Q. Why is CHERAB spelled with an A and not a U?
A. It’s all in the cheeks!
When my son Tanner was a preschool child his nickname was “cherub boy” because even strangers would call him that and say he looked like a little angel.
Tanner was first diagnosed with apraxia in 1999 when he was around 3. Back then there was little to no support for the rare orphan diagnosis called apraxia, and even less information.
I started a nonprofit and named it Children’s Apraxia Network which we nicknamed CAN -but within the first year, I saw members had children that were much older than my son, some teens. I didn’t want to limit outreach to just those with young children so wanted to have a name that didn’t have children in it even though that was my focus for my own son at the time, and clearly a huge part of my group. As you can see from this Inside Edition segment on Apraxia our outreach was large but included teens and young adults even early on (please note the crazy long website address at the time too)
Author and Executive Director of The Cherab Foundation
Lisa Geng got her start as a designer, patented inventor, and creator in the fashion, toy, and film industries, but after the early diagnosis of her young children, he entered the world of nonprofit, pilot studies, and advocacy. As the mother of two “late talkers,” she is the founder and president of the nonprofit CHERAB Foundation, co-author of the acclaimed book, The Late Talker, (St Martin’s Press 2003), and is instrumental in the development of IQed, a patented nutritional composition. Lisa served for years as a parent advocate on an AAN board for vaccines and is a member of CUE through Cochrane US. Lisa is currently working on a second book, The Late Talker Grows Up and serves as a Late Talkers, Silent Voices executive producer. She lives on the Treasure Coast of Florida.