together, organizing, and fighting against exclusion from public and social life to the forging of a common identity, the blossoming of disability arts and culture, and the embracing of disability pride. While unique, LaSpina's journey is also one with which many disabled people can identify. It is the journey to find one's place in an ableist world-a world not made for disabled people, where disability is only seen in negative terms. LaSpina refutes all stereotypical narratives of disability. Through the telling of her life's story, without editorializing, she shows the harm that the overwhelming focus on pity and on a cure that remains elusive has done to disabled people. Her story exposes the disability prejudice ingrained in our sociopolitical system and denounces the oppressive standards of normalcy in a society that devalues those who are different and denies them basic rightsMy Own Blood: A Memoir
By Ashley Bristowe. 2021
Mothering under normal circumstances takes all you have to give. But what happens when your child is disabled, and sacrificing…
all you've got and more is the only hope for a decent future? Full of rage and resilience, duty and love, Ashley Bristowe delivers a mother's voice like no other we've heard. When their second child, Alexander, is diagnosed with a rare genetic disorder, doctors tell Ashley Bristowe and her husband that the boy won't walk, or even talk--that he is profoundly disabled. Stunned and reeling, Ashley researches a disorder so new it's just been named--Kleefstra Syndrome--and she finds little hope and a maze of obstacles. Then she comes across the US-based "Institutes," which have been working to improve the lives of brain-injured children for decades. Recruiting volunteers, organizing therapy, juggling a million tests and appointments, even fundraising as the family falls deep into debt, Ashley devotes years of 24/7 effort to running an impossibly rigorous diet and therapy programme for their son with the hope of saving his life, and her own. The ending is happy: he will never be a "normal" boy, but Alexander talks, he walks, he swims, he plays the piano (badly) and he goes to school.This victory isn't clean and it's far from pretty; the personal toll on Ashley is devastating. "It takes a village," people say, but too much of their village is uncomfortable with her son's difference, the therapy regimen's demands and the family's bottomless need. The health and provincial services bureaucracy set them a maddening set of hoops to jump through, showing how disabled children and their families languish because of criminally low expectations about what can be done to help.My Own Blood is an uplifting story, but it never shies away from the devastating impact of a baby that science couldn't predict and medicine couldn't help. It's the story of a woman who lost everything she'd once been--a professional, an optimist, a joker, a capable adult--in sacrifice to her son. An honest account of a woman's life turned upside down.