As many of you know, my son Cameron has apraxia. He was diagnosed 5 years ago at 3 years old. While he has made gains beyond our wildest imagination, his apraxia will never go away. He works so very hard every day to be understood and to get his thoughts across. The Walk for Apraxia is so important to us because it is a day to celebrate him and all of his hard work with the support of his family and friends. Thank you in advance for anyone supporting the walk. It truly means the world to us. 

I walk to raise funds for the mission of Apraxia Kids – 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.

Please help me meet my fundraising goal by making a donation now or by joining our team.  You, too, can make an impact for children and families affected by apraxia!

I believe, “Every child deserves a voice”.