Reviews

I was asked by Help! S-O-S for Parents to be part of a team to review Pajaggle, a new game for ages 3 up. To access all reviews, please visit Pajaggle: A Blogger Review. My review follows below.

Their web site describes it as “Pajaggle™ (pa-jag-gul). The game that thinks it’s a puzzle.” And at one level, that’s essentially all it is. But really it’s a lot more than that, and I thought it was a blast. I was asked to consider particularly whether I thought Pajaggle was appropriate for autistic children. On that point, I’d say “it depends”, with some explanation below. But first, let me answer “What the heck is Pajaggle?” in my own words, especially since it will help me explain how I think it would work with autistic children.

Pajaggle has 61 pieces that you place into their respective slots on the Pajaggle board. That’s really it in a nutshell. But it’s deceptively challenging. Many of the pieces look similar to each other, and the variations between them can be very subtle. The spaces on the board for the pieces to slot into are an exact fit. And I really mean ‘exact’. In many cases, you’ll think you found the correct piece, but you didn’t. It’s not unusual to try to stick a piece into a slot, figure out it’s the wrong one, and then it gets stuck (or ‘Pajiggled’ in game lingo). Thankfully, they provide a separate doohickey that serves to pop pieces out of slots with little fuss (not surprisingly called a ‘Pajiggler’).

Here’s where they kick the complexity up another notch. Some of the pieces have slots within them for another piece to fit into. So some pieces just by themselves don’t actually fit into any slot on the board. They fit within another piece, which then fits into a particular space on the Pajaggle board. When I told my wife that as we were filling in the board together the first time, she said, “Oh, [expletive deleted]. Seriously?” We both laughed.

If you want to time yourself, Pajaggle comes with a digital timer. The first couple of times I solved the board, it took me forever. I was glad I didn’t time myself as I didn’t need that mark against me that day. But you know you’re going to use the timer eventually because you can’t resist, and it’s essential to the competitive, multiplayer games.

Admittedly the sample size of autistic children I considered in thinking about this review is pretty small, but I did talk with a couple of teachers along with some parents and we couldn’t think of any autistic kids we knew under age 7 who would be able or willing to sit and solve an entire Pajaggle board on their own or even with help. That said, if you gave them a partially filled in board and had them fill in the rest, that would be an option for some of them.

Our J-Man (who is 6, by the way), would mostly just stare at the board not really knowing what he’s supposed to do with it, or he might just line up or spin the pieces. We’d need to figure out how to structure it, which is hard to do with that many pieces.

So, its 61 pieces seem like too many for most younger kids. Perhaps if there were versions of the board with half that many pieces, and those pieces differed from each other a bit more than they do now, I think they’d be on to something for the younger kids.

If I could sum up in one sentence which kids I do think would respond well to Pajaggle, it’d be this. If your child enjoys puzzles and has a good attention span for them, has strong recognitions of shapes, can detect subtle differences between similar objects, and can do puzzles of two or three dozen pieces or more, then Pajaggle seems like an obvious choice to me.

This is one of those games that both parents and kids can enjoy, too. I thought it was a blast. If you dislike visual puzzles, then you might not care for Pajaggle, but otherwise I think most people would find it fun. It’s quick enough to do – somewhere between a few and somewhat more than a few minutes – versus spending hours or days working a jigsaw puzzle. Think of it like a quick brain pick-me-up if you play on your own. The possibilities for fast-paced multiplayer games are plentiful. Not surprisingly, we’re not party people, but I can see this being a great game for get togethers.

If you know of a child who likes puzzles (especially if their parents do too!), then I think Pajaggle would make a great gift. At $30, it might be a little spendy for some, but it’s fun and the variety of games and activities you can do with it to me make it a good value. You can purchase Pajaggle on their web site at http://www.pajaggle.com.

Disclosure: I received this game for free for purposes of this review.

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The recently-released Look at My Eyes: Autism Spectrum Disorders: Autism and PDD-NOS fills a much ignored gap in the growing abundance of autism and parenting titles now out there. This is author Melanie Fowler’s first book, and her insights and advice together with her husband Seth’s perspectives sprinkled in earns a spot on the short list of books parents who are either just receiving an autism diagnosis or concerned about it should have.

Look At My Eyes is in comparison to many other autism books positively svelte at 160 pages, which becomes one of the book’s greatest strengths. It’s common for books about autism to go into many levels of detail or contain copious background information, neither of which may actually be needed when parents are struggling in the early days of a diagnosis.

In hindsight, what we most needed during that time was something direct, honest, and boiled down to the essentials of what we should think about doing next at that moment. We didn’t need the whole bible, just a couple of chapters to get us started. We were too tired and overloaded to think clearly or read a ton of books back then. The Fowlers have identified the needs of this audience and distilled volumes of advice into a jam-packed book.

There are a number of online resources that offer information for this same audience – such as the 100 Day Kit from Autism Speaks – but many of these, while certainly informative, can seem rather clinical and emotionally distant. There are times you simply want to hear it from someone who knows what you’re going through, someone who’s spent a month of days cleaning poop out of the carpet and fighting with county bureaucrats on the phone. Look At My Eyes isn’t a replacement for these other resources but a complement with an understanding voice from an author who’s been down the same road as you.

If you’ve been at the autism and parenting gig a while, there may not be much new ground here for you. But I think that’s really a good thing. Too many autism books try to be everything to everybody and in doing so may not be enough for anybody. What we need now are more targeted, niche books about autism that help us addresses specific issues without the time commitment required for the hefty volumes out there. The big books, of course, fill a critical need, but often we just need to get the info and move on. It’s hard to do deep reading while you’re exhausted or constantly trying to keep your kid from escaping out the front door.

Melanie Fowler does a wonderful job weaving her personal experience and story with specific steps to put on your early journey with autism to-do list. She provides some real-world scenarios and how to work through them. Her words provide a mixture of understanding, empathy, and a swift kick in the butt. I especially appreciated the latter. We tend to treat parents with kid gloves in the early days, and obviously there’s plenty of need for understanding and compassion during that time. But there also comes a day when it’s time to put our fears on the back burner and get our tail ends in gear.

Her husband, Seth, provides his insights as a father in the “Seth Says” sections sprinkled through the book. He explores some fundamental father/son issues that could easily become another book in themselves. As men and dads, we can all be rather hit or miss about how well we deal with our emotions. We can easily get invested in our original expectations for all the ‘dad things’ we wanted to teach and do with our children, something that may or may not happen when your child has autism. Given that most autism and parenting books are written by moms (men who write autism books are often doctors and researchers; dads are very underrepresented), Seth’s insights are a refreshing addition.

I think if you pulled ten experienced parents and experts out at random, you’d find most of them nodding their heads and saying, “Yeah, what they said” to the vast majority of advice the Fowlers offer in this book. There will always be areas in which parents have differing perspectives. For example, from the lens of our experience with autism, I don’t have quite the same glowing views of ABA that were in the book, but if you asked a bunch of people about ABA you’d get about as many perspectives on it anyway. It’s a rich topic, and I think they cover the important highlights well, especially given how there are numerous, giant volumes written on the subject.

In places, Look At My Eyes may feel like it assumes certain abilities that your child may or may not have achieved yet. For example, I felt like it presupposed a level of receptive language (the ability of a child to process and respond to what you are telling them, particularly with respect to things like requests and instructions) that is noticeably higher than our son has right now. You could make a case that the book overall tilts somewhat toward the higher functioning end of the spectrum. I honestly don’t think that at all lessens the usefulness of the book, though. I mention it primarily because emotions in the early days of a diagnosis are very raw, and discussions about things another autistic child can do that yours cannot can feel isolating. This is going to happen to pretty much everyone at some point, but I think it’s an emotion worth naming so you can be aware of it when it comes up.

For those parents in the earliest stages of a diagnosis, I would recommend reading this book a section at a time. Fowler doesn’t linger on a topic for long, preferring – rightly in my opinion – to get to the point and get on with it. However, the result when you’re already overwhelmed may feel like being on the end of an information fire hose. That’s a normal feeling. Move through it steadily a piece at a time, take notes, and you will learn a lot.

Look At My Eyes has an ambitious goal and hits the mark well. Melanie and Seth Fowler bring together a wealth of practical advice, the understanding of parents who’ve been there, and wisdom on how to make sense of the emotional chaos of the early days of an autism diagnosis. If that’s where you are right now, or if you know parents in that situation or who are concerned their child may have autism, Look At My Eyes is a book you should get.

You can order a copy from their website at http://lookatmyeyes.com or at online booksellers such as Amazon and Barnes & Noble.

[Disclosures: I received a free copy of Look At My Eyes for review.]

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Book Giveaway Reminders

by Tim on April 26, 2011

Life got a bit crazy around here so I’m rather late in posting this, but you have several opportunities to win some great books over these last few days of Autism Awareness Month.

We’re giving away two on our blog: 1,001 Tips for the Parents of Autistic Boys (which actually is quite similar to the version for girls) and Love You to Pieces. All you have to do is go to those posts, read the reviews if you want, and follow the instructions about leaving a comment. Deadline is Saturday, April 30th, so enter soon!

Our giveaway is part of a larger one sponsored by the S-O-S Research blog. The Best of the Best Giveaway Bonanza includes $1,100 of giveaways offered by a bunch of different bloggers along with reviews of what you can win.

So go check it out!

Best of the Best Giveaway Bonanza

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For Autism Awareness Month, we’re giving away one paperback copy of this book! Read on to the end for more info.

Love You to Pieces is a collection of literary writings from parents who are struggling with the various issues that come with parenting a child with special needs. Parents of children with autism are the most represented in this book, but the writings here cover a sweeping range of challenges from cerebral palsy, muscular dystrophy, Down Syndrome, deafness, communication issues, and much more to rarer conditions such as Angelman’s syndrome.

In here you will find both the expression of our common challenges as parents and the unique voices of families and their children. The stories and poems are arranged mostly in order by chronological age of the children in the writings, the early ones being about birth and infancy and the later about the path to adulthood. In doing so, the editor – Suzanne Kamata – has woven these individual stories into a grand whole that will stay with you long after you finish the book.

I almost without fail love this type of book. When parents and families tell their stories, I listen. I feel inspired, wiser, more educated, and less alone when I do. Of the books in this genre, I think Love You to Pieces is among the best.

Whereas books of the Chicken Soup or Cup of Comfort series lean heavily toward inspiration and triumph, Love You to Pieces unflinchingly drives straight for the emotional core of what it means to be a parent of a child with special needs. This isn’t a how-to book or a manual of tips and tricks. This is a roller-coaster you won’t forget.

The quality of the writing is superb. The writers do an astounding job drawing you into their stories and emotionally involving you in their lives. And it’s not a glossed-over version of events either. The rose-colored glasses are nowhere to be found. There is pure, unfiltered truth at every turn. Truth can lead to triumph, joy, desperation, hopelessness, and everything in between, and these stories take you to all of them and through every hard-fought step along the way.

They regularly left me with shortened breath, quickened pulse, and in some cases gripped by an all-to-familiar fear. Many of their emotions have been mine at one point, and for some others it’s a close enough walk from my experience to theirs that imagining what they must feel like isn’t hard to do. In those cases where I don’t have that frame of reference, the writers expertly drew me in and gave me enough glimpses into their lives to blow me away.

There are more than two dozen entries in this book, but to mention a few by name, “Coming to Samsara” is a perfectly written story of a mother who gave birth to severely premature twins at 23 weeks. It’s an emotionally wrenching journey full of sadness and beauty and coming to terms with all in life that is beyond our control.

In a book filled with gut-level honesty, “Magic Affinities” may be the most unflinching of them all. To give any of it away might reduce its impact, but I will say that it is a story that will stay with you forever. (A bit of warning – if your child engages in self-injurious behaviors, you may want to be careful with this one and read it on a calmer day.)

“Lives of the Saints” elevates everyday challenges and conflicts to the level of spiritual journey – not the ethereal, pie-in-the-sky, sweet-by-and-by kind, but one much more rooted in real life. Comprised of a series of snapshots into their family’s life, conflict and tension build without resolution. Its ending may feel unsatisfying at first, but you come to realize that there simply are no clean beginnings, endings, or resolutions on this path we’re on.

The poems are masterful as well. “Form and Void” for me captures the beauty-filled moments we have had blowing bubbles with our son. This poem finds magic and perfection in this simple act. “‘Severe Language Delay’: In the Kitchen with My Three-Year-Old” reads like a poetic transcript of my brain sometimes and should resonate with all of us who desperately try to understand what our children are trying to communicate to us. And for all of us who worry about what our children’s lives will be like as adults, pieces like the poem “Victoria’s Wedding” stand for the grieving visions of our children’s futures we are reluctant to admit we sometimes have.

If you only recently received a diagnosis for your child, this may not be the book for you yet. It’s hard to bring the raw emotions of those early days into contact with similarly visceral stories and not be overwhelmed. However I do think at some point or another that Love You to Pieces should be required reading for parents. But the goal of these stories and poems is not to drag us into uncomfortable places simply for the sake of doing so. These authors encourage us to acknowledge the emotions and thoughts we deem too awful or painful to speak aloud because so often they are common to all of us on this journey. They lead us deeper into ourselves to reveal the truths inside us, whatever those may be. And only when we shine light on them do we free ourselves to be the parents we want to be.

Want to win a copy? To enter your name in the drawing for the book, please share the title of a book you like that contains stories or poems from parents of special needs children, a parent’s memoir, or a link to a personal story written by a parent that you found particularly powerful and that is available online.

But no affiliate links! We’ll hold the drawing on April 30th.

While this is optional, we like to know where people are from, so if you don’t mind, please considering including what state (if in the U.S., or province in Canada) or country you’re from. Make sure the e-mail address you fill in works so I can notify you if your name is chosen. Thanks!

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1001 Tips for the Parents of Autistic Boys.jpgI originally posted this review last November. I have one more copy to give away for Autism Awareness Month, so I’m reposting this. Read on to the end for more info! Disclosures: I have several tips in this book, and I received complimentary copies of it.

The books 1,001 Tips for the Parents of Autistic Boys and the similar, companion volume for girls were just released, and I got a chance over the last few days to read the one for boys. I only have a copy of that version, so any references to specific sections below may not be the same in the girls version.

1,001 Tips for the Parents of Autistic Boys ambitiously attempts to provide helpful suggestions and ideas across the entire constellation of issues we face as parents. The result is a 480-page guide that for the most part succeeds in providing a wealth of useful information and plenty of ‘aha’ moments from me of ideas I’d never thought about. It’s not without its weaknesses, and certainly some tips are far better than others, but one of the strengths of this format is that you can take what works for you, maybe learn from some others, and ignore the rest.

In the Author’s Note, Ken Siri states that the book is organized by autism chronology based on how long your child has had an autism diagnosis. I found that the book functioned differently for me, and perhaps this is a positive, if maybe unintended, consequence of the book’s format. I found insights in most every corner of the book, and jumping around the pages seemed as good a way to read it as any. If the author hadn’t mentioned anything about a chronology, I doubt I would have thought about it. For many of us who have a few years with autism under our belts, 1,001 Tips is a brisk skim where we can mark the tips we want to think about later and cruise by the ones we don’t. The strength in this book is that it gives you a load of ideas that I think function very well as jumpstarters that can lead to you getting several new ideas of your own that may help you figure out a problem you’ve been stuck on.

The downside to this format is that there is very little space to expound or build on the ideas provided. However, many of the tips do come with references to their original sources, many of which are freely available online, so you can read more about those if you want to. In a number of cases, I did want additional information or just some clarification that wasn’t available. I see this more, though, as a limitation to this style of book rather than a problem with the way this particular book is written. (Bonus tip: If you want a great online resource that covers individual topics more in depth in essay format, visit The Thinking Person’s Guide to Autism.)

While the following caution is echoed in the book’s introduction, I think it merits repeating. There’s a lot in this book. Some of the suggestions contradict other tips in the book. In general, I think this is OK personally as this is just how the world of autism works right now. But you really do need to read this book with this in mind. No one tip or set of tips should be considered gospel. If you read it with this perspective and your ability to think critically – and this is true for any book about autism – you’ll get much more out of it.

I believe this is especially important to parents whose children just recently got an autism diagnosis. It’s easy to get horribly confused and overwhelmed by all the information that bombards you during this time. The rapid-fire nature of how the tips are presented in this book could make you easily feel like you’re on the business end of a fire hose. Know this is a normal reaction, read a few, put it down, then come back later. And always remember, these are ideas, not verses out of an autism gospel.

So if I had to add any tips to the book, I think I would have voted to start the book with the following:

1. When it comes to autism, don’t believe everything you read.

2. Develop a healthy skepticism to advice, particularly relating to treatments.

3. There’s so much we don’t know about autism that when someone begins a statement with “We know that…” and then proceeds to suggest a treatment or course of action based on what “we know”, there’s a good chance you should be skeptical.

For those of you looking for an introductory text to autism, I think 1,001 Tips is likely going to be a daunting read. Honestly, it wouldn’t be my first choice if you’re just getting your bearings in the wide world of autism. Looking back at our family’s first days with a diagnosis, I think that’s a time when people just need support, an understanding listener, affirmation that their child is perfect and wonderful, and reassurance that they as parents aren’t crazy. After you get that and get your bearings a bit, then start swimming in the information pool.

I personally found the sections on Supporting the Family Unit, Daily Life, and Productive Approaches to Parenting to be treasure troves of good ideas. I noticed I was marking one idea after another there. Not surprisingly, these sections address many of the issues we’re struggling with right now. When you have 1,001 tips, there’s something for everybody in here. (In case you’re wondering, you’ll find me back in the Safety section sharing some tips I learned from an expert and autism mom on our local police force.)

I do have one significant issue with this book. I personally found the section Medical and Nutritional Treatment disappointing. While there is broad coverage in the book of much of what is currently offered, the information presented is often rather technical with not enough background or references to allow parents to do their own research and determine whether these approaches are appropriate for their kids. Given what felt like an excessive number of tips in this section, room could have been made for these perspectives.

In many instances, the information provided comes from tips submitted by those who provide the therapies described, which also applies to the Therapy Implementation section preceding it. This alone doesn’t make their ideas wrong, but professionals who provide certain services will always paint them in the best light. While the purpose of this book isn’t to make value judgments on how good or how ineffective a treatment or therapy might be, they all come across as having a magical quality to them that daily reality regularly doesn’t bear out. All that is to say, just know there’s more to it in many cases.

Much of the information, for example, about biomedical treatments and statements related to ‘toxicity’ issues is limited in perspective to a particular viewpoint. I did not see any tips or commentary from the numerous parents who have tried these therapies, spent tens of thousands of dollars on them, and seen no real improvement from them. Also, there isn’t any discussion from medical professionals who refute the assumptions behind some of the biomedical therapies. I’m not casting a wide blanket over the whole range of these treatments, but I think their portrayal in these sections in many cases oversells their claims while glossing over how many parents and professionals view them.

I’m not going to play doctor here and try to argue for or against particular treatments. There are other places for that. But I do think not including the perspectives of numerous parents and professionals who do not recommend at least some of these therapies and disagree with the assumptions behind them is the one glaring omission of this book. These strong disagreements exist in the autism community, and any survey of autism should acknowledge this. Those of us who have been at this a while already know about all this. It’s those who have just recently received a diagnosis that I address this to. You need to do all your homework, familiarize yourself with the disagreements and controversies, study the research, consult with properly trained professionals, and make up your mind what you think is best for your kids.

While I do realize that the author sought a comprehensive survey of autism topics, a few just really didn’t need to be here at all. Frankly I was shocked by the title of the chapter “Preventing Autism”. We barely have an inkling of what causes autism, and the chapter title presupposes that we do and here’s how to prevent it. However, if you’re reading this book you probably already have an autistic child, so the chapter just comes across as a judgment on your poor, pre-pregnancy and pregnancy, parenting choices. What’s frustrating about this is that the tips in the chapter for the most part are good suggestions in the general sense for pregnancy and when you’re trying to conceive, though some are in various degrees of left field. Putting the “Preventing Autism” label on it, however, projects all of these tips through a lens of assumptions many of which are shaky at best, disproven at worst, and most likely just to make parents feel unnecessarily guilt-ridden.

The previous ranting aside, I do applaud Ken Siri for including several topics that parents aren’t particularly comfortable even thinking about. The sections on puberty, physical maturation, and sexuality were essential inclusions in the book and ones that I thought were handled well. There’s a lot more complexity to these topics than could possibly be discussed in the confines of this book, but it gets you thinking about the issues and so does its job well.

Overall, there are a multitude of helpful tips and ideas in this book, even for ‘veterans’ who have a few years of parenting an autistic kid under their belts. I think those of us who have been at this a while may be the best audience for this book as we perhaps have a more developed sense of which ideas have a good chance of working for our kids and which don’t. I think if I had read this book three or four years ago, it would have been a lot more challenging to process.

While there are some chapters and individual tips in this book I either disagree with or would suggest removing entirely, for the most part 1,001 Tips for the Parents of Autistic Boys contains a variety of ideas and starting points to address the needs of most any parent.

You can get some introductory chapters on their website at www.1001autismtips.com.

Want to win a copy? To enter your name in the drawing for the book, please share a tip of your own in the comments section about parenting an autistic child. We’ll hold the drawing on April 30th.

Because we generally endeavor not to give medical advice around here, please focus more on tips outside medical interventions and related therapies. We reserve the right to moderate or disqualify comments that pitch therapies or products in which the commenter has some financial stake, so to those people – don’t spam. And use your own judgment about whether any tips offered here are appropriate for your child, insert standard disclaimer of liability here, etc.

While this is optional, we like to know where people are from, so if you don’t mind, please consider also including what state (if in the U.S., or province in Canada) or country you’re from. Make sure the e-mail address you fill in works so I can notify you if your name is chosen. Thanks!

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1001 Tips for the Parents of Autistic Boys.jpg[Disclosures: I have several tips in this book, and I received complimentary copies of it.]

Note: If you donate $15 or more to my Operation Orange fundraiser for our local camp for autistic kids by midnight (Eastern Standard Time, U.S.) tonight (November 10th), I’ll put your name in a hat, and the name I pull out will get a free copy of 1,001 Tips for the Parents of Autistic Boys.

The books 1,001 Tips for the Parents of Autistic Boys and the similar, companion volume for girls were just released, and I got a chance over the last few days to read the one for boys. I only have a copy of that version, so any references to specific sections below may not be the same in the girls version.

1,001 Tips for the Parents of Autistic Boys ambitiously attempts to provide helpful suggestions and ideas across the entire constellation of issues we face as parents. The result is a 480-page guide that for the most part succeeds in providing a wealth of useful information and plenty of ‘aha’ moments from me of ideas I’d never thought about. It’s not without its weakness, and certainly some tips are far better than others, but one of the strengths of this format is that you can take what works for you, maybe learn from some others, and ignore the rest.

In the Author’s Note, Ken Siri states that the book is organized by autism chronology based on how long your child has had an autism diagnosis. I found that the book functioned differently for me, and perhaps this is a positive, if maybe unintended, consequence of the book’s format. I found insights in most every corner of the book, and jumping around the pages seemed as good a way to read it as any. If the author hadn’t mentioned anything about a chronology, I doubt I would have thought about it. For many of us who have a few years with autism under our belts, 1,001 Tips is a brisk skim where we can mark the tips we want to think about later and cruise by the ones we don’t. The strength in this book is that it gives you a load of ideas that I think function very well as jumpstarters that can lead to you getting several new ideas of your own that may help you figure out a problem you’ve been stuck on.

The downside to this format is that there is very little space to expound or build on the ideas provided. However, many of the tips do come with references to their original sources, many of which are freely available online, so you can read more about those if you want to. In a number of cases, I did want additional information or just some clarification that wasn’t available. I see this more, though, as a limitation to this style of book rather than a problem with the way this particular book is written. (Bonus tip: If you want a great online resource that covers individual topics more in depth in essay format, visit The Thinking Person’s Guide to Autism.)

While the following caution is echoed in the book’s introduction, I think it merits repeating. There’s a lot in this book. Some of the suggestions contradict other tips in the book. In general, I think this is OK personally as this is just how the world of autism works right now. But you really do need to read this book with this in mind. No one tip or set of tips should be considered gospel. If you read it with this perspective and your ability to think critically – and this is true for any book about autism – you’ll get much more out of it.

I believe this is especially important to parents whose children just recently got an autism diagnosis. It’s easy to get horribly confused and overwhelmed by all the information that bombards you during this time. The rapid-fire nature of how the tips are presented in this book could make you easily feel like you’re on the business end of a fire hose. Know this is a normal reaction, read a few, put it down, then come back later. And always remember, these are ideas, not verses out of an autism gospel.

So if I had to add any tips to the book, I think I would have voted to start the book with the following:

1. When it comes to autism, don’t believe everything you read.

2. Develop a healthy skepticism to advice, particularly relating to treatments.

3. There’s so much we don’t know about autism that when someone begins a statement with “We know that…” and then proceeds to suggest a treatment or course of action based on what “we know”, there’s a good chance you should be skeptical.

For those of you looking for an introductory text to autism, I think 1,001 Tips is likely going to be a daunting read. Honestly, it wouldn’t be my first choice if you’re just getting your bearings in the wide world of autism. Looking back at our family’s first days with a diagnosis, I think that’s a time when people just need support, an understanding listener, affirmation that their child is perfect and wonderful, and reassurance that they as parents aren’t crazy. After you get that and get your bearings a bit, then start swimming in the information pool.

I personally found the sections on Supporting the Family Unit, Daily Life, and Productive Approaches to Parenting to be treasure troves of good ideas. I noticed I was marking one idea after another there. Not surprisingly, these sections address many of the issues we’re struggling with right now. When you have 1,001 tips, there’s something for everybody in here. (In case you’re wondering, you’ll find me back in the Safety section sharing some tips I learned from an expert and autism mom on our local police force.)

I do have one significant issue with this book. I personally found the section Medical and Nutritional Treatment disappointing. While there is broad coverage in the book of much of what is currently offered, the information presented is often rather technical with not enough background or references to allow parents to do their own research and determine whether these approaches are appropriate for their kids. Given what felt like an excessive number of tips in this section, room could have been made for these perspectives.

In many instances, the information provided comes from tips submitted by those who provide the therapies described, which also applies to the Therapy Implementation section preceding it. This alone doesn’t make their ideas wrong, but professionals who provide certain services will always paint them in the best light. While the purpose of this book isn’t to make value judgments on how good or how ineffective a treatment or therapy might be, they all come across as having a magical quality to them that daily reality regularly doesn’t bear out. All that is to say, just know there’s more to it in many cases.

Much of the information, for example, about biomedical treatments and statements related to ‘toxicity’ issues is limited in perspective to a particular viewpoint. I did not see any tips or commentary from the numerous parents who have tried these therapies, spent tens of thousands of dollars on them, and seen no real improvement from them. Also, there isn’t any discussion from medical professionals who refute the assumptions behind some of the biomedical therapies. I’m not casting a wide blanket over the whole range of these treatments, but I think their portrayal in these sections in many cases oversells their claims while glossing over how many parents and professionals view them.

I’m not going to play doctor here and try to argue for or against particular treatments. There are other places for that. But I do think not including the perspectives of numerous parents and professionals who do not recommend at least some of these therapies and disagree with the assumptions behind them is the one glaring omission of this book. These strong disagreements exist in the autism community, and any survey of autism should acknowledge this. Those of us who have been at this a while already know about all this. It’s those who have just recently received a diagnosis that I address this to. You need to do all your homework, familiarize yourself with the disagreements and controversies, study the research, consult with properly trained professionals, and make up your mind what you think is best for your kids.

While I do realize that the author sought a comprehensive survey of autism topics, a few just really didn’t need to be here at all. Frankly I was shocked by the title of the chapter “Preventing Autism”. We barely have an inkling of what causes autism, and the chapter title presupposes that we do and here’s how to prevent it. However, if you’re reading this book you probably already have an autistic child, so the chapter just comes across as a judgment on your poor, pre-pregnancy and pregnancy, parenting choices. What’s frustrating about this is that the tips in the chapter for the most part are good suggestions in the general sense for pregnancy and when you’re trying to conceive, though some are in various degrees of left field. Putting the “Preventing Autism” label on it, however, projects all of these tips through a lens of assumptions many of which are shaky at best, disproven at worst, and most likely just to make parents feel unnecessarily guilt-ridden.

The previous ranting aside, I do applaud Ken Siri for including several topics that parents aren’t particularly comfortable even thinking about. The sections on puberty, physical maturation, and sexuality were essential inclusions in the book and ones that I thought were handled well. There’s a lot more complexity to these topics than could possibly be discussed in the confines of this book, but it gets you thinking about the issues and so does its job well.

Overall, there are a multitude of helpful tips and ideas in this book, even for ‘veterans’ who have a few years of parenting an autistic kid under their belts. I think those of us who have been at this a while may be the best audience for this book as we perhaps have a more developed sense of which ideas have a good chance of working for our kids and which don’t. I think if I had read this book three or four years ago, it would have been a lot more challenging to process.

While there are some chapters and individual tips in this book I either disagree with or would suggest removing entirely, for the most part 1,001 Tips for the Parents of Autistic Boys contains a variety of ideas and starting points to address the needs of most any parent.

You can get some introductory chapters on their website at www.1001autismtips.com.

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Book Review – “The Game of My Life” by Jason McElwain

April 8, 2009

If you’ve been around here a while, you probably figured out that I’m a huge fan of Jason ‘J-Mac’ McElwain and everything he both embodies and symbolizes about what our children can accomplish. (See also “Autism Goes Super”, “The Unlikely, Inspiring Combination of Gatorade and Autism”, and “Swifter, Higher, Stronger” – scroll down to the [...]

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Think All Flash Cards Are Alike? Think Again! – A Review of Goosie Cards

December 11, 2008

To preview what Goosie Cards are, visit their web site at GoosieCards.com. As we’ve chronicled in recent posts (see “My God, He IS Reading!”, “Roy G. Biv”), our son is all about his flash cards lately. They’re not going to displace the Sacred Wooden Letter Blocks of Steadfast Security and Comfort anytime soon, but flash [...]

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