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Basic information for parents about Apraxia

Apraxia is a neurologically based disorder, it is pretty rare and most of the time confused with other types of language disorders. Diagnosing a child with apraxia early is one of the most important factors in treating and correcting it. It is not something that a child will simply grow out of, and takes intensive and frequent speech therapy to help your child become a verbal communicator. Apraxia is a controversial diagnosis, as not all SLP’s and doctors believe that it is a disorder recognized in children, but only caused by some type of brain assault in adults or older children (by way of blood clot in the brain, stroke etc.). It has just recently become a diagnosis for children in the past 20 years. Not all SLP’s know how to treat children for apraxia, and children with apraxia don’t normally get much help from speech therapy that is designed for late talkers. Diagnosing a child with apraxia is best done by an evaluation by a pediatric neurologist and a Speech Language Pathologist.


Some common characteristics of
children with apraxia

1. Little or no babbling as an infant.
2. Receptive speech or ability is much further ahead developmentally than expressive language.
3. Consonant sounds have a limited repertoire.
4. Some possible feeding issues during infancy.
5. Most have vowel errors.
6. The child may grope or struggle to say a sound or word.
7. The longer the phrase or word, the more errors are made.
8. They may develop gestures or sign language to communicate.

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This is Kimberly ... photo used with permission from her mother, Colleen. 
Thank you Colleen and Kimberly!!!


Verbal apraxia is sometimes accompanied by oral apraxia, but not always. Some signs of oral apraxia are difficulty with performing activities such as smiling, puffing cheeks, pucker lips, unable to move tongue correctly, licking lips, etc.

Apraxia is often times accompanied by other soft neurological signs like hypotonic (low muscle tone), sensory integration disorder, being classified as "clumsy", and not like having their faces touched, or having their hair washed or combed.

This is just some of the basic information, but there is tons more information on the next page following the links provided. For more information you can contact me by email and I will try to answer you as soon as possible.

We will also be listing times for our support group meetings on here when we get more information available.

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