Tonight was one of those nights I will remember and treasure. It's the kind of memory I will be able to conjure up the next time I'm feeling hopeless and alone. Nothing earth shattering happened, mountains didn't move but it is one of the few moments I've had where things have felt alright with the Doodle. I hate to use the word normal because I'm not convinced there is any such thing, but for a few moments it felt like what it must feel like to feel a sense of normality; to have two typical children, playing together; understanding each other and genuinely enjoying themselves without chaos and confusion. Jimmy sat down and did some serious floor time play with the Doodle with a toy and I could hear them having fun, laughing, giggling and being beautiful boys together. Jimmy kept his interest for over a half an hour which is a huge milestone,I didn't want this moment to end. The Doodle was very engaged and playful with Jimmy--he more than tolerated him.
I would look over at them and quietly observe their little happy faces because I felt if I made eye contact with the Doodle it might distract him. I kept waiting for him to be tired of playing or get annoyed with Jimmy and he didn't. He just kept on playing. He wanted more in fact. No big tantrums, no weird meltdowns or throwing of anything, nothing weird happened that punched me in the stomach of living with autism. It was a simple act of playing that I witnessed that gave me the nugget of hope I needed today.
Sigh-
Cheer Down
In a good mood? Life great? Feeling too up? Things finally going well? Having fun? I can fix that. I can help you cheer down.
Come, spend a sunny morning touring special ed kindergartens with me and you too can come home so depressed you'd like to drink a fifth of Jack and curl up in the fetal position on the bathroom floor, close to the toilet in case you might throw up. Knowing that your special needs child is getting put into the system somewhere you know he is not going to fit in, even with other "special" children, is a pretty horrifying feeling. Can't wait for our Transition IEP--that is going to be a BLAST.
Come, spend a sunny morning touring special ed kindergartens with me and you too can come home so depressed you'd like to drink a fifth of Jack and curl up in the fetal position on the bathroom floor, close to the toilet in case you might throw up. Knowing that your special needs child is getting put into the system somewhere you know he is not going to fit in, even with other "special" children, is a pretty horrifying feeling. Can't wait for our Transition IEP--that is going to be a BLAST.
Orthapedic Deja Vu
The Doodle is in a cast.........................again..............................a table top fell on the top of his foot. Not sure how long he has to wear the cast but it's definitely slowed him down a bit. We spent the better part of last Friday in doctors offices, radiology and then finished up with a 3 hour stint in the ER. Tomorrow we have our follow up with an Orthapedic specialist. A couple of years ago he fractured his shin bone and was in a cast for 3 weeks. You would need to see the Doodle in his true doodle-form to truly appreciate his activity level and to understand how this injury impacts this little guy with autism. He's taking it like a trooper but I wonder if he really understands what is happening or why he is in this cast.
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