Nashville Prepares for the 2024 Walk for Apraxia to Raise Awareness and Funds for Childhood Speech Disorder

Nashville Gears Up for the Walk for Apraxia

Nashville is buzzing with excitement as the 2024 Walk for Apraxia is set to take place on September 21st. The event will be held at Cornelia Fort Airpark and is aimed at raising awareness and support for children affected by childhood apraxia of speech (CAS). With registration being FREE, families are encouraged to join in on this wonderful day of community and solidarity.

What is Childhood Apraxia of Speech?

Childhood Apraxia of Speech is a special kind of motor speech disorder that makes it hard for kids to speak as they want to. Children with CAS know what they want to say, but they struggle with the movements needed for speech. This disorder requires intense therapy over time for children to learn how to speak effectively. Unfortunately, there is no cure for childhood apraxia of speech, making awareness and early intervention essential. Raising awareness not only helps to improve understanding in the community, but also leads to quicker diagnosis and better treatment options for families.

A Day Filled with Family Activities

The Walk for Apraxia is not just a walk; it’s a celebration! Kicking off at 9:00 AM, the event will feature a ceremony starting at 10:00 AM. Participants can look forward to a range of family-friendly activities throughout the day. This inclusive atmosphere is designed to create a sense of community, bringing together families, friends, and supporters of children with CAS.

Neil Kilby, a father of an Apraxia Star, emphasizes the importance of community support: “Apraxia Stars need a team behind them. That team includes both parents, family members, SLP’s and organizations dedicated to helping kids with apraxia.” By stepping out for this walk, community members show their support and commitment to these special children and their families.

Raising Funds for Apraxia Kids

The funds raised during the 2024 Walk for Apraxia will benefit Apraxia Kids, a leading nonprofit organization focused on improving support systems for children with childhood apraxia of speech. This organization works tirelessly to provide education and resources for both families and speech-language professionals. Their main goal is to ensure that children with CAS achieve their highest communication potential through accurate diagnosis and timely treatment.

How to Participate

If you’re interested in joining the Walk for Apraxia, participating is simple. Gather your friends and family and head to the event on September 21st. For more information about joining the cause or to learn how to get involved, visit the official Walk for Apraxia page at https://www.apraxia-kids.org/walk-for-apraxia-splash-page/.

Community Spirit Shines

The Walk for Apraxia is anticipated to be a heartwarming occasion where families come together to support one another. It creates an opportunity for families of children with CAS to connect with others who understand their journey, fostering a spirit of togetherness. This year’s event is expected to draw numerous participants eager to learn more about apraxia and show their support for those affected by it.

The event is a reminder that together, as a community, we can make a difference for children with speech disorders. By participating in the walk, attendees not only increase awareness about CAS but also provide vital support that helps children communicate better, laying the groundwork for their success as they grow up.

Conclusion

The 2024 Walk for Apraxia in Nashville is more than just a fundraising event; it’s an embodiment of community spirit, compassion, and camaraderie. Join fellow community members on September 21st at Cornelia Fort Airpark, and take part in showing support for the incredible efforts of children diagnosed with childhood apraxia of speech.

Mark your calendars, invite your friends and family, and be a part of this meaningful event that seeks to empower and uplift our Apraxia Stars!


Author: HERE Nashville

HERE Nashville

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