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Thinking Person's Guide to Autism: Everything You Need to Know from Autistics, Parents, and Professionals Paperback – November 28, 2011
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Purchase options and add-ons
- Print length355 pages
- LanguageEnglish
- Publication dateNovember 28, 2011
- Dimensions6 x 0.84 x 9 inches
- ISBN-100692010556
- ISBN-13978-0692010556
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Editorial Reviews
Review
This is a book of HOPE. The underlying message is that however tough things may be, however difficult they may get, don't give up. Things can and generally, but not always will get better and there are resources available and people willing to help you give your child the best possible life. I believe this book may be the turning point in the lives of many parents of autistic children, but what do I know? I am an autistic adult and I contributed --Rory Patton, self-advocate, Springing Tiger
When Hank got his autism diagnosis, they gave us a binder from Autism Speaks. [Thinking Person's Guide to Autism] is the book I wish we'd been given. --Colin Meloy of The Decemberists and Wildwood
About the Author
Product details
- Publisher : Deadwood City Publishing (November 28, 2011)
- Language : English
- Paperback : 355 pages
- ISBN-10 : 0692010556
- ISBN-13 : 978-0692010556
- Item Weight : 1.09 pounds
- Dimensions : 6 x 0.84 x 9 inches
- Best Sellers Rank: #1,151,878 in Books (See Top 100 in Books)
- #1,017 in Pediatrics (Books)
- #1,049 in Autism & Asperger's Syndrome
- Customer Reviews:
About the authors

Liane Kupferberg Carter is a nationally known writer, journalist and advocate for the autism community. Her work has been published in the New York Times, Washington Post, New York Magazine, Market Watch, Chicago Tribune, Next Avenue, Longreads, and numerous literary journals, blogs and book anthologies. For more information, visit www.lianekcarter.com
"KETCHUP IS MY FAVORITE VEGETABLE: A Family Grows Up With Autism" is a
*2017 American Society of Journalists and Authors Outstanding Book*
*2017 Foreword INDIES Book of the Year Awards Finalist*

Emily Willingham is author of PHALLACY: LIFE LESSONS FROM THE ANIMAL PENIS (Avery, 2020) and THE TAILORED BRAIN (Basic Books, 2021). Her writing has been published online at the New York Times, Scientific American, Forbes, the San Francisco Chronicle, the Wall Street Journal, Discover, NOVA, Science, and others. She is also co-author with Tara Haelle of the award-winning book, The Informed Parent (Perigee Books/Penguin), and the author of The Complete IG to College Biology.
Her writing focuses on the intersection where society, science, and biases meet. She specializes in examining social perspectives on mental health, sexuality and gender, and parenting, with close attention to unconscious motivations and a practical perspective.
Willingham is the 2014 recipient of the John Maddox Prize for standing up for science, a joint initiative of Nature and the Kohn Foundation, that rewards an individual who has faced difficulty and hostility in the course of promoting sound, evidence-based science on a matter of public interest. She also served on the board of the National Association of Science Writers, for which she chaired the Fairness Committee and co-chaired the membership committee. She is a recipient of an Association of Health Care Journalists fellowship award.
Willingham earned her bachelor's degree in English and her PhD in biological sciences at The University of Texas at Austin and completed a postdoctoral fellowship in urology at the University of California-San Francisco. She has taught students of all ages, primarily as a university instructor in scientific writing and biology, focusing on physiology, anatomy, developmental biology, genetics, and general science.
She has been struck by lightning once personally, on a ridge in Yellowstone N.P., and also has once been a car that was struck by lightning and in an airplane that was zapped. In other words, do not stand too near her.
Willingham keeps busy with her family, including an awkwardly comical rescue dog and a trio of sons whom she encourages to keeping asking "Why?" unless she's typing. When she's not answering their questions or her own, she's reading, hiking, eating, drinking, and generally being merry and likely argumentative. You can find her on Twitter @ejwillingham, possibly too often, and read more about her on Wikipedia.

Jennifer Byde Myers is a writer, editor, and a lover of social media. She became a special needs advocate after her first child was born. His mild cerebral palsy and later, his autism diagnosis spurred her to write her blog www.jennyalice.com, where she chronicles her family's journey from diagnosis to daily living with her son's special needs, and continues to share stories about parenting, and life in the Bay Area.
Jennifer helped create The Thinking Person's Guide to Autism (TPGA) in 2010. It has become a successful blog with information by and for autistics, parents of children with autism, and the professionals who serve the community. The book companion book was released in 2011.
In 2011 Jennifer founded the Myers-Rosa Foundation with her business partner Shannon Des Roches Rosa, allowing the work of TPGA to reach a larger audience with the benefits of non-profit status. www.myersrosa.blogspot.com
Her writing has been featured at Salon.com, Parents.com, Care.com, Dadelion Magazine, and in several books including My Baby Rides the Short Bus. Jennifer has been interviewed on NPR, most recently on Forum with Michael Krasny, and is a Parenting.com Must-Read Mom.
She lives on the San Francisco peninsula with her supportive husband, two wily children, and a dog named Gus. Follow her on Twitter at @jennyalice.
In 2011 Jennifer founded the Myers-Rosa Foundation with her business partner Shannon Des Roches Rosa, allowing the work of TPGA to reach a larger audience with the benefits of non-profit status. www.myersrosa.blogspot.com

I’m the mother of THREE terrific sons. The oldest, Matthew, is a young adult with autism. I’m an optimistic mother/autism advocate/writer, and parents like me because I tell them it gets easier and I mean it. I write an autism blog for the San Francisco Chronicle that is very popular.
I’ve contributed to several anthologies, including Voices of Autism, A Cup of Comfort for Parents of Children with Special Needs, Writin’ on Empty, Gravity Pulls You In, Writin’ on Empty, Easy to Love, Hard to Raise and the incredible Thinking Person’s Guide to Autism. My essays have appeared in many places, including The New York Times, the San Francisco Chronicle, the Contra Costa Times, Literary Mama, the East Bay Monthly, The Autism Advocate, on NPR and CNN.COM.

Shannon Des Roches Rosa's writing and interviews are featured in The New York Times, The Wall Street Journal, Redbook, Parents Magazine, PBS Parents, SF Weekly, SF Gate, AOL News, Shot of Prevention, and the Bill and Melinda Gates Foundation. She writes about autism, parenting, evidence-based approaches, iPads, vaccines, and geekery at www.Squidalicious.com, as BlogHer.com's contributing editor for parenting kids with special needs, and as a co-founder and editor of The Thinking Person's Guide to Autism. She is one of CafeMom's autism experts, and is one of Babble.com's Top 25 Autism Bloggers. Shannon's radio interviews on autism, parenting, and blogging include KQED Forum, KCUR Central Standard, and News Talk KIRO. She has been a speaker at several conferences, including BlogHer and UCSF Developmental Disabilities. She has edited several anthologies and contributed stories to numerous books, including the award-winning My Baby Rides the Short Bus. Shannon and her son Leo were featured in Apple's iPad: Year One video, which was introduced by Steve Jobs at Apple's iPad2 Keynote in San Francisco. She, her handsome husband, and their three capricious children live near San Francisco.

Susan Walton is a different kind of autism mom. She and her family tried the diets, the therapy, and even some of the voodoo, but came to know that this stuff alone wasn't going to take her family where they wanted to go. Cherry picking the parts that were helpful but then striking out for new territory, she dedicated herself to finding fun and adventure not just for her own family, but for a thousand families in the San Francisco Bay Area who are part of the group she founded. Jump on board for the ride! Whether these families are swinging from a zipline, surfing in the ocean, or hiding behind a couch, this is a group of families that have fun and want to spread the word: Life is not over after diagnosis! The adventure is just beginning.
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Trying to write a review for this book is rather difficult since the book presents me with a serious catch 22.
This book is a very complete collection of every probable piece of knowledge a parent with a severely autistic child needs to be aware of, presented in a reasonably accessible way, and coming from diverse sources, many autistic themselves.
Where lies the catch.
Parents will read this book in the hope to better know their child -BUT- to read this book correctly you need to know your child.
The sufficiently aware parent will know what information is relevant and important for his/her child and what information can be safely regarded as less relevant or important.
The insufficiently aware parent might learn and become -needlessly- very concerned of problems and their solutions because of reading about them here.
The book goes to great length to point out cures, remedies, therapies and solutions that are insufficiently proven to work, or even proven not to work. This is priceless knowledge to avoid going down a wrong track at great cost in time, money and heartbreak. The book also points out a lot of things that work, are always good to know regardless, or might require very long term planning that needs to start NOW.
What this book cannot do is point out precisely what solution applies to your child. The book does offers very good suggestions on the type, qualities and the qualifications of the professionals that can best assist you for being the best parent possible. I would therefore very strongly suggest that you start by reading up on finding the right persons to guide and help you.
Best of luck
J.
Autism is so very many different things that I think we sometimes become overwhelmed, and we resort to the parent version of squeezing our eyes shut and covering our ears. This relatively normal response is particularly unhelpful to both those individuals who work with the autistic population and our loved ones with autism.
The book is a straight-forward and far more beneficial option to the "eyes shut/ears covered" response.
One aspect of this particular book that I personally liked is that the information is presented in sort of an a la cart fashion--find for what you want, what you need, and then come later for something else when you need that. This takes the edge off being overwhelmed by a long shot. One of the clearest memories I have from when my son was diagnosed was the anxiety of being overloaded with information. Don't misunderstand me--the information is absolutely there, it is simply that the information is presented in a way that is not overwhelming.
As a parent and a teacher, I know the alone-ness of having a special needs child and I know that it is a hard and long search to find your place among parents in similar situations. I'm not entirely sure I've found mine place yet.
This book provides insight directly into that feeling--snapshots, if you will--of what other parents go through.
Wow, I would have LOVED to have that in my early days!
Finally, I think we are just now beginning to find an effective middle-ground approach to working with autistic individuals and the book focuses on that without bias or judgement. After researching and consulting with my son's doctors, it was obvious that GFCF or gluten-free was not our first, or most practical, or even ever necessary move. I still felt really, really guilty about it, and that's the last thing the parent of a special needs child needs. This book would have helped to breach the chasm between the choice and the guilt because another standout point the book makes is that there are no complete absolutes regarding autism. As Dr. stanley Greenspan said, "if you meet one autistic child, then you've met one autistic child."
True That.





