This blog is about my daughter Emily. She was diagnosed with a neurological speech disorder called Apraxia just before her 3rd birthday. My hopes for this blog are to educate people about this unknown disorder called Apraxia, to show that apraxia has no face & to reach out to other families going through the same things as we are.
Emily has too many signs for me to count now! It is absolutely amazing how fast she has picked up on them! I have to credit the Signing Time Videos. She loves them!!
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