Whether the loss is miscarriage, termination, stillbirth, or neonatal, we remember the babies we hold in our hearts. Pregnancy and Infant Loss Awareness Month honors our lost little ones. We…
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:…
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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.
Read MoreAs a service to moms with a current or prior diagnosis of HG, the HER Foundation hosts free, online support groups via Zoom on the third Thursday of the month…
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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?
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What is the best treatment for hyperemesis gravidarum? What is the cause of hyperemesis gravidarum? What is hyperemesis gravidarum and how is it treated? Is hyperemesis a high risk pregnancy? How do you relieve hyperemesis gravidarum?
Read MoreAs a service to moms with a current or prior diagnosis of HG, the HER Foundation hosts free, online support groups via Zoom on the third Thursday of the month…
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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.
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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.
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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.
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