Apraxia Awareness Month 2024 is right around the corner!
Apraxia Awareness Month 2024 is right around the corner!
Apraxia Awareness Month 2024 is right around the corner!
Apraxia Awareness Month 2024 is right around the corner!
Apraxia Awareness Month 2024 is right around the corner!

Apraxia Awareness Month 2024 is right around the corner!

Apraxia Awareness Month is May of 2024! The first EVER Apraxia Awareness Day was recognized only 11 years ago on May 14th, 2013. Right on the heals of Ashlynn’s diagnosis in 2012, this day filled my cup! Each year since it has grown bigger and bigger! One thing that’s a MUST is to wear your apraxia awareness gear! For a short time, my store is offering shirt sales through April

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Parent experience at an apraxia diagnosis

Parent experience at an apraxia diagnosis

It’s been over eleven years identifying as a parent to a child diagnosed with childhood apraxia of speech. I’ll never forget that fateful day. I missed her apraxia as an infant, despite being a speech/language pathologist before she was born. I knew she was delayed. Oh yes, I was keenly aware of it. Every well-check visit the list of milestones she was meeting grew shorter and shorter. I worked with

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New Caregiver Opportunity! Limited seating!

New Caregiver Opportunity! Limited seating!

Greetings SLP Mommy of Apraxia Community! I wanted to express my sincere gratitude for everyone who has followed my journey and Ashlynn’s journey. Many of you have been there from the start as we learned to navigate childhood apraxia of speech! The journey started out lonely and I was full of anxiety and worry. However, I slowly but surely started to learn more and find a community. I am always

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Denver Apraxia Festival!

The Denver Fall Apraxia Festival is coming back this October 7th 2023. This event is a fundraising event to benefit The Apraxia Foundation, a newer 501(c)3 founded by an individual with CAS named Jordan Levan. Since I came on the apraxia scene back in 2012 when my daughter Ashlynn was first diagnosed, I have seen the culture around apraxia change, and for the better! When Ashlynn was first diagnosed, I

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Child Apraxia Treatment and DTTC for CAS

Join me for my first episode in Season 2 of the SLP Mommy of Apraxia Podcast as I talk to Breanna Waldrup, speech/language pathologist and director of the private non-profit Child Apraxia Treatment. We talk about her role as the director of the foundation, it’s mission statement and elements of Dynamic Temporal Tactile Cueing (DTTC) for the treatment of CAS.

Woes of regression

Woes of regression

If you’ve ever watched your baby fail to meet the simplest of milestones.. If you’ve sat in meetings and offices and were told things like 1% percentile If you’ve felt a pain you can’t describe that is only eased by hope.. You know why regression hurts so much. If you’ve ever driven your child back and forth to countless therapies.. If you’ve ever felt a mix of pride, happiness, grief

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