The Health Resources and Services Administration is offering funding through the Cooperative Newborn Screening System Priorities Program (NBS Co-Propel). This program aims to strengthen the newborn screening (NBS) system to provide screening, counseling, and health care services to newborns and children with, or at risk for, heritable disorders. The funding will support up to 10 recipients to address state/territory-specific challenges and pursue priorities to enhance, improve, and expand their NBS System. It will also focus on increasing timely collection and reporting of NBS specimens to improve early diagnosis and treatment for individuals with heritable conditions identified through NBS. Additionally, the funding will support long-term follow-up for individuals with Severe Combined Immunodeficiency (SCID) and other NBS conditions, linking public health agencies, clinicians, and engaging families. The program objectives include increasing the number of NBS specimens collected within 48 hours of birth, improving the communication of presumptive positive results for time-critical conditions, and increasing the reporting of NBS results within 7 days of birth. The program also aims to develop data collection plans to measure the percentage of 3-year-old children with at least one heritable condition identified through NBS who are thriving. Organizations in the United States, including state or political subdivisions, territories, health facilities or programs operated by or pursuant to a contract with or grant from the Indian Health Services, and other entities with appropriate expertise in NBS, are eligible to apply. The deadline for applications is February 23, 2024. For more information, please visit the following link: link. For any inquiries, contact Loraine Swanson, MPH at (404)234-3557 or email LSwanson@hrsa.gov.