Títulos em Pessoas com Deficiências

A survivor of Guillain Barre Syndrome, this is the walk that led me to Tik-Tok. This audiobook recounts the events that molded me into the man that lived in your phones. Encouraged by friends and family that I had a story worth telling, I became a self-proclaimed autoimmune advocate on social media, whose ramblings captured the attention of fellow autoimmune, chronic illness, and chronic pain sufferers along the way.

My ACE (Adverse Childhood Experience) score is 6. According to numerous academic studies, that puts me at risk for over 23 negative health outcomes, including diabetes, cardiovascular, digestive, respiratory and liver disease, cancer, and mental health issues such as anxiety, depression and thoughts of suicide.

“Honey, you’ve been very ill and they’ve had to amputate…” His voice cracked. I searched his face, looking for some kind of clue to tell me why I sensed so much pain from him and in me. “…Your hands and feet.” Cyndi tried to grasp the new reality that flesh-eating disease had changed her life forever. Her recent memories of being a successful business manager and new mom seemed oceans away. It just couldn’t be true. I tried to speak, but no words came. Please God—let this be a dream.

Aos 22 anos, um acontecimento inesperado tornou Andrea Schwarz em uma pessoa com deficiência, desafiando seus sonhos e projetos para o futuro. Enfrentando as barreiras impostas pela sociedade, a autora transformou seus desafios em asas. Com coragem, disciplina e uma pitada de rebeldia, ela enfrentou as dificuldades e demonstrou que é possível construir uma vida admirável e alcançar realizações significativas.

I finished my first book, Multiple Sclerosis: A Blessing in Disguise, around the end of 1998. At that time, I was going through a lot of issues that I thought were very important to me. That book told of my discovery, my eventual acceptance of the illness, and how I dealt with what was happening to me. Like anybody else who is faced with the burden of discovery, I had a lot of questions that I felt I really needed to answer, but I never sought to answer why this had happened to me.

Written by Mark Holt-Rogers, a Wellbeing Specialist with over a decade of experience living with Parkinson’s, Shaken is one of the most insightful and practical Parkinson's audiobooks available today. Designed for patients, families, friends, and caregivers, this essential guide draws from Mark’s personal experiences and expertise to provide actionable strategies and emotional support for managing Parkinson’s disease.

"If you can dream it, you can do it!" - das ist bei Oliver Brünner keine Floskel. Dabei sah im Leben des heute erfolgreichen Speakers eigentlich alles ganz anders aus. Noch während seiner Geburt zieht sich die Nabelschnur seiner Mutter wie eine Schlinge um seinen Hals, weswegen er fortan mit einer spastischen Tetraparese lebt. Doch Oliver trotzt den vermeintlichen Widrigkeiten und kann heute auf einen Lebensweg zurückblicken, den dem schon früh als "Sorgenkind" titulierten Jungen wohl niemand zugetraut hätte. Seine Geheimwaffe: das Träumen.

Kathleen O’Neill courageously chronicles her journey through the turbulent realms of bipolar disorder, addiction, and recovery. With raw honesty and resilience, Kathleen shares the battles she fought within herself and against social stigmas, laying bare her struggles, triumphs, and the moments of grace that shaped her healing. This memoir offers a compelling look at the complex layers of mental health , the strength of the human spirit, and the transformative power of hope.

Life with Louie is a collection of coming-of-age stories about growing up with a brother who happens to have been born with Down syndrome. For the author, Mia Rotella-White, having a sibling with a disability never created hardship. The opposite is true. Growing up with Louie meant Mia’s days were full of disco balls, group hugs, fashion shows and dance parties. When adversity struck, and it did, the siblings reminded each other how ridiculous it was to think any tragedy could ever be bigger than their love.

An upcoming book to be published by Penguin Random House.

On a September night in Montreal in 1993, Curtis Pride got his first Major League hit, prompting a long, emotional standing ovation from the crowd of 45,757 fans. Profoundly deaf since birth, Pride couldn’t hear their thunderous applause. But as the cheers grew louder and more insistent, he realized he was feeling those vibrations within his chest—an undeniable acknowledgment of an extraordinary achievement.

Based on a true story, Stern by Name, Stern by Nature offers an unflinching and intimate portrayal of one of the UK's most promising and eminent philosophers. This groundbreaking work delves deep into the psyche of the protagonist as he navigates the tumultuous landscape of mental health struggles.

Rachael Kurgan is a young woman who has already experienced a lifetime's worth of trials and tribulations. From grappling with a disability from birth to the heartbreaking loss of both parents, she has already absorbed some of the most difficult blows that life can throw at a person. But through her faith in God, perseverance, and the support of friends and family, she has not only overcome all of these difficulties, but established a happy and thriving life.

Wayne Magee is on a mission to empower those who have been repeatedly told, “You can’t!” He has spent his life overcoming obstacles and negative labels intended to convince him that he could not lead a purposeful, fulfilled life. At birth, he was diagnosed with cleidocranial dysplasia, which is a rare genetic skeletal disorder that affects one in one million people. Countless medical professionals stated that he would not live beyond two years old. Wayne’s story demonstrates that for every tough blow, we have an innate ability to overcome societal and medical challenges.

Families who have supported a child with special needs will connect with this memoir about Sarah, a feisty girl with autism and a unique genetic blueprint. Her mom, Jenny, is equally feisty and determined, which leads her to make a commitment that dramatically changes her and Sarah’s lives—as well as those of many others.

While studying as a biology undergrad at UC Santa Cruz, Ian Mackay crashed his bike into a tree on campus. Paralyzed from the shoulders down, Mackay adapted to his new life with the help of his dedicated family, particularly his mother, Teena Woodward, and a group of quirky friends. After years of despair, and against all odds, he became an inspiring leader, an innovator with Apple, and a world-record-breaking athlete.

At the age of forty-three, Amy Lee Lillard learned she was autistic. She learned she was part of a community of unseen women who fell through the gaps due to medical bias and social stereotypes. A Grotesque Animal explores the making, unmaking, and making again of a woman with an undiagnosed disorder. How did a working-­class background and a deep-rooted Midwest culture of silence lead to hiding in plain sight for decades? How did sexuality and anger hide the roots of trauma among the women in her family?

Inside this moving true story, John Furniss, more famously known today as "The Blind Woodsman," along with his wife, inspiration, and fellow artist Anni share their amazing story with the mission to help and inspire others to pursue their own creative passions, regardless of the challenges they may face. The Blind Woodsman is a compelling true story that will give hope and inspiration to those dealing with disabilities, mental health struggles, addiction, chronic illness, and the anxieties and stresses in our everyday lives.

Have you ever had everything you set out to do doubted and questioned by others? Have you ever felt pressed down by the weight of others’ doubts so much that they tried to move in and overshadow your abilities? Life is not complete if you feel you have reached the end of your road and still feel an emptiness in your heart and a burning desire to go beyond the perception of others. I invite you to take this journey through the experiences that make our faith stronger and our love everlasting.

Condamné par la maladie, Olivier Goy partage avec la journaliste Anne Fulda son inlassable combat pour mieux faire accepter le handicap et lever des fonds pour la recherche, et, surtout, appelle à regarder et aimer la vie pleinement?! Olivier a 46 ans quand on lui diagnostique la maladie de Charcot en 2020. Une maladie neurodégénérative qui se traduit par une paralysie progressive des muscles, mais laisse au malade ses pleines capacités intellectuelles. Espérance de vie?: 3 à 5 ans.