Our team believes that “Every Child Deserves a Voice".
We continue to advocate for kids with the neurological disorder called Apraxia because of our son Mason. He has spent the better half of his life in intensive speech therapy with the most wonderful SLP on the planet. He works so hard every day to do something that comes so natural to everyone else, and never complains! When other kids his age are spending their mornings at the park, he's learning new motor planning skills with his therapist so he can say outside, and park, and pouch. We are really enjoying hearing all of the funny stories mason tells us, and the new words he shares every day! We couldn't be more proud to be his parents and to watch God work in new ways every single day!
We invite everyone 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.