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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.)

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Time In A Bubble

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 1 – Health Time Capsule: Pretend you’re making a time capsule of you and your health focus that won’t be opened until 2112. What’s in it? What would people think of it when they found it?

timecapsule

Sometimes, usually when I’m reminiscing about one of my grandparents, I wonder what the world was like a hundred years ago. In 1912, my maternal grandmother was nine years old. Cars were just starting to change the way people lived, and people were starting to realize that planes might be more than just a passing fad.

In 1912, the Republic of China was formed and the Titanic sank. Gene Kelly and Pope John Paul I were born, and the members of the Scott expedition to the South Pole died.

One hundred years ago, telephone communications happened over a party line and computers had not even been dreamed up. There was no such thing as a TV dinner. Indeed, there was no such thing as a TV.

It is very clear that the world was a completely different place back then. If you were to take my nine-year-old grandmother from that time and plunk her down in the middle of 2012, she wouldn’t have a clue what to do.

Now I cast my mind to the future, to the year 2112. What thoughts will the people then have about the way the world is today? What would I want them to think? What would I, the 42-year-old me who lives in 2012, want them to know about me and my life?

Maybe I should put together a time capsule, something that some random stranger can dig up a hundred years from now to get a glimpse into my life and the things that are important to me.

There would be photos, of course, a visual record of me and my family. Maybe a flash drive of family videos that the finder could watch – assuming, of course, that flash drive technology isn’t totally redundant by then.

I would include a pair of running shoes, and maybe one of my half-marathon finisher’s medals. I would print out a copy of my training plan, so whoever found the time capsule would know that I took my running seriously and tried to be healthy about it. They would know that I cared enough about my feet to use orthotics, that I ramped up my training in a way to avoid injury, and that running was my biggest stress-relieving tool.

There would, of course, be a lot of stuff about autism. A copy of George’s developmental assessment report and the autism awareness magnet that’s on my car. I would put in a copy of the very first “real” picture that George drew depicting a recognizable scene from a TV show. I would have to include one of George’s Mr. Potato Heads, along with a description of how this little character helped George’s development in so many ways. And what about a program from the biannual autism symposium? I could include one of my fundraising appeal letters for my autism runs.

Out of respect for my younger son, I would include a book about raising a child who is the sibling of a child with autism. I would throw in some of James’ artwork depicting him and George, and a leaflet about the autism centre’s sibling support program. I would want whoever found this to know that George’s autism didn’t only affect George, that we also had to make special consideration for his little brother.

And because James is an individual in his own right, I would include some stuff that’s just about him. A Lightning McQueen car. His soccer shoes. One of the T-shirts my mom has sent him from South Africa, that he always loves wearing.

Mental health is a big issue in my life. I would include some of the antidepressants I took a few years ago before the side effects scared me into stopping. I would print off some stats and information about post-partum depression – something that I suffered terribly from and that I still don’t think there’s enough awareness of. And maybe, just for fun, I would include one of my therapists’ bills. Whoever finds it can then gasp in astonishment and say, “Wow, they only paid that for therapy in 2012?”

Family is an important element in my life as well. My family, by their mere presence, enhance my physical and mental health. My husband’s support of my endeavours has an unquestionable affect on my stress levels and sense of wellbeing. So I would have to include a copy of my marriage certificate.

This time capsule is starting to get kind of full, and I haven’t even touched on some people in my life who would have to be represented, like my mom and my brother, and my best friend Jenny, and some other folks who form the fabric of my life.

I’m off to find a bigger box.

(Photo credit: http://www.flickr.com/photos/carbonnyc/2563369930/. This picture has a creative commons attribution license.)

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Home Is Where The Hat Is

I cannot say for sure when my firstborn son decided that he had to wear a hat at all times. Looking back at old pictures, it seems apparent that he spent most of his toddlerhood in a hatless state. I don’t remember him ever being resistant to wearing a hat, although from the get-go he was picky about the style of hat that he would allow onto his head.

All I know is that at some point – I’m pretty sure it was during one summer or another, the hat became a permanent fixture. It wasn’t even a gradual progression, like his preference for insistence on striped shirts was. It was an overnight thing. One day, he could take his hat or leave it. The next day, it had to go everywhere with him, even into the bathtub. Even to bed. The absence of the hat became an instant source of extreme distress for him. Taking it away from him would make him scream as if the world was ending. One day, when we forcibly removed the hat to throw it into the washing machine, a complete stranger called us from New Zealand and said that the noise had woken him from his slumber, and had we just removed our child’s kidney?

OK, I made that last bit up, but you get the picture. George will defend to the very last his right to have his hat with him no matter what.

On the surface of it, this may not seem like a big problem, but it is amazing how the full-time presence of a hat can encroach on real life. And so we had to work with George’s teachers and therapists to wean him from the hat, or at least get him to the point where he could do without it for brief periods of time.

Several years later, George is still into the hat. Whenever he outgrows a hat, my mother sends a bigger one from South Africa. We do have hats in Canada, of course, but the ones provided by my mom are so cool, so she is in charge of upgrading the hats.

We are able to persuade him to remove the hat at certain times. At bathtime it comes off his head, and remains out of his reach but always in a place where he can see it. When he is at school, he takes it off and hangs it on the hook in his cubby, only putting it on for lunch and recess. And at bedtime, the hat sleeps on the pillow beside him. To our eternal relief, he now consents (with just a little bit of protest) to having his hat taken  away for the purpose of being washed.

Although he takes it off when he absolutely has to, George still loves his hat and he always has to know where it is.

So if you’re ever in my neighbourhood and come across a shy, sweet boy who doesn’t say much and wears a striped shirt and a hat from Africa, chances are that you’re looking at my beautiful son.

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No More Teachers, No More Books!

George doesn’t want to go to school.

Big deal, I hear you say. He is, after all, an eight-year-old kid, and if I got a dollar for every eight-year-old kid who didn’t want to go to school, I’d be signing up to be the next space tourist.

His reluctance to go to school has escalated, though. It started mildly enough about five weeks ago. I was getting him ready for bed one evening when he said, “School is closed.”

“No,” I said. “School is open.”

He went to school without resistance the following day, but this became a nightly ritual. Each evening, the frequency of “School is closed” statements would increase, but as far as I could tell, there was no anxiety associated with it.

Then March break happened and everything changed. Over the course of the week-long break from school, both of the kids were sick. James recovered fairly quickly, but George had a bad cough that lingered, so I got him some natural-remedy cough syrup.

And what has cough syrup got to do with this story? Well, George hates taking cough syrup. In order to give it to him, I have to wrap him up in a blanket and give it to him with a syringe, a tiny bit at a time so he doesn’t spit the whole lot out at me. So when he reached for the cough syrup on Monday morning, indicating that he wanted that rather than school, we knew that this school aversion was serious business.

The following morning it got worse. George woke up very early and for over two hours, he constantly said, “School is closed. No school. School uh-uh.” All the time, his anxiety level was steadily rising. The pinnacle of all of this was George going into the bathroom and trying to force himself to throw up.

Despite all of this, when the school bus arrived, he got onto it without resistance, albeit looking absolutely miserable.

I sent an email to the school describing George’s behaviour and asking if anything was going on at school that I needed to know about. I didn’t think so: this is George’s third year with the same teacher, and she’s been absolutely fantastic for him. But there is, in all likelihood, something behind this and I needed to either rule out or confirm problems at the school.

Because she is so awesome, George’s teacher called me back within an hour of me sending the email. She reassured me that everything was fine, and that she would not have known that George was having a problem if I had not gotten in touch with the school.

Then she said something that was so obvious that I felt stupid for not having thought of it immediately. She said, “Did this start after you returned from your trip?”

Of course! I had been to South Africa for two weeks by myself, leaving husband and kids to hold the fort at home. The last time I had been to South Africa, when my dad died, George was 15 months old and James wasn’t even a gleam in my eye. My absence was a highly unusual state of being for both of the kids, and George, with his autism, must have had a very difficult time processing it.

And within a few days of my return, he started his nightly “School is closed” routine.  The idea that he is working through some separation anxiety makes perfect sense. The break in routine resulting from March break would have exacerbated the problem.

On the one hand, I am relieved to know that everything at school is fine. But on the other hand, I feel guilty about having been away, even though my presence in South Africa was so badly needed at that time.

I can only hope that with a bit more time and many more hugs, George will feel reassured. And if I ever have to go away unexpectedly again, I hope he will know that I am coming back.

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Running: Breaking A Personal Barrier

My Distance Enjoyment Chart

Yesterday morning I went for a 17km run.

As usual, I didn’t get enough sleep the night before. As usual, I seriously questioned the sanity of what I was doing as I got ready. And as usual, I ended up enjoying the run far more than I had thought I would.

Whenever I’m ramping up my distance, 17km is a milestone distance. If you were to plot my enjoyment of distances on a graph, the line would rise steadily from 5km to 10km. Then it would start to drop, and the lowest point would be at 16km – a distance that for whatever reason is hell for me. After 16km, the line climbs and reaches its highest point at 21.1km – the half-marathon distance.

So 17km is like a magic number for me. It means that I have broken the ugly 16km barrier at which I never really know how to pace myself, and I am free to run true to my natural style.

I knew going into the run that it might be a challenge. Two decades ago I sustained a serious injury to my left ankle that flares up from time to time. On Saturday night, I had woken up multiple times feeling as if someone was sticking a red-hot skewer right into the centre of my ankle joint. Sure enough, when I started running on Sunday morning, my foot felt a little tender. In addition, my left hamstring was a little tight, probably due to the fact that I added hill training to my routine last week.

I ran anyway, reasoning that I could always stop if I had to, and yet knowing that I wouldn’t. Little aches and pains that I feel at the start of a run have a way of disappearing as I loosen up.

Apart from a couple of little twinges, I pretty much forgot about the pain in my ankle. The hamstring never really loosened up, but it didn’t get worse either, and I was able to pace myself more or less consistently throughout the 17km. I had my usual difficulties at the usual times, and got through it as I always do: positive self-talk, upbeat music, and a reminder that my whole reason for running is to raise funds for autism.

It’s amazing how the thought of doing something for your kids can put things into perspective. My son lives with the challenges of autism day in and day out, and it will be this way for the rest of his life. Surely, surely, I can cope with the challenges of running for a couple of hours once a week.

And so I finished my 17km, and returned home to be greeted by the child who motivates me to do all of this. This little dude is the only person in the world who can hug me fiercely without caring that I have 17km worth of sweat and salt all over me. Sure, it’s a little gross, but at the same time it’s totally endearing.

After the run I may not have felt as good as new, but I was in reasonable enough nick. My hamstring hurt like the blazes for the rest of the day and I needed to stay off my ankle as much as possible, but I felt the sense of triumph that always comes after a successful long run.

My next long run will be 19km, and I say: BRING IT!

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Blog Beginnings: A Funny Guy Made Me Do It

Tim “Red Barren” Carter, who gave me the idea for my blog

Two years ago today, my blog was born. When I wrote my first post, I didn’t really give much thought to where it would all lead me. I wouldn’t have even started the blog if I hadn’t been pushed into it.

Here’s what happened:

Over a decade ago, a super-cool dude by the name of Bruce started a super-cool ezine called Really Good Quotes, and I was one of the original subscribers. In the early days of the ezine, Bruce did everything himself: the research, the writing, the sourcing of quotes, and the compilation of the issues. Five days a week he did this.

After a while, Bruce realized that it would be nice to have a life, so he cut back from five days a week to three, and he started enlisting help. He recruited a couple of writers and asked me to be the editor. And so it became my responsibility to collect everyone’s submissions and format them into something resembling a respectable ezine. When I’d been doing this for about a year, Bruce offered me my own column. I handed off the editing responsibilities to a guy named Cliff, who does it far better than I did (and writes an awesome column to boot), and I started focusing my attention on writing.

Through this whole process, I became friends with the other writers on the ezine. We were a close-knit little group from the start and our friendships started to extend beyond the bounds of Really Good Quotes. One of my fellow writers – a guy who, sadly, is no longer with us – was called Tim. Tim had a heart the size of Texas and he was an amazingly funny guy. He was also a technogeek, so in addition to being a friend, he became my unofficial tech support person.

It was Tim who got me into writing outside of Really Good Quotes. My older son’s autism diagnosis came when I was in the midst of post-partum depression, and I felt myself buckling under the weight of everything. Tim contacted me during this dreadful time and told me that perhaps I needed an additional forum for my writing.  He offered me a space on his website where I could write whenever I wanted. There was no requirement to post, there was no pressure and no expectation. I simply had a place to go when I needed to vent.

One day more than a year later, Tim told me I needed to spread my wings. He wasn’t booting me off his site, and in fact he wanted me to stay and continue posting, but he felt that my writing was good enough to warrant a wider audience. He encouraged me to sign up with one of the well-known blogging platforms that came complete with a large community of bloggers. At first I was resistant to the idea. It sounded like more hard work than I was in the mood for.

Tim’s idea would turn out to be a bug that, once planted in my mind, kept nagging at me. After a couple of months, I thought, What the hell? I signed up, and here I am, celebrating my blog’s second birthday.

Many things have happened since then, both in my blog and in the broader context of my life. I have seen all kinds of growth in my kids, I have watched my son beat out all of the doctor’s predictions, and I have done some growing up myself. I have run all kinds of races and beat my own personal best times. I have voted for the first time as a Canadian citizen, I have tied the knot with my long-time partner and I have taken on extra responsibilities at work.

As far as my writing goes, I still write for Really Good Quotes. I am also a writer and scheduling editor for World Moms Blog and I participate regularly in the Indie Ink writing challenges. I have been invited to participate in the Health Activists Writers Month Challenge which runs in April. I have been voted as one of the Top 25 Canadian Mom Blogs. And very soon, my website will be going through an overhaul. I am excited at the prospect of launching a new look to showcase my writing.

I feel like I am entering a whole new phase and I cannot wait to see where it brings me.

Happy 2nd birthday, blog!

(Photo used with the kind permission of Kristen Carter)