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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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.
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Thiamin (or thiamine) is another name for vitamin B1. It is a water-soluble, nontoxic B vitamin that is depleted within 2 weeks of not eating normally. Potentially life-threatening complications can develop for mom and baby if depleted.
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Hospitalized with a central line, TPN feeding tubes, and multiple medications at 4 weeks, the damage had begun. Four specialists said her liver would fail if she continued her pregnancy, she terminated her much wanted IVF pregnancy.
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Help us spread awareness by showing your #HGstyle everywhere you go! The Hearts of Gold gives back 10% of proceeds for this bracelet to HER Foundation.
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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.
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Thankful! Thankful is what I am. My babies and I survived Hyperemesis Gravidarum only because of the amazing support we received from the HER Foundation.
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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!
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