Títulos em Pessoas com Deficiências

Weeks after giving birth, Holly Frances went from being a healthy 26-year-old new mom to paralyzed and on life support—in less than 72 hours. Diagnosed with a rare autoimmune disorder called Guillain-Barre Syndrome, Holly was trapped in her body, unable to move, speak, or hold her newborn daughter. Life Support tells the story of how Holly struggled to overcome the despair, hopelessness and physical pain, to regain her health and get back to being a mother to her daughter.

The yard was a huge piece of property with a forest out back (or at least a few dozen trees). We had a barn and a horse (really a very small pony, but I didn’t know that then) named Romeo, because he liked to roam—often ending up out of the fenced pasture and out on the street. We had chickens, as well, in a coop by the barn up at the edge of the forest.

Af's journey starts from the exhilaration of the Rio 2016 Olympic Games to confronting a tumour diagnosis at 29. An unexpected return to the UK meant trading Olympic thrills for surgeries and chemotherapy. This isn't just a tale of medical battles but family relationships, friendships and positivity. Af shared his journey on social media with an unfiltered look into the world of cancer treatment. Set against the vibrant backdrop of Brazil and the medical corridors of UK hospitals, Af's tale is one of resilience, humour, and hope.

Embark on an extraordinary odyssey through the seasons of life in "MY MIRACULOUS HEALING JOURNEY," an engrossing memoir that goes beyond the confines of everyday life. In the spring of 2014, the author was looking forward to a new phase in his consulting career and the arrival of a grandchild. The author did not foresee the darkness that would soon envelope his path, setting the stage for a journey of resilience, faith, miracle, self-discovery, and holistic healing.

»Ich bin blind. Na und?« Dies ist das Motto der 47jährigen Sylvia, die sich trotz so mancher Rückschläge und unerwarteter Wendungen in ihrem Leben nicht unterkriegen lässt. In ihrer Autobiographie führt sie den Leser zu den wichtigen Stationen auf ihrem bisherigen Lebensweg, beispielsweise ihr Elternhaus und verschiedene Internatsschulen. Mit großer Offenheit spricht sie über Höhen und Tiefen und wie sie damit umgegangen ist. Humorvoll und einfühlsam berichtet sie über ihre Erfahrungen in Schule, Beruf und Familie, mit Freunden und in der Liebe.

Samantha Matthews was born in Texas in 1996. Not long after her birth, she was diagnosed with cerebral palsy. As a child living with this disability, she had to learn how to overcome many obstacles in life. As the years progress, she grew in determination and resilience to live her best life. Everyone has their struggles and challenges in life. It can be difficult to get people to see the person behind a disability.

Her Name Was Lola is the story of Trish Ryan’s triumphant recovery from a stroke that should have killed her. She had a successful career in the entertainment industry for over 30 years until May 5th, 2017, when she suffered a severe stroke that changed her life forever. Living a very fast-paced life had not prepared her for when it all came to a grinding halt. Lost and confused with no roadmap to follow, she relied on her faith to show her the way to embrace what happened and move forward.

A moving story about how autism and a shared appreciation for superheroes brought two brothers together. Author Josh Stehle learned everything he knows about superheroes from his older brother and best friend, Zach. From the worlds they live in, to the writers who created them, and studios who produced them--Zach is an expert in all things superhuman and heroic. He is also on the autistic spectrum.

These are a collection of new poems and some poems taken from the vault of Timothy Paul Brown. As usual they express the trials and tribulations, the glory and the pain, the grandiosity and obsession, the paranoid deluded thinking that come with having a paranoid schizophrenic disability. There is so much intensity and passion exhibited in this work of art. The author will take you to places you have never been in mind and spirit. You will feel empathy and compassion probably some sympathy. But these poems are not meant to make its listeners feel sorry for the author.

When Jim Sayre was a totally blind child growing up in Zanesville, Ohio, in the 1940s and '50s, blind children were typically steered into occupations caning chairs or tuning pianos. "Or selling pencils on street corners," Jim says. No way he was going to settle for that. With the help of a loving mother who saw the wisdom of integrating a blind child into the sighted world and Jim's own innate determination--he might call it stubbornness--Jim overcame the obstacles and prejudices blind children faced in those times.

In the haunting reality captured in this audiobook, a 13-year-old soul finds himself ensnared within the harrowing confines of a nightmarish residential treatment facility. In those 60 days, his very humanity teetered on the edge, threatened to be torn asunder. This raw and unflinching account paints a vivid portrait of a young spirit's resilience and the chilling depths of human suffering.

Already facing a wretched cancer diagnosis, a young man’s prospects for survival dim as he learns his treatments have not worked. Writing against the clock, he feverishly authors a story of profound joy and sadness exploring the life he could have lived. Desperately told, his story takes you through poignant memories, intimate relationships, and fantastical triumphs in a quest to make sense of it all and leave a legacy behind.

Embark on a transformative journey with Afi Sevor in "The Manual That Did Not Come With You." Through candid life stories, Sevor unveils the secrets to creating your life manual, guiding you through the art of self-love, effective planning, and embracing personal growth. Discover the profound impact of consistency, the wisdom of delegation, and the transformative power of sharing responsibilities. As you navigate the audio , you'll be inspired to craft your own life manual.

Lillian was a college freshman, a promising theater major facing the challenge of Stargardt’s disease, a condition that was causing her to go blind. When, in the fall of 2009, Lillian became sick, she assured her parents it was just the flu. Four days later she was in the university hospital, relying on a machine to breathe for her. Based on her father’s journal, this memoir describes what it’s like to live through a parent’s worst nightmare, conveying the heart-wrenching ups and downs of Lillian’s time in the hospital.

Kamata's adventures with her teen—who happens to be deaf, with cerebral palsy, and in a wheelchair—through subterranean Tennessee, to the islands of Japan, and to the top of the Eiffel Tower ultimately lead to a daughter's increasing independence, a mother letting go of expectations, and advocacy for travel which prohibits discrimination.

Ife Thomas’ Five Life Lessons from a Motivational Speaker’ is a deeply personal and inspiring journey through the author’s life challenges and triumphs. Ife shares her experiences of overcoming obstacles as a neurodiverse individual, from childhood rejection and grappling with an undiagnosed autism spectrum disorder to professional setbacks and personal growth. Her book weaves powerful narratives from her life with practical, actionable steps for personal development.

Sixteen-year-old Alex Noble was a high school rugby star with a promising sporting career ahead of him when an on-field injury left him fighting for his life in the ICU. Following a four-day coma and a diagnosis of C4 quadriplegia, Alex’s first words to his brother Zac were, ‘If I fight, you fight.’ These words became a war cry as Alex’s friends, family and community rallied around him, watching in awe as he fought to regain control over his body and defy his diagnosis.

Driving Myasthenia Gravis Into Remission is a book based on the personal beliefs and experiences of the author Romerol Stanton regarding the autoimmune neurological disorder Myasthenia Gravis. It is a book that provides information on all-natural and alternative treatments that have been effective in alleviating the symptoms of Myasthenia Gravis. This book also gives insight into the author's trials, tribulations and triumphs living with Myasthenia Gravis.

Marian Schembari was thirty-four years old when she learned she was autistic. By then, she’d spent decades hiding her tics and shutting down in public, wondering why she couldn’t just act like everyone else. Therapists told her she had Tourette’s syndrome, obsessive-compulsive disorder, sensory processing disorder, social anxiety, and recurrent depression. They prescribed breathing techniques and gratitude journaling. Nothing helped. It wasn’t until years later that she finally learned the truth: she wasn’t weird or deficient or moody or sensitive or broken. She was autistic.

Learning disabilities (LD) are a root cause of major problems in our society. Vast numbers of youngsters are not receiving appropriate education. Nancy Lelewer’s story began when even less was known about learning disabilities than is known today. In a gripping and fast-moving narrative style, this audiobook brings home the fact that LD persons need to receive instruction via different routes and the earlier the better.