New Caregiver Opportunity! Limited seating!
Greetings SLP Mommy of Apraxia Community!
I wanted to express my sincere gratitude for everyone who has followed my journey and Ashlynn’s journey. Many of you have been there from the start as we learned to navigate childhood apraxia of speech! The journey started out lonely and I was full of anxiety and worry. However, I slowly but surely started to learn more and find a community.
I am always looking for ways to pay it forward in the spirit of so many who were willing to help me. From my blogging, to social media, to my book, speaking events, and coordinating community events, I have been so enriched by this amazing CAS community.
Earlier this year an SLP who specializes in CAS approached me with a venture idea. Stacey Landberg desired to cultivate a similar network of support and education for parents navigating the challenges of CAS or suspected CAS in their children. She had this vision for “Apraxia Space,” in which parents and caregivers could network and learn in an exclusive online environment.
I’m excited to announce registration for this pilot program experience is now live and will be open through March 31st, 2024!!!
What is Apraxia Space?
“Apraxia Space,” is designed especially for parents and caregivers who are passionate about supporting their child with childhood apraxia of speech (CAS) or suspected CAS. Members will benefit through expert-led discussions and connecting with other parents of children with CAS. You’ll gain exclusive access to a community of like-minded individuals, resources, and events dedicated to supporting you as you become the best advocate for your child.
Here’s what you can expect as a founding member
Expert Insights: Meet monthly with Laura & Stacey, two SLPs specializing in CAS. Together we’ll lead 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.
Home Strategies: Discover actionable steps to effectively support your child at home.
To ensure that each member receives personalized attention and support, we are limiting the number of founding members for Apraxia Space. Therefore, we encourage you to secure your spot today by joining today.
Please Visit Apraxia Space to learn more and embark on this unparalleled opportunity in supporting your child with CAS.
Warmly,
Stacey & Laura
