1 in 3 HG pregnancies ends in loss. Whether your loss is due to miscarriage, termination, stillbirth, or neonatal, HER is here for you. Pregnancy and Infant Loss Remembrance Day honors the babies we hold in our hearts.
September is Sepsis Awareness Month. According to the CDC, 13.9% of maternal deaths between 2016-2018 were caused by infection or sepsis. HG puts patients at higher risk due to reduced…
22 years of Helping Generations survive HG! From 2000 to 2022, we have been building a healthier future for the next generation! Our research, support, advocacy, and education resources have reached over 2,200,000 people across the globe.
Join the celebration throughout October!
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:…
Hyperemesis Gravidarum (HG) as a disease manifests itself in different levels of severity and is not the same for every woman. Understanding the range of different experiences helps with understanding what HG is. Regardless of whether HG is mild, moderate, or severe, the mother is miserable and misses out on the joy of a healthy pregnancy.
Each year, the World Alliance for Breastfeeding Action promotes World Breast Feeding Week from August 1-7. The 2022 theme is Step up for Breastfeeding: Educate and Support. While there are benefits for breastfeeding, not all HG survivors are able to breastfeed.
The HER Foundation has partnered with ASPEN, the American Society for Parenteral and Enteral Nutrition, for ASPEN Malnutrition Awareness Week TM (MAW) on September 19-23, 2022. For more information and…
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.
I was never diagnosed with HG because of the lack of education and knowledge regarding the illness. As a result, I experienced prenatal and postnatal depression and delivered prematurely.
The HER Foundation is helping a second generation facing Hyperemesis Gravidarum (HG). If your mother have hyperemesis gravidarum (HG) when pregnant with you or siblings, we want to talk.
