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Brains, Trains & Video Games (Living The Autism Life Book 1) Kindle Edition

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Length: 246 pages Word Wise: Enabled
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Editorial Reviews

About the Author

Alicia Hart...Wife...Mother...Writer...Connoisseur of fine candies and caffeinated beverages...Recognized authority regarding comfortable pajama pants. Find me on Facebook at The Autism Life or on Twitter at @TheAutismLife or at @EwanismOfTheDay.

Product Details

  • File Size: 476 KB
  • Print Length: 246 pages
  • Page Numbers Source ISBN: 1463794657
  • Publisher: Alicia Hart (June 3, 2011)
  • Publication Date: June 3, 2011
  • Sold by: Amazon Digital Services, Inc.
  • Language: English
  • ASIN: B00548AL98
  • Text-to-Speech: Enabled
  • X-Ray:
  • Word Wise: Enabled
  • Lending: Enabled
  • Enhanced Typesetting: Not Enabled
  • Amazon Best Sellers Rank: #545,516 Paid in Kindle Store (See Top 100 Paid in Kindle Store)
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More About the Author

Alicia Hart, author of Brains, Trains & Video Games, is a wife, mother and advocate for children and adults with autism spectrum disorder. She has worked for various autism related agencies, early intervention programs, and has consulted with schools, hospitals, and other programs regarding autism spectrum disorders, feeding aversions, and augmentative and alternative communication. Alicia continues to write and has planned a series of books surrounding the autism life. The first book, Brains, Trains & Video Games details their life through infancy, early intervention, medical care and preschool. The second book in the series, Foods, Moods & Isms: Living the Eosinophilic Life, was released on March 8, 2013.

Customer Reviews

Most Helpful Customer Reviews

70 of 72 people found the following review helpful By read_read_read on January 24, 2012
Format: Kindle Edition Verified Purchase
When I saw this book, I picked it up for my Kindle right away. It looked intriguing. While I do not have a child diagnosed on the Autism spectrum, I have my suspicians that my son is an Aspie's kid. This book was interesting but it also disappointed me in a few ways.
First the good:
I like how strong Alicia is in fighting for her son. Sometimes a mother DOES know something isn't right.
I like how she tries to push her son passed doctor's expectations.
Her admission that it takes a lot of time and resources to help these children.
I like that she explains any of the terms and therapies used to help autistic kids.
Her appreciation for early intervention. Where I live that is very hard to get. All of those therapies would have to be paid for out of my pocket.

The stuff I didn't like so much:
Alicia portrays herself heavily as a martyr. She repeatedly talks about everything she sacrifices but only touches briefly on what her other children miss out on due to her hyper focus on Ewan. She also makes her husbands contribution sound almost incidental when his financial contribution (while at times not enough) was all they had.
Sections and details are repeated in the book almost as if someone else added them and didn't bother to check to see if that information had already been given. For example, the reason behind Skye's names is described twice in the book in different sections.
Making doctors out to be the enemy and that she is always right got grating after awhile. In this book, only the people who agree with her theories and methods are good, the rest are bad. But then she cautions, every kid is different so don't just copy what we did.
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15 of 17 people found the following review helpful By Allison J on January 21, 2012
Format: Kindle Edition Verified Purchase
I fully admit that I am not the parent of a spectrum child, but I am a teacher who has worked with a number of ASD kids. This book is a comprehensive insight into the life of a family with a child who is on the Autism Spectrum. However, it's not the best written thing I ever read. I would like it more if, like my high school English teachers used to stress, she would "show" instead of "tell" more of her information, and I wish someone had edited more carefully (She has used "complaisant" when she means "complacent," "persona non grata" for person who is (completely welcome but) not present, and "pronunciate." Am I being picky?). She also gives the same information several times within the book, as if she hasn't already told you before. That said, though, it's a really good story, and I'm learning a lot, and I'm quite sure that I would not have made my way through her life with as much calm and drive as she has.

I also have somewhat of an issue with the ending. She stopped the book on a very abrupt cliffhanger. It was as if she had written a 500 page book, and an editor said "this is waaaay two long. We're going to have to break it into two parts." So she just found a likely place and ripped the manuscript in half. I have no sense of closure. That said, though, I will likely read her next book when it comes out so that I can learn what happened to her son.

Overall, this book was highly engaging, but somewhat of a bumpy ride.
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11 of 13 people found the following review helpful By Amazon Customer on June 8, 2011
Format: Kindle Edition
What a wonderful, enthralling book. I was unable to put it down. A read of about 7 hours.
While the title indicates it will be about Autism, it is also more. It is a glimpse into the struggles, challenges, and ultimate finding their way saga and LIFE story of the Nees/Hart family.

If anyone has dealt with Autism they will not only relate to this book but also learn from it. Hope is given as the readers see Ewan come out of the silence and corners of Autism to share his interest in trains and gameboys and connect with the world around him.I couldn't help but cry the 1st time Ewan, through aid of a communication device, asked for pancakes. By the end of the book Ewan will be well onto his way of finding his voice.

Alicia Hart is a fighter for her child, recognizing almost instantly that something is "different" with her Ewan, which ultimately will lead to the Autism diagnosis. Her never accept less then the best for him, comes across as she seeks help from Dr. after Dr., and therapist after therapist. We read of the family's walk with Early intervention services, Speech therapy, Eating specialists, and later battles with the school system and stressful IEP meetings.

The book gives an honest,intimate look into the trials of parenting a child with special needs and how it affects everyone in the family. The ups and downs, the fears, and then the acceptance of a limitless future.

The writing also comes across as a glimpse into a personal journal. The stories come to life of those that have dealt with and survived the heartbreak of divorce, addictions, financial pressures, family stresses, miscarriage, Cancer, and even death.

Everyone will find something to relate to in this book and will be left wanting more.
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4 of 5 people found the following review helpful By J. Pollock on June 6, 2011
Format: Kindle Edition Verified Purchase
To be fair, I have been a fan of Ms. Hart's "Ewanisms" for some time, but I loved this book! I also have to commend her willingness to expose so much of her life (and that of her family) to show others how a family can and *must* cope with the search for, and then the results of, a special needs diagnosis. I found the book to have funny and touching moments that affected me as both a therapist(SLP) and as a parent. Looking forward to the next installment, and thank you for the insight into Ewan's world!
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