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.
Research initiatives to improve outcomes in PPROM. The PPROM Registry is a Patient-Reported Outcomes (PRO) registry available to those who have concluded their PPROM pregnancy. We observe trends in expectant management, outcomes, and long term effects in survivors. Research partnerships available.

The PPROM Foundation is a registered public charity 501(c)(3), legal name American Alliance for pProm Support. EIN 46-3250661.