$9.99 USD

Every month

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Support Group for Caregivers of Children with Childhood Apraxia of Speech (CAS)

Join us for this unparalleled opportunity:

What you'll get:

  • Expert Insights: Join other caregivers in meetings with Laura & Stacey, two SLPs specializing in CAS. Together we’ll host web events to deepen your understanding of CAS, while answering your questions and sharing resources.
  • Exclusive Events: Member-only meetups to foster meaningful connections and collaboration within the community
  • Community Engagement: Connect with fellow members who share your passion for apraxia advocacy and support through our private online community available 24/7. 
  • Parent Strategies: Discover actionable steps to effectively support your child holistically. 
  • Relevant Trainings: Our entire foundations course for CAS (over 6 modules) is available to you 24/7, on-demand, while you're enrolled. 

For more information about Apraxia Space, visit our website.

Final Sale. You are enrolling in a subscription and will be charged every two months. You may cancel at any time. 

What People Are Saying:

Stacey and Laura have created a great resource for parents. Having a child with CAS entails a lot of navigating and advocacy. I honestly wasn’t expecting to get so much from each webinar, but really did learn something each time. I finally felt understood and validated about the impact severe apraxia has on every area of our son’s life. Having Stacey and Laura available to provide guidance and offer insight to questions has been beyond helpful. Thank you so much for the time you have invested into this space.

Chantal, Founding Member

Being able to be part of this group has been very rewarding. I felt much more aware and empowered on how to explain my daughters speech concerns to school and what to look for in a speech therapist. I feel very grateful for this opportunity to learn more about resources and a safe place to ask questions.

Founding Member of Apraxia Space

I feel so blessed that I was able to be one of the first members of this space. This is the place I have felt the most supported since my family started our apraxia journey. I feel like the other parents in this space are truly in the same boat as me. I have never felt that way before. At first, I wasn’t sure how beneficial the monthly webinars would be. I have done so much research and try to stay informed with everything apraxia. That being said I learned SO much at every session. Laura and Stacey are so kinds and loving and they care about each and everyone one of their members. They are doing everything they can to help the community. I have been in other extremely popular support groups over the past and have never felt supported like I have in this group.

Founding Member of Apraxia Space

Apraxia Space has been an invaluable resource for me as a parent navigating the complexities of childhood apraxia of speech (CAS). The monthly webinars led by Stacey and Laura provide not only a deep understanding of CAS but also practical strategies that I can implement at home to support my child’s communication. Topics such as treatment approaches, comorbidities, and effective home strategies have given me the confidence to advocate for my child’s needs and feel more empowered in our journey. It was wonderful to connect with Laura through the open office hours who patiently answered all my queries. I am truly grateful for the support and sense of community that Apraxia Space offers and the opportunity to connect with other parents and caregivers of kids with CAS. Thank you @Stacey Landberg @Laura Smith for Apraxia Space.

Charumathi Jagannathan - Founding Member of Apraxia Space

Dealing with CAS can be an isolating journey. Advocating for a loved one with CAS can be overwhelming and...isolating! Apraxia Space was introduced as a safe place, and yes, it is! Safe and comforting. A place where it is possible to learn, share their own thoughts and listen to other people. Being in the same boat and feeling less lonely. I really want to thank the whole Apraxia Space Community and a very special thanks to @Stacey Landberg and @Laura Smith . You are fantastic!

Stefania Deiana - Founding Member

Great session, really validated my feelings and very much appreciate the leaders sharing their personal experience. That aspect makes this forum so much more valuable than other SLP-led webinars I've attended

Parent of a child with CAS

I just finished viewing the comorbidities session. It was so educational, inspiring, and motivating. Kudos to Apraxia Space and Laura Smith for all the good work you to here.

Parent of a child with CAS

Having this community of people, you know, seeing that we are all in this together and we might all have slightly different journeys, but it's just comforting to see.

Parent of a child with CAS