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The kind of self advocate that I want my child to become

Tyler and Cameron - Brothers

Tyler and Cameron – Brothers

I am writing this because I’ve had quite a few people ask me if I want my son to be an advocate like me or what I would hope he’d say. I thought this would be a good time to address those questions.

If you’ve read anything from me in the past, you likely expect the answer from me to be something along the lines of “a positive role model that is respectful and understanding of everyone.”

And yes, should he truly wish to speak up and raise awareness, understanding and acceptance of autism, that is pretty much the exact type of advocacy that I would love to see from him.

I understand that some advocates take the “fight for our rights” approach and that is very much needed as well. I won’t lie. Yes, some get caught up in the battle and it becomes hateful and negative… but this isn’t about that right now.

There’s more kinds of advocacy too. As much as some might disagree, those that fight for health care changes, particularly those surrounding vaccines, are advocates as well. Those that fight to cure their now adult sons and daughters that are still living at home or in a home, they are advocates.

There are even some self advocates that wish to be cured of their own autism. They are self advocates all the same. Even if they might not be sharing the sentiment of the “majority.”

I’ll love and respect my son and be very proud of his efforts no matter which approach he takes.

However, the honest truth is… and it’s kind of hard for me to admit is… I sort of hope that he doesn’t get into the whole thing at all.

That’s not to say that I’ll be disappointed if he does. It would be pretty awesome if he does because I think he can do a lot to improve things.

But I kind of look at it like how we shelter our kids from the 6 o’clock news. Because they don’t need to know about the wars, the murders and the state of our economy. They are happy. Carefree. The world reaches as far as their furthest friend’s house down the street and the worst thing that could happen is that they drop their ice cream cone in the middle of summer.

A self advocate (or even a parent of a child with special needs for that matter) that lives their own struggles, battles and daily disappointments and achievements will have enough in their lives to keep them both busy and content too, depending on how that day goes. For most people, that’s more than enough.

The advocacy world seems pretty great at first, getting positive feedback and support and reaching more and more people with each day’s effort you put forth. But at some point, it changes. You start reaching haters, who “come after you” where ever you may be sharing your thoughts. You get people who don’t just disagree but disagree via attacks and threats. You get people who expect more from you whether it be more effort or more time.

The best advocates are the ones that can deal with these things either by tackling them head on, rising above them or by simply paying no attention and doing what they do regardless.

But it’s taxing. It can wear you down and make you tired.

And at some point, invariably, you start to wonder…. what’s the point?

Do I hope that, should he become a self advocate, that he’ll have the strength and wisdom to over come these hurdles? Of course! I hope I can be strong enough to help him be ready should that time come or to be there for him at that time. I hope even more that he can be a self advocate and not need to experience those hurdles at all.

But the honest to goodness truth is, I would kind of rather him just not need to get to that point.

I’m one of those parents who, probably blindly and even wrongly, wants to shelter his kids from the evils of the world. To not ever have to hurt. To never know what terrible stuff is really happening out there.

But they will. One day, many days… they’ll be made all too painfully aware.

And avoiding the advocacy world won’t stop that. But it will help him to avoid extra hardships. Some extra hurdles that he need not worry about.

Not much would make me more proud than seeing him pick up a metaphorical sign (or a real one for that matter) and fight for himself and others like him, for what ever reasons and in what ever manner he chooses. I believe that he would inspire many and do great things.

But I’d also be quite happy and every bit still just as proud to see him go about his life, focused on what matters most to him, what ever that may be.

Because in the end, that’s what this is all about. Being accepting of what others do, even if it’s not what we did, or what we want them to do. To let them be their own person, whether it’s some other advocate or someone that refuses to be an advocate.

Because if my own advocacy is to mean anything, if it’s to have any value at all, than it has to start with me.

That means having my own hopes and dreams, even hopes and dreams for those that I love, and having the understanding and respect to accept that not only do they not have to fulfill those hopes and dreams of mine but that I will be every bit as happy and proud of of them for having their own hopes and dreams.

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Conversations within the autism community

Miscommunication

Miscommunication

Before I begin, you should know that I’ve altered these to be a bit more… generic. As in, not specific.

Also, I recognize that these types of conversations happen in any community and basically in general on the internet but this is an autism blog and thus, it’s my topic “du jour”.

But if you’ve been a part of the autism community for any decent length of time or even just been on the internet for more than say… 5 minutes, chances are you might recognize some of these.

Be sure to let me know which conversations seem most familiar to you in the comments.

 

Reading Comprehension

Person 1: Would you like to go for a drink after the movie?
Person 2: I’m not hungry.
Person 1: I didn’t say food, I said a drink.
Person 2: Listen, I don’t even like steak so just stop.
Person 1: What? When did I say steak would be involved?
Person 2: Great, now you’re talking in circles. You don’t even know what you’re saying. Man you’re stupid! This conversation is over. I’m out.
Person 3: What just happened?
Person 1: I have no idea.

Mis-association

Person 1: Hockey looks like fun. It’s fast paced and full of action. It’s a lovely sport.
Person 2: So you’re saying that baseball is a terrible sport, is that it? You prefer hockey over baseball??
Person 1: No, I didn’t say that. I didn’t even mention baseball.
Person 2: I can’t believe that you hate baseball!! It’s a perfectly great game and you have to come and rain all over it.
Person 1: I don’t hate baseball. I was just commenting about hockey, that’s all.
Person 2: People who hate baseball shouldn’t even be on the internet. I hope you die.

Condone-sation?

Person 1: They really should try to put a stop to the fighting in hockey.
Person 2: So what, you think it’s ok to fight in baseball?? All the players rushing the field and hurting each other is suddenly fine with you?
Person 1: What?? No. I don’t think fighting is ok in baseball either.
Person 2: Well that’s what you’re saying. Suddenly fighting in hockey is bad but all this time, you never said a word about the fighting in baseball so obviously you condone it!
Person 1: That is some twisted logic you’ve got going on right there.
Person 2: You’re the one who’s twisted. I can’t believe you actually think it’s fine for there to be all kinds of fighting in baseball but when hockey does it, it’s all rules and regulations with you.
Person 1: Wait, what?? I didn’t say any of what you just said.
Person 2: I’m going to go tell everyone what a bigot you are… how you want there to be more fighting in baseball but none in hockey. God I hope everyone learns to hate you as much as I do.

Para-flipflop-phrase

Person 1: This ice cream sure is cold!
Person 2: So you’re saying that it’s too cold to eat? It’s not that cold, you know.
Person 1: No, that’s not what I’m saying. I’m just saying it’s cold. You know, like, I might get brain freeze if I eat it too fast.
Person 2: That’s like saying that a steak is so hot that you might get heart burn. You know you can’t get heart burn from something that’s too hot right. You do have an IQ high enough for that, right?
Person 1: No, it’s not like saying that and yes I do know that. What does my IQ have to do with it?
Person 2: So what, now you question my intelligence? That’s like saying I didn’t even go to high school. I’ll have you know I went to college and was on the honor roll! You probably didn’t even finish elementary.
Person 1: Wait, what? Of course I did. I finished college too. I don’t understand what our IQ has to do with the temperature of ice cream.
Person 2: I knew it, you’re a moron. I can’t talk with someone so stupid.

Victimizer

Person 1: Science is better.
Person 2: No, religion is better.
Person 1: No, science is better.
Person 2: No, religion is better!
Person 1: Listen, religion is all nice with it’s fluffy clouds but science is based on facts.
Person 2: Ah, Fluffy!! How dare you remind me of my childhood hamster!!
Person 1: What? What does your hamster have to do with this?
Person 2: You’re the one who brought it up. And you keep mentioning it!! Don’t you know I was horribly traumatized by the stench of my uncle farting on it and killing it?? It was death by gas cloud man!!
Person 1: Ooooo…. k. Well, I’m sorry I brought up Fluffy.
Person 2: You keep saying his name!! Are you intentionally trying to hurt me!! Is this how you win an argument??? You’re so cruel!!!
Person 1: Wait… what? I just said I was I sorry.
Person 2: You’re a vile and evil person.
Person 1: Ok… well, anyway… back to science vs religion…
Person 2: You don’t even care!! You jab a knife into my gut and then just go on like nothing happened!! Is this how you’re mother raised you!?!?
Person 1: Look, I said I’m sorry about the Fluffy thing. Let’s move on.
Person 2: You’re still talking about it!!! I can’t believe you keep saying his name when you know how much it hurts me!! I’m like, unable to stay seated in my chair right now because I’m just so furious!!
Person 1: I am very sorry that you’re so mad, I’m sorry for what ever I said… can we get back to the topic at hand?
Person 2: Oh no, I’m not leaving until this is resolved. You are going straight to hell and I’m going to see to it that I’m driving the bus mister!!
Person 1: Ok well, this really isn’t going anywhere productive for me so I’m going to go now.
Person 3: What happened here?
Person 2: Religion totally won that argument.

ASSumption

Person 1: Aww…. my baby just sneezed.
Person 2: YOU’RE A TERRIBLE MOTHER!!!!!!

 

Sound familiar to you? Have any to add?

Leave me a comment below!

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The start of something finished

Well, 2012 really sucked for the world of autism. Between 50 cent and his dumbass remarks on twitter, doctors placing a lower value on an autistic life, Jenny McCarthy calling autism moms “victims” if they aren’t trying to find a cure and what has to be the absolute worst, the media attempting to find a correlation between the Sandy Hook shooter and Aspergers.

Even for me personally, it really sucked as my wife decided we need to get a divorce… just before Christmas.

The good news? The past is the past. 2012 no longer exists.

This is 2013 and things are going to change.

Ignorance is being forced to apologize, the only moms that are victims are the ones that believe McCarthy’s stupidity. And the media were falling all over themselves with articles about how there is no connection between autism and violence.

As for Paul Corby and his heart transplant… I sincerely hope that the doctors received a good firm slap in the face and changed their minds. But I haven’t heard anything.

The autism community is getting the message out there. People are talking and when they’re wrong, there’s someone there to correct them.

Autism is not something to be feared, laughed at or used as a way to guilt moms into doing what you want them to do.

Not the media, celebrities, lynch mobs or even divorce can stop the wave that is heading towards governments, communities and audiences everywhere.

It’s a wave of truth, understanding, positivity and love that is a much needed set of emotions in this ever increasingly dark world.

It’s so easy to find the wrong information, to spread the wrong information, to be a hater and to ignore what you don’t want to hear.

But a force, such as the autism community is becoming, can’t be ignored and it can over come any misinformation that the media or celebrities can fling no matter how wide their audience is. In fact, the larger the audience, the more likely the backlash.

2013Don’t let up though. Don’t coast that wave.

Rise up out of your seat and correct those people that are getting it all wrong. Write and phone those media outlets, those celebrities, the government and anyone else that isn’t getting it right.

Shut down the haters, force the ignorers to listen and don’t give ignorance a free pass.

A lot went wrong in 2012 but a lot went right too. And I’m proud of most of the aftermath.

But more can be done. More can be achieved. More people can be reached. More that is broken can be fixed.

2013 might not be the end of the story but after what I’ve seen in 2012, I can see the start of the finish on the horizon.

People will accept all differences.

In the world around them, themselves, in our loved ones, in ourselves.

They’ll have to. Because we won’t stop.

And we’re just getting started.

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Father’s Day in the autism community is becoming something amazing

Since getting involved in the autism community, particularly with my blog, I’ve gained a little extra attention simply for the fact that I’m a father. I knew, going in, that fathers speaking out was a rarity but I really had no idea just how rare. And while I enjoyed being given a little extra oomph to my voice by people willing to help get fathers heard a little more, I also kind of felt that I shouldn’t be taking it because… well, it’s really not fair. My voice was new, not yet established and even I wasn’t sure if I should be reaching a wider audience yet.

Still, as the years passed, I did get to meet some other fathers and I did get some more extra attention by those who were eager to hear from a dad for a change and started to feel more comfortable in my role… the autism father.

I was getting emails from other dads telling me how nice it is to hear that they’re not alone. Some of them even started blogs of their own. I was getting comments from moms telling me that they passed on something I wrote to their husbands and that they really liked it.

But this year… this year really takes the cake.

And I’m going to write now, a lot about me, but it’s not to gloat. Honest. It’s just that mine is the only perspective I have and don’t follow all of the mentions/articles/features that other dads have. But I will still highlight a few that I did notice.

Anyway, skip passed this next section if you want to get straight to the point because I am trying to make a point here.

A Father’s Point of View

something special magazine

Click for full size

This year, months ahead of time, I was contacted by Something Special Magazine because they wanted to feature a few “Dynomite Dads” for their June issue. It’s a magazine that distributes in only a few states but it’s growing and doing well and to be honest, for a guy sitting at home in a 10×10 room with no windows while my kids are playing, being in a print magazine is pretty awesome.

You can read the whole issue here or click on the thumb to the right to read the page that was about me.

A little closer to Father’s Day, I was contacted by Your Beautiful Child to be the guest featured father for Father’s Day morning. What an honour! And it really was a great show too, I think. Although the hour went by far too fast.

You can listen to my interview here.

On Father’s Day itself, I got mentions from fellow bloggers such as from Lou at Lou’s Land and also from resource sites including:

I even had a blog post of my own that was shared about quite a bit and another blog post of mine featured over at http://SpecialHappens.com as well.

 The rise of the fathers

The point is, which I alluded to earlier, is that father’s are getting noticed and being heard. It’s not that no one would listen before but that we just never tried. Well, ok, some did but not enough. Not nearly enough. There’s still not enough but this proves that more and more dads are getting out there and speaking up.

This proves that more and more people like what we’re saying and want to hear more.

So yes, I shared mostly links to what I had going on but many of those links include more links to other fathers and to other resources with more fathers. Check them out!

Go find those dads… you might not agree with some, that’s to be expected. But some of them may have some very fresh perspectives which may really grab your attention.

And if you’re a dad and you see all these other dads out there, jump right in! Start your own blog, start commenting on other’s blogs, start up a Twitter account.. what ever.

Just, let us hear you. I’ve already proved that people want to.

If you’re still not convinced, check out this video from ABC where they talked to Lou from Lou’s Land… a father.

For more incentive, check out these other great dads:

Yeah, I’m pretty thrilled with the attention I got this Father’s Day. How can I not be? Still, the best part of the day wasn’t all the hoopla at all.

The day started with an email from a man in Florida who simply said that he read my story and now, no longer feels alone.

I can’t even begin to describe to you how great that feels. What a brilliant way to start the day!

Father’s Day is over now, but there’s a whole year to find more dads that are willing to speak up, to give more dads the attention they deserve and to make next Father’s Day even better.

It’s very exciting to me. I’ve seen so much change in so very little time.

Fathers, you rock!

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The subjective relativity with which we define “normal”

Normal… that peculiar notion of fitting in with those around us. Not with society… but with those around us. In highschool, some people felt it was normal to be with the cool kids, others with the nerds and so on. At work, for me, the designers tend to fit in with other designers more so than programmers and programmers tend to fit in with other programmers better than designers.

For parents, we want our children to be normal in the sense that they feel comfortable fitting in with other children that are good influences. If they tend to fall in with “the wrong crowd”…. then perhaps normal to them is something that we (the parents) won’t be too comfortable with.

For those of us with special needs children, we think of normal in an entirely different context.

Normal is much more abstract than all of that.

Normal is a conflicting array of all that we could ever wish for and the last thing we’d ever want.

not normalWhen our child is born

A funny thing happens when we have a child. I like to call it “their life flashing before your eyes.” They’re born, you flash a glimpse of their entire life… in contrast to when you are dying and you flash a glimpse of your own entire life.

Essentially, we see a fresh new start with limitless possibilities and all of the ways our child’s life can be so much better than our own was.

With that comes a very strong desire for our child to be anything but normal.

We see them standing against the crowd, standing up to bullies, being able to think differently and creatively… all of the wonderful qualities that makes an innovator, trail blazer and leader.

The last thing we want for our child is to be… mediocre… average… normal.

Growing up normal

The whole problem with the dream of bringing a child into the world that will be anything but normal is that we teach them from day one to be exactly that… normal.

Do as your told, eat all your food, say please & thank you, respect your elders and on and on and on… they’re all good things for people to know and do. But without really putting much thought into it, you are setting your child on the path to being normal.

We send our child to day care, school, play dates, the park… all in an effort to make friends like everyone else. To go to birthday parties like everyone else. To just fit in.

Oh, we still want for them to be great… to be smarter than the other kids, to get straight A’s in school and to be the cool kid that others want to hang out with.

But we sort of want them to do it the ‘normal’ way.

Then comes the diagnosis

Chances are, if your child has autism, you knew before the diagnosis that something wasn’t… dare I say it… normal.

But receiving the official word from the doctor is usually the moment that it truly sinks in for us and our notion of just what was and wasn’t normal is completely changed.

It’s pretty much at that point where all of the optimistic dreams of limitless possibilities leave us and we look at our child wishing for exactly the one thing that we didn’t want for them… to be normal.

The talking comes later, if at all, the toilet training comes later, if at all, the friend making comes later, if at all… and each step of the way, you’re thinking “not normal”, “not normal”, “not normal.”

But then…

Hopefully, if we learn how to help our child, where to get help, what works best and what doesn’t and we figure out what our child is truly capable of… we start to realize that all of this time, through all of these dreams and doubts… we got exactly what we wanted.

Our child is not normal.

We wanted it from the start, we dreamt of it and we wished for it… we just didn’t picture it this way.

But that shouldn’t get us down. Our child is beautiful and wonderful and amazing!

We find ourselves taking great appreciation in the nuances of speech, our senses, the patterns around us, the finer details, the strengths and weaknesses in others and ourselves, the world around us and in the power of unconditional love.

Our children continue to grow and show us just how much we’ve been missing in our lives. Just how much we were completely unaware of all around us.

We missed it… because we’re normal.

Our children are not.

Thank goodness.

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