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WHAT YOU SHOULD KNOW ABOUT CHILDHOOD APRAXIA OF SPEECH. This is an easy to read brochure, explaining apraxia of speech in simple terms for the lay reader. This can be a great brochure to give parents, extended family, neighbors, friends and community members. DOWNLOAD.
Our Brochures and Downloadables are an essential tool for raising awareness and educating about childhood apraxia of speech. From simple, visual explanations for kids to helpful information for teachers, our resources are helping families across the world!
This page contains the foundational information about childhood apraxia (CAS) of speech for families who are at the beginning of their journey. Answers to those important first questions as well as detailed information and resources about assessment and treatment of CAS are found here!
Understanding Childhood Apraxia. by Becky Spivey, M.Ed. Childhood Apraxia of Speech (CAS) is a very specific motor speech disorder. Children with this diagnosis have difficulty planning and consistently producing sequences of speech movements using their tongue, lips, jaw, and palate.
This list of books for parents, children and professionals has been compiled by the apraxia community. It includes books to help with sound practice, stories about children dealing with speech difficulties and books to inform parents and professionals about childhood apraxia of speech.
These parent handouts for childhood apraxia of speech will help families of children with apraxia by teaching general knowledge and tips they can use at home. This is the packet I give my own student's families when they get a CAS diagnosis.
People also ask
How can we help children with childhood apraxia of speech?
What is childhood apraxia of speech?
How can I spread awareness of childhood apraxia of speech?
Can apraxia of speech be treated in children with idiopathic CAS?
These parent handouts for childhood apraxia of speech will help families of children with apraxia by teaching general knowledge and tips they can use at home. This is the packet I give my own student's families when they get a CAS diagnosis.
