You can mail  this form and a check made payable to Apraxia Kids to:

Apraxia Kids
P.O. Box 899
Wexford, PA  15090

Attn:  Walk for Apraxia

Please specify the Walk and Participant/Team you want credited for your donation.

If you raise $50 on or before Walk Day, your shirt MUST be picked up at the event so that you can wear it proudly on Walk Day! Participants who raise $50 after the Walk will be mailed their shirt. All additional fundraising incentive prizes will be awarded and mailed by the end of March, 2027.

Please keep in mind incentive prizes are awarded based on individual fundraising, NOT team fundraising. Contact apraxiawalk@apraxia-kids.org if you need help allocating funds to the correct individual participants.

The official Walk for Apraxia T-shirt is only given as a token of recognition to registered walkers that raise $50 or more. All registered Apraxia Stars will get their shirts for free!

Yes, you will still receive the official Walk for Apraxia shirt if you raise $50.  

Individual fundraising focuses on one’s personal efforts and is tracked through a participant’s personal fundraising page. This total determines the individual’s eligibility for individual incentive prizes, such as the official Walk t-shirt and a variety of other prizes at different fundraising levels.

Team fundraising focuses on the collective efforts of the team. The sum of all individual members’ totals plus any general donations made directly to the team page contribute to group recognition, such as the Champions or Grand Champions clubs. Donations towards the team do not count toward an individual's incentive prize eligibility.

Although Walk courses vary by location, our Walk events are typically one mile or less in distance and are accessible to individuals of all abilities.

We encourage you to reach out to your local Walk Coordinator as each venue has different rules surrounding animals.  

Although each Walk event may differ on their day of logistics, all Walks do provide drinks and snacks for participants. 

The Walk for Apraxia® is the largest fundraiser of Apraxia Kids supporting children with childhood apraxia of speech (CAS). We walk in over 60 locations across North America to create a world where every child with apraxia of speech receives the help and care they need.

The Walk celebrates the lives and incredible efforts of our kids (our Apraxia Stars), who work so hard everyday to overcome CAS. Every Apraxia Star attending the Walk is individually recognized for their accomplishments. 

Apraxia Kids is the leading nonprofit that strengthens the support systems in the lives of children with childhood apraxia of speech (CAS) by educating professionals and families; facilitating community engagement and outreach; and investing in the future through advocacy and research.

Apraxia Kids began in 2000 as a virtual support group for parents looking for answers about apraxia, a relatively unknown motor speech disorder. Since that time, Apraxia Kids has grown to be the leading nonprofit in apraxia education that supports children, families, and speech-language professionals worldwide.   We encourage you to visit our website to learn about all of the programs and services that we provide.   

Your donation to the Walk for Apraxia makes an incredible impact for Apraxia Kids.   Your support provides our Apraxia Stars, their families, and the professionals who serve them with vital resources, expert guidance, and evidence-based programs.  

Click here to see how your donation makes an impact.  

YES!  We want to recognize all of our Apraxia Stars on Walk day during our ceremony. 

All registered Apraxia Stars receive a FREE medal, personalized certificate, and Walk shirt. 

Yes, registration is a requirement to participate. We encourage you to share your team link with all your friends and family to have them pre-register for the Walk, whether they are attending in person or supporting your team virtually.  

All minors attending the Walk must be registered as well.  

We are sorry you are having difficulties registering for your local Walk for Apraxia.   

Please contact us at apraxiawalk@apraxia-kids.org or you can watch this easy how-to video to assist you through the registration process.  

Do you have a passion for event planning, fundraising, or forming new relationships? Are you interested in making a difference in the lives of children with apraxia of speech? Are you looking for a way to give back and get more involved with Apraxia Kids?

If the answer to any of these questions is YES, we want to connect with you about a Walk in your community.

Please fill out the short survey and we will be in touch with more information!

Each of our local Walk for Apraxia events has its own unique elements, but they all follow a similar structure.  Walk Day begins with a window of time for registration and check in. Then the day will kick off with a special ceremony recognizing all Apraxia Stars in attendance. Each Apraxia Star will receive a medal and certificate honoring their accomplishments. After that, its time to walk! Everyone in attendance will join together walking as a show of support and to raise awareness in your community.

What makes the Walk for Apraxia truly special is the people. Walk Day is all about celebrating the Apraxia Stars in your community and bringing together their support network to cheer them on!

No Problem!  You can still register for your local Walk and receive incentives based on your fundraising.   

You also have the choice of registering for the Virtual Walk for Apraxia! Registering for the Virtual Walk for Apraxia means you can create your own day-of experience - anywhere, anytime. Participating virtually is as simple as it sounds: Register for the Virtual Walk, fundraise, and celebrate from the comfort of your own home! Take a walk around the neighborhood, have a party in your backyard, take advantage of our Celebration Kit, and do whatever else you choose to make sure your Apraxia Star feels celebrated!

To register for the Virtual Walk, visit the Walk for Apraxia homepage and click on the Virtual Walk.