Birthing people build the foundation for long-term health and well-being in the weeks and months after birth, yet data on postpartum health and health outcomes are inadequate to support clinical and policy efforts to ensure optimal postpartum health. Key information is inconsistently measured, often poor in quality, and lacking in continuity throughout the postpartum year. Such data deficits disproportionally impact Black, Indigenous, and People of Color, who experience greater risk for adverse maternal health outcomes compared with non-Hispanic White patients and for whom better data collection and use could have a great impact (DeMeester & Mahadevan, 2014;Hoyert, 2021;Huyser, Horse, Kuhlemeier, & Huyser, 2021). These data deficits also negatively impact rural residents, who face decreasing access to obstetric care and for whom better data to inform and evaluate rural-specific policy solutions are necessary (Kozhimannil, Interrante, Tuttle, & Henning-Smith, 2020). In addition, many individuals, especially those covered by Medicaid during pregnancy, lose insurance in the weeks and months after birth. Without consistent access to care, data to track and improve postpartum health outcomes among this population is largely absent (Romano & Kleinke, 2021). Better data are urgently needed to support a new standard of postpartum care.