EIN: 47-2459997 · Washington, DC
In September 2014, Monica Dudley-Weldon and families of children with SYNGAP1 mutations united to form the SYNGAP1 Foundation. Their shared experiences drive the mission to raise awareness and seek treatments that enhance the quality of life for affected children.
The SYNGAP1 Foundation has created the largest SYNGAP1 Patient Registry in collaboration with the FDA, serving as a crucial resource for advancing research on SYNGAP1-related Disorders.
Your contributions to the SYNGAP1 Foundation fuel essential research initiatives that improve the lives of families impacted by SYNGAP1-related Disorders.
Support the SYNGAP1 Foundation by donating cryptocurrency or cash. Your generosity helps provide resources, advocacy, and education to those in need. Together, we can bridge the gap for families affected by SYNGAP1-related Disorders.
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