Mehreen Kakwan first emailed me a couple of months ago to simply ask if I could be listed as a resource for her new book on apraxia, “Billy Gets Talking.” I asked to read the book and she sent me a PDF version, in which I was instantly hooked. I don’t just say that lightly either…. I get a lot of pitches in my email to review or promote a
It’s Halloween, 2018. You are a freshly turned nine-year old. You are 9 years old. My mind immediately repeats a phrase from my dad, “Mr. Baskall, here’s your little baby girl.” I remember I would roll my eyes and scoff at him. “Ugh dad!” I would lament as he looked at me with eyes brimming with pride. I don’t have any words to describe or memorialize your entrance into this
This weekend I was the guest speaker at the Nevada Walk for Apraxia and stayed with the walk coordinator Alyssa Hampson and her family. I flew in the day before the walk, and her house looked very typical of any other walk coordinator. It was bursting with items such as goody bags for the kids, prizes for the silent auction, food and beverages for breakfast, signage, T-shirts, and so much
In my opinion, Ashlynn’s birth history was significant. No, she wasn’t born premature. No, there wasn’t a dramatic rush to the ER. However, I was failing to dilate or efface and the labor was taking so long that vaginal fetal electrodes were placed on her head. In addition, every contraction brought concern to the fetal hear monitor. My OB recommended at least three times that I get a C-section; but
Old faces, new faces, and the passing of the torch. The selfless individuals who had been there before were still there giving back like they always had and a new wave stood by their sides ready to continue the mission. I have so much respect and love for the past, and I’m so excited for the future!
The mission has never changed and was never about any one person. It’s about Apraxia and Kids.
Every Child Deserves a Voice.
Let’s see this mission continue to spread!