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
Will you be their voice?
SATB2 Awareness Day: Will you be their voice? We are on a critical mission to discover treatment(s) for individuals affected by SATB2-associated syndrome. Our community works to understand the impacts of SAS on
Research Grant Open Call
Research Grant Proposals Open Call This year we are pleased to announce that we have $50,000 in funding available for research grants which prioritizes the following areas of research, based on high
SPEECH AND LANGUAGE SURVEY
SPEECH AND LANGUAGE SURVEY Have you ever asked or wondered: what kind of speech therapy should we be doing with our SAS child? How many words do other individuals with SAS have
Virtual Meet Up for Children ages birth – 5 years old
VIRTUAL MEET-UP Join us on Saturday, June 12, 2021 for one (or both) virtual meet-ups for families of SAS children aged newborn through 5 years old! Connect with other families during these