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Ava Sanders: A Journey of Hope and Advocacy for Childhood Apraxia of Speech

Updated: 8 hours ago

Ava Sanders celebrates a first-place dance competition win on stage with her teammates.

At One Voice Arkansas, we believe that lived experience is powerful. Few stories reflect that truth more clearly than that of Ava Sanders, one of our very own junior board members.


Ava's Early Years with Childhood Apraxia of Speech


Now 16 years old, Ava was diagnosed with Childhood Apraxia of Speech (CAS) just before her third birthday. Like many children with apraxia, she knew what she wanted to say long before her speech could keep up. Those early years were marked by frustration, and Ava often relied on gestures to communicate when words wouldn’t come.


The Role of Speech Therapy


What helped Ava most was consistent speech therapy paired with daily practice at home. From an early age, her family fought to ensure she received treatment from professionals who truly understood apraxia. This advocacy effort shaped the course of her progress and made a significant difference in her journey.


Ava remained in speech therapy through elementary school and officially graduated in second grade. Some of her most meaningful therapy experiences extended beyond the therapy room. She loved opportunities that pushed her to use her voice in the real world—surveying people, going into stores, and practicing communication in everyday settings. These moments helped build not just speech skills but also confidence.


Building Confidence Through Dance


Today, Ava’s confidence shines in everything she does. She is deeply passionate about dance and is a company member at Dance Dynamics Arkansas, as well as a member of her school’s Pom team. Dance gives Ava another way to express herself—through movement, rhythm, and presence.


Ava understands that CAS is a lifelong diagnosis. As she puts it, apraxia can improve, but it cannot be cured. Progress takes time, consistency, and support. Still, her message to younger kids with apraxia is filled with hope: where she is today once felt unimaginable to her family, but steady effort made it possible.


Ava's Role at One Voice Arkansas


As a junior board member for One Voice Arkansas, Ava brings something incredibly valuable to the table: perspective. She represents what long-term growth with CAS can look like and reminds families just starting their journey that progress doesn’t end in childhood.


Ava’s story is one of persistence, advocacy, and belief—belief from her family, her therapists, and now from a community she helps shape. She is proof that kids with CAS don’t just find their voices—they grow into leaders who use them.


The Importance of Community Support


In our journey, community support plays a crucial role. Families, friends, and professionals all contribute to the growth and development of children with CAS. It’s essential to create an environment where children feel safe to express themselves, whether through speech, dance, or other forms of communication.


Encouraging Open Dialogue


Encouraging open dialogue about CAS can help demystify the condition. It creates a supportive atmosphere where families can share experiences and strategies. We can learn from each other and build a stronger network of support.


Resources for Families


One Voice Arkansas aims to provide resources for families affected by Childhood Apraxia of Speech. We strive to raise awareness and empower every child to find their voice. Whether through workshops, informational sessions, or community events, we are here to help families navigate their journey.


Celebrating Progress


It’s important to celebrate every milestone, no matter how small. Each step forward is a victory worth recognizing. By highlighting these achievements, we inspire hope and motivation in others facing similar challenges.


Conclusion: A Bright Future Ahead


We are honored to have Ava as part of One Voice Arkansas and grateful for the strength, insight, and hope she brings to our mission. Her journey is a testament to the power of perseverance and community support.


Together, we can continue to advocate for children with Childhood Apraxia of Speech and ensure they have the resources and encouragement they need to thrive. Let’s work hand in hand to create a brighter future for all children, helping them find their voices and share their stories with the world.


As Ava reminds us, progress is possible, and with dedication and support, every child can achieve their dreams.

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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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