Marvin One Too Many

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.

Life is especially tough for Joey. Not only does he struggle with ADHD, his family is truly dysfunctional. Readers will sense that Joey is a good kid who’s trying to do the right things, but often without much support. Readers will likely laugh and weep for Joey.

With a positive, friendly approach, this guide defines learning disabilities, illustrates the different types, and explains where they come from, all the while providing reassurance without overwhelming the child. Many Ways to Learn describes the effects learning disabilities have on young people’s behavior, performance, and emotions, and offers solid, proven suggestions for coping at home, in school, and with friends. It features a first-person account from a child with learning disabilities, a chapter on computers and an extensive resource list for parents. The message in Many Ways to Learn is that kids with learning disabilities have average or above-average intelligence; they just find it difficult to learn in a particular area or areas. With some help from school and family—and a little extra work on their part—they can do as well as anyone else.

Research shows that if these children do not “close the gap” before they finish third grade, they are likely to remain functionally illiterate throughout their lives. See Johnny Read! is the first book to offer practical, proven, and timely ways for parents to help their boys with this critical skill. Written by an expert teacher and educational consultant, this much-needed book answers essential questions, including: When does a reading delay become a reading problem? How, when, and where should I look for tutoring? How can I get the best help from the school? How can my son avoid (or overcome) the “Bad Boy” label? How can I help my son learn to read — and enjoy reading — at home?

Kids with sensory processing disorder SPD may seem unduly sensitive to physical sensations, light, and sound, and they may react strongly to sensory events that adult and other children take in stride or totally ignore. SPD can make it hard for kids to do well in school, participate in social events, and live peaceably with other family members. Until now there have been only limited resources for parents of kids with this condition, but in this book a child advocate and child psychologist offer this comprehensive guide to parenting a child with SPD and integrating his or her care with the needs of the whole family.

The book introduces SPD and offers an overview of what it means to advocate for a child with the condition. It describes a range of activities that help strengthen family relationships, improve communication about the disorder, and deal with problem situations and conditions a child with SPD may encounter. Throughout, the book stresses the importance of whole-family involvement in the care of a child with SPD, especially the roles fathers play in care-giving. Many of the book’s ideas are illustrated with case stories that demonstrate how the book’s ideas can play out in daily life.

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.