検索キーワード： 制作 "-- Kevin Wright --" 障害者

This true love story follows Lars and Amanda, two twenty-somethings who fall deeply in love, with big plans for their future together, only to have the rug pulled out from beneath them when Lars is diagnosed with Acute Lymphoblastic Leukemia at age 24. They must learn to adapt to "medical life", putting their hopes and dreams on pause, navigating side effects and difficult emotions, and missing out on the beauty of every day moments that some may take for granted.

Written in first-person, from the emotional perspective, My Quiet Fight for Home emphasizes Johnnie's lifelong efforts to develop communication and career skills, as well as essential character traits, like honesty, courage, kindness, and loyalty.

Una vita perfetta in ogni minimo difetto. Una storia che ci insegna a guardare al di là dei pregiudizi, delle paure e delle. discriminazioni, per ricordarci come si arriva al cuore delle cose. Alessandra è una nutrizionista che ama viaggiare, Luca è un ingegnere. appassionato di cucina. Sono una coppia normale, che vive con serenità una. gravidanza perfetta, fino a pochi istanti dopo il parto, quando ai neogenitori viene. un sospetto: gli occhi a mandorla della piccola Luna vogliono forse dire qualcosa? La diagnosi arriva subito: Luna ha la sindrome di Down.

By age 25, Tracie Bork is a rising scientist and half of a power couple who throws lavish faculty parties. But beneath the perfect surface lurks the chaos she’s tried to control since childhood—and alarming physical symptoms she’d rather dismiss. Each year, she works more fiendishly than the one before as the complications to her health compound and become more mysterious until finally, she hits a wall, body, mind, and soul. In a series of honest inquiries and reflections, Bork chronicles her journey as a patient, academic, former military brat, and woman in search of faith.

I grew up believing that perfection was the only way to gain approval and feel safe. Every item in my room had to be aligned just right, every deadline met without fail, and every mistake felt like a personal failure. It wasn’t until adulthood that I realized these behaviors went far beyond simple neatness or discipline. They were signs of Obsessive-Compulsive Personality Disorder (OCPD)—an unyielding drive toward order and control that had slowly taken over my life.

Ausgezeichnet mit dem Leipziger Lesekompass 2023. Superheldin mit Hörgerät. ÄTT MÄN ONA UBA MÄN? Das ist alles was Cece versteht, wenn sich die Nachbarjungen über Superhelden unterhalten. Schon als kleines Kind hat Cece ihr Gehör verloren. Seitdem trägt sie ein Hörgerät und hat gelernt, Worte und Sätze von den Lippen abzusehen. Aber Cece hasst das Hörgerät. Es ist riesig und Cece ist sich sicher, dass jeder sie deswegen anstarrt. Bis sie herausfindet, was das Phonic Ear noch alles kann. Denn als "El Taubinio" ist Cece damit selbst schon fast eine Superheldin.

To the special person reading this: Hello Beautiful!!! Hope that you are doing well. When God created you he made one of his best decisions. You are unique, giving, loving, and very special. What does having mental health wellness coping strategies mean to you? After years of suffering from not having a way to cope mentally, having mental health wellness coping strategies means everything to me today. That's why I wrote Do I Look Bipolar?

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.

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.

They were part of the Baby Boomer vanguard, three boys thrown together in a 1950s Southern California subdivision looking like most other boys of that era. Under coonskin hats they ran free all summer long inventing their own games and endless challenges, fought imaginary Indians and pirates in a nearby orange grove, and on occasion battled a neighborhood bully or two. Their greatest enemy, however, was an infectious disease called polio – a paralyzing scourge that maimed and too-often killed little kids.

From the remarkable man whose life inspired the heartstopping film, ‘I Swear’, a book that offers extraordinary insight into what it’s like to live with a severe form of Tourette’s Syndrome: a fascinating, complex condition that’s more common than most of us think (1 in 100 schoolchildren have the condition), and yet is chronically misunderstood.

One fine April day, Mary Ann Kenny’s husband died suddenly while jogging near their family home. In the months that followed, Mary Ann – who had no history of mental illness – began suffering from depression, and then from a terrifying succession of physical and psychological symptoms, including the delusion that her young children had been harmed by her medications.