Why I walk for Apraxia Kids!
Wyatt was diagnosed with apraxia of speech at around 2 years old. We have never even heard of apraxia until his diagnosis.It is important to walk, fundraise, and spread awareness because this is a rare and very unheard of neurological speech disorder. Everyone with apraxia deserves all of the help and support to be able to talk.
Wyatt works hard every single week in his therapy that is specific to apraxia motor planning.
You can tell it is exhausting for him, but he try’s so hard and has made so much progress.
Apraxia is something Wyatt will have for the rest of his life. We want to make sure everyone around him supports him and helps spread awareness for this taxing disorder.
Please donate, walk, and share any apraxia facts you see on social media!
And be on our team for Wyatt the Warrior!
We are Wyatt’s Warriors!
Thank you to our Donors
$50
Laura Reed
$28
Linda Flores
$28
Michelle Allen
Rock on!!
$28
