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Just wanted to introduce ourselves. We are and . We live

in western Michigan. We just adopted our daughter, Grace, from

China at 20 months old. She is now 27 months old. we knew she had

a cleft lip and palate, and she had palate surgery in December. We

knew it would take a while for her to begin talking because of the

palate and the language switch, but it is becoming apparent that

there is something else going on.

She was not speaking at all in China, and is still only saying Mama

and Dada, but only sporadically. Her receptive speech is coming

along well and she has learned close to 50 signs. She responds to

spoken English and doesn't appear to have any hearing loss. We've

been going to speech therapy twice a week since January. Our

therapist just began talking about apraxia, saying that she should

be making more sounds by now. So now we are trying to inform

ourselves as much as possible about apraxia, since we had never

heard of it before.

So that's why we're here. We also subscribe to the cleft palate

list and the special needs adoption list from China. We look

forward to hearing about everyone's experiences here in the future.

and Dave

dd Sophie 6

dd Lily 4

dd Grace 2

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