We've
gone to the same doctor since the boys were about 13 months old, so the
office staff and nurses know them on sight. They know both boys have
Autism Spectrum Disorder (ASD). It helps because they've seen how the
boys react to different things over the years, so they will ask when we
get there if we'd like to be put in a room or stay in the waiting room.
It always depends on how many people are there, what movie's on the
television and how long the wait is going to be. They know there could
be a meltdown if something isn't just right.
When it was time for Daniel's appointment, we take off his shoes an try
to get him to stand still long enough to get his weight. Yay! Got it
pretty quickly with no outburst. I wish I could say the same for his
height. That took quite a bit of convincing and he still proceeded to
fight. He hates to stand straight against the wall and have that
("measuring thing" they use) touch the top of his head. We've worked on
it and some days he does ok with it... some days not - but we did manage to get an "approximate" height.
Then comes the wait in the room
- the nurse comes in and asks the usual questions... then comes time to
take his temperature, check his blood pressure and check his pulse. The
nurse is relatively new and keeps telling Daniel what she needs to
do... ok. I say, "Daniel - look at me. The nurse (her name) needs to...
you can do it. Just like at home... touch the thermometer, we need to
"tickle" under your arm... watch the baby crawl." Daniel, of course,
decides he wants no part of it. So for the next 5 minutes or so I hold
him and tell her to "just do it", while I continue to explain to him
just what she's doing. I can only imagine what someone must think if
they walk by the room and don't know who's in there.
Once
everything is done of course, Daniel is just fine. No tears, no sign
that he had a problem with anything. He's ready to wait for the doctor
now... he's gotten some energy released. He's let us know that just how
he feels about being there. Daniel proceeds to walk around and around
and around. He touches everything he can reach, he's stimming (self
soothing behavior). He'll try to swing things with cords in circles, run
water in the sink. I have to move the doctor's chair out of the room
because he's never content to just spin it around and around with his
hands. He'll want to sit on it and spin around... shoot, I'd like to
sometimes too.
Then the doctor comes in and asks the usual "checkup" questions... Sick lately? Appetite? Diet? Problems with any meds? Asthma under control? Drinking milk? Potty trained?
Then the doctor comes in and asks the usual "checkup" questions... Sick lately? Appetite? Diet? Problems with any meds? Asthma under control? Drinking milk? Potty trained?
Daniel's
gotten pretty good at letting the doctor "listen with his ears" (that's
what we call the stethoscope). He'll let him listen to his heart and
lungs. He'll start to contest when the doctor wants to look into his
eyes, his nose, his mouth, which... he... is... not... going... to...
open! Then the ears, which involves a really, really big hug - holding him so he can't move. Otherwise everything is fine.
No
checking vision, no hearing test, at least not at the regular doctor's
office. Those require specialists. Being non-verbal and autistic makes
for a very interesting combination when it comes to specialists.
At the end of the visit, I am completely reminded of the differences between my son and stereotypical kiddos. All of these tasks that many parents take for granted that their children just do - all reminders of what my babe doesn't or can't do. That's ok, I have never considered myself "normal" - whatever that means, so I don't expect my family to be either. I do wish that certain things were easier for him though. The best part is that he is "healthy" and growing well. That makes me very, very happy.
At the end of the visit, I am completely reminded of the differences between my son and stereotypical kiddos. All of these tasks that many parents take for granted that their children just do - all reminders of what my babe doesn't or can't do. That's ok, I have never considered myself "normal" - whatever that means, so I don't expect my family to be either. I do wish that certain things were easier for him though. The best part is that he is "healthy" and growing well. That makes me very, very happy.
From a mother's heart - those subtle reminders we receive that tell us our children are different than the "average" can also remind us that our children are indeed special. And sometimes special isn't bad at all.
God Bless!
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