STXBP1 Foundation is dedicated to finding a cure for STXBP1-related Disorders while improving the lives of our patients and families. Founded in 2017, STXBP1 Foundation is a parent-led advocacy organization. STXBP1 Disorder is a rare epileptic and neurodevelopmental disorder caused by changes in the STXBP1 gene. With an incidence of approximately 1 in 30,000 live births, STXBP1 Disorder is one of the most common genetic causes of epilepsy.

The STXBP1 Foundation is focused on:
* Creating awareness in the disorders associated with STXBP1 mutations
* Funding and drive research to accelerate discovery of a cure
* Providing families with tools to help them understand the disease & how to get involved
* Advocating to improve early detection
* Fostering activism to help change policies in favor of orphaned diseases
* Improve the lives of our STXBP1 Family

For more information, contact info@stxbp1disorders.org and visit http://www.stxbp1disorders.org/.