Why I walk for Apraxia Kids!
When my son was diagnosed with childhood apraxia of speech (CAS) at age 2, it was overwhelming but it also gave us answers. Because he was diagnosed early, he was able to start intensive speech therapy during a critical time in his development.
Now almost 5, I’m so proud of how far he has come.
Children with apraxia know what they want to say, but their brains have trouble telling their mouths how to make the movements for speech. Every word takes effort, practice, and determination.
Watching my son has shown me what resilience looks like. He has faced frustration with courage and never given up.
This walk is for him.
It is also for every child with childhood apraxia of speech and every family on this journey. We were fortunate to get an early diagnosis and access to great therapy, and every family deserves that chance.
I’m walking to raise awareness that childhood apraxia of speech is real, early diagnosis matters, and these kids deserve every opportunity to find their voice.
I’m also raising funds for Apraxia Kids, whose work supports families, educates professionals, expands awareness, and advances research.
If my son’s journey has touched your heart, please consider donating or sharing this fundraiser. Every contribution helps children with apraxia and their families.
Thank you for helping give children with apraxia a voice.
Every child deserves to be heard. Every child deserves a voice.
