Showing posts with label myself. Show all posts
Showing posts with label myself. Show all posts

Monday, December 13, 2010

Letter to D

This was inspired in part by my talk at the Children's Development Center. In the interest of safety, I will not reveal who D is, but I will say that he was there when I was talking to parents like his about autism, which D has.

Hello D,
A couple of nights ago, I was talking to moms and dads like your very own mom and dad. They were asking me all about people like you and I: My hobbies, my favourite foods, my dislikes, my favourite thing about myself, and what I think is the best possible path for them to take to raise kids like you, kids who are like I was at your age. You were off in the corner with your legos, and I felt like joining you and answering their questions while building a totally awesome fortress. But I sat at the table and just talked, while clicking my tongue occasionally, sighing, and rocking gently back and forth in my chair. Occasionally I cracked a joke.
When I was talking with them, I saw them smiling, laughing, and there was something in them that I was able to faintly detect, though I'm not so good at this type of thing: A mixture of relief and gratitude.
I think I know why they're grateful, D, but I can't be sure. I think they were glad to see me. See me there, dressed nicely, hair combed, but still wearing my totally comfy old scruffy black addidas shoes, mismatched socks, and rocking back and forth like I do. I was clearly like their own kids, but I was happy, content, and at ease (somewhat) in the world of adult conversation and adult responsibility. I had goals, dreams, and a tangible type of happiness, the kind that playing with those legos used to give me.
I think, more than anything, that's what they want for you, and their own kids. That happiness. For a long time now, they've been told that that's beyond your grasp, that your autism means that there's no hope, no future for you beyond living at home in your own filth and their shattered dreams. That's the image the media and not-so savoury folk have fed them about our autism. But that night, I could practically feel it break away. There was something different taking root there, and it was this idea that not only was happiness possible for you and I, it was all possible without having to force us into a way of life we were never meant to adhere to.
It's important that people like those parents know I exist, that others like me exist. When I was your age, I didn't know there was anyone like me out there. When I was your age, what I "was", would often be dubbed a mystery, a puzzle, or unsolvable. I had people call me horrible names and tell me horrible things. I've never managed to shake it off, and it forms a weight on me that sometimes makes my words, thoughts, and deeds drag along the ground, like a ball and chain. I know that this still goes on, and it makes me shudder and wince with a pain you'll grow familiar with as you age.
But I want a better future for you. Both myself and my parents want it. If the world took off its pity-tinted glasses and saw you do what I see you do, they'd be amazed. I love your intricate lego designs, towering high. I marvel at how you, like me,love to blow on cold glass and trace along letters and numbers in them. I'm amazed at your prowess with your finger as you write out these sums and words. But most of all, I love seeing you stimming quietly or not-so-quietly in the corner of the room uninterrupted. No attempts to jerk you out of it, no worries about how weird you look.
I love it because it's the world you created for yourself, and now, nobody wants to intrude in and deflate it. Never lose that world, D, it's your safe haven.
I promise you, I am going to do everything in my power to make sure that safe haven is yours to keep. I was luckier than others yesterday and today, and I want the very best of luck for you and all your friends. There's a little bit of me in all of you, and you all have something you share with me. Treasure it. And I'll make sure that it is seen for the precious gift it is, until you're old enough to protect it yourself.
Hopefully by then, nobody will be fighting to rob you of it though.
Leah Jane


Saturday, May 29, 2010

A small (re)introduction

Welcome, everyone! This is my new blog, named because I love wordplay, and because my attitude towards life is, through the eyes of many, overly idealistic. I feel it's just coloured by the radically romantic ideal that I, as an autistic woman, am deserving of my own voice to speak with. My language, mannerisms, and ideals are filled with flourishes of dreams and thoughts.
Before I get started, I want to make my reasons for starting this project clear.
Ask yourself this: If you are neurotypical, think back to all the stories on autism you have seen in the media actually featured an autistic person or interviewed someone who was autistic? How often did stories on autism portray it as a tragedy, a nuisance, or a horrible epidemic? Or, on the other hand, how many portrayals of autism display autistic people as savants (Savant syndrome differs from autism, though in some individuals, like Daniel Tammet, they overlap) with near inhuman abilities?
I do not have superhuman abilities. I cannot count cards like Rain Man. I am not an object of pity or sickened by vaccines.
Other autistic people will note similar experiences of seeing an extreme dearth of representation and accurate portrayal in the mainstream media. We're almost never asked about our own opinions on our conditions and life, the opinions of our doctors and our parents are sought, while we are pushed out of the way and only pulled into the limelight again when the story calls for us to be seen but not heard.
Well, this blog is my way of being heard, even if it only reaches an audience in the single digits. I have lived for nearly a quarter of a century as an autistic person. In this lifetime, I have come across some horrifying and unacceptable experiences and statistics that are the norm in how people like me are treated. To add insult to injury, many autistic people are denied the chance to explain their experiences, either because we are assumed incapable of doing so, or because our truth is uncomfortable for neurotypicals to hear. It shatters their back-patting self-assurance that disabled people now live comfortable privileged lives, and forces them to confront their own prejudice. We need to keep chipping away at that façade until it's blown away like so many motes of dust.
My blog is my chance to fight against that forced ignorance and silencing. My weapons are ten knobby fingers and a keyboard. I'm going up against a mighty enemy of forced ignorance. I hope you enjoy it.