She had so many questions about her daughter’s future—and no one to turn to. When Bea was just six months old, their family moved home from California to Watertown, NY, still searching for connection, answers, and hope. Then they found the Spina Bifida Association of New York State (SBANYS). At their very first event—the Walk-N-Roll in Schenectady, three hours from home—Jess felt relief. Surrounded by people of all ages living with Spina Bifida, she finally saw what was possible for Bea’s future. Jess continued to attend SBANYS programs including the State Conference and Adaptive Recreation Expo held in Syracuse, closer to home. Jess and her family have found more than support—they’ve found a community. A community that offers education, empowerment, and hope at every program. Jess shared: “Living with Spina Bifida doesn’t mean you’re unhealthy. With the right care, people with Spina Bifida can lead a happy life. SBANYS gave us the confidence to advocate for Bea.” This hope is only possible because of generous supporters like you. Your gift ensures families like Jess and Bea’s never feel alone—and that they have the tools, resources, and community they need to thrive. Will you make a gift today to bring hope and connection to more families across New York State?