April 2022 Newsletter

Dear Friends,

Spring is a busy time at Apraxia Kids. Together we are mission-driven with a shared vision.   The remaining nine months of 2022 are filled with opportunities for you to get involved with Apraxia Kids. Together, we can make an impact this month and throughout the year.

Together we are a powerful voice spreading awareness about CAS and Apraxia Kids. As we look forward to celebrating our 10 year anniversary of Apraxia Awareness Day, we encourage your voice to be loud this May 14th and the rest of the month! Utilize our Official Apraxia Awareness Month Calendar all month long to celebrate and honor those individuals that make up your support system on social media. We also invite you to join us online for live educational opportunities, share our resources, and help us raise critical funds to further the mission of Apraxia Kids.   

Together we are planning to learn more about evidence-based practice by making plans to be a part of the National Conference taking place July 7-9 in Las Vegas. Registration is now open to attend in person or virtually, providing education on treatment, diagnosis, and methods to help children with CAS.  We encourage you to check out our line-up of sessions and speakers and register today. 

Together we are a community in action. Walk for Apraxia events across North America have opened and just like last year, registration is free for all participants. Walking together, we are growing our network, spreading awareness, and celebrating the Apraxia Stars that inspire us every single day. If you do not see a Walk in your area and have a passion for event planning, complete this survey and we will be in touch with more information about what goes into Walk planning!

As the leading nonprofit focused on childhood apraxia of speech, our commitment to spreading awareness, building a strong support community, sharing evidence-based resources, furthering research, and empowering families to better advocate for their child remains strong. Together we are partners in achieving the mission of Apraxia Kids and with your continued support, our vision becomes a reality.   

Best, 

Angela Grimm
Executive Director

Click here to subscribe to the Apraxia Kids monthly newsletter!

Dear Friends,

Spring is a busy time at Apraxia Kids. Together we are mission-driven with a shared vision.   The remaining nine months of 2022 are filled with opportunities for you to get involved with Apraxia Kids. Together, we can make an impact this month and throughout the year.

Together we are a powerful voice spreading awareness about CAS and Apraxia Kids. As we look forward to celebrating our 10 year anniversary of Apraxia Awareness Day, we encourage your voice to be loud this May 14th and the rest of the month! Utilize our Official Apraxia Awareness Month Calendar all month long to celebrate and honor those individuals that make up your support system on social media. We also invite you to join us online for live educational opportunities, share our resources, and help us raise critical funds to further the mission of Apraxia Kids.   

Together we are planning to learn more about evidence-based practice by making plans to be a part of the National Conference taking place July 7-9 in Las Vegas. Registration is now open to attend in person or virtually, providing education on treatment, diagnosis, and methods to help children with CAS.  We encourage you to check out our line-up of sessions and speakers and register today. 

Together we are a community in action. Walk for Apraxia events across North America have opened and just like last year, registration is free for all participants. Walking together, we are growing our network, spreading awareness, and celebrating the Apraxia Stars that inspire us every single day. If you do not see a Walk in your area and have a passion for event planning, complete this survey and we will be in touch with more information about what goes into Walk planning!

As the leading nonprofit focused on childhood apraxia of speech, our commitment to spreading awareness, building a strong support community, sharing evidence-based resources, furthering research, and empowering families to better advocate for their child remains strong. Together we are partners in achieving the mission of Apraxia Kids and with your continued support, our vision becomes a reality.   

Best, 

Angela Grimm
Executive Director

Click here to subscribe to the Apraxia Kids monthly newsletter!



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