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A Voice for the Voiceless: Arkansas Declares May 14th as Childhood Apraxia of Speech Day

Updated: Jun 2

May is National Childhood Apraxia Awareness Month, a time dedicated to amplifying the voices of children with Childhood Apraxia of Speech (CAS) and shining a light on the challenges they face. This year, Arkansas joins the growing movement of recognition and advocacy in a deeply meaningful way—thanks to the courage and determination of one remarkable student.


Paisley Pettus Thomson Leads with Heart


Paisley Pettus Thomson, a freshman at Little Rock Christian Academy, took it upon herself to make a difference—not just for her family, but for children across the state. Moved by the journey of her younger sister, Rowen Pettus, who has been diagnosed with Childhood Apraxia of Speech, Paisley penned a heartfelt letter to Governor Sarah Huckabee Sanders, urging her to recognize the importance of CAS awareness.


Her advocacy paid off.


Arkansas Makes It Official


In response to Paisley’s moving letter, Governor Sanders signed a formal proclamation declaring May 14th as Childhood Apraxia of Speech Day in Arkansas. This marks a significant moment for families and advocates in the state, spotlighting a condition that is often underdiagnosed and misunderstood.


Understanding Childhood Apraxia of Speech


CAS is a rare neurological speech disorder in which children know what they want to say but struggle with the motor planning required to produce clear, articulate speech. These children require intensive speech therapy, early intervention, and a supportive community to thrive.


Throughout the month of May, organizations, families, and educators nationwide rally together to:


  • Educate the public and professionals about the nature of CAS

  • Encourage accurate diagnosis and effective treatment strategies

  • Offer support and build awareness for affected children and their families


The Role of Apraxia Kids


A national leader in this mission is Apraxia Kids, a nonprofit organization that provides resources, education, and community support for those affected by CAS. Their work continues to empower families, train clinicians, and elevate public understanding of this complex disorder.



A Personal Victory, A Statewide Impact


Paisley’s advocacy is more than a personal act of love for her sister Rowen—it’s a beacon of hope for countless families in Arkansas. Her voice has helped make sure that children like Rowen are not only seen, but heard.


As we approach May 14th, we celebrate this historic step for Arkansas and honor the young leaders—like Paisley—who are changing the future of CAS awareness, one voice at a time.

 
 
 

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One Voice Arkansas is a growing hub for families, caregivers, and professionals seeking trusted, Arkansas-centered information and support around Childhood Apraxia of Speech (CAS). Our mission is to raise awareness and connect families with stories, resources, and insights specific to CAS — including early signs, evaluation, therapy options, local services, and advocacy. We aim to be an invaluable support for parents, speech-language pathologists, educators, and anyone walking alongside a child with apraxia.

Disclaimer: Consistent with our mission, One Voice Arkansas does not promote any single method, therapy, or approach. Instead, we share a wide range of experiences and resources to help families and professionals in Arkansas make informed, personalized decisions as they support children on their journey to finding their voice.

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