Preeclampsia Foundation News

2013 Vision Grant Recipients to Study the Underlying Mechanisms of Preeclampsia $25,000 research grants will be presented to two preeclampsia research studies Melbourne, FL – September 12, 2013 – The Preeclampsia Foundation announced today that Ana Sofia Teixeira de Cerdeira, MD of the Harvard Medical School and Mandy Bell, PhD, RN of the University of Pittsburgh School of Nursing are recipients of its 2013 Vision Grants. Vision Grants are awarded to the strongest scientific proposals recommended by the Foundation’s scientific review committee with a further review by a consumer advisory board. The Foundation’s Board of Directors renders the final decision based on those recommendations. Preeclampsia is a major cause of maternal and fetal pregnancy related disease and death worldwide. Both recipients have the goal of better understanding the underlying mechanisms of the disease and translating their research findings to clinical application. Study #1 is working on the immune mechanisms (NK cells and Tregs) of regulation of placentation in health and preeclampsia. Study #2 is designed to clarify the role that soluble endoglin (sENG) plays in preeclampsia by investigating if differences in the genetic code of the endoglin gene and related genes account for increased sENG in women with preeclampsia. Click…Continue reading Preeclampsia Foundation News

Preeclampsia Foundation News

Screening Tests for Preeclampsia Preeclampsia Foundation News – August 16, 2013 If there were a way to learn your risk of developing preeclampsia in the first trimester of your pregnancy, would you want to know?  What if that test result wasn’t 100% accurate? We asked almost 1,000 women – some who had had preeclampsia and some who had not – these and other questions to better understand patient preferences around the need for screening (or prediction) tests. Eighty-eight percent of women with a history of preeclampsia agreed that an early test was important, even if it was imperfect. Even those without a history of preeclampsia – 74% – still agreed it would be important. Click here to view more: Screening Tests for Preeclampsia (www.preeclampsia.org) © Preeclampsia Foundation 2013 | www.preeclampsia.org

Creating a Community of Hope

It’s talked about in little circles. It’s discussed in hushed tones amongst family and friends. It’s brushed aside as a sad part of life that one should not dwell on and certainly should never be talked about with strangers. What am I talking about? Miscarriage. I am starting this blog because I recently experienced my fourth loss in three years and I no longer want to hide it and be ashamed of it. Why is it that people can post every detail of their pregnancies on facebook and other social media sites, right down to the sex of their baby months before the baby is even born, but talking about miscarriage, another part of pregnancy, is taboo? After my most recent miscarriage, I really hit an all time low. This was my third miscarriage in two years and I delivered a baby boy prematurely at twenty-eight weeks due to preeclampsia the year before. He died after three and a half months in the NICU. These were four incredibly painful events in my life. I was tired of it all. I was heartbroken. I was angry. I asked, how could this happen again. I wondered how it is possible that there…Continue reading Creating a Community of Hope