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.
Read More
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.
Read More
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.
Read More
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.
Read More
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.
Read More
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.
Read More
Hyperemesis gravidarum (HG) does not look the same for every patient. Learn about the severity levels.
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…
Read More
We frequently receive questions about why HG patients need more thiamin than their healthy counterparts. A pregnant Hyperemesis Gravidarum (HG) patient cannot eat a nutrient rich diet and may not be able to eat at all. A healthy pregnant patient can eat a nutrient rich diet that includes a variety of foods.
Read More