A child with ASD is like a snow flake or finger print in the sense that, from a distance they look similar or even the same but upon closer examination they are in fact, quite different. Each unique in their own way with no two being the same.


Thursday, February 16, 2012

Something about hearing.....

"I'm going to go ahead and put this in medical records" makes everything feel real.

Don't get me wrong...I hadn't been doubting that D had Aspergers but knowing it's officially official brought up a lot of emotions that I really wasn't expecting.

Yesterday was Dylan's appointment with Dr. T, the child psych.  I really, really liked him and felt like he listened to what our concerns were and offered a lot of good help.  It's funny how I could tell exactly what he was doing as far as Dylan was concerned the minute we met him in the waiting room...the questions he asked him, etc.  I will say that Dylan didn't hold back...he showed the good, the bad, the ugly and the really, really ugly.  If we had been anywhere else, I likely would have been holding back tears and been incredibly embarrassed by his behavior but I was almost relieved...I wanted the doctor to see what we struggle with....not just hear me say it or read it in a report.

We were there for close to 2 hours.  It was a good mix observing, talking and interacting with Dylan.  Dr. T. had a resident with him who spent a lot of time interacting with D.......good thing because otherwise I would have had a really hard time talking with the doctor.

He agreed 110% with the dx of Aspergers but he also strongly felt that D has Oppositional Defiant Disorder.

We spent a good chunk of time talking about what supports we need to try to have in place for D before he starts kindergarten in the fall and thankfully, he is going to write a letter for me to share with the school district as we work to have services in place.  I fear that this may not be an easy task but I do know that I will fight for what I KNOW he needs to succeed.  Ready, set, go! :-)

Like so many things we've gone through with Kira, we can't go around this journey....we have to go right through it.  I know it's not going to be an easy one at times but we're going to take it one step at a time and put one step in front of the other.  It's not what  I would have picked, obviously and I know there will be times, as there have been already, where this Mommy's heart will break......but we'll figure it out.

I'm reading a book right now called Ten Things Every Child with Autism Wishes You Knew and it's been really eye-opening for me.  One line has really stuck in my head though.....

"........when your dreams break into a million pieces, you can either fall apart or get yourself a new dream."

I am not saying at all that I'm falling apart because of either diagnoises......maybe a little sad and yes, I've cried some tears but I'm not falling apart.  I am realizing, like I said before and like Dr. T said, it's going to be a long road and it's going to be a few steps forward and lots of steps back but we'll get there.......wherever "there" is.

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