The Preeclampsia Foundation envisions a world where preeclampsia no longer threatens the lives of mothers and babies.
The Preeclampsia Foundation reduces maternal and infant illness and death due to preeclampsia, HELLP syndrome, and other hypertensive disorders of pregnancy by providing patient support and education, raising public awareness, catalyzing research and improving healthcare practices.
Established in 2000, we are the only national 501(c)(3) not-for-profit patient advocacy organization serving the 5-8% of pregnant women - 300,000 women each year in the U.S. - who are affected by hypertensive disorders of pregnancy such as preeclampsia (formerly known as toxemia), eclampsia and HELLP syndrome.
We are advised by a medical board comprised of the top medical and scientific experts in preeclampsia and related fields, additionally partnering with other non-profit organizations, governmental agencies, academic institutions, and corporations to achieve our mission and provide educational content.
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