Apraxia Awareness

Raise awareness of childhood apraxia of speech in your community! Whether it is during Apraxia Awareness Month in May, or year-round, there are many opportunities to inform others of CAS!

Apraxia Kids envisions a world where every child with apraxia of speech reaches their highest communication potential through accurate diagnosis and appropriate timely treatment. We believe that every child deserves a voice.

However, we know that the first time many people hear “childhood apraxia of speech,” is when their child is receiving the diagnosis. Raising awareness means that upon receiving a diagnosis, a parent is aware of what that means, and the speech therapist is aware of how best to support the child and the family.

“The more people that know and understand Apraxia, the more support children and families will have. Early intervention is crucial. A team supporting a child with Apraxia is crucial. I’ve learned along the way, we don’t know what we don’t know. Let’s help people know about Apraxia!”

How can YOU raise awareness?

You can make a difference in the lives of children with apraxia of speech by raising awareness in your community! Below are some ideas to share your story!

  • Oftentimes parents present information on their child’s diagnosis to classmates and teachers! Schedule a time with your child’s teacher to go into the classroom either at the beginning of the school year or during Apraxia Awareness Month!
  • One parent’s school created a wall of stars where every member of the school including teachers, cafeteria staff, and support staff signed their name in recognition of a student that had apraxia. We love this idea!
  • Make spreading awareness easy with printable letters, brochures, cards and more with our new Brochures and Printables web page!
  • Print out our coloring pages to get the students involved! Coloring Page One | Coloring Page Two | Coloring Page Three
  • Encourage your coworkers to show their support to children with apraxia of speech!
  • Employee Matching Gifts are donations an employer makes to match its employee’s charitable contributions. You can give your employer and coworkers information about making an ongoing matched gift to Apraxia Kids, to help strengthen the support systems in the lives of children with apraxia of speech.
  • One parent organized a “jeans day” where coworkers could wear jeans in exchange for a small donation to Apraxia Kids! During Apraxia Awareness Month, workplaces around the country wear blue to celebrate children with apraxia of speech!
  • Order free brochures from our print store to pass out to your coworkers, and contact your employer to organize a workplace event!
  • Plan an awareness event or organized a community fundraiser!  Be the Voice in your community.  Please click here to register your event with us so we can support your event!
  • Download our Apraxia Awareness Month post cards to distribute to community members!
  • Every child deserves a voice, and your stories help give a voice to families affected by childhood apraxia of speech. The easiest way that you can inform others of childhood apraxia of speech is to post about it on social media! Share YOUR story of how CAS has affected your life! Make sure you tag us using #ApraxiaAwareness so that we can read your story!
  • Want to share your story around the world? If you are an apraxia blogger, advocate, or just someone with a story to tell, we need you! You can be featured on our parent blog!



If you’ve been looking for an opportunity to raise awareness of childhood apraxia of speech in your community, here is your chance! File a proclamation for your state, county, or city!

A proclamation is a public or official announcement issued by your local government. Our community files proclamations every year to make May 14th Apraxia Awareness Day!

Learn More


Raise awareness of childhood apraxia of speech (CAS) in your local community!

Use our Letter to the Editor template to contact your local paper! You can also use this format to write to a local church newsletter, school newspaper, or parent guide.

When you see your story featured, please make sure to share on social media and tag #ApraxiaAwareness so that Apraxia Kids can share your accomplishment! Together, we can inform more and more people about CAS!

Download Letter to Editor
letter to the editor stock image

Write To Your Representative

Sharing your story with your legislators allows them to understand the reality of CAS. Your story can strengthen relationships with elected officials and raise awareness for CAS in your state. You can be their resource for advice on CAS! Find your elected officials here –

Download Letter to Rep.


Raise awareness for CAS by contacting your local TV news outlets and sharing your story. Use this template to inform local anchors of your story and how you’ve been impacted by CAS.

News outlets in your community are easier to contact and obtain coverage because they cover a niche area, so there will be less competition. Your story is likely to be about someone in the community, so it’s very relevant and therefore, very likely to be covered.

To contact a news outlet, you must first find their contact information. For most sites, the contact page is located in the footer.

Do NOT send your email or letter to more than two reporters from the same site. It is recommended to just send to one reporter plus general tip or editorial email.

Download Letter to News Anchor
news anchor

Raise awareness on social media!

During Apraxia Awareness Month and throughout the rest of the year join the conversation about apraxia on social media! With a single post, you can let your friends, family, and followers know about your apraxia journey! Tag Apraxia Kids and use #ApraxiaAwareness when you create your posts to increase your reach and spread awareness.

Apraxia Day of Giving

Make a donation: CLICK HERE

Additional Resources

Download the Apraxia Awareness Day press release here!

Download Apraxia Awareness Day Flyer here!

Download custom official Apraxia Awareness Month Zoom backgrounds here!



Families of children with apraxia of speech continue to face a world where most people they encounter have never heard of CAS. Your donation helps ensure that apraxia is not only recognized but diagnosed and treated appropriately.

Donate Now!