Journey to Gameland: How to Make a Board Game from Your Favorite Children’s Book

Leo isn’t reading, or writing, or drawing, or even speaking, and his father is concerned. But Leo’s mother isn’t. She knows her son will do all those things, and more, when he’s ready.

This anthology is comprised of two major components: thirteen full-length, autobiographical essays written by persons with learning disabilities and five analytical chapters written by education and psychology scholars. Speaking in terms alternately intimate and analytical, the autobiographical essays each tell of a sustained personal encounter with the challenges and mysteries of living with a learning disability. But these autobiographies are not merely personal, concerned solely with their writers’ private lives. Rather, they are also in various ways consciously analytical, offering astute critical readings of culture and society. The scholarly essays are written by such noted educators and psychologists as Lisa Delpit, Robert Kegan, and Janet Lerner. For any educator or parent of students with learning disabilities.

The prevalence of learning disabilities has provoked both the growth of research into the field and the development of educational interventions to assist those with learning disabilities. This book’s aim is to present the current state of this research and intervention ideas and programs. It includes updated material on the 1997 re-authorization of IDEA (Individuals with Disabilities Education Act) and expanded coverage of ADHD and its relationship to learning disabilities. This book presents the latest information on the characteristics of persons with learning disabilities, the causes of their problems, and educational interventions to help them succeed in school and at work. The book is research-based, user-friendly, and practical. 

*This text refers to the Hardcover edition.

There was something wrong with my brain. What had previously been a shadowy suspicion that hovered on the edge of consciousness became certain knowledge the year I was nine and entered fourth grade. I seemed to be like other children, but I was not like them; I could not learn to read or spell.

In this first account of what it is like to grow up dyslexic, Eileen Simpson vividly recreates the frightening world of a child living in the limbo of illiteracy. Simpson’s lack of reading skills so exasperated her teachers and relatives that they began to think she was mentally retarded. She could get lost walking to the grocery store; at times she felt as if she had no control over her speech. It was not until she was twenty-two that her future husband, the poet John Berryman, finally named her mysterious ailment.

Simpson intersperses her narrative with nontechnical explanations of dyslexia and what is being done to treat it. But despite growing public awareness and advances in research, dyslexia remains a frustrating and frightening disorder.

An ADHD boy helps rescue his dad because he pays so much attention to what is going on around him. He is the one who knows where to go get help.

Samantha Abeel couldn’t tell time, remember her locker combination, or count out change at a checkout counter — and she was in seventh grade. For a straight-A student like Samantha, problems like these made no sense. She dreaded school, and began having anxiety attacks. In her thirteenth winter, she found the courage to confront her problems — and was diagnosed with a learning disability. Slowly, Samantha’s life began to change again. She discovered that she was stronger than she’d ever thought possible — and that sometimes, when things look bleakest, hope is closer than you think.