Showing posts with label disability. Show all posts
Showing posts with label disability. Show all posts

Wednesday, June 10, 2009

Snacktime! and a Turning Point for me

John Michael is almost 19 months old. He's drinking more from a sippy cup these days -- milk and OJ and sometimes diluted apple juice. He can use a straw very well, too, but these lightweight disposable cups are easier for him to maneuver. Psst, don't tell him it's an older girly princess cup of Greta's. He hasn't noticed yet. BUT! Yesterday, I gave him milk in a Dora the Explorer cup and I asked, "Where's Dora?" With his middle finger, he pointed to Dora and said Dih Dih. Another word! Yay! Now we have Dada, Bap for bath or water, Eh Duh for Greta, "K" for big brother Nic and Cat, and Dih Dih for Dora.

Check this out! He can reach and put his sippy cup in the cup holder of his high chair tray. We're beginning to work on simple puzzles now.

He loves snacking on graham crackers or baby Gold Fish crackers and orange juice. His pincer grasp is getting better. He used to pick up food with 3 or more fingers and shove it in. He's working on using his index finger more, although he still points with his middle finger more often than not.

It looks like he has a headache, but he's actually playing peek-a-boo and trying to hide his eyes from me. It's so funny, I can never keep a straight face! John Michael also will shake everyone's hand and give high-five's. He's very social and loves to get peoples' attention by forcing eye contact.
So here's my "Turning Point." I brought Anna to the racquet club this morning for summer tennis camp. BJM (before John Michael) I used to play tennis at least once a week, on a team or just fun doubles matches. Somehow as he's grown and his delays are more obvious, I haven't had the courage to put him in the play care room at the club so I could play tennis or exercise. As a result... well, I'm not physical enough.
On our way out, I decided to pop in the play care room and ask the woman there if there were slower times and whether they would take JM. It turns out that every morning from 9:30 to 11, the 4-6 year olds go outside to play on the basketball courts so the room would be quieter with kids more his size.
I went through the diagnosis, explained he's healthy as a bear -- just delayed in some areas. I was choked up and on the verge of tears the entire time I was talking with her. She watched him crawl over to the shelf, pull out some big plastic dump trucks and start pushing them around. She asked a few questions about whether he could eat Gold Fish (yes) and drink from a sippy cup (yes) and whether he was OK with strangers (not always, but a Binky will help). She remembered Greta from the past and asked if she would be joining him (yes!). After watching him play contentedly for a few minutes, she said he'd do fine in there and that it would be good for me and him. Before we left, she knelt down, looked John Michael in the eyes, and spoke directly to him and welcomed him to come anytime. I smiled, thanked her and said, "I promise!"
I left there with a load lifted off my shoulders. I'm still emotional typing this. It's been 2 years since I've played tennis. It's the only sport I thoroughly enjoy and I miss the physical and social aspect of it. Last year Nic and Anna got to play while I stayed home with a baby. Now it's my turn. I think this might be a great summer.

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