(Not to distract from the topic at hand, but this is my 500th

I’ve been in my cave this week, so to speak, but I’m ready
to poke my nose out and growl.  (Nice
growling, though. Growling to start conversations, not end them).  For those of you who have read my blog for a
while you know that we were having issues with Chance (you can read about them here, here
and here,
and even some here).
 Well, we’ve had some developments

Right before I went to BlogHer, we made the decision to pull
Chance out of preschool for the rest of the summer session.  Basically, he was still biting; not all the
time but it was still enough that we decided a break was needed.  A break would give me more time to get
assessments done and/or work with him on specific issues, and a break for him from the place where he kept getting in trouble (although he did NOT want to leave school).  He continues to be more physically rough,
more active, less focused than the kids around him.  (We also have a vacation planned so it just
made sense to pull him out.)  

This has been a long road to get assessments done.  I’ve been working on this process since
February.  I was getting a lot of feedpushback
and random advice, the two most frustrating being “just wait until he’s older,”
and “read this parenting book.”  (This from professionals, some of them who
hadn’t even seen Chance.)  It’s not as if
I wasn’t open to trying different methods – I read the books, I implemented
some of that advice – but a lot of it just didn’t feel right.  For example, people advised that I give
Chance something to do every single day to “burn off energy”, when my instinct
(and experience) was that he would get increasingly wound up if he didn’t have
“downtime” days.  When I talked about how
Chance always wanted to be on top of people, the advice I got was “just don’t
ever let him climb on you and he’ll learn,” when my instinct was telling me
that he somehow needed that physical
touch.  Although it was suggested that I
do hearing and/or speech screenings, when I asked about other sensory
processing issues I got pushback. 
Frankly, I needed some help (now, not six months from now) and my gut
said some form of physical therapy.

A couple of weeks ago I said fuck it and I found a place
that would do both speech and occupational (physical) screenings.  It was private and out of pocket, but waiting
for referrals or help from the school district was getting ridiculous.

Chance had his assessments yesterday.  The therapists immediately could see, and
point out, behaviors leading to the issues we’ve been having with him.  Suddenly, things we didn’t understand made a
lot more sense.  Chance is showing symptoms
of apraxia and dyspraxia, which are problems with motor-planning.  Essentially, when a person wants to move their
body: 1) you get the idea of moving, 2) you plan the movement, and 3) you do
the movement.  People who are dyspraxic
get stuck at the planning movement stage and need a little extra time for the
thought process.  Apraxia is similar but
has to do with verbal motor planning, trying to get the words out.  Chance also seems to be hyper-aware of sound
and it’s distracting the hell out of him. 
The confusion of trying to process everything can cause a lot emotional
buildup, anxiety or lashing out. 

Finally feedback that felt right.  Or at least a lot closer to what could work
than anything before.  There have been a
lot of communication disconnects between what I hear people say about Chance
and what I observe.  For example, his
school would tell me he can’t do such and such, when I would see him do such
and such all the time at home.  The apraxia
accounts for when he doesn’t respond to questions or instructions or when he
sometimes avoids eye contact when you’re talking to him; he understands
everything but he needs the extra time to process.  He could learn something at school and not do
it there at all, but come home and do it perfectly.  Chance has problems with “on demand”
instructions or requests, both physically and verbally.  This can also mean difficulty with group

As for his activity level and rough playing, the
occupational therapist pointed out that kids with these issues sometimes run
around "wild" because running around is either easier than the
processing or gives them time to process. 
Chance seeks out a lot of physical contact because it helps him
"ground" himself, releasing physical and emotional energy.  The biting was/is an unfortunate component of
that. (Everyone who has ever observed him has said that his aggressive behavior never seemed vindictive, but like "he couldn't help himself".)

The apraxia/dyspraxia is not a definitive “diagnosis” by any means, but I feel
like these are elements that we can specifically address that may help get our
arms around his behavior.  We will be doing speech and occupational
therapy and I have high hopes.

So that’s where we’re at.  Having a plan in place, hearing specific targeted
techniques…this feels so much better
than reading another book*.  

the weirdgirl

P.S. I went to the Parents of Children with Special Needs
panel at BlogHer ’08 and I felt a lot of love and support from that community,
especially being a “newbie” to this process.  I’ve also spoken to and asked advice from other
blogging parents out there.  Your stories and encouragement mean a lot.  Thank you.

*Though, yes, I will be reading Out of Sync Child.