Anything but Silent book review and GIVEAWAY!

By Laura Smith|May 5, 2017|Anything but Silent review and giveaway, Apraxia, Apraxia Awareness Day|10 comments

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I’m continuing on with giveaways leading up to Apraxia Awareness Day on May 14th! Today I am reviewing the book ANYTHING BUT SILENT by Kathy and Kate Hennessy.  Kathy Hennessy is the mother to Kate who has pure CAS and another son Andy who has global apraxia and SPD.  Kathy is also the educational director at CASANA!

The book rotates chapters from Kathy’s point of view to Kate’s point of view.  First of all, I just have one piece of advice: if you are a parent or professional

READ THIS BOOK.

READ THIS BOOK!

Yes, people.  It’s that good.  I read it in one night!  I couldn’t put it down.  I laughed, I cried, but mostly I related.

It starts with the diagnosis:

“I decided that day I could beat myself up about the unfairness of life or I could educate myself and help my daughter move her own mountains.”

I could not have said it better.  This is EXACTLY how I felt.  How I feel! Kathy wasn’t kidding either.  She’s now the education director at CASANA (apraxia-kids.org).

It captures the need for others who are going through the same thing:

“What I needed at this point in my life, more than anything, was another parent, and that was the one thing I couldn’t find.”

I can’t even imagine.  My fellow women I have met through facebook are my saviors.  Seriously, I don’t know what I would do without them.

They capture the fears at simple holiday traditions:

“When you have someone in your family with childhood apraxia of speech, things that are everyday occurrences for other families are moments for you that aren’t very normal at all.”

She’s referring to the tradition of seeing Santa.  Kathy would fret and worry that Santa wouldn’t understand them, among other things.  Let me tell you, EVERY mommy of apraxia has been there.

From fighting insurance companies, to therapy sessions as a lifestyle, these two amazing women tell their incredible story and as Kathy puts it, “Today both kids are doing great and I’m still standing.”

This story was inspiring beyond my wildest imagination.  I can’t believe I waited this long to read it!  Read it people!!  That’s my review.  You won’t be disappointed!

To win this book, enter below. Open to U.S. residents only!  Good luck.

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10 Comments

  1. Our 5 year old son was recently diagnosed with dyspraxia… hardest thing so far has been helping him to be confident and to always keep trying!

  2. Would love to read this book!

  3. Love your blog, would love this book!!

  4. The hardest part of having a kido with CAS is getting him the therapy he needs and deserves. It shouldn’t be so hard and so expensive to teach kids basic skills.

  5. The hardest part of having a kido with CAS is getting him the therapy he needs and deserves. It shouldn’t be so hard and so expensive to teach kids basic skills.

  6. The hardest part has to be finding specialized services that are able to provide the frequency and specialty treatment than children with CAS need.

  7. My son was diagnosed with Apraxia a couple months ago and he just turned 3 last Sunday. The hardest part is watching his classmates talk to each other at school while he plays by himself. 🙁

  8. My son was diagnosed with Apraxia a couple months ago and he just turned 3 last Sunday. The hardest part is watching his classmates talk to each other at school while he plays by himself. 🙁

  9. My oldest son was diagnosed with “expressive and receptive language disorder” ~ but, it’s so difficult getting him the therapy he needs. I work with him every day.

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