22 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:…
The 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.
The HER Foundation continues the breakthroughs with publication of “Whole-exome sequencing uncovers new variants in GDF15 associated with hyperemesis gravidarum” in BJOG.
Individual 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.
21 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…
November is Prematurity Awareness Month. Hyperemesis Gravidarum (HG) is one of the leading causes of prematurity. 15% of HG pregnancies result in premature birth (a 4-fold increased risk) are more…
In honor of HG Awareness Month 2021, we are launching a new Patient Treatment Brochure and have expanded our HG treatment algorithm.
Hyperemesis gravidarum (HG) is characterized by severe and persistent nausea and vomiting during pregnancy. Even though not well understood, there are some signs that there is a relationship between HG…

