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what will happen at dev ped visit?

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I just started reading all the information this wonderful group has to offer

last week and have learned an incredible amount about apraxia. I am convinced my

daughter could have this, and we are going to dev. Ped. next month. Please tell

me what will happen. I am afraid to go and have my 2 year old labeled, but at

the same time can't wait for someone to tell me what's wrong. Maybe I will be

able to sleep and not have nightmares every night about what could be a possible

diagnosis for my little girl. Please let me know what to expect. Also, we speak

Spanish at home only. Should we have a translator at the meeting? Or is this the

type of thing where I won't need one?

Guerrero

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