Do you believe, “Every Child Deserves a Voice?”

Our son, Myles, was diagnosed with Apraxia in May of 2024.  He is an expressive, smiley, loving little boy and we are so grateful he is ours.  He has many challenges to overcome with CAS but we believe that he is a strong and capable little boy who will overcome these hurdles and do great things.

Our team name, "Myles of Smiles" is a play on his name and personality! :) 
 
We invite you to join our team at the Walk for Apraxia.  By joining our team, you will walk beside us as we celebrate all the Apraxia Stars and support our efforts to raise funds for Apraxia Kids.  With these funds, Apraxia Kids will continue to strengthen the support systems in the lives of children with apraxia of speech by educating professionals and families; facilitating community engagement and outreach; and investing in the future through advocacy and research.

Unable to walk?  That’s ok!  You can still participate in helping our team meet our fundraising goal by making a donation now.

Together we can accomplish amazing things for our Apraxia Stars.