Along with good medical care, surviving Hyperemesis Gravidarum (HG) means finding others who understand. Here are some ways to make connections. Facebook Support Groups The HER Foundation offers multiple support…
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21 Years of Hyperemesis Gravidarum (HG) Impact was made possible by the support of our amazing community. And there is such hope for change. Don’t you feel it! Here at HER, we are ready for a BIG day in the nonprofit world: Giving Tuesday, November 30, 2021. Giving Tuesday (GT) is the largest giving day of the year, and we want to make this year’s GT our best yet!
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HER Board members, Marlena Fejzo, PhD, and Patrick Mullen, MD, are running the first study of GDF15 in HG patients in the United States.
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Hyperemesis Gravidarum (HG) is a risk factor for premature birth. On Prematurity Awareness Day, meet Crew and Tru.
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Join us in honoring Maria and her twins on Thursday, November 25th. Maria’s voice was silenced due to preventable complications of Hyperemesis Gravidarum (HG), and we all must be a voice for her. No mother should be silenced by HG!
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In HER Words: Thank you for sharing your Hyperemesis Gravidarum (HG) journey. I had baby fever. I wanted a baby so bad it hurt. I was jealous of others who were…
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We have a special treat for you! LIMITED EDITION premium Yeti cups with the HER Ribbon or 1 MOM is 2 Many™ logo, so you can share your HG story…
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At the end of November 2020, I found out I was pregnant with our third child. The day after my doctor called me to confirm I was indeed pregnant, the…
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