16 Aug August 2023 Newsletter
Dear Friends,
It seems like only yesterday we were kicking off a new year. Seven months later we have so much to be proud of with much more to share as we move towards the remainder of 2023.
Walk season is in full swing with 63 in-person events this fall. The Walk for Apraxia is so much more than your average walk. Our events inspire hope, whether you are a new family seeking information and support or a family who has been on this journey for a while. The main focus of our walks is celebrating each Apraxia Star and all their accomplishments throughout the year. It is a time to raise awareness, meet other families, have lots of fun and support the mission of Apraxia Kids.
We hope that each of you will join us this fall as registration is free for everyone! It has never been easier to invite your friends, family, and community to be a part of your Walk team in support of your Star. You never know who might be interested in walking, donating, or fundraising until you ask!
We continue to offer our Virtual Walk if there is not a Walk in your community. Once again this year, we will share a virtual ceremony so that all of our Apraxia Stars are celebrated no matter where they are located. We invite you to move our mission forward and join our incredible Walk community today!
The Walk for Apraxia is critical to the mission of Apraxia Kids. Funds raised through Walk support education, programs, resources, research, and advocacy initiatives like our NEW & FREE IEP Road Map. This interactive tool provides information and resources about the IEP process enabling you to be your child’s best advocate!
In addition to supporting our mission through fundraising, attending and sharing information, the Walk for Apraxia spreads awareness to new families throughout the communities we serve. When a new family learns about Apraxia Kids and the resources we provide, they are empowered to expand their knowledge, seek appropriate treatment, and advocate for their child.
As you prepare for back to school, we encourage you to visit our IEP Road Map, order a Be the Voice Kit for your child’s classroom, or check out our brochures and printables to share resources with your child’s teacher and school community.
Everything that you do to support Apraxia Kids, large or small, makes a difference. Thank you for your continued support of our organization, our mission and our vision Every Child Deserves a Voice.
Wishing you all well as we enjoy these last few weeks of summer!
Angela Grimm
Executive Director
Click here to subscribe to the Apraxia Kids monthly newsletter!
Dear Friends,
It seems like only yesterday we were kicking off a new year. Seven months later we have so much to be proud of with much more to share as we move towards the remainder of 2023.
Walk season is in full swing with 63 in-person events this fall. The Walk for Apraxia is so much more than your average walk. Our events inspire hope, whether you are a new family seeking information and support or a family who has been on this journey for a while. The main focus of our walks is celebrating each Apraxia Star and all their accomplishments throughout the year. It is a time to raise awareness, meet other families, have lots of fun and support the mission of Apraxia Kids.
We hope that each of you will join us this fall as registration is free for everyone! It has never been easier to invite your friends, family, and community to be a part of your Walk team in support of your Star. You never know who might be interested in walking, donating, or fundraising until you ask!
We continue to offer our Virtual Walk if there is not a Walk in your community. Once again this year, we will share a virtual ceremony so that all of our Apraxia Stars are celebrated no matter where they are located. We invite you to move our mission forward and join our incredible Walk community today!
The Walk for Apraxia is critical to the mission of Apraxia Kids. Funds raised through Walk support education, programs, resources, research, and advocacy initiatives like our NEW & FREE IEP Road Map. This interactive tool provides information and resources about the IEP process enabling you to be your child’s best advocate!
In addition to supporting our mission through fundraising, attending and sharing information, the Walk for Apraxia spreads awareness to new families throughout the communities we serve. When a new family learns about Apraxia Kids and the resources we provide, they are empowered to expand their knowledge, seek appropriate treatment, and advocate for their child.
As you prepare for back to school, we encourage you to visit our IEP Road Map, order a Be the Voice Kit for your child’s classroom, or check out our brochures and printables to share resources with your child’s teacher and school community.
Everything that you do to support Apraxia Kids, large or small, makes a difference. Thank you for your continued support of our organization, our mission and our vision Every Child Deserves a Voice.
Wishing you all well as we enjoy these last few weeks of summer!
Angela Grimm
Executive Director
Click here to subscribe to the Apraxia Kids monthly newsletter!
Credentials:
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Overall Treatment Approach:
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Professional consultation/collaboration:
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