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Patient Advisory Council

Patient Advisory Council

The Patient Advisory Council (“PAC”) serves as an advisory resource to the Board of Directors and staff of the Preeclampsia Foundation, for the purpose of maintaining and furthering the Foundation’s position as a patient-centered, patient-driven, patient advocacy organization. The patient voice and experience are integral to the mission of the Foundation; therefore, the PAC operates to directly engage patients, the Board, and staff, in meaningful, ongoing communication, and keep the patient at the forefront of all we do. 

The PAC is currently taking applications for US-based membership. If you experienced preeclampsia, postpartum preeclampisa, eclampsia, or HELLP syndrome during pregnancy and/or the postpartum period and want to use your representative voice to help improve understanding between patients, providers, and researchers...Apply to join the PAC

Dads, partners, and grandparents who can closely speak to the patient experience are also welcome to join.

Please click here to apply before November 6, 2024 to serve for the January 2025-December 2026 term. Membership may be renewed for a total of four years of service.

The PAC works to reflect the great diversity in patient experiences through its membership. Therefore, not all applicants may be selected to serve at this time, but all applications will be considered on an annual basis by the PAC's membership committee.