The PPROM Foundation aims to provide resources and support for those who have experienced Preterm Premature Rupture of Membranes (pProm) in their pregnancy and beyond. We will promote awareness of pProm through: *Advocacy conducted by local and regional contacts who will lead Support Groups and provide One to One Support to mothers given the diagnosis of pProm *Partnerships with healthcare providers, hospitals, and organizations who support Fetal and Neonatal Health and research with a goal of ensuring more consistent expectant management and neonatal care *The pProm Registry of individuals with the diagnosis of pProm in pregnancy. Through the collection of self-reported data by volunteers who have endured a pProm diagnosis in pregnancy, we will survey trends in expectant management, outcomes, and long term effects in survivors. A database of information about this syndrome will be critical in bringing new therapies to the market through research and advocacy.