Archives for April 2012

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A Letter To My Younger Self

I am participating in the Health Activist Writers Month Challenge, in which I publish a post every day for the month of April, based on health-related prompts.

April 10 – Dear 16-year-old me: Write a letter to yourself at age 16. What would you tell yourself? What would you make your younger self aware of?


Dear 16-year-old me,

I am writing to you from 26 years in the future. I am 42 years old, and a lot has happened in the last two and a half decades. The world is a different place now, and I have grown up a lot since I was – well, you.

I don’t want to tell you too much about the next few years of your life, because as painful as some of it will be, it wouldn’t be right for me to change it. I am who I am today because of some of that stuff. You have to live through it, knowing that you will survive your worst times and come out stronger for it.

However, there are a few things you should know, that will make it a bit easier for you to navigate the next 26 years.

1) You are not fat, no matter what anyone tries to tell you. You are a beautiful young woman, and this body image problem that you have is just going to cause problems for you later in life.

2) When you go to that birthday party that’s coming up and drink a truckload of beers, Mom will smell your boozy breath from a mile away when she picks you up. Especially when you open your mouth to make lame excuses for why you’re tripping over your own big toes.

3) When they bring in the school’s first computer later this year, pay attention to it and learn how to use it. Computers will become a massive part of your life so you may as well start now.

4) That hairdresser appointment you have next week? For the love of God, cancel it. Believe me, you do not want a perm. It will take the phrase “big hair” to a whole new level.

5) If you meet a good-looking guy in the hallway of the medical centre, don’t talk to him. He’ll just cause trouble for you. Don’t fall for his flattery.

6) You’re allergic to mangoes. Like, seriously allergic. If you avoid mangoes, you will avoid anaphylaxis and a trip to an Israeli hospital where they’re very nice but don’t speak good English.

7) Things will happen during your University years that will be very hard on you. You will not be as alone as you will feel, and if you ask for help, you will get it. Don’t try to go through it alone.

8 ) Just because one therapist is mean and judgmental, that doesn’t mean they will all be like that. Don’t try to deal with depression alone for twenty years before you get help.

9) Find out as much as you can about autism and take your first child for screening as soon as you see the signs. The doctor will try to get you to wait for another year. Don’t listen to him. Threaten to sit in his office gathering dust until you get a referral.

10) Post-partum depression is a terrible, scary thing, especially when it goes undiagnosed for over a year.

11) Take care of your feet. You’re going to be getting plenty of use out of them. When you really get into the running, your feet will not be your most attractive feature. Wear your callouses and blackened toenails with pride.

12) You don’t realize yet that you are a runner. When your inner runner emerges, go running with Dad every opportunity you get. Later in life, you will hold onto the memories of those runs like treasures.

13) You deserve happiness, and you deserve to be treated with true respect. Don’t settle for anything less.

14) Enjoy your sleep while you can. When you become a mother, you will yearn for it.

15) In a few years’ time you will go to Israel. It will be one of the best times of your life and you will meet some people who will become lifelong friends. Enjoy it and store as many memories of it as you can.

16) The degree you do at University will have no relation to your eventual career. That does not matter. The degree will be useful to you in other ways.

17) Spaghetti mixed with ketchup does not make a gourmet meal, and you will get some very strange looks if you make it for your parents as a special treat.

18) Don’t try going on antidepressants without the guidance of a therapist. As the depression lifts, some other feelings will emerge that will seem scarier. You will need help managing those feelings.

19) The person who has been your best friend since you were ten will still be your best friend when you are 42. Your friendship will survive a rift and you will be there for each other through many major life events. Treasure this friend, because she really is a gem.

20) Life is too short for bullshit. Don’t bear grudges, don’t procrastinate, and make the most of every opportunity you have.

21) Take care of your teeth. When Mom lectures you about flossing, she’s right.

Enjoy your youth, Younger Me. It will be gone all too quickly, and you want to have some good memories of it to carry you through the darker patches of your life.

I’ll see you in 26 years’ time. Enjoy the ride!

Regards,

Older You

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Poster Child

I am participating in the Health Activist Writers Month Challenge, in which I publish a post every day for the month of April, based on health-related prompts.

April 9 – Keep calm and carry on: Write (and create) your own Keep Calm and Carry On poster. Can you make it about your condition? Then go to http://keepcalm-o-matic.co.uk and actually make an image to post to your blog.

Today I got to unleash my inner artist. There’s no need to mention the fact that my inner artist can barely draw a stick figure. With the Internet being what it is these days, you don’t have to be any good at drawing in order to create pretty posters. All you need is a few photographs and enough imagination to come up with some lines of text.

For today’s post, me and my inner artist made three posters. One about autism, another about mental health, and a third about running.

I’ll probably never be featured in London’s Tate Gallery, but this was kind of fun.

What would you put on your Keep Calm posters?

Autism

 

Mental Health

 

Running

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Autism Through A Child’s Eyes

I am participating in the Health Activist Writers Month Challenge, in which I publish a post every day for the month of April, based on health-related prompts.

April 8 – Best conversation I had this week: Try writing script-style (or with dialogue) today to recap an awesome conversation you had this week.

I’m not much of a person for conversations. I suffer from social anxiety, so talking is difficult. I tend to be more comfortable finding my voice in the form of the written word.

Obviously, this is less of a problem when I am among friends and family. I am married to a man who, in addition to having a totally off-the-wall sense of humour, has no “inside voice”. The conversations I have with him range from the baffling to the downright hilarious.

I also have some great conversations with my younger son, James. For a six-year-old, his vocabulary is astounding, and his imagination knows no bounds. He weaves in and out of topics at will, and you can never tell where the conversation will go next. One moment he seems to be wise beyond his years; the next, we are reminded that he is still a kid finding his way in this world.

A few days ago, we had this conversation while I was cooking dinner:

James: Mommy, can you buy me a water gun?
Me: Why do you want a water gun?
James: So I can spray Granny on the nose.
Me (after snarfing on my coffee): Why do you want to do that?
James: Because her nose is dry and that means she’s sick. Roger (a classmate) said so.
Me: Roger said that Granny is sick if her nose is dry?
James (looking at me as if I’m nuts): No. He was talking about his dog.
Me: Ummmm, James? Dogs and people aren’t the same. Granny’s nose is fine.
James: I think Roger’s dog has autism.
Me: What makes you think that?
James: He doesn’t talk and he knocks down Roger’s Lego towers. It’s not his fault, though. He doesn’t know what he’s doing because he has autism.
Me: James, that’s just the way dogs are. Dogs don’t have autism.
James: How do you know?
Me: Ermmmmm (thinking: the kid has a point)
James: Mommy?
Me (wondering about James’ sudden sombreness): Yes, buddy?
James: Will George always have autism?
Me: Yes, baby, he will. Autism is not something he can grow out of.

I want to pause this account briefly to say that where autism discussions with James are concerned, I find that honesty is the best policy. I don’t try to sugar-coat anything, and I answer questions without elaboration. This approach seems to be the one that works best with James.

James: That’s OK. I love him.
Me: I know you do. And he loves you too.
James: Yeah! Mommy?
Me: Yes?
James: Will George die from autism?
Me: No, people cannot die from autism. We just have to make sure we keep him safe.
James: It’s OK, Mommy. I’ll take care of him.

Yes, I cried.

(Photo credit: Kirsten Doyle)

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Book Review: My Brother Sammy Is Special

I am participating in the Health Activist Writers Month Challenge, in which I publish a post every day for the month of April, based on health-related prompts.

April 7 – Health Activist Choice: Today, I get to write about anything I like. I decided to take the opportunity to review a book that should really be on the bookshelf of every child who has a brother or sister with autism.

I tend to feel a lot of angst when it comes to parenting my younger son, James. James, who is six going on thirty-two, is the neurotypical child in my family. He is the one without autism, the one who is very socially engaging and never stops talking, even when he’s asleep.

James himself does not make parenting difficult. He is as well-behaved as a boisterous six-year-old boy can be, he is making good progress at school, and he gets along famously with his big brother George when they’re not throwing Lego at each other.

What makes it hard is the fact that due to George’s autism, I have to use completely different parenting styles with my kids. What I do makes perfect sense to me, but it can be hard for a six-year-old to grasp why he is being treated differently to his brother. Although my husband and I try our best to explain things to James, a lot happens that James perceives to be unfair.

And so when I got the opportunity to review a book written specifically for the siblings of children with autism, I wasn’t going to pass it up. Written by Becky Edwards and illustrated by David Armitage, My Brother Sammy Is Special tells the story of a boy who is angry about his brother being different. He doesn’t want a brother who is different. He wants a brother who can talk to him and play with him, and who doesn’t wreck his stuff.

In a beautiful twist, Sammy’s brother has a revelation, and instead of trying to force Sammy out into his world, he ventures into Sammy’s world. And so Sammy’s brother achieves the brotherly bonding that he so desperately craves, but not in the way that he had expected.

Having read the book myself, it was time to test it out on a member of the target audience. I snuggled up with James, opened the book, and started reading. The story, with its flowing narration and beautiful illustrations, engaged James’ attention throughout. He was very concerned about where this brotherly relationship would go, and he was visibly relieved that it all worked out in the end.

My Brother Sammy Is Special is written in language that is simple enough for young children to understand, yet descriptive enough to convey the complexity of the special needs sibling relationship. Although the blurb in the dust jacket says that the story is about a boy with autism, the story itself makes no specific mention of the condition. This makes it flexible enough to be effectively used within many kinds of special needs families.

The book is a great launch-pad for discussion. It flows in such a way that parents and their children can pause to ask questions and talk about aspects of the story without losing the flow. For children who may be bewildered by the special needs of their siblings, the story can serve to provide both comfort and understanding. It also describes practical ways in which a typically developing child can try engage with his or her special needs sibling.

I highly recommend this book for any family that has a mix of special needs children and typically developing children. It is a gem – a treat for parents and children alike.

My Brother Sammy Is Special is available for purchase at Amazon.

Many thanks to Skyhorse Publishing for allowing me to review the book, and for providing the cover image.

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Grandpa And The Floozie: Good Friday Ten-Miler

Running is the one area of my life where all of my health interests intersect. It is good for my general health, it does a lot to keep depression at bay, and it is the means by which I raise funds for autism services.

It is no wonder that I take my running so seriously, nor that I’ve been anxiously awaiting my first race of the season: the Good Friday Ten-Miler, which happened today. I had watched the weather forecast throughout the week, and I was excited about the prospect of running in shorts to herald the arrival of Spring.

When I arrived at the start, the bitterly cold wind caused me some anxiety. I could deal with the shorts but I didn’t know if I would be able to take off my jacket. It was sunny, though, and it was only cold when the wind blew. And so I decided to stop being a sissy and leave the jacket in the car.

I headed to the registration area to pick up my race kit, and the first thing I had to do was look up my bib number. When I saw what it was, I actually snorted with laughter.

666. The number of the beast.

Seriously? I was going to have to run ten miles with the number 666 on my shirt? Where people could see me? The man who gave me my bib had a good laugh and told me to “run like the devil”.

I got to the start line with about a minute to spare, and all of a sudden we were off. I was aiming to beat 1:45:00, and in my eagerness to have a good race, I flew out of the starting blocks. I ran my first kilometre in 6:05, and realized that if I was going to meet my target I would have to dial it back a little.

A big hill in the second kilometre took care of getting my pace back in line, and through the rest of the race my pace was more or less consistent. Somewhere between the third and fifth kilometres, I saw my friend and coach Phaedra, who was a couple of kilometres ahead of me in the race. We waved and exchanged a high-five and went on our respective ways.

About six kilometres in, I tucked in behind a tall elderly man who was running at just the right pace. After a while I picked up my pace and passed him. Two kilometres further, at about the halfway mark, I slowed down and the man caught me.

He ran with me for a little while, and then we got to the big hill again, and he turned out to be better at tackling it than me. Off he went into the distance. I saw Phaedra again, but by this point she was entering her final mile and I still had about six kilometres to go.

Throughout the race, me and the elderly man were passing each other but staying more or less within spitting distance of each other.

With about three kilometres to go, I caught up with the man again. Sensing that we were going to be running alongside each other for a while, he started chatting to me. Jovially, he said, “I’ll race you to the finish!”

In wonderment that I could talk at all, I said to him, “You’re on!”

“Well, I gotta tell you. You may be young and pretty, but there’s no way I’m allowing myself to get chicked in a race.”

God bless him. He had called me young and pretty! I’m 42 years old, and having run 13km pretty hard at that stage, I looked anything but pretty. Still, it was nice of him to say so.

There is a fine but steely thread of competitiveness that runs through my veins, and I decided then and there to take on the man’s challenge. I said to him, “Well, you may have a ton more running experience than me, and you certainly look like you’re in better shape, but I’m not letting myself get beaten by someone who’s clearly a lot older than me.”

With a twinkle in his eye, he said, “Let’s see who gets home first. The grandpa or the floozie!”

Like a shot, he was off. And I wasn’t having any of it. I picked up my pace and chased him. I caught him and stuck with him for the next kilometre and a bit. I have to say, he put up a hell of a fight. Every time I sped up, so did he. But that little bit of competitiveness in me refused to lie down and die, so I kept trying.

All of a sudden, I could smell the finish line around the corner. I dug deep and found the biggest finishing kick that I’ve ever had. With about 500 metres to go, I finally passed my elderly friend and sprinted to the finish line, clocking a time of 1:43:10.

Not only had I beaten my target time of 1:45:00, I had absolutely smashed my previous personal best time by almost ten minutes.

And the floozie had beaten the grandpa.

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Poetic License

I am participating in the Health Activist Writers Month Challenge, in which I publish a post every day for the month of April, based on health-related prompts.

April 6 – Health Haiku: Write a haiku about your health focus. 5 syllables/7 syllables/5 syllables. Write as many as you like.

About Autism

Mysterious boy
You always make me wonder
Beautiful strange mind

Touched by autism
You are locked in your own world
I reach into you

He doesn’t say much
His mind is always busy
Silent but present

The room rocks with screams
Communication fails him
I hold him with love

About Mental Health

My mind tortures me
I know I should be happy
Sadness fills my soul

Postnatal darkness
Drowning in new motherhood
Do not be ashamed

Memories flood me
The past seeps into the now
Accept who I am

Look in the mirror
See the beauty within you
Know that you are loved

About Running

Feet hit the sidewalk
Legs are aching, I am tired
No way I can stop

Start line at the race
Getting high on energy
My legs want to run

It’s more than the legs
The body must be healthy
Eat like an athlete

Running keeps me sane
Time to myself, time to think
The stress melts away

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Butterfly

I am participating in the Health Activist Writers Month Challenge, in which I publish a post every day for the month of April, based on health-related prompts.

April 5 – Ekphrasis Post: Go to flickr.com/explore and write a post inspired by the image. Can you link it to your health focus?

When my son was first diagnosed with autism, we enrolled him in a local daycare centre on the advice of his speech therapist. He needed the social aspect of it, she said. He needed the group lunchtimes, the circle times, and all of the other elements of being part of a group of children. We were nervous about letting our sensitive, vulnerable son out of our immediate orbit, particularly since the daycare had never had a child with autism before.

To their eternal credit and our eternal gratitude, the daycare welcomed George with open arms. The director of the centre arranged for all of her staff to be trained in how to work with special needs kids, and George was very happy there.

During the summer months, the kids would be taken to play outside at the end of the day while they were waiting for their parents to pick them up. I would get off the bus from work, pick up my boy, and walk home with him. One day, I picked up his backpack from the darkened daycare classroom as usual, and went out to the playground. I always tried to arrive undetected so I could watch George at play for a few minutes. In typical autistic fashion, he always did his own thing. He played among the other kids, but not with them.

On this particular day, I got to the playground just in time to see a few of the other kids preparing to have a race from one tree to another. George stood apart from the kids, watching them shyly. When the daycare teacher said, “GO!” the kids scampered away from the start line while George stood by on his own.

My heart constricted with unbearable sadness. The whole thing seemed to underscore the isolation of autism, and I felt a sense of unjustness that my child was standing there on his own. With his lanky frame and long legs, he is a natural runner. He might have won that impromptu little race.

Damn autism, I thought. I knew these other kids well enough to know that prior to lining up for the race, they would have tried to encourage George to participate. But being locked in his own world, he would not have known how to. Outwardly, he seemed perfectly happy, but I couldn’t help wondering about that. What was going through his mind as he watched those other kids at play together? Did he feel any sense of isolation? Did he wish he knew how to join in?

I started thinking about sports teams and group activities. Was George ever going to be able to be part of a soccer team or a high school band? Would he travel in a pack of teenage friends or would he sit by himself in the high school cafeteria? Would he be excluded from birthday parties? Or would some group of well-meaning kids include him in their group and look out for him?

How was my child, with his autism and his social communication deficits, going to survive in a social world?

This is a concern that is with me more or less all the time, despite assurances from his teacher that he is starting to tentatively reach out socially at school, that he is getting better and better at participating in social activities, and that he is, in fact, an extremely well-liked member of the student body.

A few days ago I saw something that made my heart soar. Me and my husband were out for a walk with the kids, and we saw the teenage boys down the road shooting hoops in their driveway. Before we could stop him, George ran up to the boys and held out his hands for the ball. The boys good-naturedly obliged, and like a true natural basketball player, George bounced the ball on his knee and then threw it towards the hoop as if he did this every day.

The hoop was too high for George to have any success, and the boys offered to lower it for him. We told them not to worry and we went on our way, but not before the boys had invited George to play basketball with them any time he wanted.

When things like this happen, my vision of the future shifts, as if I’m looking at my son’s life through a kaleidoscope. I start to see possibilities that were previously hidden to me, possibilities that simply may not have been there before George grew and developed into them. Instead of seeing the kid who stood on his own while everyone else had a race, I now see the boy who, just for a few moments, joined other boys in a basketball game.

If I had, just a year ago, seen the picture that inspired this post, I would have thought, “George is probably never going to do that. He’s probably never going to romp around with friends or be invited to take part in impromptu soccer games.”

Now I look at that picture and realize that I am seeing the emergence of George as a social being. Maybe he’ll always be shy, and it is very likely that he will always need to be surrounded by people who will look out for him.

But his personality, his character, the very essence of who he is – that is emerging bright and beautiful, like a butterfly coming out of a cocoon.

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The Stories I Tell And Why I Tell Them

I am participating in the Health Activist Writers Month Challenge, in which I publish a post every day for the month of April, based on health-related prompts.

April 4 – I write about my health because…: Reflect on why you write about your health for 15-20 minutes without stopping.

When I was young, I had a somewhat cavalier attitude towards my health. This was partly due to the invincibility and stupidity of youth, and partly because there were some things happening in my life that relegated my health to the backseat. I really had better things to think about than whether I was eating enough spinach.

Of course, my lifestyle through my early twenties didn’t really lend itself to healthy thinking anyway. I was fond of pasta, Coca Cola and beer. I was not fond of vegetables, exercise or moderation. Water was for swimming or showering in, not for drinking. My daily life was punctuated with cigarettes. I didn’t really care whether I had enough money for groceries as long as I had a six-pack in the fridge and some cigarettes in my purse.

One morning I woke up and realized that I was tired of being a smoker. And just like that, I decided to quit. I reasoned that while I was quitting, I may as well fix up the other troublesome aspects of my lifestyle. And so I gave up the soft drinks, reduced the alcohol consumption and took up running.

In the years since then, more things have happened that have forced me to take a close look at the health of myself and my family. I have learned better ways of running, I have battled some mental health issues, I have lost family members to cancer and I have become an autism mom.

The subject of health is not something I can ignore or take casually. So much depends on it, and it has far-reaching effects on my children. I am mindful of the fact that for the next few years, I am making decisions about food and activity on their behalf. And for their sake, I have to get it right.

Through my journey, I have learned a lot and discovered that there’s so much I still don’t know. Through my writing, I can share what I have discovered and reach out to people who very often have answers that I need. I have come across people who know exactly what I’m going through, making me feel less alone. In sharing a piece of my life, I have found a voice that I might not otherwise have.

I write because I love to, and because – hopefully – I tell stories that people can either relate to or be informed or entertained by. And as long as I think my voice is touching at least one other person, I will continue to write.

(Photo credit: Kirsten Doyle)

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Superhero Wannabe

I am participating in the Health Activist Writers Month Challenge, in which I publish a post every day for the month of April, based on health-related prompts.

April 3 – Superpower Day: If you had a superpower – what would it be? How would you use it?

superhero

A couple of weeks ago I posted something on Facebook about a long training run I had just been on, and one of my friends responded by asking if I run while wearing a cape and a big “S” on my shirt.

Well, no I don’t. It would be highly uncomfortable and let’s face it, people would stare. I don’t want to be responsible for any traffic accidents. And besides, being a distance runner might set me apart in some small way from non-runners, but it certainly doesn’t make me a superhero. If I was wearing an “S” on my shirt, it would stand for “sweaty”.

But what if I was a superhero? What if I could choose any superpower I wanted? What would that superpower be and how would I use it?

As an autism mom – indeed, as a plain old mom – there are so many areas in which I feel woefully inadequate. There are so many things that I wish I could do better, or faster, or with less grief. There are, of course, things I would like to do that in the real world are simply impossible.

And now, for the purposes of this article, I have to choose just one superpower.

The ability to cure autism? This may seem like the obvious choice, but it is not what I would want. If I cured my son of autism, I would be changing who he is. And while I am on a permanent quest to help him with the aspects of autism that cause him pain and frustration, I would never, ever want to change who he is.

What about bottomless reserves of patience? Those who know me well know that I am don’t exactly have a Zen-like aura of calm about me. I tend to get a little fraught at times. But changing that would surely change who I  am, and while I would never claim to be perfect, I’m reasonably OK with the person I am.

No, the superpower that I would order would be the ability to instantly soothe my children. At a touch, I would be able to calm my son from his meltdowns, and in the midst of his inability to communicate that causes him such frustration, I would make him feel safe and secure. I would brush my hand lightly on his forehead, and immediately, he would know that everything is OK, and inner turmoil he was feeling would disappear.

I would use this superpower on my younger son as well. The neurotypical child, the sibling to the special needs child. The one who, while knowing that his brother is different and needs special care, sometimes feels overwhelmed by it all. It is a rough deal, being the brother of a child with autism. My two boys unquestionably love each other, but still, it is hard for the sibling.

With my superpower, I would soothe my younger son when things got too much for him. When something happened that he perceived to be unfair, I would gently stroke his hair, and he would instantly feel a sense of calm. He might not fully understand his brother’s autism, but he would feel that everything was right with the world, and he would feel the love that we all have for him. He wouldn’t feel overwhelmed, and above all, he would know that his brother adores him and never, ever wants to hurt him.

I strive to make my kids feel these things – usually, it just takes longer than I would like.

(Photo credit: http://www.flickr.com/photos/globalismpictures/5723668328/. This picture has a creative commons attribution license.)

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A Place To Stand

I am participating in the Health Activist Writers Month Challenge, in which I publish a post every day for the month of April, based on health-related prompts.

April 2 – Quotation Inspiration: Find a quote that inspires you (either positively or negatively) and free write about it for 15 minutes.

move the world2

Give me a place to stand and I can move the world. ~ Archimedes ~

While I was labouring with my first child, I channelled some of my pain by yelling out swear words about Ontario’s new premier, who had been appointed after the resignation of his predecessor. I did not have much interest in Canadian politics at the time: I had only been in the country for three years and I did not have the right to vote. Adjusting to living in a new country and being pregnant had pretty much taken up all of my energy.

I didn’t know anything about this man I was yelling obscenities about, except that he had this irritating whiny voice that made me wish my head would just explode.

At some later point, after Mr. Whiny Voice had been ousted from office, I asked someone how Toronto’s problem with homelessness had originated. The answer horrified me. Apparently, the former Ontario government – the one led by Whiny Voice’s predecessor – had cut funding to a lot of services, mental health care being one of them. As a result, patients with mental illness suddenly found themselves being ousted from programs that they could not afford to pay for themselves, and in the absence of homes or job prospects, they had ended up on the streets.

When I heard about this, I just wanted to cry for these people. I mean, is that any way to treat a human being? Stop their treatment and put them out in the street?

As an autism parent, I know all about the difficulties with funding. Governments do not have unlimited money, and increasing – or in some cases, merely maintaining services comes with raised taxes, and that never goes down well with the public.

I could offer up a thousand suggestions as to what could be cut instead of services that allow people to have basic dignity and quality of life, but this post is already in danger of being more political than I’m generally comfortable with.

Instead, I will say this: that every single person has a place in this world. No matter what challenges they face, no matter what their strengths and weaknesses are, and no matter what level of functioning they ultimately achieve, they are all rightful members of the communities in which they live, and they should be respected as such.

I often tell the story about the day we received George’s autism diagnosis. In the midst of the devastation that goes with this kind of thing, the doctor started talking about his prognosis for George’s future. He didn’t hold out much hope, and we left his office that day thinking that as an adult, George wouldn’t be able to do much more than sweep floors.

The reality has turned out to be very different, and although George is an eight-year-old with some profound challenges, he is also an eight-year-old with a great deal of intelligence and a ton of potential.

But that is not the point. The point is this: so what if George grows up to sweep floors or clean toilets? Can you imagine what the subway station or the airport or the shopping mall would be like if there was no-one to sweep the floors or clean the toilets?

Whether my son sweeps floors, becomes a computer programmer, works in a library, or wins the Nobel Peace Prize for revolutionizing heart transplant surgery, he has a place in the world.

It is my job to help him reach his full potential, whatever that may turn out to be.

It is up to me to help him find a place to stand so that he can move his world.

He already totally rocks mine.

(Photo credit: http://www.flickr.com/photos/sporst/6914330609/sizes/m/in/photostream/. This picture has a creative commons attribution license.)