My Nonprofit Reviews

I am a preeclampsia and HELLP Syndrome survivor who became aware of the Preeclampsia Foundation after my near-death pregnancy experience when I was resarching the medical facts behind what happened to me. I found the Preeclampsia Foundation website and learned of a vounteer training that I attended in 2006. At that conference, I was impressed with the professionalism and organization of the group. I was surprised to learn, however,that at that time, the organization was entirely volunteer led. Since that time, the Foundation has evolved to the next step in hiring professional staff but still operates with a high level of fiscal responsibility. More personally, the Foundation and its volunteers helped me significantly during a key point of my recovery. The Preeclampsia Foundation works to reduce the risks of adverse maternal and fetal outcome resulting from preeclampsia and other hypertensive related disorders of pregnancy by raising awareness about the conditon, providing professional education opportunities for healthcare providers, acting as a catalyst for and funding research, and providing outstanding patient/family support in person, through a dynamic online Forum, and via a toll-free hotline.

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