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 promote awareness of PPROM through:
Advocacy in Expectant Management, conducted by PPROM parents through support groups and individual consultations.
Partnerships with healthcare providers, hospitals, and organizations who support maternal, fetal / neonatal health, research, and person-centered care in Expectant Management.
The PPROM Registry of individuals diagnosed with PPROM in pregnancy. This Patient-Reported Outcomes (PRO) registry is available to mothers who have concluded their PPROM pregnancy. We observe trends in expectant management, outcomes, and long term effects in survivors. Research partnerships available. More > >
The PPROM Foundation is a registered public charity 501(c)(3), legal name American Alliance for pProm Support
The PPROM Foundation has earned the 2019 Platinum Seal of Transparency, the highest level of recognition offered by GuideStar, the world’s largest source of nonprofit information. By sharing metrics that highlight progress The PPROM Foundation is making toward its mission, the organization is helping donors move beyond simplistic ways of nonprofit evaluation such as overhead ratios.