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For me, the issue with being able to speak begins inside my head. Let me use an example to explain.
My family enjoys playing a game called "Scattergories". In the game each player fills out a category list with answers that begin with the same letter. If no other player matches your answers, you score points. Players determine the letter used by rolling a die with all of the letters on it. Oh, and there's a time limit.
I give myself some credit....I'm pretty good at this game. (Most of the time.) I think it's because I can be creative with my answers and because I have such unique interests that no one else knows about. My weakness, as with everyone else, is the time limit.
Today, however, I discovered a new weakness. Language processing. This frustrated me to the point where I nearly said "just forget it, I can't play". But I didn't want to be left out. So I just played a miserable game. You would think that it would be obvious that I was having some issues when I went from getting LOTS of points to getting one or two. But right from the start of that last round, I knew I was going to struggle. I could SEE the objects in my head. I KNEW what I wanted to write in as my answer, but the words wouldn't come to me. THIS is how it feels when I have trouble speaking.
I really wish that I could have been given some extra time. Or I wish I could have just left and gone home right then and there. But I didn't want to be left out. I wanted so badly to have fun. Yet, I couldn't. I can only imagine the frustration felt daily by those who are completely non-verbal. I've experienced this frustration to a degree, but never fully.
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Hopefulaspiemommy says...
Hi, As a mom of a Aspie 8 yr old I want to thank you for weiting this blog to help us understand our kids. In my wishful thinking, I thought he'd be over these things like food sensory issues, language blocks when he gets excited, and other things you describe. Then I saw your age and was a bit heartbroken, realising that slthough my son has made so much progress, some of these issues he will carry into adulthood. In the long run, our main worries are avoiding him depression and feeling assured that he will be able to lead an independent, self-supported life as an adult (study in the University, hold a job he can live on, etc). Have you been able to? Talk to us a bit about how to support our aspie kids socially and emotionally please, from your perspective. What would you have preferred as a kid: to know you were an aspie or is it best to not be labeled at a young age?
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