The HER Foundation’s staff, clinicians and referral coordinator volunteer many hours each year to respond to thousands of emails, messages, and calls for help with Hyperemesis Gravidarum (HG). This is core to our mission, and we want to share why we want to expand this service. Enjoy these heartwarming messages and stories.
The HER Foundation’s breakthrough psychosocial study shows that Hyperemesis Gravidarum (HG) is not self limiting and has societal implications.
We put together this list of highlights from 2021! These are some of the people, the work, and the campaigns that made this HER’s best year yet! We are making Hyperemesis Gravidarum (HG) progress!
The HER Foundation is thankful for our business partners who support our mission.
We created this tool to help guide HG patients through the steps of self advocacy.
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…
Marlena Fejzo, PhD, HER Board Member and Research Advisor, presents at the American Society of Human Genetics Annual Meeting on the genetics of Hyperemesis Gravidarum (HG).
The Champions for Change Summit is dedicated to empowering our community with the education, training, and resources needed to make necessary changes in maternal health, hosted by MoMMA’s Voices. This…
21 years of Help & Hope! From 2000 to 2021, we have been building a healthier future for the next generation! We have offered research, support, advocacy, and education resources…
November is Prematurity Awareness Month. Hyperemesis Gravidarum (HG) is one of the leading causes of prematurity. 15% of HG pregnancies result in premature birth (a 4-fold increased risk) are more…
