I have faith though that this next decade will be one of overcoming! I know ten years from now I’m going to be writing another success and triumph story, much like I did in the book I published this year called “Overcoming Apraxia.” I also want this next decade to be one of exponential growth in apraxia awareness and information so all children have the access to the best therapy.
On my facebook page SLP Mommy of Apraxia, every Sunday I post a kids being kids moment. The idea was to show the world that kids with apraxia or other invisible disabilities enjoy doing the same things as neurotypical kids. One day, a mom remarked she felt bad she didn’t have the money to give her kid all the experiences other parents seemed to be giving their children. I told
I’ve created a (not exhaustive) list of questions to ask a potential SLP about their knowledge and experience treating childhood apraxia of speech.
I’ve compiled a list of trainings and resources on childhood apraxia of speech for speech-language pathologists.
Almost seven years ago to the day, before my daughter Ashlynn’s 3rd birthday, I received news so significant, my life has never been the same. Though devastating at the time, the life lessons I have learned from it have far outnumbered any loss. What was this news? My daughter Ashlynn was diagnosed with one of the most severe neurological speech disorders in children. It is called “childhood apraxia of speech
I’m so excited to have some of the two largest apraxia social media influencers with me today to talk about what it is like to be “Adulting with Apraxia.” Mikey Akers from Mikey’s Wish and Jordan LeVan from Fighting for my Voice are both young men living with verbal apraxia. In the UK, verbal apraxia is known as verbal dyspraxia. Jordan and Mikey were talking one day about various issues