We're Walking for Apraxia Kids — And We'd Love Your Support
What Is the Walk for Apraxia?
If your child has been diagnosed with childhood apraxia of speech, you already know something that most people don't.
You know what it looks like when a child has something important to say — and their body just won't cooperate. You've watched your child concentrate harder than any adult you've ever met just to produce a single word clearly. You've sat through the appointments, the evaluations, the "let's wait and see" conversations, the moments of breakthrough, and the moments of heartbreak.
You know exactly why this matters.
This year (2026), CloudSpeech is participating in the Central Texas Walk for Apraxia — and we're asking our community to walk with us, cheer us on, or support us with a donation.
How to Support Our Team
There are a few ways to get involved:
Make a donation. Every dollar raised goes directly to Apraxi Kids' research, training, and family support programs. You can donate to my personal fundraising page at act.apraxia-kids.org/fundraisers/christinaburnham. No amount is too small — even $10 makes a real difference.
Join our team. If you're in the Central Texas area and want to walk with us, join the CloudSpeech team at act.apraxia-kids.org/fundraisers/cloudspeech.
Share this post. If you know a family affected by CAS — or a clinician who works with these children — share this post and our fundraising page. Awareness matters as much as dollars.
A Note to Our CAS Families
If your child is currently receiving therapy for apraxia of speech — at CloudSpeech or anywhere else — this walk is for them. Your child is the reason this community exists. The research being funded today will shape the treatment options available to kids like yours tomorrow.
Thank you for trusting us with your child's voice. Walking for them is the least we can do.
With gratitude and excitement,
Christina Burnham, MS CCC-SLP Founder, CloudSpeech: Online Therapy
How to Support Our Team
There are a few ways to get involved:
Make a donation. Every dollar raised goes directly to Apraxia Kids' research, training, and family support programs. You can donate to my personal fundraising page at act.apraxia-kids.org/fundraisers/christinaburnham. No amount is too small — even $10 makes a real difference.
Join our team. If you're in the Central Texas area and want to walk with us, join the CloudSpeech team at act.apraxia-kids.org/fundraisers/cloudspeech.
Share this post. If you know a family affected by CAS — or a clinician who works with these children — share this post and our fundraising page. Awareness matters as much as dollars.
A Note to Our CAS Families
If your child is currently receiving therapy for apraxia of speech — at CloudSpeech or anywhere else — this walk is for them. Your child is the reason this community exists. The research being funded today will shape the treatment options available to kids like yours tomorrow.
Thank you for trusting us with your child's voice. Walking for them is the least we can do.
With gratitude and excitement,
Christina Burnham, MS CCC-SLP Founder, CloudSpeech: Online Therapy
