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…
Read MoreJust in time for the holidays!!! We partnered with The Hearts of Gold to create a limited number of beautiful sterling silver logo necklaces with an amethyst stone to honor…
Read More21 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!
Read MoreThe HER Foundation is thankful for our business partners who support our mission.
Read MoreHER Board members, Marlena Fejzo, PhD, and Patrick Mullen, MD, are running the first study of GDF15 in HG patients in the United States.
Read MoreWe created this tool to help guide HG patients through the steps of self advocacy.
Read MoreHyperemesis Gravidarum (HG) is a risk factor for premature birth. On Prematurity Awareness Day, meet Crew and Tru.
Read MoreJoin 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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