Eleni Tsigas, CEO of the Preeclampsia Foundation, talks about her personal experiences that drive her passion. Eleni further discusses the important work the Preeclampsia Foundation is engaged in, including the 10th anniversary of the Preeclampsia Registry and how it is impacting research. Also, covered is the future of maternal care and the Preeclampsia Foundation’s impact on it, including the growing Cuff Kit program, and the new initiative, the Take 10 campaign. Launching soon, Take 10 will work with partners to increase diverse representation of all people in the registry.

The Preeclampsia Foundation was designed to be a “place to come to, to get reliable information, to find a community that [people] can connect with…”

We are a “collaborator, a partner…to work hand-in-hand with you to make the world a better place for those who experienced hypotensive disorders of pregnancy”

There are many ways to get involved: Become a MoMMA’s Voices Patient Family Partner, get involved with Promise Walks, volunteer with the foundation, or even do DIY fundraisers.

Contact the Preeclampsia Foundation and we will try to help match you with opportunities “where you are.”

About MoMMA's Voices
MoMMA’s (Maternal Mortality and Morbidity Advocates) Voices is the first-ever maternal health patient advocacy coalition established in 2018, to amplify the voices of people who have experienced childbirth complications or loss - especially those who have been historically marginalized - ensuring they are equipped and activated as partners with providers and researchers to improve maternal health outcomes.

This is a program of the Preeclampsia Foundation, a 501(c)(3) non-profit organization, and is supported by a grant through Merck for Mothers. For more information, visit mommasvoices.org and preeclampsia.org.