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Ten Pieces of Stuff About Blissdom

October 31, 2012 By

 

The Pantry Girls with Top Chef Carl Heinrich

Ten days after The Bliss, I am finally sitting down to write about it, and I find myself not knowing where to start. It is impossible to capture everything about an event like Blissdom in a single blog post. Should I talk about the ten best things I learned? A chronological account of the whole weekend? Selected highlights? Profiles of some of the people I met?

Initially, I was going to cheat and collect tweets about Blissdom from fellow delegates. Having just come off a half-marathon, Blissdom, and a three-day autism symposium all in the space of two weeks, I was tired, and I was tempted to write my Blissdom post using the words of other people. With full accreditation, of course.

In the end, I decided to keep it simple – and in my own words –  and talk about Ten Pieces of Stuff About Blissdom, in no particular order. Because putting these into any kind of meaningful sequence could make my brain explode.

1. If you’re planning to leave your kids and husband at home in order to have a relaxing Blissdom weekend, it’s not going to happen. The relaxing part, that is. When you have a gathering of a couple of hundred moms who don’t get out much, the socializing and wine drinking gets a little intense. You will have an awesome time, but you will not be relaxing.

2. There were microsessions on the Saturday morning that I absolutely loved. The microsessions are round table discussions with a small group of people, facilitated by an expert, and it’s an opportunity to really focus on the specifics that apply to you. It was such an honour to meet and talk to renowned Canadian writer Ann Douglas, and I learned a lot from her.

3. I collected many business cards, each representing a new contact. Said business cards are currently sitting in my purse, and I need to spend a bit of time going through them and getting in touch with everyone, so that those contacts stay active. The people I met were awesome, and there is potential to do great things with them in the future.

4. On the Friday morning, some of us were in the studio audience of the Marilyn Denis show, which is a popular Canadian daytime TV talk show. It was fun to be there, and it was interesting to get a behind-the-scenes look at what happens during these shows. Also, my co-workers got a kick out seeing me on TV during my three seconds of fame.

5. At blogging and social media conferences, there is free stuff. A lot of it. I really needed to allow extra space in my bag to bring home the books, the coffee mugs, the pillow, the samples of food, and so on.

6.The costume and karaoke party was a blast. I got into the spirit of things and dressed up as The Flash, but no amount of money would make me take part in the karaoke. It was fun to see other people take the stage, though. It was also fun to see the creative costumes that people were wearing. There was a Christmas tree, Facebook, Cher, Mitt Romney’s binders full of women, and much more. I was one of a posse of superheroes, but on that particular night, we all took a much-needed break from fighting crime and saving the world.

7. As a slightly neurotic person with social anxiety issues, I was not wild about the idea of sharing a room with people I did not know. But my roomies – Nolie and Jenn – were fantastic to spend time with. They were an essential part of my Blissdom experience and I am immensely grateful to them for putting up with me.

8.Due to the aforementioned neurosis and social anxiety, I tend to feel a little out of place when I’m among other people. I envy the ability of others to converse with ease with complete strangers, and I feel awkward as I stand in a quiet corner with my wine, desperately scanning the room for someone I might know. At Blissdom, I did not feel this way. I was among other writers, many of whom are just as introverted and socially anxious as me. I felt as if I was hanging out with my own kind. Ironically, being with fellow introverts helped draw me out of myself a little.

9. On the Friday night, I went out to dinner as part of a group that christened itself the Pantry Girls. Our dinner was prepared by the winner of Top Chef Canada, and it was outstanding. The food was good, the wine was good, and the company was a lot of fun. We were in an alcove area that appeared to function at least partially as a pantry, hence the name of our little group.

10. The whole weekend was capped off with a wine-tasting excursion in the Niagara region on the Sunday. I almost bailed – I had gone to bed at about two in the morning and woke up with a hangover for the second consecutive day. Was more wine really what I needed? In the end, my inner wine affectionado prevailed and I had a great day.

Now I am left with memories, a ton of people to contact, Blissdom swag. I am also left with the goal of losing some weight before next year’s Blissdom with the intention of being a slicker looking Flash!

(Photo credit: Kirsten Doyle)

Filed Under: Blissdom Canada, blogging, Conference, Social Media, Uncategorized Tagged With: , , , , ,
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GUEST POST: Fighting With My Shame

June 6, 2012 By

Kerry White has a few things in common with me. She was also born in South Africa, and she also lives in North America (Texas, to be exact). Like me, she knows what it’s like to parent a small energetic boy. And like me, she knows what it’s like to live with mental illness, including depression and social anxiety.

I first got to know Kerry through a now mostly-defunct Yahoo group called Homesick South Africans. During its heyday, this group was the venue of some lively discussions – a few of them controversial, many of them humourous, almost all of them supportive. Several friendships that formed during the group’s active existence have continued through social media. I am so grateful to the Internet for existing, because without it, my friendship with Kerry would not have evolved in the way it has. This is a woman for whom I have a great deal of admiration and respect.

As I strive to talk about my own struggles with mental illness, I am immensely grateful to Kerry for this post, in which she frankly and courageously shares her own journey.

So I think I’m crazy. Absolutely strait-jacket-heavily-medicate-me-and-lock-me-up crazy! I have felt this way for a very long time, probably since I was about ten years old and reading my first Stephen King books. I recognized the signs of madness in my mind from the characters in some of his books.

As a much more jaded adult, I now recognize myself for what and who I am. I have severe depression, social anxiety, obsessive compulsive disorder, and it all comes bursting forth in the less than neat and tidy package of major panic attacks. I live with mental illness, and I am terribly ashamed of it. I feel broken, less of a person, less of a woman, and worst of all I feel like a terrible mother because of it.

Growing up in South Africa in the 80s, my mental illness was not recognized for what it was. My anxiety, and shyness, and my odd acting out behaviors gave the impression that I was a difficult child; not that I was a child in dire need of some thought of help.

Don’t get me wrong, my childhood was not unpleasant at all. My parents were hard-working and loving individuals who did the best they could for us during rocky financial times. But there was no such thing as depression, anxiety, panic attack, mental illness. There was just doing what needs to be done, threatening electroshock therapy when I refused to communicate about an assault when I was a teenager, and threatening to send me away to a mental institution. At 16 I was admitted to a psychiatric hospital for teenagers who are in crisis. I felt normal! I felt accepted! I felt safe! I was there for two weeks and then released, but promptly tried to kill myself because I didn’t get the support I needed at home. I spent another several weeks in there, but soon learned that I was better off shutting the part of myself I thought to be crazy away. I was never going to get support outside of the walls of that mental health hospital. I was always going to be told to just suck it up and get over it. Because that was just the way things were handled.

I have spent the better part of my adult life trying to just get over it, trying to avoid the idea that I have a problem that no amount of “getting over” will fix. I have tolerated abusive partners, abusive bosses, and abusive coworkers; because I felt I wasn’t worth more.

When I had my son, my depression and anxiety kicked into high gear – but I expected it to. I refused to take the prescribed antidepressants, in case they made me worse (as others have done in the past), or someone saw me as too weak to raise this child. But I do recognize now that I should have not only taken the medication but sought out help. Help wasn’t offered for my “baby blues” and I didn’t go find it. It got to the point, several times, where I wanted to end my life because I was so miserable and felt like such a failure.

I’ve found myself mentally standing on a ledge, with nothing behind me, not even one hand to reach out and pull me to safety. But then the knowledge of the small body pressing against me, raising out a hand and calling out for “mommy” reminds me that if I jump off of this mental ledge then he loses himself, too.

As my son’s needs have changed, so has my mental illness. It has to. I have to get us dressed and get him to daycare so that I can work. I work at home, which just encourages my social anxiety. We need to go to the store and get milk and the occasional toy car, so I steel myself and leave the house. For him.

I’ve made myself get on a plane to visit family; I’ve made myself go visit friends. But it is hard. I have to find a way to change this, for my son.

So what is my next step then? I have more anxiety than will allow me to even see a therapist. What if they deem me to be as unfit of a mother as I feel some nights when sobbing over a panic attack or crying in my office when he is at school? I can’t just “suck it up and get over it.” I have tried. Believe me, I have tried.

I feel crazy. Insane. Broken. But this is my normal. I just wish I didn’t feel so much shame and fear along with it. How do I find the inner strength I need to get help and not feel so broken? Help that will not judge me as being weak or unfit as a single parent?

My heart breaks for others who feel like I do, and I do my utmost to help them. I even write helpful blogs and books for a counselor who helps women like me!

Why then can’t I find what I need in order to help myself work through this? At what point will my son notice that his mommy isn’t like other mommies? I do not want to continue trying to bury my mental illness, but I do not know any other way to function. I am not strong, I am doing what I need to do in order to provide for this boy that the universe has seen fit to place in my care.

To find out more about Kerry and the children’s books she is writing, visit her website!
 
(Photo credit: Kerry White)
Filed Under: anxiety, Depression, Guest Posts, Kerry White, Mental Illness, OCD, parenting Tagged With: , , , , , , , , , ,
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The Good And The Bad

April 26, 2012 By

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 27 – 5 challenges, 5 small victories: Make a list of the 5 most difficult parts of your health focus. Make another top 5 list for the little, good things (small victories) that keep you going.

Autism can be a very complicated thing to live with. Its manifestations change from day to day. One day, my son will be able to tolerate loud noises but a small change in routine will send him into meltdown. The next, we’ll be able to turn his entire routine upside down but anything louder  than a whisper will set him off. Different strategies work for different kids on different days, and everyone you might see guidance from is convinced that their opinion is the right one.

The things I find most challenging about being an autism mom don’t really have to do with the autism itself. Whatever might be going on with my child on any particular day, I just deal with it. Sometimes it’s hard, but I always know that I’m doing my best, my son is doing his best, and at the end of the day we’ll all survive.

My challenges tend to come from sources other than my son and his autism. I list them in no particular order.

  1. The judgmental critics. It’s a moment every autism parent has lived through at least once. You and your child are in a grocery store, which let’s face it, is a mecca for sensory overload, and your child is getting more agitated by the second. You throw things into your cart at quickly as you can, but just as you get to the checkout, your child reaches his breaking point and explodes. As you are trying to calm him down, some snarky stranger loudly proclaims, “What that child needs is a good hiding.” I once heard someone say (referring to me), “If that mother was doing her job properly, this wouldn’t be happening.” Like I’m not already carrying around enough angst with me. With my social anxiety, I’m not great at the quick comeback, although I’m definitely better than I used to be.
  2. The third-person talker. These are the people who will talk about someone who is present as if that person were not in the room. The chances of this happening increase exponentially if the subject of conversation happens to have autism. I get it all the time. “Would George like a hamburger?” they will ask. My answer always seems to throw them a little: “Ask him,” I say. Yes, it is true that George is not the world’s greatest talker, and may not respond to everything that is said to him. But, you know. At least give the kid a chance to try. If he struggles to answer, I will help him.
  3. Guilt. I was educated at a girls-only Catholic school run by nuns, and I am married to an Irish Catholic man. I can therefore say with some authority that the Catholics turn guilt into an art form. And some of the guilt that I feel as a special needs parent (hell, forget special needs – just as a plain old parent) almost makes me think I should just convert. I feel guilty about everything. Did the Taco Bell I ate during pregnancy cause George’s autism? Did I give him enough affection as a baby? Am I paying enough attention to my other son? Did I get too mad at George when he tipped over the laundry basket?  The list goes on and on, and my guilt makes me constantly second-guess myself when I should just be following my parental instincts.
  4. Time. Time very often seems to be my enemy, so much so that I sometimes regard it as a person. Time with a capital T. No matter how much I try, Time seems to run away from me. At the end of each day, there is always something that remains undone. Parenting is my absolute number 1 priority, so my kids’ needs are always taken care of. But I tend to let other areas of my life slip occasionally, and that is detrimental to my physical and mental health.
  5. The Internet. When George was diagnosed with autism five years ago, the first thing I did when I got home was Google autism. I obsessively read web page after web page. Every link that I clicked on seemed to have some information that flatly contradicted something I’d read somewhere else, and in the end my brain was hurting from information overload. I was overwhelmed by not knowing what information to trust. Since then, I am wiser in my use of the Internet and I have learned, for the most part, how to tell the good information from the noise. But the Internet, with all of its gazillion theories about the causes of autism, can still hinder more than it helps a lot of the time.

In my house, there is no such thing as a “small victory”. Every single accomplishment, all of the positive things in our lives – are massive, big things. That’s the way it often is in special needs families. We tend to place extra stock in things that other families take for granted. And as hard as it can be to live with autism, there are many things that I am grateful for, that enable me to keep chugging along even at times when I just want to cry.

  1. Love. Love really does make the world go around. Out of all the challenges my son has, lack of affection is definitely not one of them. Both of my sons give the best hugs that I can carry around with me all day. My favourite moments are when my boys somehow manage to squeeze onto my lap together to give me a hug. I sit there, with my arms full of squirmy, giggling kid, and never want the moment to end.
  2. Running. Yes, running keeps me sane, and when something stops me from doing it – like illness or injury – depression starts to creep in. The fact that it keeps me in good physical health is almost a by-product of running. My prime reason for doing it, along with raising funds for autism, is to keep my mental health on an even keel. I struggle with mental illnesses like depression and anxiety, and there’s no better way to combat my darker moments than a good long run. I am stubbornly resistant to using medication to deal with my issues, and running acts as a decent substitute for chemicals most of the time.
  3. Therapy. It has been said that running is cheaper than therapy, and while that is certainly true, I actually do need both. The therapist/client relationship is a very strange one. It involves the client placing complete trust in someone they actually know nothing about. I have been going to my therapist for a little over a year now, and it has taken me almost all of this time to build up my trust to a level where I can really open up during my sessions. Sometimes the sessions are very hard and they make me feel all weirded out for a while, but the truth is that once a week, I get the opportunity to talk without reservation in the sanctuary of my therapist’s office. I can say whatever I like and there will be no judgment or anger.
  4. Writing. I am somewhat inept as a verbal communicator, and I experience high levels of anxiety in social situations. When I am talking to other people, I hold back a lot, not only because of my natural shyness, but because my brain actually doesn’t work well during conversation. I can formulate a completely coherent thought in my mind, and even mentally phrase how I want to say it, but when it comes time for me to speak, my words get lost somewhere between my brain and my mouth. With writing, that doesn’t happen. I truly have a voice, and I treasure the opportunities to speak my mind on things that are important to me.
  5. The Internet. The Internet is both a blessing and a curse. Despite the evils described in my “bad” list, the Internet is a haven of sorts. I belong to two Internet support groups – one for moms who have suffered pregnancy or infant loss, and one for parents of children with autism. Both of these groups are places where I can vent my concerns, ask for advice, or celebrate good news. Some of my best friends are people who I have known online for a long time, but have never met in person. Here’s the wonderful thing about the Internet: no matter what I am going through on any particular day, I will always be able to find someone who knows, at least to some extent, how I feel.
Filed Under: autism, Challenges, Communication, Health Activist Writers Month Challenge, Mental Health, running, Victories, WEGO Health Tagged With: , , , , , , , , , , ,
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Finding The Path Of Healing

April 18, 2012 By

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 18 – Open a book: Choose a book and open it to a random page and point to a phrase. Use that phrase to get you writing today. Free write for 15-20 minutes without stopping.

My random phrase comes from a book called Watermelon, written my Marian Keyes – one of my favourite chick-lit authors. The sentence I pointed to with my eyes closed was strangely appropriate. “I was no longer carrying my humiliation like a weapon.”

I am a natural-born late bloomer. I have done many things in life after most people: I was 24 before I selected a career, my first child was born when I was 33, and I finally got married at the ripe old age of 41.

Now that I am old and wise, it doesn’t bother me that I tend to lag behind other people in some respects, but when I was in high school it was a great source of embarrassment for me. Socially speaking, I was streets behind most of my classmates. I was not exactly ostracized by my peers, but I was definitely not one of the “cool kids” either.

I got invited to parties from time to time, but I always felt so awkward when I got there. While my peers were laughing and chatting effortlessly, or retreating to private corners to snog their boyfriends, I was sitting by myself trying, and failing, to look as if I belonged. I could only really enjoy social gatherings if my best friend was there too. My best friend was the one who stopped me from drowning completely, and bless her heart, she is still my best friend today.

I had a couple of half-hearted boyfriends as a teenager, but compared to my classmates, I was geeky and socially inept. At an age where people are desperate to fit in and be accepted by their peers, it was painful. I was an unhappy teenager, although I never really admitted that to anyone.

When I graduated from high school, I went to a university 1400km away from my hometown. I figured that being among people I didn’t know would allow me to turn myself into the person I thought I wanted to be. I had always felt slightly inadequate and I didn’t like myself very much, and I wanted more than anything to reinvent myself.

Even though I made friends at university and had some kind of reasonable social life, the truth was that I was lonely. Never really a party girl, I tried to shoehorn myself into a party lifestyle because that’s what college students did, and I wanted so badly to fit in. And so I found myself immersed in a social group who were a laugh to be around, but I yearned meaningful contact. In those days before the Internet made the world a smaller place, I was not able to confide in my best friend. When waves of depression hit me, I had to get through them alone, with no-one to talk to.

And so, when a man started paying attention to me in my second year, I was flattered enough to fall for him. I do not want to share the details, but I will say that the whole thing was an absolute disaster from beginning to end. I was immersed in a situation that I had no ability to deal with.

The effect on my life was catastrophic. It was as if my future had been mapped out for me, and then a tsunami had come along and wiped everything away, changing the landscape of my life.

I floundered in the wake of this personal disaster. I completely lost all sense of who I was and what I wanted. I vacillated between depression and anger, and I blamed myself for having allowed my life to veer so far off the course I had planned. I drifted for a while, literally and metaphorically, and eventually washed up in a career, albeit one far away from what I had originally wanted.

One day, after having carried around the baggage of my past experiences for twenty years, I looked around me at all I have today. I have a solid job and my dream to be a paid writer is starting, in small but definite increments, to come true. I can run half-marathons in spite of not having a “typical” runner’s body. I managed to move halfway across the world and establish myself in a place I had never been to. I have a husband and two miraculous children. Although I make my mistakes, I think I’m doing well as the parent of a child with autism.

That tsunami that had swept so much away also created a new landscape with new paths for me to follow and new goals to shoot for.

This realization, when it hit me, was like a breath of fresh air. Although some scarred remained, I was no longer carrying the humiliation like a weapon.

For the first time, I felt that I owed it to myself to try to heal.

(Photo credit: http://www.flickr.com/photos/kudumomo/3140538425/. This picture has a creative commons attribution license.)

Filed Under: Depression, Health Activist Writers Month Challenge, Letting Go, Memories, Mental Health, Possibilities, Second Chances, Social Anxiety, Success, WEGO Health, Youth Tagged With: , , , , , , ,
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Getting It Write

April 15, 2012 By

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 15 – Writing with style: What’s your writing style? Do words just flow from your mind to your fingertips? Do you like handwriting first? Do you plan your posts? Title first or last? Where do you write best?

The fact that my older son’s childhood development is almost a carbon copy of my own leads me to believe that I am somewhere on the autism spectrum. I had the same speech delays, the same geekiness with numbers, and the same tendency to play by myself in spite of being in a room full of other kids.

To this day, I experience social anxiety, although I have learned how to mask it well enough for other people not to notice. I am not fond of social gatherings where I do not know at least one person very well. During times of stress or conflict I struggle to coherently express my thoughts verbally. Let’s not even get started on the telephone. I am downright terrified of the telephone.

My ineptitude and discomfort with the spoken word is what led me to the written word. Writing is marvelous. It gives me a voice. It provides an outlet for the creativity that I have, to my complete surprise, discovered within me, and it eliminates the problem I have with conversation, where my words frequently get lost between my brain and my mouth.

When I was in high school, I used to get somewhat disillusioned when my creative writing projects were marked down “for lack of structure”. We had it drummed into us that our stories had to have a beginning, a middle, and an end. We were supposed to rigidly plan our essays and then stick to the plan. If the ending did not clearly tie in to the beginning, that was the mark of a Bad Essay.

The problem was that this whole beginning-middle-ending thing didn’t work for me. I understood the theory, but I couldn’t make my mind work in such a linear pattern. As long as the stuff I wrote made an impact, and as long as my readers were engaged throughout, did it really matter? Whenever I tried to write in the prescribed way , the finished product came across as stilted and awkward, and just not me.

When I started this blog just over two years ago, I promised myself that I would remain true to my natural style. I try to make sure my writing flows, and that it’s easy on the eye. I have a goal to leave my audience with some kind of message, whether it’s an idea, a call to action, or an emotion. How I accomplish that depends on my subject matter and what my state of mind is like as I’m writing. Sometimes my posts do follow a traditional structure, and when that happens, it’s just because the topic lent itself to that.

Many times, I will change direction midway through a post. I will allow my train of thought to drive my writing. In that sense, my blog posts are often a true reflection of how I think. They are a glimpse into the part of my soul that’s open for public viewing. I may struggle from time to time to come up with the first sentence, but usually, once I achieve that, I’m off and running. I don’t always go to where I had intended. My destination can be a surprise even to me.

The journey is always a lot of fun too.

(Photo credit: http://www.flickr.com/photos/kharlamovaa/6016780468/. This picture has a creative commons attribution license.)

Filed Under: Communication, Structure, Style, Thinking Differently, Train of thought, Uncategorized, Writing Tagged With: , , , , , , ,
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Why Autism?

July 19, 2011 By

“Why do you think he has autism?”

This question is posed to me quite a lot by friends and strangers alike, people who for the most part intend no malice, but are genuinely curious about the origins of George’s autism.

That they are asking the question at all is something that I see as a positive sign. It tells me that increasingly, people are wanting to be educated about autism instead of blindly believing every tidbit of information – right or wrong – that is thrown their way.

Over the years, I have done research on a variety of theories.

Was it vaccines? No, I don’t believe it was. Deep down, I knew from the time George was a tiny baby that he was not on the trajectory of “typical” development. I don’t buy into the dietary theory either, for the same reason. George was exclusively breast-fed for four months, and by then I was seeing some little signs that something was not quite right.

No, whatever happened within George’s brain to result in his autism, it was a done deal by the time he came out of the womb.

Even with that knowledge, the title of Primary Cause is wide open. I have read a couple of recent studies suggesting that environmental factors in utero could have more of an effect than previously believed. As if moms of children with autism didn’t have enough guilt on their shoulders already. But that is neither here nor there.

When I was expecting George, I did everything that was considered by pregnancy gurus to be “right”. I ate lots of leafy greens and took my prenatal vitamins every day. I ate lean protein and avoided foods with a high fat content. Accustomed to eggs “over easy”, I ensured that my eggs were fully cooked, and I did not touch deli meat or anything else that could be a potential listeria risk. I did not touch a drop of alcohol, I stayed away from places where I might be exposed to second-hand smoke, and my body pretty much bullied me (through the magic of the laughably known “morning sickness”) into kicking caffeine to the kerb. I went to all of my OB/GYN appointments and followed the advice of my doctor. I did not take so much as a headache pill through my entire pregnancy. The only tablets going into my mouth were vitamins and Tums.

I don’t think I could have created a better environment for my baby if you had paid me a million bucks. Of course, there is the possibility that fifty years from now, someone will prove that some obscure enzyme in, say, oranges, has been linked to autism. But I think it is safe to say that the prenatal environment is an unlikely candidate for the cause of George’s autism.

Leaving aside other environmental factors like air pollution, there are two other possibilities: genetics, or the circumstances surrounding the birth itself. Or maybe a combination of the two.

When I was a child, I was developmentally delayed. I didn’t talk until I was five, and I had some motor skill delays. My body was physically capable of doing anything my peers could do, but the communication between my brain and my muscles was out of synch. It was clear – especially in the early years – that I had some kind of learning disability, although I was never formally diagnosed with anything. As I navigated my way through childhood and adolescence, I was able to compensate for my learning difficulties by simply thinking in a different way and leveraging areas that I was strong in. But as my academic performance got better and better, my social awkwardness and anxiety among people became more and more apparent.

To this day, I suffer from social anxiety, although in general, I have found ways to adapt and mask it so that people don’t really notice. I’m not so much a stickler for routine, but once plans are made I get very uncomfortable – almost panicky and kind of, well, spectrummy – if they are changed. Although I am now fully verbal – sometimes, downright talkative – there are times, usually when I’m stressed – when I lose the ability to communicate through speech. It’s as if the words get lost somewhere between my brain and my mouth.

Am I on the autism spectrum? I don’t know. I have never been for screening, and frankly, I don’t really see the point. But if I were to learn that I have Aspergers, I would not a bit surprised. When I look at the way George has evolved through his early childhood, and the way he is at this point in his life, I do see a lot of parallels with my own early years. So, genetics? It’s a strong possibility.

The other possibility is that something happened to George’s brain while he was being born. For the most part, my labour was pretty standard. Everything happened more or less when the Medicals said it would. When I was in the thick of contractions, I heard someone use the word “textbook”. When the time came to push, though, the going suddenly got a lot tougher. Even though the baby was perfectly positioned for birth, no matter how hard I pushed, nothing budged. The Medicals kept telling me to push harder, push harder, but I just couldn’t do it. After what felt like an eternity but was probably only a couple of minutes, the Medicals gave me an episiotomy (if you don’t know what that is, look it up, because I ain’t describing it here). Once that was done, I gave one more almighty push, and an eternal second later, I was rewarded by the sound of a baby crying.

Here’s the thing, though. While I was pushing to no avail, the baby’s heartbeat – usually in a range of 130-150 beats per minute – dipped to below 40 beats per minute. Only for a couple of seconds, mind. Like a momentary blip in the radar. But could those couple of seconds have been enough to alter the wiring in my baby’s brain?

In the end, I suppose it doesn’t really matter. George has autism, and knowing the cause with crystal clarity would not change that.

No matter what the cause, George has autism, and I love every inch of him for who he is.

(Photo credit: http://www.flickr.com/photos/macbeck/4146730230/)

Filed Under: Aspergers Syndrome, autism, Autism Spectrum, Causes of Autism, Childhood, Developmental Delay, Environment, Genetics, Learning Disability, Social Anxiety, Speech Delay, Vaccines Tagged With: , , , , , , , , , , , , , ,
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Lost For Words

January 13, 2011 By

I think the Internet was the best thing ever invented.  OK, make that the second best thing, after coffee, which when you think about it, wasn’t actually invented in the true sense of the word.  One reason the Internet is so great is that it enables me to keep in touch with people without actually having to talk to them.

Lord, that sounds awful, doesn’t it?  It makes me sound like an arrogant, antisocial jerk who doesn’t care about the people in her Facebook friends list.  Let me assure you that this is not the case.  I care about people a great deal, and my friends are very, very important to me.  I realize that this is the kind of thing that anyone would say, even people who would sell their grandmothers to the devil.  But I really do mean it. I have my fair share of faults, but I believe that the people I care about would describe me as a good and loyal friend.

So when I say that I want to keep in touch with people without talking to them, it’s not the actual people that I have an aversion to.  It’s the talking.

Let me pause for a moment to say this: what I am sharing today is a glimpse into a part of my life that I have difficulty with.  It is something that, while not exactly earth-shattering, is not easy or comfortable to talk write about.  And while there are certain aspects of my life that I will never share publicly, I just-about-kind-of-sort-of feel brave enough to discuss this.

You see, all my life I have suffered from pretty intense social anxiety and awkwardness. While I always enjoy being around people, I frequently don’t know what to say when I’m with them.  Or to put it more accurately, I know what I want to say but I find myself unable to say it.

Are you confused yet?

Here’s what it’s like for me.  I often find, when I am talking to people, that I am able to formulate an idea in my head.  I can script the words I want to use in order to verbally express that idea.  But when it’s actually time for me to utter those words, I cannot.  The best way to describe it is that the words get lost somewhere between my brain and my mouth.  It’s as if the synapses in my brain that are responsible for translating thought into speech just aren’t firing.

Picture yourself sitting in your car in your driveway, intending to drive to the post office, and suddenly discovering that all of the roads between your house and the post office have suddenly disappeared.  So you sit in your car at home, at a loss as to what to do.

Or if you’re me, you sit there not taking part in the conversation, and people just assume that you don’t have anything to say.  And you get more and more frustrated because you do have something to say, but you are unable to say it. Or when you can say it, you sound awkward and stilted, and because this whole conversation effort is so stressful, you come across sounding abrupt or disinterested or babbling in an uncomfortable way.  If I’m in a situation of conflict with another person, this problem multiplies a hundredfold.

Some people who know me personally are probably reading this and going “Huh?”  This verbal debilitation I experience is not visible to everyone – a lot depends on who I’m talking to and what the circumstances are.  This problem is a disability of sorts, and people with disabilities learn how to adapt, and how to live life as seamlessly as possible without letting the disability take over.  But even at times when I give the appearance of having a normal conversation, I am capable of feeling a level of anxiety that most people probably cannot relate to.

Although certain events in my life may have exacerbated this issue, it is really something that I have always lived with.  I had a variety of developmental delays as a child, and only developed a reasonable level of functional speech at the age of five.  Throughout my childhood and adolescence, my social development was far behind that of my peers.  At an age where most of my contemporaries were going to parties, acquiring boyfriends, and traveling in large, noisy packs, I was the quiet, awkward one who never said much.  My social anxiety was frequently misconstrued as shyness.

As an adult, this has impacted my life in a number of ways.  Certain events in my life can be attributed at least partly to the fact that I did not have the social skills I needed to deal with things differently.  These events have ranged from the minor events that you forget about the next day to the bigger events that stay with you for life.

My social interactions tend to vacillate between two extremes: one the one end, I kind of clam up and don’t say anything.  On the other end, I talk non-stop, saying inconsequential stuff to cover up the anxiety I feel.  In the middle of these two extremes are the “normal” interactions I enjoy with my family and my closest friends; with people that I have a high degree of trust in.

Telephones terrify me.  Seriously.  I hate the things.  If I could get through life without ever talking on the phone, I’d be happy.  When I do find myself on the phone, I get the hell off as fast as I can.  Again, there are exceptions.  My Mom?  I could talk to her on the phone all day.

I love to write.  Love, love, love it.  My tendency to lose words does not extend to my writing – in fact, I have a theory that my writing skills have developed pretty well in order to compensate for the difficulties I have with oral communication.  This is a good outlet for me.  It is a way for me to share a part of myself with the world, without going through the anxiety that I might otherwise experience.

I find my social anxiety issues to be disabling at times, but being the eternal optimist, I strive for things to be better.  I adapt, I compensate, and I seek opportunities to overcome.

(Photo credit: Flickr Creative Commons Attribution License)

Filed Under: Communication, life, postaday2011, Speech, Uncategorized Tagged With: , , , , , , , , , , , , ,