You know you need awareness when you know more than the “experts.”

By Laura Smith|August 16, 2017|Apraxia, apraxia blog, developmental coordination disorder, dyspraxia, Executive Functioning Skills, global apraxia, Sensory Processing Disorder, special needs, special needs parenting|

About a year ago I switched insurance from my husband’s to mine, in order to leave no stone left unturned.  I know that kids with apraxia can have some sort of positive indicator on a brain MRI, or genetic marker.  I had yet to do any of that testing, and so I decided this was the year to do it. My husband questioned why.  Is there a reason to know?

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Apraxia would have destroyed me

By Laura Smith|March 19, 2017|#knockoutapraxia, Apraxia, apraxia blog, Childhood Apraxia of Speech, developmental coordination disorder, dyspraxia, language disorder, Sensory Processing Disorder, special needs, special needs parenting, specific language impairment|

I often think about what would have happened had it been me who had apraxia, dyspraxia, SPD, dysarthria, and a learning disability when I was young.  It’s pointless I know, but I was/am a perfectionist.  That’s not a good thing.  I learned early I was really good at spelling, reading and writing, but math I had to work for.  I won a math award in 3rd grade and I looked

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It’s like juggling 8 balls at one time desperately hoping one doesn’t roll away

By Laura Smith|February 14, 2017|Apraxia, apraxia blog, developmental coordination disorder, dyspraxia, global apraxia, Sensory Processing Disorder, special needs, special needs parenting|

There is not one day that goes by I don’t think of Ashlynn’s disability (ies).  As a basis of comparison, I have my four year old son.  He has some concerning behavior issues, and I do think (worry) about them often; however, I do not think of it EVERY SINGLE DAY. Apraxia and dyspraxia make that impossible.  There is always something else to worry about.  Something else in which I

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The problem with school SLP’s.

By Laura Smith|January 23, 2017|Apraxia, apraxia blog, Childhood Apraxia of Speech, special needs, special needs parenting, Speech/Language therapy, Therapy for apraxia, Uncategorized|

I only realized after being a part of the special needs community that school SLP’s have a bad rap.  Like a really, REALLY, REALLY bad rap.   I’m preparing a talk next month for Colorado school SLP’s, and every time I prepare a talk for this demographic, I have to tell you they have a special place in my heart.  No, it’s not just because I started as one and

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