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)
Apraxia is a rare diagnosis and unlike autism there is very limited research. We used to have a lot of in-person meetings and events out of 2 hospitals in NJ and I noticed that like my son Tanner the majority of the kids with apraxia have these adorable round cheeks that make them look like little cherubs -just like my son. This is because most of them have something called hypotonia (low tone) in their body and typically also their face. (
see this page for more info) When it’s in the oral area it may be diagnosed as dysarthria which is not uncommon as a dual diagnosis with apraxia. You can see a TV segment with Tanner when he’s 5 along with Haily, also diagnosed with apraxia and see what I mean about the cheeks.
We called it Cherab with an A vs. a U to stand for Apraxia. Cherab stans for what we’d provide support in Communication Help, Education Research, and the AB stands for Apraxia Base
You may not be aware that 64 percent of those with autism have apraxia according to
one study and this is probably why so many of our members have children with autism. We joke we should call it Communication Help, Education, Research, Apraxia Autism Base -but the base of the Cherab Foundation is still the rare orphan diagnosis apraxia.
LISA GENG
Author and Executive Director of The Cherab Foundation
Lisa Geng is an accomplished author, mother, founder, and president of the CHERAB Foundation. She is a patented inventor and creator in the fashion, toy, and film industries. After the early diagnosis of her two young children with severe apraxia, hypotonia, sensory processing disorder, ADHD, and CAPD, she dedicated her life to nonprofit work and pilot studies. Lisa is the co-author of the highly acclaimed book “The Late Talker” (St Martin’s Press 2003). She has hosted numerous conferences, including one overseen by a medical director from the NIH for her protocol using fish oils as a therapeutic intervention. Lisa currently holds four patents and patents pending on a nutritional composition. She is a co-author of a study that used her proprietary nutritional composition published in a National Institute of Health-based, peer-reviewed medical journal.
Additionally, Lisa has been serving as an AAN Immunization Panel parent advocate since 2015 and is a member of CUE through Cochrane US. Currently working on her second book, “The Late Talker Grows Up,” she also serves as an executive producer of “Late Talkers Silent Voices.” Lisa Geng lives on the Treasure Coast of Florida.
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Consumers United for Evidence-Based Healthcare (CUE) is a national coalition of health and consumer advocacy organizations committed to empowering consumers to make the best use of evidence-based healthcare (EBHC).
Why is CHERAB spelled with an A?
Posted: August 3, 2018 by lisa
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)
LISA GENG
Author and Executive Director of The Cherab Foundation
Lisa Geng is an accomplished author, mother, founder, and president of the CHERAB Foundation. She is a patented inventor and creator in the fashion, toy, and film industries. After the early diagnosis of her two young children with severe apraxia, hypotonia, sensory processing disorder, ADHD, and CAPD, she dedicated her life to nonprofit work and pilot studies. Lisa is the co-author of the highly acclaimed book “The Late Talker” (St Martin’s Press 2003). She has hosted numerous conferences, including one overseen by a medical director from the NIH for her protocol using fish oils as a therapeutic intervention. Lisa currently holds four patents and patents pending on a nutritional composition. She is a co-author of a study that used her proprietary nutritional composition published in a National Institute of Health-based, peer-reviewed medical journal.
Additionally, Lisa has been serving as an AAN Immunization Panel parent advocate since 2015 and is a member of CUE through Cochrane US. Currently working on her second book, “The Late Talker Grows Up,” she also serves as an executive producer of “Late Talkers Silent Voices.” Lisa Geng lives on the Treasure Coast of Florida.
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Category: About, Disorders, News Tags: apraxia, cheeks, Cherab, hypotonia, name