Apraxia? How does that affect her vision and hearing?

So today I took Ashlynn to her 5 year checkup at the doctor’s office.  Her pediatrician is one I met at a pediatrician’s office, but who decided to go work at a family medicine facility.  I love the pediatrician, but having her housed in a general practice creates some challenges….such as today. The regular physician assistant was out on vacation, so  another one was there to fill in.  Though she

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A tale of two roles: navigating my role on both sides of apraxia.

A tale of two roles: navigating my role on both sides of apraxia.

I first met a fellow mommy of apraxia at the Denver Apraxia Walk.  She was pleasant with kind eyes, and said she felt her 5 year old son needed a change up in speech therapy services. The next week her son was scheduled for therapy at the private clinic in which I work. In most cases, I have my parents come with their child into my office.  I NEED them

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Working our way out of the apraxia tunnel

Working our way out of the apraxia tunnel

Ashlynn has been saying things lately that are really showing higher level thinking. You’d think this would be glaringly apparent to me, but it really IS crazy how much language gives us an idea of what is going on in their brain. She’s been VERY interested in her schedule, and where she is going the next day.  I still haven’t made our visual schedule, but it’s on my to do

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September Specialty Series: Using AAC (Alternative and AugmentativeCommunication). A mother’s story.

September Specialty Series: Using AAC (Alternative and AugmentativeCommunication). A mother’s story.

To continue my September Specialty series, I want to introduce Merry. Merry is an amazing mom, and I wanted to feature a mother because in my opinion, parents are the experts on their child.  I think it’s important professionals keep this in mind, so I’ll say it again. Parents are the experts on their child. Her daughter is using an AAC (Assistive & Augmentative Communication) device at the age of

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Turning Pain into a Purpose

Turning Pain into a Purpose

Two years ago, I found out my almost three year old first born had Childhood Apraxia of Speech (CAS).  Despite being an SLP and treating CAS at the elementary level, I failed to recognize it in my baby. It was a VERY difficult time filled with overwhelming sadness for my daughter and guilt as her mother…an SLP who didn’t realize she had CAS. It rocked my world.  Not only did the

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Last year of Pre-K

Last year of Pre-K

Today was Ashlynn’s official first day to her last year of preschool.  It was also two years ago today I heard the words, “Laura, this is apraxia.”                                                                                      

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