Be a part of finding answers about Hyperemesis Gravidarum (HG). Currently, the HER Foundation has three active research surveys. Please participate!
Read MoreIn 2023, we will continue our support of families across the globe, continue our groundbreaking research, advocate to change policy to improve maternal and fetal outcomes, and launch an exciting new education program!
Read MoreWhat causes hyperemesis gravidarum? How is hyperemesis gravidarum treated? How do I find an HG doctor?
Read More22 Years of Helping Generations survive HG is made possible by the support of our community. Here at HER, we are ready for a BIG day in the nonprofit world:…
Read MoreThe third Thursday of every month from 12-1 PM/Central, the HER Foundation hosts an Online HG Support Group facilitated by licensed professional who are also HG survivors as a service to people with a current or prior diagnosis of hyperemesis gravidarum (HG). These groups are facilitated by volunteers Sarah Coffman and Elizabeth Lowder, HER Foundation Advisory Council members and HG survivors.
Read MoreThe HER Foundation continues the breakthroughs with publication of “Whole-exome sequencing uncovers new variants in GDF15 associated with hyperemesis gravidarum” in BJOG.
Read MoreIndividual response to Hyperemesis Gravidarum (HG) medication varies due to many factors including genetics and hydration. If a patient is vomiting constantly, oral dosing of medications will likely be ineffective and alternates such as sublingual, transdermal (patch/cream), subcutaneous (subQ), intravenous (IV), or other routes should be considered along with hydration.
Read More21 Years of Impact was made possible by the support of our community. And there is such hope for change. Don’t you feel it! Here at HER, we are ready…
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