08/21/2026
DYRK1A Syndrome Awareness Day!
Today, we raise awareness, spread love, and show our support for individuals and families impacted by this rare genetic condition. This cause is especially close to our hearts because DYRK1A Syndrome affects one of our very own, Everlee (7), the youngest daughter of our Marketing Specialist, Dakota Wilson!
Did you know? DYRK1A Syndrome is a rare genetic condition caused by a mutation or change in the DYRK1A gene. It can affect many parts of development, leading to speech delays, intellectual disability, unique facial features, feeding difficulties, and motor skill challenges. Because it is so rare, raising awareness helps foster better understanding, research, and support.
Read below to learn more about DYRK1A Syndrome and Everlee’s journey. They celebrate 5yrs since receiving the diagnosis this year!
