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!
My doctor said I could afford to lose weight with being fat. The mental struggle of watching my body deteriorate and wondering if me or my baby would die was traumatic.
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…
The HER Foundation is thankful for our business partners who support our mission.
HER Board members, Marlena Fejzo, PhD, and Patrick Mullen, MD, are running the first study of GDF15 in HG patients in the United States.
We created this tool to help guide HG patients through the steps of self advocacy.
Hyperemesis Gravidarum (HG) is a risk factor for premature birth. On Prematurity Awareness Day, meet Crew and Tru.
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…
