2019 Detroit Walk for Apraxia

Team ChloBuggs

Welcome to our team fundraising page for the Walk for Apraxia

 Chloe has come SO far since her diagnosis in 2013/2014. She has a moderate case of it, however there are children out there who are severe and have no words. I cannot explain the joy I feel when Chloe is able to say a new word or when she expresses what she wants and how she feels perfectly. I want to cry every time. It's a time I thought would never come. At 3, Chloe was almost completely non-verbal. She had about 50 words, if that. And only limited family could understand her. Now she's a total chatterbox and I rarely, IF EVER, need to translate for her!!!!

We’re helping children find their voice! We need your help!  By joining us, you are a partner with the Childhood Apraxia of Speech Association in its efforts to provide support to children and families on their journey with apraxia. You can participate even if you are unable to be at the Walk by making a donation to support our efforts.

Check out how our team is progressing towards its goal and keep pushing to help us achieve it. Your donation goes to fund amazing programs like iPads for children who need it to communicate, parent and speech therapist workshops, research, and a program to assist families in need with speech therapy costs. 

Thank you again for your support in this very important cause.  


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