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Schuyler’s Monster is an honest, funny, and heart-wrenching story of a family, and particularly a little girl, who won't give up when faced with a monster that steals her voice but can’t crush her spirit.
When Schuyler was 18 months old, a question about her lack of speech by her pediatrician set in motion a journey that continues today. When she was diagnosed with Bilateral perisylvian polymicrogyria (an extremely rare neurological disorder caused by a malformation of the brain.), her parents were given a name for the monster that had been stalking them from doctor visit to doctor visit and throughout the search for the correct answer to Schuyler's mystery. Once they knew why she couldn’t speak, they needed to determine how to help her learn. They didn’t know that Schuyler was going to teach them a thing or two about fearlessness, tenacity, and joy.
Schuyler’s Monster is more than the memoir of a parent dealing with a child’s disability. It is the story of the relationship between a unique and ethereal little girl floating through the world without words, and her earthbound father who struggles with whether or not he is the right dad for the job. It is the story of a family seeking answers to a child’s dilemma, but it is also a chronicle of their unique relationships, formed without traditional language against the expectations of a doubting world. It is a story that has equal measure of laughter and tears. Ultimately, it is the tale of a little girl who silently teaches a man filled with self-doubt how to be the father she needs. Schuyler can now communicate through assistive technology, and continues to bethe source of her father's inspiration, literary and otherwise.
The monster in this heartfelt memoir is polymicrogyria, an extremely rare brain malformation that, in the case of Rummel-Hudson's daughter Schuyler, has completely impaired her ability to speak. During her first three years, as her parents seek to find out what hidden "monster" is causing her wordlessness, they endure "two years of questions and tests and at least one unsatisfactory diagnosis." But while Rummel-Hudson initially rages at God for giving Schuyler "a life that would never ever be what we'd imagined it to be," his depiction of her next four years becomes a study not only in Schuyler's vivacious and resilient personality, but also in the redeeming power of understanding and a "stupid blind father's love." As he describes how Schuyler eagerly takes to various forms of communication, such as basic sign language and an alternative and augmentative communication device that provides whole words she can type to express her thoughts, Rummel-Hudson effectively and compassionately shows how the "gentle strangeness about her, like a visitor from some realm where no one spoke but everyone laughed," leads him to understand that "she was the one teaching me how to make my way in this new world." (Feb.)
Copyright 2007 Reed Business Information More Reviews and RecommendationsRobert Rummel-Hudson has been writing online since 1995. During that time, his work has been recognized by the Diarist Awards at diarist.net, including citations for Best Writing (1999 Q4), Best Overall Journal (2000 Q1), Best Account of a Public or News Event (2001 Q2, on the execution of Timothy McVeigh), Best Dramatic Entry (2002 Q3), and the Legacy Hall of Fame Award (2004 Q4). He has served as a featured panelist at JournalCon, an annual conference for online writers, in 2001, 2003 and 2004. His online writing has been featured in articles in the Austin Chronicle (August 2000), the Irish Times (summer 2003) and the New Haven Register (April 2003).
Robert and his family currently live in Plano, Texas, where Schuyler attends a special class for children who use Augmentative Alternative Communication devices. Much of her days are now spent in mainstream classes with neurotypical children her age. More of Robert’s observations on life with Schuyler can be found on his blog at www.schuylersmonsterblog.com.
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November 07, 2009: I found this book at a Goodwill, not knowing anything about it ... As I began to read, I was amused by the author's sense of humor. But after a few dozen pages, it began to be apparent that there was nothing wrong with the little girl except she couldn't pronounce vowels. An ENTIRE BOOK dedicated to the "ups and downs" of living with a little girl who cannot pronounce vowels. At page 171, I just couldn't go on reading about this little girl who apparently stopped the worlds of both of her parents by not being able to speak. You'd think she had a terminal illness. I bothered to watch two videos of Schuyler on youtube to see how bad off she was/is ... the videos were ridiculous. So much footage and of what?! One very spoiled little girl obviously accustomed to everything around her also being ABOUT her. I wonder how much more her father can possibly write about her not being able to say vowels. I'm guessing two or three more 300 page books.
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August 01, 2009: Intrigued by the title and curious about a "wordless daughter", I journeyed with Robert Rummel-Hudson through Schuyler's life thus far with sympathy, surprise and a renewed appreciation for the parents of special children. The book is informative about a rare brain malformation that produces a not-so-rare speech problem. In a world that takes for granted the internet, I-phones, and all the other electronic toys we have, it is not surprising that a computer can help the wordless to speak again. I plan to use this book in my women's book group, and highly recommend it to anyone who has children, knows children, or was a child...that's pretty much everyone. Read, enjoy and learn a new appreciation of parental love.