About Stuart Duncan

My name is Stuart Duncan, creator of http://www.stuartduncan.name. My oldest son (Cameron) has Autism while my younger son (Tyler) does not. I am a work from home web developer with a background in radio. I do my very best to stay educated and do what ever is necessary to ensure my children have the tools they need to thrive. I share my stories and experiences in an effort to further grow and strengthen the online Autism community and to promote Autism Understanding and Acceptance.
Author Archive | Stuart Duncan

Do what you need to do, I won’t sue

By on February 16, 2012 in Autism, Parenting

I often hear horror stories in the news, from other teachers and all over the internet about parents being in some epic battle with their child’s school or day care because their child had to be restrained, separated from others or other cases like that.

Most of the time, everyone sides with the parent in a unanimous cry of outrage in the complete and total mistreatment of their child. Most of the time, that comes with very little information as the schools are often unable to comment on the situation, same with any enforcement personnel. This means that we only have the parent’s information to go on.

I won’t argue however that most of the time, that’s all we really need. What’s wrong is wrong.

Still though, this creates a situation in society that basically ties the hands of those teachers and care givers should they truly have the right or need to handle a situation where those circumstances arise.

Dear care givers

What I’m trying to say is, if you care for my child and he is in danger of hurting himself or someone else, please do restrain him. Please do send him for a time out, even to some other room if need be.

I won’t sue. I won’t call the media.

If my son hurts himself… in a private area… please do check it out. He’s hurt, he needs attention, give it to him. I understand that it’s not sexual, I understand that you have his and my best interests at heart.

I won’t sue. I won’t call the media.

But be warned

If my trust is abused or my understanding is taken advantage of, I will hunt down the person and make sure that no one finds them until skyscrapers start going up in remote parts of northern Canada.

My children are that important to me… but they’re also that important to me that I don’t want to see his care givers afraid to touch them for fear of me being the type of parent to make it a national news story.

time out chairThe reality

The reality is that when my son completely loses it and hurts himself or his little brother, or is breaking things, or is just generally out of control… I will put him in his room. I will drag him there if I have to.

And I fully understand… no, I expect… that anyone else that I have entrusted with the responsibility of watching him would do the same.

I won’t call it barbarism when someone does the exact same thing that I would have done in the same situation. I won’t give my story to the first reporter that will listen to me.

The reality is that I understand how it’s come to this but I also feel disappointed that it has.

Somewhere, lines have blurred… and it’s often due to those who take advantage of the situation or react too harshly to the situation. Those care givers who go overboard and actually hit a child, or do something else that is completely inappropriate.

There’s also the “not knowing” that we must face… since our children aren’t great at relaying the details, we have to just hope that the teacher’s telling the truth. And if they did do something wrong, what would be the likelihood of that?

In a perfect society, every person that comes into contact with a child would be certified do-gooders with halos and wings that could never do any harm… but there is no perfect society and that leaves us skeptical and scared.

But I refuse to hand cuff those who care for my children by never letting them do what I would do myself to ensure their safety.

If I wouldn’t do it, damn straight I won’t let them do it. But if I would take an action, such as dragging my kid, kicking and screaming to a time out… then I fully support his teachers/care givers doing the same.

I know a lot of parents won’t agree with me, or simply aren’t willing to let “strangers” do those sorts of things… I can understand that. But it is how I am and how I feel about it. If I don’t trust the person that my son is with, he won’t be with that person. It’s that simple.

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If you believe in yourself, the magic will happen

By on February 15, 2012 in Autism, Parenting

In 2007, a wonderfully fun little movie called Mr. Magorium’s Wonder Emporium came out featuring Dustin Hoffman, Natalie Portman and Justin Bateman. While this movie will never hold a candle to films such as the Wizard of Oz or Willy Wonka and the Chocolate Factory, it does shine in it’s own special way.

Dustin_Hoffman_in_Mr._Magoriums_Wonder_Emporium_Wallpaper_3_800

Just Believe

The Premise

Dustin Hoffman plays the magical being, Mr. Magorium… and by magical, I mean that he’s 243 years old and brings toys to life. His assistant is played by Natalie Portman who is struggling to find herself. She tells Mr. Magorium that she “feels stuck” and he responds by giving her the Congreve Cube… uh… a block of wood.

As you get accustomed to the magical world within the store, Mr. Magorium throws in a shocker in announcing that he has to leave… effectively, he’s going to die tomorrow.

This leaves her with a store that she’s not sure she wants, an accountant that hasn’t even seen a toy in years and a fun little boy sidekick type that is in the peak of his magic believing life.

The Magic

It’s a wonderfully fun movie for the kids… Cameron was mesmerized through most of it but did get bored a few times as the discussions about life would take away from the store and the magic.

But that was the thing, I think, in that this movie held so much more magic for the parents than it did for the children. I think that is what holds it back from being a classic like Oz or Willy Wonka but it’s also what makes it so important for parents to watch.

You see, as Mr. Magorium “leaves” and his assistant has to figure out her life, the store begins to lose it’s colour, the toys stop coming to life… essentially, it dies. It becomes a dark, dreary place that no one wants to step foot into.

It’s not until Molly (Natalie Portman’s character) realizes what it is that she has to do that everything comes back to life. She believes in the magic, she believes in the toys, she believes in the store and most of all, she believes in herself again… and the Congreve Cube begins to move.

It’s her belief that causes the cube to move, it’s her belief that brings back the colour and it’s her belief that leads the viewer to believe that, providing she always does believe, she too will live to be over 240 years old.

The Lesson

As Molly dances around the store and the toys begin to move, dance and fly, the colours come back, the music builds and builds and the children come running in the front door to see all of the magic, my son sat on the couch, hugging the couch cushion with a huge smile on his face.

I love to see him being so happy that he can hardly contain it. It’s a rarity.

So I decided to see if Cameron got it:

Me: So what did she have to do to make the magic come back?

Cameron: …  believe?

Me: Right! …  And what did she have to believe in?

Cameron: … magic?

Me: Nope… herself! She had to believe in herself!

Cameron: believe in herself?

Me: Yes, that means that she had to be happy being her. She had to know that she was smart and a good person. She had to know how awesome she is!

Cameron: and that makes the magic?

Me: Exactly. If you believe in yourself, the magic will happen.

While I don’t know just how much of that will stay with him, I know that it will stay with me. And I hope it stays with every parent that watches the movie.

Never stop believing in make believe. Never stop believing in silly, childish, wild and wacky fun. Never stop believing in magic. And most importantly, never stop believing in yourself.

It’s this that I will always remind my boys and will always do my utmost best to remind myself.

Autism or not, if you believe in yourself, the magic will happen.

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Birthday parties, autistics, parents and choices

By on February 9, 2012 in Autism

While many parents feel a great deal of pain in accepting the reality of a birthday party-less life for their autistic child, I have found that there are in fact some parents, a small number, that just don’t seem to get it.

The usual problem


birthday partyThe problem that most autism parents face is isolation… that feeling you get when your child is never invited to birthday parties. The parent feels this through osmosis, meaning, they feel isolated because their child feels isolated. They know that the question is coming one day: “Mom/Dad, how come I never get invited to birthday parties?”

It’s a terrible feeling, and not just because it is saddening, but it’s also maddening. Because deep down, you know the reason. In fact, in a way, you probably don’t even want your child to go to those birthday parties. So loud, so bright, so much excitement, socializing, awkwardness…. yes, for many children with autism, it’s far more a nightmare than a dream and yet… the child doesn’t know that. They just know, or one day will know, that they are missing out on a world of fun.

And so, as a parent, you are left with a twisted up stomach, knowing your child feels alone, knowing your child feels like they’re always left behind, knowing that one day your child will ask you and knowing that one day, you’ll have to answer.

The unusual problem

In my son’s (Cameron) case, we don’t have the usual problem because of the great school that he attends. He is in a “regular school” but they have dedicated 5 classrooms to children with autism, which means that his friends all have autism as well.

So when his friends have a birthday party, he’s invited. Or when he has a birthday party, he has friends to invite. It’s actually pretty awesome in many respects because, not only are they not missing out, but they’re gaining those valuable party skills that they’ll need in college (hey, I can dream, can’t I?).

Here’s the thing… even though the other kids in all of those 5 classes have autism, not all of their parents really “get it”. What I mean is, they don’t realize how lucky they are to have their kids going to birthday parties.

The problem that I face, is whether or not to invite certain other autism children from those classrooms. They’re the ones that easily meltdown, easily get aggressive, have little verbal ability…  you have to understand, they’re great kids and I love to see them when I stop in at the school, but it’s obvious that they will need some extra help and attention at a place like a birthday party.

What I expect, and this is probably where I am going wrong, is that their parents would understand this and do something as simple as… stick around. You know, go to the party and be there with their child to help out should a meltdown occur, to say to me “oh, don’t do that because my child doesn’t like that” or “my child can’t eat that”…  stuff like that. I don’t mind changing things up on the fly, I’m an autism parent too!

But they don’t do that. They leave.

And to be fair, I’m not talking about the parents who honestly and truly have something they need to do, like work. But the ones who see it as a break…. a chance to be free.

It’s not a chance to be free. It’s a chance to learn valuable socialization skills. It’s a chance to do something that many other children with autism can not. And this parent is taking it for granted. They’re taking advantage of it.

What to do?

So at my son’s next birthday party, I have a choice to make.

Do I invite that child even though I know that things could be… well, let’s just say, more of a struggle?

Should the child miss out because of their parent? Should the child be punished? Or, would it be more of a punishment to actually invite the child to a place that he/she won’t be able to cope with? I mean, if I don’t invite the child, the child stays home with their parents, where they’re comfortable and at ease, right?

I’m not really sure what the right answer is… all I know is that it would be so much easier if the parent just took it more seriously. If the parent would see it for what it is.

To those parents:

Don’t make me have to choose whether or not to invite your child just because you can’t be bothered to stick around.

Birthday parties aren’t the same for you or I, compared to “other parents”. Not for the person throwing the party nor for the parent of the child that is invited.

I’m sorry that it’s not happy, fun, break time for you like it is for other parents. But that doesn’t mean that it can’t be a really great time.

You need to step up.

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The brilliance of the innocence

By on February 4, 2012 in Autism

While out shopping yesterday, my son (6 years old with autism) said something that is so profoundly brilliant that it took a little while to realize the whole scope of it.

You have to realize that this is a boy who really has no concept of the value of money except that we parents make it and use it to buy them stuff. He doesn’t really get that some things can cost more than others or that sometimes we just don’t have the money for what he wants.

cameron ambition

Award winner for Ambition


So what did he say?

“Stuff that we need shouldn’t cost anything because we have to have it and that way, we’d have more money for the stuff we want.”

Simple right? Makes sense too. I mean, you start to think about all of the homeless people, the hungry people… the people who need basic necessities that simply can’t get it because they have no money. They should have these things because they need these things. We all should.

The things we want, now that’s what we need to work for. That’s what we need to earn.

The things we need, we deserve… simply by being human. The things we want, we have to work hard to deserve.

So it stands to reason that, if society could be revamped, from the ground up, the things we all need should be made available to everyone while the things we want would cost money.

The problem, as my wife and I saw it, is that most people don’t really know what they need. For example, most people think they need their cell phone. They don’t.

Many women think they need a good hair-do and make up while many men think they need access to sports or a fast car/big truck. They don’t.

It’s a bit of a warped mentality that we’ve all become accustomed to.

But I think that a system as my son envisions it, would really help to put things into perspective and firmly place that dividing line between needs and wants for us.

Another problem would be that those people that provide the shelter, food and other basic needs need to be compensated for their hard work…  but with enough thought, I’m sure that could be worked out.

Anyway, I’m not trying to work out the foundation for a new society, I’m just demonstrating how sometimes the most simple, yet profound, thoughts can really get you thinking.

And it came from, of all the unlikeliest of places, my 6 year old son who really has no grasp of needs vs wants nor that of money/value on things.

Or at least, I thought he didn’t.

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The complications of having delayed sensory overload problems

By on January 31, 2012 in Autism

I have a bit of a booming voice, it can get loud… so when my dog is particularly bad or my boys stop listening and I raise my voice… it gets attention. I’m not yelling or screaming out of control by any means, it’s just… raising my voice is… loud.

The problem with this is that my son Cameron is especially affected… since a sudden loud voice like that can send him running to hide under some blankets.

At least when that happens though, it’s instant. I’m done, he’s done… we go about our day. No worries.

The real issues come into play when it’s not done and over in an instant.

A positive is a negative

Cameron shows some pretty amazing resilience sometimes when it comes to being able to handle himself. Yesterday was a perfect example of this.

My boys were invited to a birthday party at an indoor playground where kids were free to just go anywhere and do anything. There were games all around, flashing lights and a huge network of netting and tubes to climb and go through.

A child’s paradise!

house of wee

Cameron is in green

When we arrived the place was full which meant the entire place was just a wall of noise. An occasional crying child somewhere in the distance, lots of screaming and a bit of laughing mixed in.

Cameron and his little brother jumped right in and played just as any child should… it was quite nice to see. They had a lot of fun.

But I knew, I just knew that this was going to be too much. It was too much for me and I wasn’t right in the middle of it.

See, Cameron won’t just have a meltdown right in the middle of the place… instead, he’ll store all that pent up energy until he’s back home where he feels safe.

So, even though he can have a great time and handle himself quite well for quite some time… it comes with a price.

Solving the mystery

At first, this presented quite the challenge for us as parents as we’d have to figure out why our little guy was completely out of control for a day or two. To us, it would seem completely random that he’d just be really moody, extremely hyper and very much unwilling to listen to us or do the things we asked of him.

But it wasn’t random. It was actually very much a cause and effect situation (which most things are), where the effect was hyperactivity, irritability and lack of control… and the cause was over stimulation that no one had noticed.

What would happen is that my son would go to school and they’d have an assembly, or go on a field trip, or a party like the one I just described… something somewhere would happen and even though my son had a wonderful time and everyone thought he was just the most perfect little boy… there was actually a time bomb building up pressure, waiting to get home.

The biggest thing is, it’s entirely up to us as parents to solve that sort of thing too because no one else will ever see it. They only see the boy that holds it all together during the day.

Over time, I’ve come to recognize the clues though. For example, at that birthday party, when it came time for everyone to sit and have cake, all of the kids were excited.. but only Cameron bounced in his seat. Literally.

He had so much pent up energy in him, beyond what the other kids had, that he quite literally could not keep his butt on his seat. And while he was still quite happy and having fun, I knew that if he can’t keep his butt on his seat even after I ask him too, that it’s a sensory problem that’s been building up.

Something he just has to do for himself

This is one of those cases where, we as parents, could decide to just not go to those places so that we don’t have to deal with the after effects but that’s not very fair to him. He loves going to those places and doing those things.

We could read every book we have and talk to every professional we can find and try to set up systems and procedures to deal with the after effects at home in a constructive way.

But ultimately, this is something that he has to learn to deal with. I can help to guide him as best I can, help to calm him, focus his energies somewhere… but this is something that is likely to stay with him for the rest of his life.. unlike me.

And to be honest, I think he’s starting to get it. When he gets home, he’s still moody and hyper but he’s learning to take time for himself to go off and make believe something on his own. His little brother gets mad sometimes that he can’t go be with his brother but it’s obvious that it has to be that way.

When he’s given his space and allowed to get that energy out through pretending his favorite video games, pokemon or bey blade battles… what ever it is he needs to envision… it works for him. At least usually.

It’s great that he’s able to do that. And it’s even greater that he’s able to put it all aside in the moment and be “just one of the kids” when there is fun to be had.

It’s been hard for us to figure out and to deal with… I’m sure it’s been even harder for him… and we’ll always get people asking questions about it as it’s not quite ‘normal’… even by autism standards… but it is what it is and it works for us.

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