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.
What is the best treatment for hyperemesis gravidarum? How do you treat hyperemesis at home What is the first line treatment for hyperemesis gravidarum? What are the drugs of choice for hyperemesis gravidarum?
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.
My name is Sally. I have three children: Rachel (born 1988), Timothy (born 1991), and Emilia (born 1997). I suffered from HG with all three pregnancies, before the HER Foundation began.
I’m pregnant with my second baby right now. My first pregnancy was a healthy, and I wasn’t expecting Hyperemesis Gravidarum (HG) at all!
