It's time.
Dr. Waters wanted us to wait to do the surgery until Quinn's mobility and range of motion stopped improving. He still is showing some very gradual improvement, but in the meantime he's developing a series of work-arounds that result in him using his right arm less and less.
We shared the latest range measurements and these details with Dr. Waters' staff, and they decided it's time to go ahead. April 29 is the first opening, and of course we couldn't get tickets with our frequent flier miles that week. We didn' want to push it much later and subject Quinn to a summer of hell in a cast and brace. So I called American Airlines hoping to get a mom I could appeal to, and lucked out! She agreed to appeal on our behalf, and her supervisor agreed, and that guy's supervisor agreed, so we got the tickets.
I'm relieved, but nervous.
My unvarnished story about adopting a boy who turned out to have autism.
Saturday, March 13, 2010
Ice cream - yum!
I ordered some ice cream the other day because it's something I can eat despite my broken jaw. Quinn has shown very little interest in hard-packed ice cream (he does like soft-serve) so I didn't think he'd take too much. Ha! He took a bite, then slid the whole parfait glass in front of him and wouldn't give it back.
I thought he'd give up when he ate through the vanilla and got to the green tea ice cream. Ha! He loved that, too. He did finally stop when he hit the cut-up roll cake at the very, very bottom of the glass. Finally I got some!
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