Apraxia, special ed, and grad school. One woman’s remarkable tale.

By Laura Smith|April 8, 2017|Apraxia, apraxia blog, developmental coordination disorder, dyspraxia, global apraxia, Sensory Processing Disorder, special needs parenting|

One day I was perusing The Mighty to see if any new apraxia articles had been posted, and I ran across an article by Kelsey Belk, a graduate student studying to be an SLP.  I was so inspired by her article I just had to reach out and thank her.  I found her on facebook and saw that she was currently attending the University of Northern Colorado! I live in

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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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The Rise

By Laura Smith|March 9, 2017|Apraxia, Apraxia Awareness Day, apraxia blog, Childhood Apraxia of Speech, developmental coordination disorder, dyspraxia, language disorder, specific language impairment, Uncategorized|

I have Ashlynn on a new game plan.  We had to take a break from her private speech because of unforseen financial issues in our life, but now we are back and better than ever. She’ll be seeing her awesome private SLP again on Tuesdays (who just happens to be my mentor, friend, and speech mom), and then Wednesdays we have insurance finally paying for 20 sessions, which is not

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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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Neurology, delays, a dream, and a miracle.

By Laura Smith|January 29, 2017|Apraxia, apraxia blog, Childhood Apraxia of Speech, developmental coordination disorder, dyspraxia, special needs parenting|

Most parents of kids who have a child with global apraxia will at some point visit the neurologist.  It’s usually before the age of 7, which is the age Ashlynn is today. I remember the referral, although the dates are a little fuzzy.  We were either at Ashlynn’s 6 or 9 month checkup and I had to fill out one of those dreaded developmental screens.  Don’t get me wrong, as

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SLPMommyofApraxia Top Ten Posts of 2016

By Laura Smith|December 29, 2016|Apraxia, apraxia blog, Childhood Apraxia of Speech, developmental coordination disorder, dyspraxia|

This year was a little rough on me.  However,  positives and good things still happen in any bad year. I personally believe the life we are given, your life, my life, Ashlynn’s life…we are given this life to learn to and to grow.  Christians may refer to this as a “cross to bear.”  I know at times, life has seemed incredibly unfair, but in that unfairness I have met some

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