Last year we learned that Avery has a diagnosis of apraxia. Since then, we have learned so much about this speech disorder and we are still learning a lot. I am receiving an amazing opportunity to attend the apraxia conference on a scholarship in July 2024. To be honest I can’t wait to attend, I’m so excited!
It hasn’t always come easy. Learning your child has a severe speech disorder and struggles with speech as much as Avery does, it is hard to witness. It has motivated me to become an even stronger advocate for Avery, to help him and be a voice on his behalf and educate others on apraxia.
I think it’s important to acknowledge that speech is hard! I’m driving Avery 3 times weekly to his private speech therapy sessions. I’m sitting in all of his speech sessions. I’m listening to him practice, practice and practice some more. It has taken a lot of energy out of my family. I couldn’t be prouder of my star Avery. He is determined, motivated and has such a strong will. He has found his voice!
We are excited to participate in another walk to contribute to the apraxia community.We hope you will support us in our journey and join us in the walk for Brave Ave!
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