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 MoMMAs 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 MoMMAs VoicesMoMMAs Voices (Maternal Mortality & Morbidity Advocates) is the first-ever maternal health patient advocates program bringing together real patient and family voices. We're made up of dozens of maternal health organizations who represent all types of maternal health conditions, as well as cross-cutting topics like maternal mental health, racial equity, healthcare delivery, and patient-provider partnership. We sit at the center of maternal health improvements, connecting and training patients with lived experiences, providers, quality improvement leaders, researchers, and policymakers to move forward improvements in maternal care. We are a program of the Preeclampsia Foundation.

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