Sparrow,
I read your post about your lad and the trials and tribulations of needing to get a haircut and I sighed in recognition of the emotions that you must go through over, what seems to us, the insignificant details of life. To our children, though, and to children on the Autism Spectrum in general, these things aren’t simple; getting a haircut, going out into society in general with its plethora of sounds, sights, colours, and smells, can be a sensory overload that can throw a child into a literal panic. I wonder what people, who don’t know about Autism, or Autism Spectrum, think when they read our postings about our kids. Do they think we’ve gone off of the deep end or can they actually commiserate?
Your most recent posting, "Haircut"(http://birdieandsparrow.blogspot.ca/2013/01/haircut.html), received a beautiful comment from a reader empathizing with you on this issue and encouraging you forward and I was deeply moved by it and the fact that this person could be so feeling, but it made me wonder how many others really understand what it is like to have children like ours. If they don’t, they must read postings like yours, or the one I wrote about Chronic Sorrow(http://birdieandsparrow.blogspot.ca/2013/01/uncontrollable-weeping-and-chronic.html), and think we are over dramatic. Heck, they must wonder why we even feel the need to blog, altogether. For anyone that is interested, here is a link with information pertaining to Asperger’s Syndrome and Autism Spectrum Disorder: http://kidshealth.org/parent/medical/brain/asperger.html
On our end, we always knew that our youngest was “different” somehow. Her drummer tapped out a beat unlike most and we recognized, from a very early age, that the world, through her eyes, was unlike anything we could experience. We started the process of diagnosing her when she was only 6 and, while many a possible label was thrown our way, it wasn’t until yesterday, January 22 2013, that the official label came through: Asperger’s Syndrome.
There it is - High Functioning Asperger’s Syndrome(the high functioning aspect refers to her higher than average intelligence level). We are no longer “potentially” on the Autism Spectrum with a “potential” disorder. My daughter has Asperger’s Syndrome. If you imagine a line drawn horizontally across a page, much like a historical timeline, we have a definitive spot now marked with a great big red dot. It’s further down the line from Classic Autism but it shares many of the same traits and quirks and it is that big red dot which allows my daughter to see herself, and her needs, in a concrete, “this is me” kinda way. And, for those that don’t believe in “labelling” a child, let me say this: try to walk through the world knowing that the world, as others experience it, is so vastly, grossly, monumentally, different than the way you experience it that you think there must be something wrong with you, and then tell me that a label doesn’t matter. A simple label truly does have the power to not only explain your behaviours, but also to help you understand and forgive yourself for them, and to appreciate them. The label is just a word, sure, I get that, but it allows a child to say: “That’s Why!”. It allows parents to say: “Now I get it!”. It gives, to a degree, a guideline of how to proceed and a chance to start again, with understanding. Never underestimate the need to “understand” and to be understood. My child couldn’t be happier to finally know, “This is who I am, this is why, and this places me in a group of people that I understand and who will understand me”.
Asperger’s Syndrome, I welcome you to my world as a label, but you don’t phase me because you have, technically, been in my life for almost 13 years via my Kidlet. You have challenged us but this family has met you head on. You have introduced us to beauty, and to heartache, you have dragged me kicking and screaming into a world of Chronic Sorrow but also into one of stunning happiness. I welcome you as an official label and we, as a family, will banish the preconceived prejudices that such a label brings with it and we will continue to love our Kidlet, respect her, and marvel in her as we always have. I just wish, Asperger’s Syndrome, I just wish that you didn’t make my little lady THAT intelligent cause she rolls her eyes at me, way, way, way, too many times a day!!!!! Actually, I take that back, BRING IT ON!
Love Always,
Mother of an "Aspie Girl"
Red Bird
Love Always,
Mother of an "Aspie Girl"
Red Bird

I have a Goddaughter with Asberger's Syndrome. When she was 6 it was almost normal for her to wander off and she could not walk straight. It was very frustrating when we took her to the Super Ex as almost every 10 seconds she would wander to the right. As she is a little older being 8 years old now she is really good with puzzles, and very determined with scavenger hunts. One thing's for sure, she loves horses so we'll probably take her for riding lessons soon. It's a never ending process and we hope that she could function on her own when she gets older but were just not sure right now. i guess we'll just wait and see.
ReplyDeleteThat's the constant worry for Sparrow and myself, Pierre; how will our kids function in the world on their own one day? Kids like ours, and your Goddaughter, they're lucky because they have love and support. That's part of the battle won to get them to leading a succesful happy life. They will always have issues, but we can train kids with Asperger's to take an active part in their own lives and be successful. Thanks for sharing your story
ReplyDeleteWith your love and support, she will be successful, Pierre. It just depends on how you define success. We work from a different playbook as parents of autistic children, but our children bring so much to this world, never underestimate her abilities and the value of those abilities. She sounds like a lucky girl, an open and caring family by her side. It's great to hear your story. Thank you. Perhaps we'll see her riding in the Olympics one day?!
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