05 Apr April 2021 Newsletter
Dear Friends,
Spring is my favorite time of year! The days are getting longer, flowers are beginning to bloom, and Awareness Month is soon approaching. As we look to the coming month, we are excited to share educational opportunities, resources, and activities to help expand awareness about childhood apraxia of speech (CAS) and Apraxia Kids. Childhood apraxia of speech impacts 1 in 1,000 children, and we estimate that many children are either misdiagnosed or not diagnosed at all. Our vision is that every family impacted by CAS knows about Apraxia Kids and has access to our resources. We need your help to make that happen!
The month of May brings renewed excitement to our organization as we engage with old and new friends, spreading our mission locally and afar. We are so grateful for your continued commitment to Apraxia Kids as we work to grow our community. What better way to help us grow than to “Be the Voice” for a child with apraxia? Whether you share our Awareness Month calendar, post your personal story on social media, or choose to be 1 of 1,000 donors by creating a fundraiser during May, you are making a difference in the life of a child with CAS.
Last month, we shared the National Conference schedule with you, detailing the sessions available along with our speaker lineup. With the conference being virtual this year, you will have the unique opportunity to watch the sessions live during July 8-10 AND have continued access to a majority of the recorded sessions for a limited time following the conference to catch up on anything you might have missed.
Apraxia Kids is so thankful for every member of our community. Because of you, families do not have to feel alone as they navigate their apraxia journey. Your generosity provides: Hardship Grants for families to attend the National Conference, resources such as our parent folder, free educational webinars, and so much more. By investing in our future, you are providing support to the 1 in 1,000 families impacted by childhood apraxia of speech today, tomorrow, and for years to come.
Wishing you and your family health and happiness this spring season. We look forward to seeing each of you decked out in blue next month!
Best,
Angela Grimm
Executive Director
Click here to subscribe to the Apraxia Kids monthly newsletter!
Dear Friends,
Spring is my favorite time of year! The days are getting longer, flowers are beginning to bloom, and Awareness Month is soon approaching. As we look to the coming month, we are excited to share educational opportunities, resources, and activities to help expand awareness about childhood apraxia of speech (CAS) and Apraxia Kids. Childhood apraxia of speech impacts 1 in 1,000 children, and we estimate that many children are either misdiagnosed or not diagnosed at all. Our vision is that every family impacted by CAS knows about Apraxia Kids and has access to our resources. We need your help to make that happen!
The month of May brings renewed excitement to our organization as we engage with old and new friends, spreading our mission locally and afar. We are so grateful for your continued commitment to Apraxia Kids as we work to grow our community. What better way to help us grow than to “Be the Voice” for a child with apraxia? Whether you share our Awareness Month calendar, post your personal story on social media, or choose to be 1 of 1,000 donors by creating a fundraiser during May, you are making a difference in the life of a child with CAS.
Last month, we shared the National Conference schedule with you, detailing the sessions available along with our speaker lineup. With the conference being virtual this year, you will have the unique opportunity to watch the sessions live during July 8-10 AND have continued access to a majority of the recorded sessions for a limited time following the conference to catch up on anything you might have missed.
Apraxia Kids is so thankful for every member of our community. Because of you, families do not have to feel alone as they navigate their apraxia journey. Your generosity provides: Hardship Grants for families to attend the National Conference, resources such as our parent folder, free educational webinars, and so much more. By investing in our future, you are providing support to the 1 in 1,000 families impacted by childhood apraxia of speech today, tomorrow, and for years to come.
Wishing you and your family health and happiness this spring season. We look forward to seeing each of you decked out in blue next month!
Best,
Angela Grimm
Executive Director
Click here to subscribe to the Apraxia Kids monthly newsletter!
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