Truth Hurts: What To Do When Your Kid Always Speaks The Bitter Truth

Children with autism have the uncanny habit of speaking the truth all the time. This results in really embarrassing situations sometimes!

Autistic children (and even adults) have minds that tell them that being honest is more important than being polite. So you may hear sentences like “You’re fat”, “You’re ugly”, “I don’t like this Christmas present” or “I hate this grilled chicken.”

The book reading

When my son, Jonathan, was in the fourth grade, we took him to the library, which turned out to be quite an eventful trip! All the little kiddies and their moms were sitting on the library floor listening to a new author, Mrs. Spalding. She was reading a children’s dinosaur story that she had just finished writing and had not yet published. The children were all behaving so nicely, sitting with their legs crossed in perfect form. When Mrs. Spalding was talking about the dinosaur book, she asked the kids a lot of questions as well. The children would raise their hand and reply and it was all very interactive and engaging. At the end, the children started raising many of their own questions.

During this time, Johnny, who was in the back of the room, was frantically waving his hand in the air trying to get Mrs. Spalding’s attention. Finally, she called on him and out of his mouth came words that not only embarrassed me, but probably embarrassed her as well. “Mrs. Spalding, well, um, this is boring.” I looked around to see what all the other parents were thinking and, sure enough, they were glaring holes through me! I’m sure they were thinking, “What kind of a mother does this child have?” Jonathan was just being very truthful and said it the way he felt it, which is so typical of kids with autism.

Teach them to apologize

I took the opportunity as a way to teach Jonathan how to apologize to people for things that might hurt their feelings. I also explained to Mrs. Spalding a bit about autism and how there was nothing meant to hurt her feelings. It all worked out well in the end, even though the parents probably still thought I was in need of parenting skills! Well it was never going to be the perfect situation now, was it?

Sometimes, the truth just makes you laugh

But it’s not all bad. This literal telling of the truth also means that autistic children expect that everything you say is literally true too.

In the first grade, Jonny was just learning how to apply sentences to a context and not always take them literally. He did not like to go outside to play, probably because of the social challenges on the playground. One day, he decided to tell his teacher, Mrs. Shincaryk, that he was too sick to go outside to play because he had a tummy ache.

Johnny’s aide, Caraly, heard this news, went to him and said “Johnny, a birdie told me that you don’t want to go outside to play because you have a tummy ache. Is this true?” Johnny replied “What? I didn’t know Mrs. Shincaryk was a bird! It’s really cool to have feathers though.”

Johnny’s literal understanding of what Caraly said was very endearing to us all. It’s times like these when you thank God for having such special little ones.

Identifying And Understanding Hyperlexia in Autism

Hyperlexia is a syndrome characterized by an intense fascination with letters or numbers. Children with hyperlexia show a very advanced ability to read, much higher than kids their age. Hyperlexic children often begin reading at very young ages, sometimes at age two.

Mix this condition with a child with autism and you’ve got yourself a whole lot of confusion. Between 5 – 10% of children with autism are estimated to be hyperlexic as well.

My oldest child, Jonathan, was all of two and a half when this incident happened. My husband and I took him to the park at Edmonton, Alberta for a family outing. We were both holding each of Jonathan’s hands and playing with him. “1-2-3 weeeee!”, “1-2-3 weeeee!” we went. That’s when Jonathan spotted a truck with the words ‘recycle’. The next thing we heard out of his mouth was “re-cy-cal”. My husband, Jim, and I looked at each other in amazement as we realized he had just read his first word.

Now Jonathan was autistic and just barely learning how to talk, let alone read. We were so taken by surprise that we actually didn’t believe it at first. We thought, “Wow! We have a gifted child in our hands.”

We were so excited that we called the Autism Society to tell them all about it. We spoke to a lady called Anita who, after hearing us patiently, informed us that this was hyperlexia and while it was certainly wonderful that Jonathan was able to speak, he may not be comprehending what he’s saying. Poof!

Hyperlexic children are brilliant at visual and auditory memorization. This means that they easily pick up things that they see and hear. They do not learn language the way that most other children do – sounds to words to phrases to sentences to conversations. Instead, they memorize what they hear and have a challenge in deconstructing sentences to find the meaning of smaller phrases within them. Therefore, they cannot comprehend what they read. In fact, they also find it very difficult to create original expressions.

Long story short, some children with autism demonstrate this phenomena and can lead many parents down the wrong pathway. What Jonathan was doing was showing an innate ability of repeating things that he heard other people say when they saw the visual construction of the word ‘recycle’.

Such kids are amazing readers and with the right communication strategies, you can gradually increase their comprehension skills. With hyperlexic children on the autism spectrum, enhancing their comprehension skills will give them a boost that can even make them surpass their peers in language and communication. That is really something you should be aiming for!

For me, I’m glad that we were given the right direction to recognize it for what it was. Thanks to that, we took immediate measures to get Jonathan into a proper intervention program to encourage his comprehension skills.

Early Intervention Can Do Wonders To Your Child’s Functioning And Communication

My youngest son, Alex, has had many, many challenges in his life. He was diagnosed with mild ataxic cerebral palsy at the age of six months. Thankfully, we were able to dig up and use resources to help our newest born. This included speech and language therapy that meant that we had to shell out to the tune of $350 from our pockets three times every week.

While these resources are by no means easy to accumulate, we soon started seeing the benefits of our decision. Thanks to this early intervention, we now call him Mr. Chatty Cathy. We are sure that had he not had an early intervention, he may not have ever spoken.

Children with autism have a lot of trouble communicating. They often don’t start babbling at the age they’re supposed to and show a lot of delay in starting to talk. You start realizing this when all of the similar aged kids around you start talking but your child wont. Instead, your child starts engaging in repetitive behavior like staring at certain objects like their feet or other people.

Sally Rogers at the UC DAVIS MIND INSTITUTE in California conducted a small pilot study on early intervention of autism. The study showed that 5 out of 7 babies between the ages of 7 and 15 months who showed signs of autism were able to catch up with the developmental growth of other kids their age after an early intervention program.

Today, statistics show that 25 – 50% of autistic kids who receive early intervention can move into general education streams by Kindergarten. Additionally, several others move into general education by the next few grades. Many others need significantly less service provision in the future.

During his early years, one of the major challenges Alex had in his communication was an inability to hold concepts together in to a complete thought. This was one of the problems that we tried to deal with. For example, when pictures of a baseball bat, a football, a softball, a cash register and a pair of skates were shown to Alex, he had a difficult time understanding that that was a sporting goods store. Slowly, but gradually, we trained his mind to read these patterns and make conclusions. He’s still not great at this stuff, but the bottom line is that we’re happy he can talk and communicate with us. His life would be much more difficult without having this type of early intervention.

Subsequently, Alex’s doctor stated that Alex no longer qualified for cerebral palsy and we were elated. “Alex is not a CP kid”, he said. This was great news at the time.

Not many families are able to diagnose or afford early intervention. It would definitely be helpful if parents had a DIY kit on strategies to use for their kids. Our goal with Autism Today is to make resources available for everyone through early recognition, diagnosis and subsequent strategies for improvement of an autistic child.

A Personal Message from Karen Simmons

When I co-authored “Chicken Soup for the Soul, Children with Special Needs” with Jack Canfield, Mark Victor Hansen and Heather McNamara, the biggest dilemma we faced was what to call the book ,as folks both did and did not want to be labeled in certain ways. It was reported to be the most challenging title the Chicken Soup people wrestled with to date. What we learned was that people on the autism spectrum and other spectrums for that matter, are people first before their condition!

Some of my favorite people are on the autism spectrum! My dad, my son, Stephen Shore, my sister (maybe) and even a bit of me! When my son was diagnosed in 1992 I embraced his autism and mostly tried to focus on his gifts, strengths and talents rather than the deficits he displayed at the time, after I got over the initial denial of it all. Of course I had the same challenges families face in those beginning years and could have chosen to have a negative attitude and chose instead to focus on the positives as much as I could. As part of his early intervention, before the days of behavioral interventions, I wasn’t about to wait around for science to prove to me whether certain methodologies were legit or not. I just wanted to find tools that would enable him to have the best life he could have.

Of course I used my own “mom” common sense compass, built into most moms, though I tried things to help my son that were not necessarily science based. They were “mom” based. My real question is who are we to “fix” people? All people are broken in some way, and to different degrees. ALL people have different ways of being though certainly no one is “better” than the next person. If we feel with our hearts and souls while helping people through tough times, in whatever way makes sense at the time, the world will be a better place!

Our time on the planet is all-together too short to waste on efforts that take an extraordinary amount of time to prove one way or the other. Often, by the time double blind studies are concluded, methodologies have changed. Don’t get me wrong, I’m not a Polyanna, with an altruistic view, and I do believe in research with a true return on investment. I propose that we focus to create a better overall society that promotes everybody flourishing.

Autism is not a disease, an illness or a disorder, it’s a different order and people on the spectrum as well as other spectrums, are wonderful souls and deserve the best, most successful lives, whatever that might look like. Thanks for being you, John!

Karen Simmons
CEO, AUTISM TODAY

Be part of the Art! Exploring our Autism Arts Website, ArtismToday.com

Be part of the Art!  Start by exploring our autism arts website, ArtismToday.com

The Art of Autism is universal.  For so many of our kids, art is that first inspiration that lures them out, into a world of fulfilling social interactions, through their exceptional, autism-enhanced ability to connect to others through art.  That’s why Autism Today has teamed up with author Debbie Hosseini, to create Artism: The Art of Autism, a magnificent coffee table book, packed with beautiful art by artists who happen to have autism.  As you enjoy the book, Hosseini takes you on a journey into the lives of 54 artists from around the world, and how each has used art to overcome the challenges of living on the spectrum.  In the process, she dispatches, one by one, with common myths about people with autism, perceptions among neurotypicals for example that people on the spectrum lack emotion, creativity, sensitivity, and empathy.

But Artism: The Art of Autism is not just a book.  It’s a community!  Be sure to check out our website, ArtismToday.com.  Interact with Debbie Hosseini, who curates the site.  Follow Artism artists in the news.  Each artists continues to attract interest and media coverage now that Artism: The Art of Autism is now available.   Learn about Keri Bowers’ upcoming Art of Autism Tour dates and how to participate, www.normalfilms.com.  Share YOUR story or that of a friend whom art has helped to cope or to transcend the challenges of autism.  Best of all — have fun!  Our goal is for ArtismToday.com to be an online crossroads for everyone interested in art and, yes, autism too.

We look forward to seeing you, interacting with you and learning about you and your art soon, on ArtismToday.com!

Every Autism Mom is a Star: But there is only one Eustacia Cutler

What can I say about Eustacia Cutler?  It is impossible to know Temple Grandin‘s story without intuitively knowing the strength, the dogged determination of the woman who never gave up on her daughter.  Even if you knew nothing of Eustacia, her background, her own beautiful telling of her story, A Thorn in My Pocket, you would know her through Temple.   And if you talk to Temple, you learn how much Temple herself is the product of an ethical, and maternal act of faith, in Temple’s inherent worth, autism and all.  At a time science would have instructed her to abandon her child to an institution, she embarked on a deeply personal equivalent of the Apollo mission, sacrificing her own ambitions (which were many for a Harvard-educated young woman of the 50s), and focusing on Temple’s potential.  How richly that journey has paid off – for Temple, and for all of us.

Temple Grandin honored her mother so beautifully at the Emmy Awards.  Even those not entirely familiar with the autism story, or even the movie Temple Grandin, remember the moment when the lady in the cowboy gear brandished an Emmy statuette and gave her mom a shout out.  It was an electrifying moment for autism moms.  Those tributes to Eustacia Cutler have continued to flow since the Emmys.  I wanted to be sure everyone has seen this one. In it, Julia Ormand, the actress who played Eustacia in the HBO movie, gives Eustacia her Emmy statuette at a conference last November.  Noting that Eustacia had once hoped to be an actress, Ormand jokes that Eustacia can use the Emmy as a door stop.  But then, unscripted, Ormand says: “I want you to have it for all the doors you have opened.  I want you to have it for the thing you let go – that you gave to me.”

See video of Eustacia’s Tribute to all mothers http://www.youtube.com/watch?v=_ykBWPpHDsc

Ormand’s explanation of an autism mom’s sacrifices is a restatement of a code we all are familiar with, as autism moms.  “This mother met the challenges of motherhood with such courage.  She did not attempt to be her kid’s best friend.  She said ‘I’m here to give you boundaries.  I’m here to do the tough stuff so you can walk through life empowered.”  Eustacia, in accepting the award, drives the point home.  “This is for all the mothers who work in silence.  Autism is a family disorder — everyone is affected.”

Eustacia, thank you for joinning us in Vancouver.  We can’t wait to welcome our favorite mom – and to be warmed by your triumph.

It’s a Personal Question: Are You Behavioural or Biomedical? Or Both?

Dear friends,
Welcome to this special Autism Vancouver edition of the Autism Today newsletter.  In just two weeks, I will stand up at a podium at the magnificent Vancouver Convention Centre, on the harborfront of one of Canada’s most beautiful cities, and open our 3rd Biennial Behavioral and Biomedical Congress.  I am thrilled by how far we’ve come since our first Biennial Congress.  And imagine our speaker line-up: Temple Grandin’s mom, Eustacia Cutler; Sheila Wagner of Emory University, one of America’s top autism educators; Dr. Bill Shaw, CEO of Great Plains Laboratories, and one of the top advisors to health professionals on the biomedical aspects of ASDs; popular behavioral experts like Stephen Shore and Doreen Granpeesheh; and many others.

I won’t kid you – it’s not easy to combine the true believers from either the purely behavioral or purely biomedical schools of thought at a single event.  Some people feel deeply antagonized by the mere suggestion that both sides could have something to teach us.  Some speakers don’t like the format, some families and teachers don’t understand it.  And imagine trying to explain the significance of such a happening to the mainstream media!  But at Autism Today, we are deeply focused on empowering individuals – people with autism spectrum disorders and their families – on the most complex, personal journey they will face – the path of emergence (some even say, “recovery” and even, “cure”).

The argument over how to define a fulfilled, fully expressed life is as varied and endless as the human race.  Our job, as we see it at Autism Today, is to equip each person and his or her family with information about every legitimate tool they might use to find their own way.  There are not top-down answers in autism.  It’s not only grass roots; it’s deep in the soil.  Success depends in part on a willingness to get dirty!  And on some level, love that process.  Watch the HBO movie about Temple Grandin, or listen to painter Keri Bowers describe her work with her son Taylor Cross, literally spending hours, dipping him bodily into paints, and creating art, or listen to almost any narrative of successful intervention, and you learn – it’s a hands-on process.

Autism Vancouver is still two weeks away.  But it is not too early to give thanks to our champions who will make this such a special event.  None of this could happen without a dedicated staff and the support of our Autism Today friends and family.  We especially wish to thank Keri Bowers, founder of Normal Films, and director of Normal People Scare Me, Debbie Hosseini, author of our newest title, Artism: The Art of Autism – both tireless champions of the arts as a vehicle of emergence — Kelly Lebrock, who has donated her star power and agreed to act as honorary hostess of our Gala, and Diana Graling, of Helms-Briscoe, whose invaluable logistical counsel is helping us to run a tight ship in Vancouver.

For those unable to join us in Vancouver, I hope you won’t mind this special Congress edition of the Autism Today newsletter.  Please remember we will be broadcasting segments of the Congress via webcast every day of the Congress, April 7-9, and for those who wish to experience the complete program, we will make this available in DVD for purchase.

Soon, we will have the capacity in place to make all of our programming available by live webcast, so you can enjoy and benefit from it without the expense of travel, and in the company of family, students or colleagues.  Keep an eye on our newsletters for announcements about these enhancements to our program offerings.

Thank you again for your friendship and support.

Warm regards,
Karen?

Free Live ABA Webcast with Doreen Granpeesheh, Founder of CARD

You’re invited to join us for a Special Live Webcast on March 14th, 2011 presented by renowned Dr. Doreen Granpeesheh on Applied Behavioral Analysis (ABA): A Flexible and Affordable Intervention for Autism! This web-cast is being brought to you from Autism Today and is Absolutely FREE! With the 3rd Autism Vancouver Biennial Congress just around the corner we’re extremely excited to give you this no-cost gift featuring one of our amazing event speakers.

The Live FREE Webcast Details are Listed Below:

Applied Behavioral Analysis (ABA): A Flexible and Affordable Intervention for Autism
Dr. Doreen Granpeesheh, Executive Director and Founder of the Centers for Autism and Related Disorder (CARD)

March 14th, 6pm PST / 7pm MTN / 8pm CST / 9pm EST

The webcast can be viewed at the following URL:
http://www.ustream.tv/channel/autismvancouver

As you know, Doreen is one of the world’s leading ABA practitioners and will be a featured speaker at the Autism Vancouver Biennial Congress, this coming April 7-9 2011!

What you will learn on the Live Webcast…

Internationally-renowned pioneer of Applied Behavioral Analysis (ABA), Dr. Doreen Granpeesheh, provides a practical, informative introduction to this powerful treatment methodology. Widely practiced in North America, intensive ABA has been scientifically proven effective as a means of improving social and intellectual function in pre-schoolers.  Dr. Granpeesheh will also explain how  online tools and services now enable parents and educators to apply ABA more affordably and conveniently.

See you there!

Karen’s Survivor Story

Based on my book, Surrounded by Miracles

When I woke up, I couldn’t believe the pain shuddering through my entire body.  I wanted to die.  But wait, where was the baby?  I knew I was pregnant and that I had just delivered a beautiful baby boy, but he was nowhere in sight?  As I glanced out the window I noticed the grass was green, but just yesterday snow had covered every square inch of the landscape.  How could this be?  As my nurses came into focus, as well as the faces of my husband and mother, a story began to unfold as miraculous as those angels that surrounded me. They began to tell me what had happened during the past 57 days. I had almost died, was given a 1% chance to live, and was even read my last rites, but I had somehow managed to live again, against all odds.

Yes, I had survived, and so had my son.  But our real story was just beginning. My new baby, Alex, was soon to be diagnosed with ADHD.  His brother Jonathan, my two-and-a-half year-old, had just been diagnosed with autism.  It was a double-whammy!  Along with these two special boys and so many children like them, I had survived for a reason that would soon become very clear.

Where a life starts and why it starts again is the question every survivor faces. My story actually began fifty-three years ago when I was born in Oklahoma City.  Six years later our modest family of four packed up and moved to Florida where I grew up, from one hurricane season to the next.  This must be the reason for my attraction to high-energy people and my fearlessness, which both have served me well.
Dad had his own aeronautical engineering company, and mom worked for Pan Am Airlines, so my sister and I got to travel the world at an early age.  I loved the picturesque, quaint communities and the unique perspective others had in the many different cultures I visited.  I remember one woman in Ratnapura, Sri Lanka, being totally content sitting on top of a pile of rocks and breaking the big rocks into little rocks.  That’s what she did all day long and she had the biggest grin on her face I’d ever seen!  This is also where I fell in love with gemstones, which would become one of my callings in life.

After graduating from high school I attended college in north Florida and then decided to join the U.S. Air Force where I was stationed in Panama City, Florida. But four years was more than enough time for me to realize that the military life was not for me, so I received an honorable discharge and enrolled in the Gemological Institute of America in Santa Monica, California to become a Graduate Gemologist. Upon graduation I started a company in Bellevue Washington.  I later sold the company when, at age thirty-one, I met my current husband and moved to his home in Canada where I set up a jewelry store called The Gem Gallerie.

Jim and I had a wonderful life together. When I was younger, I would never have thought I wanted children, but at age thirty-four, Jim and I began our large, happy family.  We had our first three children in three consecutive years, one right after the other. I had my fourth child, Jonathan, when I was thirty-nine years old. He was rather quiet from the start, which was fine with me since I had three other kids in diapers.  I never noticed anything was different.  How could I?  Kim, Matt, and Christina consumed all of my energy, and I was still running the jewelry store.  Jonathan, I thought, was the perfect baby.  He would lie quietly in his crib, apparently perfectly content with the world.  In fact he didn’t really like to be held much.

It was my sister-in-law, Anna, who insisted that Jim and I get Jonathan evaluated for autism after she happened to listen to a radio talk show on the subject. How could I have known he was autistic?  I didn’t even know what autism was or what symptoms I should be looking for.  This was 1992 and autism was still relatively new territory, even for specialists.  It turned out that Jonathan did have autism and I was told to bring him back in a year, when he would be three-and-a-half years old.

For the next two years I met with special needs counselors and teachers who helped us work with Jonathan and I attended special needs conferences all across Canada.   We also went on to have our fifth child, Stephen, who was perfectly healthy. We thought we had faced our major hurdle in life and had come through it together as family.  We never guessed what lay ahead.

On April 18, 1994, I checked into the hospital for what I thought would be another routine childbirth like all the others. I was ready to deliver what would be our sixth and—though we didn’t know it at the time—last child. I had had a typical, healthy pregnancy.  I expected to go home in a couple of days and resume our busy, fun-filled life together.  But just minutes after Alex was born, I started to hemorrhage.  Nothing could be done to stop the bleeding.  What happened in the next 57 days was an unimaginable fight for my life. My family, friends, doctors, and nurses tried everything to pull me through—including a few “wild” schemes to get through to me in my comatose state.  It was ultimately just a few words from my husband that, unknown to him, gave me an ironclad will to live and to return to my family.  His words still ring in my ears.

“Don’t worry, honey.  I’ll take care of the kids”

After I woke up from my near-death experience, or “back-to-life experience” as I like to call it, one thing after another began to happen.  I had an internal drive and relentless passion first to write a book for my autistic son, Jonathan, called Little Rainman so he could understand his own autism as well as the people and the world around him.  I had six children at home at the time, so it’s not like I had extra time on my hands!  In fact every spare moment went into my urge to share my experiences with Jonathan with the world.

Shortly after the book was published I started a non-profit organization.  I would wake up in the middle of the night with visions of what this would be and the words “Key Enrichment for Exceptional Needs” would appear in my head.  In 1996 the KEEN Education Foundation was born as a driving force behind the effort to serve not only autism but also all types of special needs. Today, KEEN continues to support the educational goals of people with exceptionalities by providing them with the tools, research, and resources they need to thrive.
After this I started Autism Today, a small company that became the exclusive Canadian distributor for the worlds largest publisher of autism books and resources at the time.  I attended conferences and workshops to learn as much as I could about autism and special needs.  We’ve now grown from a simple one-computer, home-based business to an international organization that receives close to three million hits a month on our website, www.AutismToday.com.  Parents, educators, and more come to us for resources, coaching, and the latest news and articles from the top experts in the field. When baby Alex was diagnosed with ADHD, I expanded Autism Today to offer information and resources for the parents and educators of all special needs children.

Looking back now, I believe that breaking open my own rocks to see shining gems emerge from what look like only rough stones has always been part of what makes me smile as well–even today–only the stones have changed. What we experience when we are young and what we gravitate to as we grow is preparing us for everything life has in store for us.  Our new banner headline for Autism Today is “Shining New Light on Special Needs.”

As far as surviving, I suppose it is only in looking back at where we’ve been that those meaningful patterns start to emerge.  A new phase in my life is starting Healing Attitudes Seminars, which redefine perfection to share the secrets of the survivor’s story with others who have been there and for those who realize there will always be challenges in the road ahead.  In one way or another, we all are or at some point will be survivors. Here are just seven of the secrets I have learned and now develop and share with others through this program:
What doesn’t kill us makes us stronger–for a reason.

We all teach what we need to learn most, and by doing so everyone’s life is enhanced.
We all have special needs—some are just more obvious than others.  Do what you can to help others heal.
At any given moment, choose peace rather than conflict, love and acceptance rather than fear, and compassion and understanding rather than guilt and judgment.

Practice empathic listening and hearing your own inner, intuitive voices as well as  “true” voices of others.
Transcend all “types” of spirituality to embrace and teach the underlying message of love.
Bring others “up” to shine, acknowledging each person’s special gifts–the beauty and the hope.

I am certainly no angel, but I feel to the very depth of my being that I’m surrounded by miracles.

Karen Simmons is the parent of six children, ages 10 to 20, two of whom have special needs.  She is the founder and CEO of the internationally recognized Autism Today© non-profit organization, established in 1998, one of the world’s leading resources for all special needs, both online and at numerous conferences and events worldwide.

Karen is also the author of four celebrated books, including her soon to be re-released survivor’s story, Surrounded by Miracles.  Currently based in Alberta, Canada, Karen is a dual citizen of the U.S. and Canada, which gives her and her organization a uniquely expansive network with the special needs community worldwide. For more information about Karen’s Healing Attitudes around Special Needs Seminars, her books, and other special needs resources, please visit www.AutismToday.com

“Different Son” by Susan Werner – A Song about a Boy with Autism

Dear friends,

I launched Autism Today as an online community in 1998. For families touched by autism, and facing so many challenges already, the Internet is more than a tool, it is a lifeline, connecting us with other families, expertise and resources, inspiration, and yes, good old entertainment.

Every week, something truly magical pops up on YouTube.  This week we received a video by Susan Werner, a deeply personal song about autism, entitled Different Son. It is from her album,  Kicking the Beehive, which will be released March 1st.

Her agent says he fears Different Son will not get radio play, because it deals with too serious a subject.  But with one in 110 children born with the disorder in the US, we feel this is, for all the right reasons, music for all ears.

At Autism Today, we have a special love for artists.  Something magical happens when a child on the spectrum is moved to create art.  Properly cultivated, art can be the key to unlock exceptional gifts.

This is why we created the Artism series; and will soon publish Artism: The Art of Autism; and celebrate Autism Vancouver with a wonderful arts carnival.

So, today, instead of my usual blog, I decided it would be enough to share a beautiful song, about something we all are passionate about. Sometimes a picture — or a song — is worth a thousand words.

Have a lovely week!
Love,
Karen

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1 in
45

Diagnosed with Autism

Over
100

Autism Diagnosis a Day

Costs
238

Billion per Year

Boys are
4

Times More at Risk