After my last video, some people asked for a video from a child’s point of view. I thought about it from the point of view of Cameron’s brother and what he might say… this is the result.
I hope you like it:
After my last video, some people asked for a video from a child’s point of view. I thought about it from the point of view of Cameron’s brother and what he might say… this is the result.
I hope you like it:
When I started the project ‘Autism Understanding and Acceptance’, I did it with the intentions of helping those without Autistic children to better understand and accept people with Autism as well as the parents that do have children with Autism.
I knew though, that it also meant doing the same for parents that do have Autistic children. Far too often I’ve seen parents disagree, quite vocally and with much anger, where one has a child with Aspergers or “high functioning” Autism and the other has a child that is far lower on the spectrum, much more severe (nonverbal, not toilet trained, etc.).
This morning, I saw this news story where a woman abandoned her 10 year old, severely Autistic son to a hospital. He was just left there to wander the halls. When they found him and talked to her, it turned out that she was bi-polar, unemployed, has 2 other children, going through a divorce and being evicted.
Along with the story were a lot of comments, including extra comments from those who posted it on Facebook and so forth. Some were with some level of understanding while most were very judging…. some were even full of a lot of hate.
So I copied the link and shared it in a couple of places, asking what people thought… and one such place was my Autism Understanding and Acceptance fan page. I picked this place in particular for a reason.
In the article, it states that the authorities are not pressing charges. They are instead, focusing on the child and making sure that he gets the help and care he needs.
Parents on the other hand, not all, were pretty quick to pass judgment. Many stating “you just dont leave your kids” and “our kids aren’t throw-aways”.
Many parents, feeling for the child, imagine his loss, his confusion… he no longer has any semblance of his past routine, he no longer knows anyone at all and he no longer knows where he is. He must feel terrible and afraid.
The truth is though, that not one of us has walked a mile in her shoes. The truth is, not one of us knows her story, his story or what preceded that day.
The article tries to paint the picture with a quick list, as I did above (eviction, divorce, unemployed, etc) but that only gives us an idea.
The fact is that we don’t know how hard it really was for her, we don’t know for how long she struggled with this decision, who she talked to about it, what advice she was given, what her other choices were (or weren’t).
For that matter we don’t know what other assistance she tried to receive. Did she exhaust all of her financial options (there’s not always a lot of support from the government if you’re unemployed), did she exhaust all the options her local charities/groups could afford her? Did she get turned away from medical facilities for having no insurance or even for having her own disorder (bi-polar) to contend with?
We all know how hard it can be to get proper services and yet we’re quick to suggest that it would have been so simple for her to have the resources handed to her to avoid her having to resort to abandonment.
Another truth is, we don’t know just how hard it really was. I know it’s hard raising my 2 boys, one with Autism (not severe) and one without. This woman had 3 children… and one had severe Autism.
And in our minds, we can picture that… but some small part must also be saying “I don’t really know because I’ve never met him.” The reason for this is that it’s exactly what we tell teachers, doctors, professionals, other parents and everyone else when they tell you “I know what it’s like”… no, they don’t, because each child is different.
Furthermore, each parent is different. Some people simply aren’t good parents. Some people are really NOT good with special needs children. Not everyone has the same patience, tolerance, understanding, stress, anxiety and coping levels that we might have.
Would I have been able to do better than her? Would I still be caring for that little boy? I’d like to think I could but you know what, I can’t say that. I can’t possibly know.
My children aren’t like hers. My situation isn’t like hers. My life isn’t like hers.
It’s not exactly hypocritical but it’s pretty close, to judge this woman harshly and then ask others not to judge us.
When my son hits the floor at the grocery store, kicking and screaming, I deal as best I can but most likely I’m just paying the cashier to get us out of there. Other parents judge me. I can see it, I can hear it, I can feel it. And I hate it.
I make a very conscious and concerted effort to not judge others in the same way. When I see a screaming child, I look at the parent and smile. They know I’m thinking “It’s ok.. don’t worry about it.”
This situation is far more extreme but it’s no less different. We can not ask for others not to judge us all the while quickly, and vocally, judging another parent at the first media story we read of her.
Media stories seldom tell the whole story, media stories rarely are as accurate as they should be. But even still, from this media I can take a few points:
I would never give up my children but it doesn’t take a lot of television watching to realize that not everyone is parenthood material. Not everyone that has children should have children. And many of those people recognize that. It might not be right, but I can respect that. If they’re willing to do their best, and fail, and admit that they can’t do it.. I’d rather they gave up that child.
Adoption agencies are there for a reason. You can judge a person for giving up their child but for some people, they just have to. They aren’t you. The child may very well be better off with someone else than with a parent that only pretends to be a good parent… someone that may end up hating that child enough to do harm.
A person that snaps is a dangerous person. People can be pushed over the edge and that edge isn’t the same distance for everyone.
As part of understanding and acceptance, I recognize that not everyone can raise a special needs child. Not everyone can live through the same stresses that I can. Not everyone has it as easy or as hard as I do. And no one… not one person, is the same as me or my child.
Maybe I don’t always understand and maybe I can’t always accept… but that doesn’t give me the right to judge.
Understanding and Acceptance isn’t reserved for those without special needs children. I think we all could do with a little more of it.
Update 10:26am: This news piece shows the mother in court, explaining why she did it: http://www.wsvn.com/news/articles/local/21004795218839/
If I could snap my fingers and become nonautistic I would not do so. Autism is part of who I am. – Temple Grandin
This topic tends to come up a lot and tends to cause some tension between people when really it shouldn’t. The truth is that, just as much as Autism is a spectrum, so are the thoughts on whether or not to cure Autism.
I mean, obviously there’s really only two answers.. yes or no… but the reasons for these answers are quite wide ranging. And none of them are wrong.
There are some people who benefit from the way their brain is wired, becoming known as savants. They are extremely gifted in math, music, art… usually one specific thing out of a wide range of abilities.
However, that’s not usually the case. Still though, many Autistics and even parents of Autistics feel that there is nothing to cure. Autism is a part of who they are, who they will be and is perfectly natural. Yes, it may present some challenges but removing their Autism would be like removing their sense of humour, or their unique way of thinking.
Sadly, this isn’t true for everyone. For a very large part of the Autism community, Autism is a very real disability that renders a person unable to speak, function… live an independent life. It can make a person very aggressive, fearful and even, as some would call it, locked in their own world.
For people like that, for the people who have to make the hard decisions on behalf of those people… it’s quite easy to understand why they would want a cure. It’s quite understandable that they’d see very little to no benefit of having Autism and would never hesitate for a second in wishing they could go back and take it away.
These are just some examples, as I said, there’s actually a LOT of reasons for answering yes or no.
None of this is really new to anyone, however it should be pointed out that a big part of understanding and acceptance also includes doing so with each other. We can’t judge and condemn those who would choose differently from us when their circumstances are very different from our own.
Recently, my wife asked me “If you could turn back time and go back to under Cameron’s Autism, would you?”
My first reaction was, and I’m sure if you’ve read my blog for a while, you’d agree with this: “Have you met me?”
The truth is though, from a strictly curiosity stand point… like, let’s say there was a preview button, where you could simply see how different your child would/could be without Autism… I’d love to hit that button and see.
But would I remove the Autism? Or, to put it another way… would I take Autism away from him?
The answer is no. I would not.
I believe, for me and for Cameron anyway, that he’s actually doing very well and will likely have a good life ahead of him. It will likely be filled with his fair share of struggles and maybe even some very depressing moments… I know my life was… but I think he’ll turn out just fine.
The thing is, I do believe that Autism is a part of who he is. It shapes how he sees others and the world around him. It shapes every bit of the input that he takes in as well as his output.
It will give him unique insights into the world, a very different point of view.
For better or worse, the struggles and turmoils that he’ll very likely have to endure, thanks to that Autism, can make him a stronger person.
With proper guidance, lots of love and tons of encouragement… he can learn to focus the negatives into positives, in time. He can learn that all the greats throughout history saw the world differently, it was that gift that made them great.
And those people were outcasts, they were seen as different.
Would I go back and remove Autism from him if I could? No. He has the potential to be great with or without Autism. He has the potential to overcome any adversity that life presents him.
You may feel differently than I do, I can respect that. It’s a personal opinion that each of us makes for different reasons.
I say no because I believe that Cameron can be a wonderful human being because his potential is limitless.
I also say no because I dedicate my life to being there to help him up when he’s down, to help him see the positives in the negatives, to help him recognize the opportunities and to help him learn how to break down the walls that try to get in his way.
And I know that my wife, his teachers and the people that we have in our lives will support Cameron in the same way.
One day his dog will die, one day he’ll have his heart broken, one day he’ll feel very alone, one day he’ll have financial trouble…. one day, me wife and I won’t be here any more.
And as much I’d like to protect him from all of that… I can’t. And I shouldn’t. These things are a part of life and these things can build character or ruin a person. They’re the trials of life.
And as much as they suck, they’re a part of life.. and for Cameron, that includes Autism too. For all it’s benefits and even for all the incredible drawbacks, it is what it is and protecting him from it would be taking away a part of who he is and who he has yet to become.
Sometimes a blog post just can’t properly convey how a conversation would go, so I decided to put together this little video as an example conversation between two parents.
I’m quite happy with how it turned out and hope to make some more soon. It’s less than 4 minutes, I hope you like it.
Have you ever noticed that you never see Superman and Clark Kent in the same place at the same time? That’s rather odd, isn’t it?
They both exist, although you only see Superman from time to time where as you see Clark Kent quite often. They definitely do seem quite different though… Superman holds his shoulders up high, stands tall… seems to handle people well. Clark Kent on the other hand tends to slouch, keep his head down and isn’t exactly the coolest person in the group.
I got to thinking about it, if my son was that guy… then empathy would be his Superman persona and his Autistic traits would be his Clark Kent.
My wife and I have had a very trying couple of weeks… mounting stresses over mounting stresses. Nothing life threatening, we still have our health however, eventually, stresses have a way of breaking you down.
This is what happened to my wife. Eventually, one day, it became too much and she began to cry.
As I held her, my two sons sat on the couch… playing games.
After a couple of minutes, Tyler, my 3 year old without Autism, put down his game and came to us. He put his arms around us and asked his mommy what was wrong. “Mommy, why are you crying?” he asked.
Meanwhile, there on the couch sat my little Clark Kent. He knows his mom is crying. He knows that there must be something wrong, but he doesn’t even give us a second look. He just sat there, playing his game.
From time to time, I get to see the superhero emerge… when he’s needed.
Most of the time, it’s for his little brother. When Tyler is hurt, or upset… Cameron is there. Whether it be due to actual empathy or Cameron not wanting to get into trouble…. he consoles his little brother. It’s not always for one reason or another but it can be hard to tell which is which sometimes.
There’s something you need to understand about Clark Kent… even though all you can see is the slouched shoulders, lowered head and introverted nature, Superman is in there.
Clark Kent won’t stand up tall but he’s still bullet proof. You just can’t see it.
Nobody looks for Clark Kent. When someone is hurt or in need, nobody expects Clark Kent to answer. They want Superman. And it can be so disappointing when he doesn’t come.
When Cameron sat on that couch, it was disappointing that he didn’t come to his mother. Not surprising, but disappointing.
We are never upset by it though, never judging. We understand… we know… empathy is in there. Inside that little slouched boy with his head down, playing his game… Superman is in there.
He didn’t give us a second look… but he did look once. He did show his concern, in his way.
When you don’t know that Clark Kent is Superman, you don’t look for Superman within him. But when you do know, you can see it plain as day. You no longer see the glasses or the posture… you see Superman, in a disguise. You see him look to the danger and make the decision to show up as Superman, or to let it be as Clark Kent.
I see empathy in my son. I see it every day and I see him make those decisions every day.
Never assume something isn’t there just because it’s well disguised. When he’s ready, Superman will be there.
© 2024 Autism from a Father's Point of View. All Rights Reserved.
Powered by WordPress. Designed by