Wednesday, July 27, 2005

One in a million...

Dear Nicky,

Today we went to the Judy Center, a medical facility devoted to the study of kids with T21, and their associated developmental and health requirements. We met with this doctor who thought you were just great. And not just great, but he said things like he bet few people could ever tell you had T21 just by looking at you, and he also said--get this--in his thirty-five years of practice, he has never seen a kid with an A/V canal defect look as good as you. He and the nurse who assisted were very impressed with you, and with Mom and me I might add, for taking such good care of you. Well, of course we're going to take care you; we're crazy about you. We spent a good long time there, and they looked you over thoroughly. We also received a lot of information about state agencies and the like that might be able to help us with whatever, should we need them on down the road. All in all, we were very glad we went. It made Mom and me feel really good to hear that you are doing well. In other news, when we came home, the maids were just starting to clean the house, so we went to a restaurant downstairs. I had a burger, Mom had a turkey club, you had some formula. It was extremely hot out today, so we didn't spend much time outside. Tomorrow is supposed to be better.

Love,
Dad

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