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Apraxia Kids
@Apraxia_KIDS
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National 501(c)3 nonprofit for children with #apraxia of speech and their families. Dedicated to up-to-date, reliable information for parents & professionals.
Worldwide
Joined March 2009
We are so excited to announce our NEW Parent Portal! The #ApraxiaKidsParentPortal came out of the need for info on #CAS topics from diagnosis into adulthood that is in one place. Learn about the Parent Portal: Parent Portal:
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Hey SLPs! Looking for a way to raise awareness for #CAS? Order an Apraxia Kids Be the Voice SLP Brochure Bundle! Raise awareness at your clinic, school, or private practice by placing informational resources in common areas. Learn more:
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The Path to Soaring to New Heights – by: Kim “Apraxia Kids has made such a positive impact on our lives.” #findhope #givehope #apraxia #apraxiaawareness
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Are you preparing for your child's #IEP (Individualized Education Program) meeting? This free, interactive tool has the answers to the most commonly asked questions surrounding ways to prepare for your child's IEP meeting! Learn more here:
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We want to make sure that all speech-language pathologists listed in our SLP Directory have a reasonable level of experience and skill in evaluating and treating #CAS. To learn more and find an SLP check out our website:
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Have questions regarding #CAS? Apraxia Kids is here to help! We recruited some of our SLP Boot Camp Graduates and caregivers to answer some of the most common questions surrounding apraxia, insurance, and so much more! Check out our vlog series here:
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Recently our friend Mikey Akers was interviewed by BirminghamLive where he talked about his journey with #CAS. Read more:
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