Títulos em Pessoas com Deficiências

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.

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.

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!"

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.

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.

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.

Look at It This Way answers questions we all may have been reluctant to ask, it gives us a glimpse into what blind people experience living in a sighted world, and it breaks through barriers that may cause people to think that differences equate to superiority or inferiority.

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.

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.

If you're skeptical about changing society's discriminatory treatment of people with dwarfism and other disabilities, Van Etten offers hope with these words: "Advocacy makes change possible when people call out what is wrong, care enough to stand up for what is right, commit to the cause for as long as it takes, and have confidence in God's power to change hearts". Van Etten repeatedly demonstrates the power of advocacy in this audiobook.

Bill Rush lived with a significant disability of quadriplegic cerebral palsy. He did not have use of his arms, hands, or voice. Society’s prejudices proved to be a greater obstacle than his disability in attaining his first life goal of completing college. Rush chronicled his extraordinary life from childhood until graduation from the University of Nebraska - Lincoln in Journey Out of Silence, first published in 1986. This second edition brings back into print Bill's original chronicle. It also contains an introduction to Our Life Our Way, the sequel.

Love for a Deaf Rebel introduces listeners to a vivacious Canadian woman who was born into a silent world and with the foundation for schizophrenia. With pathos and nostalgia, the author recounts his roller-coaster ride with Pearl, a vivacious deaf maverick, who, unknown to him, had paranoid schizophrenia. We follow their encounters through actual notes written before Derrick learns sign language; we go on their motorcycle ride to Mexico and Guatemala; we watch as the happy couple moves to Bowen Island, a British Columbia community with just three paved roads.

When a tragic accident crushes her dreams, can a young woman fight to thrive once again? As a teen growing up in the '80s, Jenny Smith loved life. But, when a spinal cord injury paralyzed her from the chest down, her days of gymnastics and playing music came to an agonizing end. Completely reliant on others for her most basic needs, privacy and independence became things of the past. Refusing to give up, Jenny struggled along the exhausting, painful, and endless road to living as a quadriplegic.

I realized, at age 70, that I had no memory of being inside my home, where I grew up, or ever being inside a school classroom. I began to write then, and have continued over the last 24 years, as one painful memory after another was slowly revealed. Recently I figured out what had happened to my mother, and therefore to me. Two more major insights totally freed me. I could then finish Missing Pieces.

The day Ms. Meadows walked out of court victorious after her 15-year-long struggle to regain her Constitutional rights from the state of Montana and her four parents, she knew one thing for sure.... She would one day get even with the lawyers. After more than 30 years of this insanity, they have instead succeeded in creating a deeply passionate, intelligent, driven, broad-minded and crafty machine - a lady-genius with an unstoppable force. Ms. Meadows has mastered the secret of how to beat them. Join her as she embarks on this epic journey of Changing My Perspective.

After 30 years as a professor in the field of communication studies, Dr. Smith reminisces about some of his experiences and how his race and differently abled intersectionality have influenced documented encounters. As a Black and totally blind individual, he muses about how this distinction has both colored and shed light on what might have been innocuous or unremarkable encounters otherwise.

Everything happens for a reason; I truly believe writing these words was one of the primary purposes of my life. Father God gave me this disability - I’m just trying to make the most out of it. This is not your typical autobiography or memoir. I’m sharing my life experiences as more of a commentary on humanity as a whole. I do my best to sprinkle bits of comedy throughout the composition so it feels more like a conversation between friends than me just talking at you.

Trente-deux ans, c'est le nombre d'années qu'il m'a fallu pour mettre un nom sur ma différence. Comment ai-je pu "passer au travers des mailles du filet" durant tout ce temps ? Je vous révèle, au travers de ce récit parsemé d'anecdotes, comment j'ai grandi dans l'ignorance de mon syndrome. Plongez dans mon quotidien et découvrez chacune des étapes clés de mon évolution ainsi que les moyens mis en œuvre pour survivre dans ce monde parfois difficile à appréhender.

One September day in 1955, Rita’s life changed forever when polio struck her family. She was five years old. Rita became totally paralyzed; her brother was partially affected, and she lost her mother to the virus. The hospital became her home, and the ward sister her mother. Hospital life was harsh in the 1950s: Crying was a punishable offence and meant solitary confinement. Rita struggled to walk again using leg callipers and a spinal brace, and later became mobile with the use of a wheelchair.