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Birth Defect Research for Children, based in Orlando, FL, is a 501(c)(3) non-profit organization dedicated to providing information and support services for parents and expectant parents regarding birth defects and childhood disabilities. The organization operates the National Birth Defect Registry, a comprehensive data collection project aimed at uncovering the causes of non-genetic birth defects to prevent future occurrences and enhance treatment options. Through research, community resources, and legal advocacy, Birth Defect Research for Children strives to empower families with knowledge and resources to address the complexities of birth defects. The organization's mission is supported by generous endowments and donations, enabling ongoing efforts to advance understanding and support for individuals and families affected by birth defects.Generated from the website

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