Blue Man Group’s reputation for kids with special needs

Blue Man Group’s reputation for kids with special needs

We went to Vegas for Spring Break, and we took the the kids to see the Blue Man Group.  I had heard great things about the show in my parent support groups, so I thought it would be the perfect show for my kids. Ashlynn has a formal dx of SPD, and my son, well, he definitely has sensory issues.  Not sure if they fit a formal dx or not,

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The day she had enough!

The day she had enough!

When I was in 1st grade, a little boy kept kissing me on my head.  After the third time, I told my mother in exasperation.  I explained that even though I kept telling him to stop, he still kept doing it.  That night, both my parents had decided my mom would go to school the next day and let the teacher know and put a stop to it. “Nooooo,” I

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International Women’s Day includes my “apraxic, IC kid”

International Women’s Day includes my “apraxic, IC kid”

I practice person-first language.  I make sure I use it in every setting.  If you’re not familiar with person first language, it’s the idea that you put a person *before* their disability.  The idea is that when we put the disability first, we define a person by their disability.  However, no person is defined by their disability.  A person is just…..a person first. So, instead of saying that bipolar guy, you

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Finding all the wrong words or no words at all.

Finding all the wrong words or no words at all.

I think one thing, well actually I KNOW one thing I never knew about CAS before Ashlynn, was the significant difficulty kids with CAS tend to have with word finding. Ashlynn and all of my clients struggle with this to varying degrees.  Sometimes, Ashlynn’s seem innocent.  She’ll call me grandma after she’s been with her grandma all day.  She’ll say “today” when she really meant “tomorrow,” or say “tomorrow” when

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Tips for carryover in Childhood Apraxia of Speech: Part 2 of 2

Tips for carryover in Childhood Apraxia of Speech: Part 2 of 2

We all know Childhood Apraxia of Speech is rare!  The odds then of having a mother who is an SLP?  Probably substantially rarer right?  When I first started on this journey, I knew of none.  Now I know at least 30!  We have a unique perspective for sure, and I wanted to team up with two other moms to tell you what we do in our own homes with our

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Tips for Carryover in Childhood Apraxia of Speech: PART 1 of 2

Tips for Carryover in Childhood Apraxia of Speech: PART 1 of 2

  Thanks to the internet, I went from feeling I was the only SLP mommy of apraxia in the world, to meeting one other, to now knowing many others!  One year ago, I teamed up with one of them to write “Strategies to Promote Speech and Language in the minimally verbal or pre-verbal child with suspected Childhood Apraxia of Speech.”   Today, I’ve teamed up with two other SLP moms

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