My sweet Mason we wear blue for you

I finally decided to share a very special private part of our lives because I want to bring awareness to a condition that is rarely ever talked about.

Mason was diagnosed with Apraxia (CSA) at the age of three. He did not talk until the age of four. He has consistent speech therapy four days a week and has an amazing support team at home and at school.

Apraxia is a neurological disorder that affects the brain pathways-it means that the brain has difficulty sending signals for accurate movement of the lips and tongue to create sounds and language.

Apraxia is a lifelong disorder that cannot be cured, though with consistent speech therapy improvements can be made.

Our world turned upside down when we heard of Mason’s diagnosis but despite the unknown, we are super proud of his accomplishments and how hard he works everyday to communicate with the world around him. We will continue to support him though this journey and help spread awareness. I have included a link in my bio if you would like to donate and assist with raising awareness.

Why I walk for Apraxia Kids!

I walk to support all children diagnosed with apraxia of speech - our Apraxia Stars. To show these children they are not alone and to acknowledge all the hard work they must do to overcome communication challenges that affect their day-to-day lives.  

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”.