OUR MISSION
The SATB2 Gene Foundation, Inc. was established to enrich the lives of individuals with SATB2-associated syndrome, including those diagnosed with the condition and their families, through support, research and education. Our mission will be met by raising awareness about the characteristics of SATB2-associated syndrome, providing support to families, and supporting research in a wide range of issues related to SATB2-associated syndrome.
SATB2 NEWS & ARTICLES
Regional Rep Open Call
We need YOU! We are looking for volunteers to launch our Regional Representative program in North America. This program is designed to be a support and resource program for our our SAS families to help
SAS Family Support Group
SAS Family Support Group Virtual Meet Up Calling all SAS caregivers! Join us for our first bi-monthly Family Support Virtual Meet Up on Tuesday, February 8th at 8pm EST / 5pm PST!
SAS Adult Families Virtual Meet Up
SAS Adult Families Virtual Meet Up If you are a family member of an adult loved one with SAS, please join Bill and Terry Regan for a time of discussion and support
SAS Speech and Language Survey Report
SAS Speech & Language Survey Report In order to support families with a SAS diagnosis, in June 2021 an independent study supported by the SATB2 Gene Foundation was launched to better understand