Zeigt Titel in Menschen mit Behinderung

Many people give up on God. It’s easy to trust in his goodness and strength when life is easy. But how do we persevere in our faith when life gets hard? Few people can show us how to do that better than Allan Schwartz.

See? is an inspirational autobiography that describes how God's grace and the firm, loving support from family, friends, neighbors, an exceptional teacher, and caring supervisors guided the author through life's challenges. It also debunks common myths of blindness and discusses adaptive equipment used by the author on her journey.

Inizia con un formicolio nella parte destra del corpo. E una strana stanchezza. L’equilibrio che si fa precario. Quando, mesi dopo i primi sintomi, arriva la diagnosi di sclerosi multipla, Marco ha trent’anni e una carriera da tenore appena avviata. Come gestire i concerti e le audizioni in giro per il mondo senza sapere come ci si sveglierà domani? Marco mantiene segreta la sua nuova, scomoda compagna di viaggio. Almeno fino al 2013, quando, nella prima apparizione di Sintomi di felicità, decide di rivelarla al mondo.

Jean-Baptiste Dethieux est le père d'une enfant porteuse d'un handicap qui la rend à certains moments toute petite et démunie et à d'autres, grande et forte, si forte qu'elle semble embrasser le monde dans son entier, s'en amuser ou s'en réjouir dans une innocence désarmante. Elle est alors, non seulement cette enfant souffrant d'un handicap, mais aussi l'incarnation d'une joie simple et d'une force de vie irradiante.

"We all have trapdoors in our lives. Sometimes we jump off just in time: we defuse an argument with a joke; we swerve to prevent a traffic accident. But sometimes we are unlucky enough to be on the trapdoor when the lever is pulled. My own trapdoor was hidden in the consulting room of an Oxford neurologist." When the trapdoor opened for Robert Douglas-Fairhurst, he plummeted into a world of MRI scans, a disobedient body and the crushing unpredictability of a multiple sclerosis diagnosis. But, like Alice tumbling into Wonderland, his fall did something else.

When someone would tap along and rescue me from being sandwiched between these two hardbacks, sorry, did I frighten you? You never heard or seen a talking book. Well, me either. The majority of the time, I am the only one in the room, or shall I say, “on the shelf”? So many humans walk right past me, playing blind games by pretending not to see that the struggle is real. Talk about the lack of accessibility.

I Sverige finns mer än en miljon anhöriga som vårdar eller stöttar en närstående med fysisk eller psykisk ohälsa eller funktionsnedsättning. Även om var och en har sin unika historia är det mycket som förenar oss. Anhörig i ett hav av känslor ger röst åt våra berättelser. Om ovisshet och oro, otillräcklighet och frustration, skuld och skam, sorg och maktlöshet. En situation som kan utveckla oss som människor, men också utmana och slita ut oss. Det handlar om avgrunder och guppande känslohav, men också om stillsamma solgläntor och fascinerande utsiktsplatser.

Steph Hammerman has been motivating herself and others her entire life. Since defying the odds by surviving as a one-pound, fifteen-ounce baby and weeks later being diagnosed with cerebral palsy, to beating Hodgkin's lymphoma stage 3B cancer in 2016, Steph has been a living example of overcoming seemingly insurmountable objects in order to achieve the impossible.

Escrito quando Naoki Higashida tinha apenas 13 anos, o conjunto de ensaios reunidos neste audiolivro conta, do ponto de vista do próprio Higashida, a experiência de ser autista. Preso em seu mundo individual, muitas vezes ele exibe comportamentos vistos como estranhos, peculiares, “inadequados”. Seja repetindo palavras e frases aparentemente sem sentido ou evitando contato visual com outras pessoas, Naoki tem uma enorme dificuldade de se comunicar e de socializar.

Poetic Madman showcases and celebrates the creativity and the ability to express my innermost thoughts, ideas, emotions, philosophies, and raw experiences that come with having paranoid schizophrenic disorder. Poetic Madman is sure to open the minds of those who don't understand mental illness and hopefully help to dispel some of the stigmas. The purpose is to give the listener a different take on what they understand to be true about the illness. You may even identify with some of the experiences expressed throughout this work of art.

2020 was a hard year for everyone. In this journal, learn how one woman experienced the pandemic while also having to deal with the effects of having bipolar disorder. From the book: "Truth is best expressed as silence. Words are our creations. They come and go, live and die. They are incapable of expressing what is real. This has been a journal of a false identity assuming itself to be real. From this new vantage point, I see how I am creating this story. Today I start a new chapter. Or maybe it is just a page. Even if I could just cobble together a sentence. Make it meaningful!"

Jeremy Schreiber was on top of the world—athletic, newly married, successful. And then something went terribly wrong. In this moving memoir, he shares his journey after he received a terrifying diagnosis: ALS. As the devastating disease robbed him of movement and speech, he was abandoned by his wife and betrayed by a society that shuns people with disabilities. But it’s not all doom and gloom. He found love, support, and a powerful purpose. While fighting for his independence and then for his life, Jeremy gave his all to the ALS and disability communities.

Love Is Blind is the memoir of Ruth Vallis. Blind before the age of three, Ruth was the youngest pioneer of integration in the public school system in Canada, blazing a trail for many to follow. At every stage of her extraordinary life, Ruth defied the low expectations of others, and took on such challenges as biking from Ottawa to Toronto, completing a master’s of science degree online before technology accessibility was legislated, and more. Through it all there was her tender, tough-loving mother, Peach.

In this powerful new history, New York Times bestselling author Max Wallace draws on groundbreaking research to reframe Helen Keller’s journey after the miracle at the water pump, vividly bringing to light her rarely discussed, lifelong fight for social justice across gender, class, race, and...

Sarah’s story is one for any parent; it is not just about the highs and lows of having a child with additional needs, but also simply as a mum of three. She talks candidly about coming to terms with the decision to move Oscar to a SEN (Special Educational Needs) school, another big milestone in Oscar’s young life. Whilst Sarah may have found herself on a different path to the one she’d imagined for herself, it has not been a bad one. There is sadness, certainly; and there have been struggles along the way; but there has been so much laughter and happiness, too.

My neurologist stunned me when she said, “You have multiple sclerosis, and looking at your MRI, you are a walking time bomb. You may not have symptoms today, but it’s just a matter of time.” As the MS tightened its grip on my body, I plunged deep into a myriad of strange feelings—denial and depression for over a year.

This book is based on real-life events and is a raw and authentic account of a true fight for life and justice—a memoir of a mother’s love for her daughter, Rachel, who is diagnosed with severe cerebral palsy, a condition which makes her incapable of voluntary movement or speech. It tells of hopes and fears, and the true meaning of what it’s like to be the mother of a daughter with severe cerebral palsy. It portrays Rachel’s passion for life and her mischievous sense of fun.

Jump in the passenger seat as I navigate you through my journey of blindness, sexual abuse, mental illness, and various other medical conditions and tragedies. I will take you on the twists and turns of single motherhood and dating with a disability, all while only having the use of one arm. Join me for an emotional, yet exciting, ride to see how I end up at my current destination.

Do you like sex, drugs, and rock 'n' roll? Do you know what jails, institutions, and death are all about? I don't want to be controlled, but can I control myself? Who says I have to live by society's rules?

When you hear the word “disability”, what comes to mind? Cheryl Schiltz tells her story of being introduced to disability. She shares her journey from a silent world to one that encased her in constant anxiety. Her life as she knew it had disappeared. It became one of a continuous fight between psychological and physical change. Noise. From her childhood, you’ll find yourself traveling with her as she discovers the power to gain control. She shares her story openly and honestly, raw and sensitive.