June 2022 Newsletter

Dear Friends,

It is hard to believe the month of May is in our rearview mirror and June is upon us. Together, we are a strong community who made a significant impact during Apraxia Awareness Month by spreading awareness and supporting the mission of Apraxia Kids. We want to share some highlights below as well as look ahead to all the great things we have coming in the next few months.   

Throughout Apraxia Awareness Month, we had 13 different events, including Ask an SLP events and CAS book reading events. You can still view most of these events on our Facebook Page! We also wrapped up our Lecture Series that provided 12 hours of FREE evidence-based education to families and SLPs on various topics centered around CAS. All of these recordings will be available later this summer on our website. In addition, we launched our NEW Parent Portal, filled with information, education, and resources for families all along their apraxia journey.   

A total of 210 proclamations were filed in 2 countries, 39 states,155 cities and counties, 2 provinces, and 12 municipalities. Countless city landmarks turned blue, and various awareness and fundraising events took place, all while we launched our first partnership with Taco Cabana.

On the horizon, we are excited for our in-person National Conference, taking place July 7-9 in Las Vegas, Nevada. This unique conference experience allows parents and SLPs to learn together and further their knowledge of CAS. We understand that not everyone can attend in person, so once again this year, we will offer a virtual option for those who cannot make the trip to Las Vegas. If you have not registered yet, we encourage you to do so today

We are thrilled to announce that our Walk for Apraxia events will be in person this fall. Together we are the strength and support for our Apraxia Stars and Walks allow our community the opportunity to celebrate each Star for all their hard work. Please visit our Walk for Apraxia page to find a Walk closest to you. Remember, registration for the Walk is FREE.        

Together, we are a support system sharing resources, education, and programs for everyone who is on an apraxia journey. As we look to the summer and fall, we encourage you to continue making an impact. Sharing your story, joining a Walk, sharing our organization’s resources with a new family, or making a financial gift are all ways you can make a difference 

Together, we are mission-driven. Thank you for being our partner and for your continued commitment to Apraxia Kids!

 

Angela Grimm
Executive Director

Click here to subscribe to the Apraxia Kids monthly newsletter!

Dear Friends,

It is hard to believe the month of May is in our rearview mirror and June is upon us. Together, we are a strong community who made a significant impact during Apraxia Awareness Month by spreading awareness and supporting the mission of Apraxia Kids. We want to share some highlights below as well as look ahead to all the great things we have coming in the next few months.   

Throughout Apraxia Awareness Month, we had 13 different events, including Ask an SLP events and CAS book reading events. You can still view most of these events on our Facebook Page! We also wrapped up our Lecture Series that provided 12 hours of FREE evidence-based education to families and SLPs on various topics centered around CAS. All of these recordings will be available later this summer on our website. In addition, we launched our NEW Parent Portal, filled with information, education, and resources for families all along their apraxia journey.   

A total of 210 proclamations were filed in 2 countries, 39 states,155 cities and counties, 2 provinces, and 12 municipalities. Countless city landmarks turned blue, and various awareness and fundraising events took place, all while we launched our first partnership with Taco Cabana.

On the horizon, we are excited for our in-person National Conference, taking place July 7-9 in Las Vegas, Nevada. This unique conference experience allows parents and SLPs to learn together and further their knowledge of CAS. We understand that not everyone can attend in person, so once again this year, we will offer a virtual option for those who cannot make the trip to Las Vegas. If you have not registered yet, we encourage you to do so today

We are thrilled to announce that our Walk for Apraxia events will be in person this fall. Together we are the strength and support for our Apraxia Stars and Walks allow our community the opportunity to celebrate each Star for all their hard work. Please visit our Walk for Apraxia page to find a Walk closest to you. Remember, registration for the Walk is FREE.        

Together, we are a support system sharing resources, education, and programs for everyone who is on an apraxia journey. As we look to the summer and fall, we encourage you to continue making an impact. Sharing your story, joining a Walk, sharing our organization’s resources with a new family, or making a financial gift are all ways you can make a difference 

Together, we are mission-driven. Thank you for being our partner and for your continued commitment to Apraxia Kids!

 

Angela Grimm
Executive Director

Click here to subscribe to the Apraxia Kids monthly newsletter!



Credentials:
Hours of Operation:
Treatment locations:
Address:

,
Phone:
Email:

Overall Treatment Approach:
   

Percent of CAS cases:

Parent Involvement:
   

Community Involvement:
   

Professional consultation/collaboration:

Min Age Treated:

Max Age Treated:

Insurance Accepted: