Títulos em Pessoas com Deficiências

"Dandelion Roots Run Deep" is the true story of three generations of tenacious Midwestern women, one in Illinois and two in Michigan. Merry is the third generation, and her mother Merrill, fought for organic agriculture and Michigan's environment from 1967 - 2009. Merrill developed Alzheimer's before finishing her book, so Merry took her story to fruition.

Sumérgete en la extraordinaria vida de Gerardo Schmedling, un hombre cuyo poder espiritual inquebrantable desafió las adversidades de la parálisis de Guillain-Barré en su juventud y las secuelas que afectaron su movilidad de por vida. Este relato, narrado por su prima María Mercedes Olivares Schmedling, conocida como Mechas, quien compartió con él desde su infancia, revela cómo Gerardo se convirtió en el arquitecto de un movimiento global de transformación personal y social.

With evocative storytelling and incisive research, Katie Rose Guest Pryal brings a new eye to the mental health crisis that higher education has faced for decades. Written from the perspective of a bipolar-autistic professor, A Light in the Tower is both a bracing account of the mental health crisis in higher education and a passionate and informed proposal for how to teach with mental health in mind. Pryal contends that higher education's mental health crisis is the result of long-term systemic problems in education that demand nothing short of a revolution.

Elaine, What Happened? A History follows the thirty year life of Elaine who was born without eyes and had other deformities. Besides trying to find out what caused her defects, it is a history of the changes that took place in the medical field, in public education and most notably in society's customs and attitudes regarding people with disabilities.

Esta autobiografía cubre muchas facetas de la experiencia humana: raza, salud, discapacidad, religión, pobreza, inmigración, acceso a la atención médica, educación, derechos de las personas con discapacidades, aborto espontáneo, adopción y mucho más.

Sugar Mamas is a book of personal stories of women who have a condition called lipedema, which affects 11% of women in the world and results in often debilitating fat deposits in the legs, thighs, hips, arms and other areas. While lipedema is primarily a woman's disease, the research on the condition has only in the last five years really taken off, so the causes and treatments are still in early research stages.

When I was six years old, I started wearing glasses. My view of my low vision quickly changed when I was twenty years old and found out that my brother had suddenly gone blind. He was told that he was suffering from Retinitis Pigmentosa (RP), a disorder that slowly destroys the pigment cells in the eyes. So far, there are no known cures. At the tender age of twenty-one, I was also diagnosed with RP. Since then, I have been slowly going blind, not knowing when my world would finally fade away forever. Battling against such a crippling disease led me through a labyrinth of challenges.

This book is written by the husband of a stroke victim. The husband is the caregiver of 25 years to his wife in helping her in her battle to recovery from a massive stroke. It describes some of her challenges over the years and the tools that she has used to meet these challenges to make her life easier in the world that she knows of it today.

Pascuala Herrera, a Mexican immigrant woman with a physical disability resulting from childhood polio, had the odds against her, yet she conquered simply by working hard, having unfailing faith, and finding her own life purpose. Although her mother always told her that life was a valley of tears, Pascuala learned that although there were many difficult moments in her life, there were also beautiful miracles that happened every day.

What would you do if it happened to you? If you awoke one day when you were twelve years old to be informed that your life was suddenly over? Well . . . Here is what I did. If you became the wealthiest person you would ever know just three and a half years later? What would that be like? Well, this is what it was like when it happened to me.

Jessica Knight grew up on a dairy farm in rural Victoria, her crib next door to where all the cows were milked. It's a loving Mormon household, a god-fearing home. While they don't have very much, it's their values and good humor that allows them to laugh at what scares them. All young Jessica wants is to be good and make her parents and her Heavenly Father happy. She cleans the house and helps out with her siblings; all the while being subjected to intensive medical tests and major surgeries. Doctors consider her a puzzle and a medical mystery.

Born deaf and discovering encroaching blindness at the age of 16, Anthony Lawton’s future appeared to be full of locked doors. Prejudice. Delayed education. Distorted speech. Limited sight. But when benign strangers intercede and inner gifts reveal themselves the opportunity to pursue a childhood dream of speaking and participating in mainstream society become a realisable vision. He would need to do this before the consequences of dual sensory loss would again close the doors.

At the age of thirty-one, Dave Kelly lost his eyesight to a rare disease called retinitis pigmentosa (RP). Up until then, he had lived a life like any other young man, albeit one blessed to be growing up in Liverpool during the heyday of The Beatles and Liverpool FCs win against Leeds in the 1965 FA Cup. But then, one day everything changed. Dave was faced with a choice. He could either let blindness defeat him or he could face it head-on and live as fulfilling a life as he possibly could.

DEMENTIA and OUR LOVE, Caregiving as spiritual practice, is the story of Gary and Heather's love that sustained them through an unusual and courageous life across continents, including tending Gary and his onset of dementia at 73 years. The story helped them remember their love and use this energy to move through the hard times. We will always remember us this way, a song by Lady Gaga, was pivotal in keeping Heathers focus.

Join Onya Page as she gently guides you through the struggles of living with bipolar disorder II, helping you better understand mental health. This book explores a world of emotions through simple yet powerful poetry. With heartfelt verses, this collection offers comfort and companionship to those going through the process of their inner struggles. Through each poem, discover the courage to confront the shadows and embrace the light within.

A journey from darkness to acceptance is a raw and compelling memoir chronicling one woman's harrowing personal struggle with mental illness. When a severe psychotic break abruptly derails Elisa's stable life as a wife and mother, she finds herself plunged into an unpredictable world ruled by the terrifying whims of her mind. This powerful personal account traces Elisa's odyssey through the fragmented mental health system, oscillating from psychiatric holds to outpatient programs and back again as doctors struggle to control her volatile mood cycles.

You are more than your limits. Choosing to see herself as more than a person with a disability and wheelchair user, Lolo chooses to live a bold and courageous life now because representation matters. She created this intersectional guide to provide tools for people with disabilities to thrive in personal growth, independence, and community building. Add this guide to your list of inclusion books!

In this candid, humorous, and insightful book, author, political science lecturer, and “Dudeist Priest” Arch Grieve provides listeners with a first-hand account of the many lessons he has learned (often the hard way) as a person living with bipolar disorder. This guidebook is a must-listen for anyone who has recently been diagnosed with bipolar disorder or knows someone who has.

Splendid Agony is an informative, illuminating, and encouraging book that offers valuable insights for people with dyslexia, parents and teachers of people with dyslexia, and anyone who wants to know more about what it's like to go through the American educational system with dyslexia.

This book is a reflection of a mother’s experience when her daughter, after a sudden severe headache, was diagnosed with a torn brain aneurysm and arteriovenous malformation in the cerebellum. TJ, Evie’s brother, also shares his experience.