06 Jul July 2022 Newsletter
Dear Friends,
Greetings from Las Vegas, Nevada, where we are kicking off the Apraxia Kids National Conference today! It is hard to believe it has been three years since our last in-person event. We are excited to meet over 270 parents and professionals joining us in person and over 350 virtual attendees this year. As we look ahead, please mark your calendars for July 6-8, 2023 as we embark upon Plano, Texas, for our 2023 National Conference. We have much to be thankful for as we finish out the first six months of 2022 and a lot to look forward to as we continue through the rest of this year.
Walk season is in full swing with 60 in-person Walk for Apraxia events across North America this fall. We also remain committed to offering the flexibility to celebrate virtually for those communities where a Walk is not taking place. We want all of our Apraxia Stars to be involved in the Walk for Apraxia and to be celebrated for their hard work!
There is still time to take part in the Summer Team Challenge! Our Walk teams will have the opportunity until July 31st to earn a custom team sign to carry proudly on Walk day. We encourage you to visit the Walk Facebook Page to learn more. Remember, you can register for the Walk for Apraxia for FREE. It has never been easier to join the Walk, raise awareness and funds, celebrate your Apraxia Star, and help us support Apraxia Stars nationwide!
In an effort to expand our resources, our NEW Parent Portal is available on our website. The Parent Portal is an all-inclusive resource for parents to find answers to the many questions they have about childhood apraxia of speech. The Portal also provides additional information and resources on different ages and stages of verbal development in the areas of Speech Therapy, Education, Support/Social, and Developmental, Academic, and Learning Challenges.
We rely heavily on the support of our community year-round to further the mission of Apraxia Kids and to develop new resources such as our Parent Portal. We encourage you to continue spreading awareness about childhood apraxia of speech and Apraxia Kids by inviting your friends and family to join the Walk for Apraxia, sharing the link for the Parent Portal with a newly diagnosed family as they begin their journey, sharing our SLP Kit with a therapist in your community, or making a donation to help further our mission.
Together, we are a strong community, making a difference so that Every Child Will Find Their Voice!
Angela Grimm
Executive Director
Click here to subscribe to the Apraxia Kids monthly newsletter!
Dear Friends,
Greetings from Las Vegas, Nevada, where we are kicking off the Apraxia Kids National Conference today! It is hard to believe it has been three years since our last in-person event. We are excited to meet over 270 parents and professionals joining us in person and over 350 virtual attendees this year. As we look ahead, please mark your calendars for July 6-8, 2023 as we embark upon Plano, Texas, for our 2023 National Conference. We have much to be thankful for as we finish out the first six months of 2022 and a lot to look forward to as we continue through the rest of this year.
Walk season is in full swing with 60 in-person Walk for Apraxia events across North America this fall. We also remain committed to offering the flexibility to celebrate virtually for those communities where a Walk is not taking place. We want all of our Apraxia Stars to be involved in the Walk for Apraxia and to be celebrated for their hard work!
There is still time to take part in the Summer Team Challenge! Our Walk teams will have the opportunity until July 31st to earn a custom team sign to carry proudly on Walk day. We encourage you to visit the Walk Facebook Page to learn more. Remember, you can register for the Walk for Apraxia for FREE. It has never been easier to join the Walk, raise awareness and funds, celebrate your Apraxia Star, and help us support Apraxia Stars nationwide!
In an effort to expand our resources, our NEW Parent Portal is available on our website. The Parent Portal is an all-inclusive resource for parents to find answers to the many questions they have about childhood apraxia of speech. The Portal also provides additional information and resources on different ages and stages of verbal development in the areas of Speech Therapy, Education, Support/Social, and Developmental, Academic, and Learning Challenges.
We rely heavily on the support of our community year-round to further the mission of Apraxia Kids and to develop new resources such as our Parent Portal. We encourage you to continue spreading awareness about childhood apraxia of speech and Apraxia Kids by inviting your friends and family to join the Walk for Apraxia, sharing the link for the Parent Portal with a newly diagnosed family as they begin their journey, sharing our SLP Kit with a therapist in your community, or making a donation to help further our mission.
Together, we are a strong community, making a difference so that Every Child Will Find Their Voice!
Angela Grimm
Executive Director
Click here to subscribe to the Apraxia Kids monthly newsletter!
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