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Tuesday, 09 June 2009

  • 8th grade promotion

    Last night I watched my son (and his 8th grade class) get "promoted" to 9th grade. It was awesome to hear his name announced, followed by "with honors". I think I got goosebumps! To think that two years ago at the end of sixth grade, my son's teacher had pulled me aside and talked to me about his concerns for M's future. He was not doing so well, the teacher had told me... and he was worried that he would not be able to adjust to junior high. Imagine how I felt to be told that about my son. Not that it matters now...

    WITH HONORS!

    Ha! I wish those who doubted him could see him now. I'm so proud of him, not just because of his grades... but because he adjusted to junior high so well. I remember asking him in 7th grade what was so much better in junior high that he seemed happier and was doing better in his classes. M said he liked having a separate teacher for each subject, instead of one teacher for everything (in elementary school). He also liked having a schedule with a set amount of time for each subject.

    He's so excited for high school. I'm not going to lie and say I'm not worried about this upcoming transition, but if he's not worried then I'm going to try and relax a bit.

    How have your kids handled school transitions?

Wednesday, 13 May 2009

  • sensory overload

    My son usually takes the bus to school, but I have today off so I drove him. As he stepped out and waved goodbye, I noticed how a lot of the boys at the junior high had long hair. M's hair is long, but it's always been long... now it's actually "cool". Funny how that works out.

    The few times it's ever been cut were always an ordeal. In his earlier years, I used to be the one to cut his hair... or his grandpa would. He would fight us, squirm about, climb off the chair, and cry. My happy, usually compliant child absolutely hated it! I often resorted to begging then bribery. To no avail. There were times he'd end up with a crooked haircut and I'd have a super-cranky kid.

    I had the brilliant idea of taking him to a pro. Surely it was just me, I must have been doing something wrong. Someone who was trained could do it faster and better, right? Well... I still had to beg and bribe through his tears, but for the most part if they were patient enough with him it would work. Though, one barber did refuse to cut his hair... due to "safety issues"... which is understandable.

    "You just have to do it more often so he gets used to it," was the advice given by friends and family.

    I didn't know then what had bothered him about it, but as the years went by, and after much torcherous hair cuttery, he found his words. He found his words and he told me why he didn't like it. The hair, he said, felt like it was poking him... the prickly feel of each individual hair falling on the nape of his neck, on his ears, and face as it was cut was too much for him to handle. And the sound of the scissors, the snip snip snip... he said it felt like it would cut into him. Oh and the clippers, the constant buzzzzzz... it made him cringe, tighten up his neck and shoulders. He couldn't stand the sound and the vibration, it reverberated through him.

    So I let him keep his hair long. It's only hair, after all... there's nobody to impress, no dress code against long hair on boys at school. My relatives may cringe at the long hair, but who cares? Nowadays, he'll ask if we could go to get his hair cut or trimmed. I always make sure it's his choice... I might suggest it but I never force it on him. I no longer have to beg or bribe, but sometimes we still go get ice cream afterwards just for old time's sake.

    What is an instance of sensory overload you or someone you know has had?

Monday, 11 May 2009

  • My son and AS

    Aspergers Syndrome is part of the autism spectrum. Some people might call it "high-functioning autism" but I believe that's another dx of its own. These are the DSM IV criteria for Aspergers:

    Diagnostic Criteria For 299.80 Asperger's Disorder

    A. Qualitative impairment in social interaction, as manifested by at least two of the following:

    1. marked impairments in the use of multiple nonverbal behaviors such as eye-to-eye gaze, facial expression, body postures, and gestures to regulate social interaction
    2. failure to develop peer relationships appropriate to developmental level
    3. a lack of spontaneous seeking to share enjoyment, interests, or achievements with other people (e.g. by a lack of showing, bringing, or pointing out objects of interest to other people)
    4. lack of social or emotional reciprocity

    B. Restricted repetitive and stereotyped patterns of behavior, interests, and activities, as manifested by at least one of the following:

    1. encompassing preoccupation with one or more stereotyped and restricted patterns of interest that is abnormal either in intensity or focus
    2. apparently inflexible adherence to specific, nonfunctional routines or rituals
    3. stereotyped and repetitive motor mannerisms (e.g., hand or finger flapping or twisting, or complex whole-body movements)
    4. persistent preoccupation with parts of objects

    C. The disturbance causes clinically significant impairment in social, occupational, or other important areas of functioning

    D. There is no clinically significant general delay in language (e.g., single words used by age 2 years, communicative phrases used by age 3 years)

    E. There is no clinically significant delay in cognitive development or in the development of age-appropriate self-help skills, adaptive behavior (other than social interaction), and curiosity about the environment in childhood

    F. Criteria are not met for another specific Pervasive Developmental Disorder or Schizophrenia


    My son M is 13-years old and he has Asperger's Syndrome (AS). I am not an expert on AS, but I am an expert on my son. I don't often share with others that my son has AS. I suppose I'm trying to protect him from stigma and avoid having him labeled by others, which is quite a challenge since anyone who spends a moderate amount of time with him can easily see that he is a bit quirky (to say the least). He speaks quite loudly, has difficulty maintaining eye contact, talks about his favorite things to the point it's almost a monologue (or he doesn't talk at all), lacks a filter... I could go on and on. But I guess that's what this blog is for.

    This blog will be a place where I would like to share my experiences as his mom, my beliefs, frustrations, expectations, hopes and dreams, etc. First a quick background...

    M was lucky enough to spend his elementary school years at a GATE (gifted and talented education) school, where most of the kids seemed a little odd anyway. There he was able to be himself. He still didn't make friends like you and I would think friends would be: coming over to play, getting invited to parties, etc. This made me sad, but then again he didn't seem to care so I didn't make a big deal out of it. If he was invited, we went.

    Before he was diagnosed with Aspergers in 3rd grade, they thought he might have ADD (2nd grade). They were quick to label kids with ADD/ADHD back then so they thought to just throw him in the same group. I disagreed with them, rejected the Ritalin, and eventually got a second opinion. While this dx is neither more nor less favorable, I felt it was more fitting than attention deficit disorder.

    He made the biggest steps in 5th grade, when he decided to join band, choir, and intramural basketball. (He had already been in chess club since 3rd grade.) I think having found success in chess club boosted his self-esteem or at the very least it made him less shy to try new things. That's my theory anyway.

    So now fast-forward to 8th grade. (I know I skipped a lot.) He still plays chess in tournaments (even though there's no club at school), he's still in band (and will continue in high school), and he joined a video game club (LOL). His three loves: chess, band, and video games. I love that he's involved in extra curricular activities.

    Some family and friends have wondered why I would "do that" to my son... like it's such a bad thing to play chess and be in band. It might be "less" to be proud of in their eyes of because it's not sports, but not in mine. (Btw, we tried T-ball and soccer... it didn't take.) To me it's such a huge deal to let him be where he feels the most comfortable... To find his place. I feel this is why, as a result, he is doing better with interacting with people, has better eye contact, is better able to share his accomplishments, etc.

    Do you know anyone with Aspergers?

  • I've been visiting Autisable from my main blog and I've finally decided to join! I'll have to work on a much better intro post that this. But this should do for now.

chessmom

  • Visit chessmom's Autisable Site
    • Member Since: 5/11/2009

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