Today is Apraxia Awareness Day. In place of my usual Wordless Wednesday photo post, I am sharing a book about one family’s experience with childhood apraxia of speech. If your life has been touch by apraxia in some way, I hope you read it too.
It’s been over five years since our daughter Anna was diagnosed with childhood apraxia of speech, and before she was diagnosed we had never heard of this surprisingly common motor-speech disorder. We felt so alone. But we found help from fellow parents online and we found the Childhood Apraxia of Speech Association of North America (CASANA). We weren’t as alone as we thought.
Fifteen years earlier, Kathy Hennessy had to grapple with this same diagnosis twice. Both her daughter Kate and her son Andrew had apraxia. Fifteen years earlier there was nowhere to go for support. The internet was in it’s infancy, and apraxia was little known even among speech language pathologists. I can’t imagine how alone she felt.