We knew something wasn't right when our son wasn't talking by 2. We went to Many pediatricians and was told "boys talk late -don't worry about it." After being persistent we were hooked up with an excellent speech pathologist who finally gave us the proper diagnosis of apraxia of speech. Max continues to make strides every day he has therapy seven times a week and is constantly our speech warrior. We will never take advantage of the gift of speech ever again.
Do you believe, “Every Child Deserves a Voice?”
We do… and 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.