Aiden’s Coaster Crew

Twin Cities Walk for Apraxia

Welcome to Aiden’s Coaster Crew! 🎢💙

Welcome to Aiden’s Coaster Crew! 🎢💙

Thank you for visiting our team page!

We’re walking in honor of our amazing son, Aiden, who was diagnosed with childhood apraxia of speech (CAS) at just 2 years old. Childhood apraxia of speech is a motor speech disorder that makes it difficult for a child’s brain to plan and coordinate the movements needed for speech. Children with apraxia know what they want to say, but getting the words out can take an incredible amount of hard work.

Aiden is now almost 5 years old, and every day he amazes us with his determination, courage, and resilience. We were fortunate to receive an early diagnosis, which allowed him to begin intensive speech therapy during a critical time in his development. Because of that support, we’ve watched him grow in confidence and find his voice one word at a time.

We named our team Aiden’s Coaster Crew because Aiden absolutely loves roller coasters—and his speech journey has been a lot like one. It has had exciting highs, challenging climbs, and moments that felt overwhelming, but through it all, he has faced every twist and turn with a smile and incredible bravery.

We’re walking to celebrate everything Aiden has accomplished, to raise awareness of childhood apraxia of speech, and to support other children and families on this journey. Every child deserves the opportunity to communicate, be understood, and have their voice heard.

If you’re able, please consider making a donation or joining our team. Every contribution helps support education, advocacy, research, and resources for families affected by childhood apraxia of speech.

Thank you for cheering on Aiden and every child working so hard to find their voice. Your support means the world to our family.

Every child deserves a voice. 💙

Thank you to our Donors

$56

Tess Selander

$56

Joshua Owens

$56

Catherine Mielke