Showing results by publisher "----RM Alexander" in People with Disabilities

Genius or Lunatic goes deeper into the mind of a paranoid schizophrenic. There is so much confusion in there. So much contradiction. So much religiosity. And there is much desire to know, understand, and find the truth. Along the ride you will find yourself saying, "But in this poem didn't he just say this"? It will bring out emotions that you won't expect. This brings you into his pain and lets you experience it firsthand.

Emily Owen was a highly intelligent teenager who was also athletic and a skilled musician. Tragically, in her late teens she was diagnosed as suffering from Neurofibromatosis Type 2 (NF2). Since then, Emily has survived many complicated surgical procedures, been close to death, and seen the gradual erosion of all the abilities that defined her personality including the total loss of her hearing. Despite this, she has a remarkable sense of humor and has coped with everything she has been through due to her strong Christian faith, her supportive family, and indomitable personality.

Disabled with polio from the neck down aged 5, Mark Esho was told he would never walk again. Although he partially recovered, he had to battle against an abusive father and discrimination as a black and disabled person. But not only did he survive, Mark thrived! In an extraordinary story that starts with polio, discrimination, adversity, racism, abandonment and child abuse, Mark takes us through his amazing achievements, from working as a senior manager for a charity and creating several successful businesses, to winning awards and gaining his Masters Degree in Administration.

Robert Mercer's life could have been very different. He was born with very low vision and as a youngster struggled in school. But through the intervention of a caring teacher and the support of his family, he found his way to the Halifax School for the Blind and into the classroom of Mrs. Beaton. It was there he discovered his voice, a voice he uses to recount his remarkable journey from a shy little boy to a community leader.

I don't know whether this is the story of Jeff the autistic individual, Jeff the man of God, or Jeff the medical enigma; but I do know it is the story of Jeff, my son. Jeff was so autistic, and yet not autistic at all if you used the textbook definition. He had huge sensory integration issues and appeared to be living inside of himself, but he cared so much for God and other people that their needs always came above his own. He had severe speech issues, only spoke one-word answers, but wrote beautiful papers and prayers when given the Canon communicator.

This book explores the untold story of a war veteran's journey with transcranial magnetic stimulation treatment.

Life is never easy, but there are times when it feels like everything is against you. Tyra Hodge grew up feeling the world's weight pressing down on her. A nagging feeling awakened, whispering how she would never amount to anything the older she got. Daunted by the increasing demands of education and her private struggles, Tyra turned away.

Unser heimlicher Star in der Hörbuchreihe "Die Runde Ecke" hat das Tourette-Syndrom. Eine Krankheit, die durch sogenannte Tics charakterisiert ist. Jean-Marc sagt über sich: "Wenn es morgen eine Wunderpille gäbe, ich würde sie nicht nehmen." "Tourette in my head" ist eine berührende Mischung aus motivierenden Gedanken und tiefem Vertrauen in das Leben. Das Hörbuch erzählt von persönlichen Abstürzen, Neuanfängen, skurrilen Momenten und besonderen Triumphen.

Rick Werry was living the good life in beautiful Monroe, Utah. He was a young, athletic man who woke up every morning doing what he loved for work, and he had been lucky enough to marry his college sweetheart. A year after their marriage, all of that suddenly halted when an onsite construction injury nearly claimed his life.

In "Not Now Please: Living through Racism, Ableism, and Grief," Elizabeth takes you on an intimate journey through the intersecting worlds of adversity, resilience, and transformation. This compelling narrative is a candid exploration of personal experiences that touch upon the deep-rooted issues of racism, ableism, and the complexities of grief.

This is a story about a mother and son on a road trip along the Pacific Coast of Southern California. Asher is a 19-year-old child/teen/man who is diagnosed with severe cerebral palsy and a visual impairment rendering him nonverbal, wheelchair bound, and visually impaired. Stacey is his devoted mother and a neuropsychologist who specializes in the assessment of children with neurodevelopmental disabilities.

When fourth grader Alex Schwartz first met his cello, his eyes lit up with wonder, and a smile appeared on his face as bright as the potential his new cello teacher saw within him. The cello positively impacted all aspects of his development, including focus, fine motor, and gross motor skills.

Life moves fast. Too fast for some people. This is the true story of what it's like to live in a world where you can't keep up. Bobby was ten months old when my mom and dad rescued him from birth parents who were slowly killing him. He was adopted into our family after a lengthy custody battle. Instead of that settling him, it set off a lifelong struggle to find a place to belong, a place to call home. Like an old-fashioned merry-go-round, the world moved at a speed that was just too fast for Bobby. He couldn't keep up, which prevented him from keeping a job.

Isaiah was eighteen years old when he was diagnosed as being on the Autism Spectrum along with having OCD. It was a relief for the young man to finally have a name for what he had been feeling and experiencing for so long. For his parents, it was a different story. They had never observed any signs or symptoms that would have led them to believe their son might be autistic. At least, there were none they knew to look for. Autism in Hindsight is a conversation between mother and son about getting diagnosed, working through it the process, and learning to connect the dots. Along the way they ...

I am continuing with a genre of poetry that I created that I call schizoetry. It is a literary work fusing poetry with the thoughts, feelings, and perceptions of one who lives with a schizophrenic or schizoaffective disorder. I have been writing poetry since the age of 10. My poems go deep into my mind, emotions, and my spirit. They are very revealing to say the least. I wish to reach those living with this illness.

"Ich bin einer derer, die die Jahreskarte gezogen haben. Wenn ich abrutsche oder hochfliege, dann für eine lange Zeit. Dann bin ich nicht mehr zu halten, ob im Flug oder im Fall." Die fesselnde Chronik einer manisch-depressiven Erkrankung: ein autobiografisch radikales Werk von höchster literarischer Kraft.

For many years, Jeffrey Demitrack searched for a meaningful and fulfilling relationship and, most of all, hoped that one day he would find a significant other who understood and unconditionally accepted his struggles with epilepsy. People have their insecurities, and relationships already are hard without throwing seizures into the mix, so his search has been a challenging one.

When Ellie Goldstein was first diagnosed with Down Syndrome, her mother was soon told that her new-born would amount to nothing. For 21 years and counting, Ellie Goldstein has been defying the odds and overcoming every hardship thrown at her. Told she wouldn't walk, Ellie has danced on mainstages. Told she wouldn't learn, she has gained a college education. And told not to dream, Ellie has gone on to become the first model with Down Syndrome to be photographed for Gucci and continues to change the face of fashion from the inside out in countless international campaigns.

Andrea struggles to mourn a man who is still alive as she witnesses her father decline into the depths of Alzheimer's. Denial and devastation color her life when she learns her father, Richard, a recently retired surgeon, is diagnosed with Alzheimer's at the age of 67. Her dream to grow closer to him is crushed as the reality of his disease is fully realized. Andrea, a mother of three young children, learns to balance motherhood with daughterhood as she grapples to accept her father's fate.

In 2012, combat engineer Curtis McGrath was serving in the Australian army in Afghanistan when, in the line of duty, he stepped on a mine. Seriously injured but still conscious and aware he'd bleed out and die within minutes, McGrath, as the unit's chief first-aid officer, directed his comrades to apply tourniquets and administer an IV and morphine. Then, as he was stretchered to a helicopter, fearing he would never see his family again, he joked that he planned to become a Paralympian.