My entire pregnancy was traumatic, and I still suffer from PTSD due to HG. My son is now 3 years old, and we are all happy, healthy, and thriving. My husband and I made the decision early on that our son would be our one and only.
Read More
Candace Renee, Maxwell’s mom, TV Personality, Actress, and Host and star on Floribama Shore talks with HER about Hyperemesis Gravidarum (HG) and her son’s premature birth.
Read More22 years of Helping Generations survive HG! From 2000 to 2022, we have been building a healthier future for the next generation! Our research, support, advocacy, and education resources have reached over 2,200,000 people across the globe.
Join the celebration throughout October!
Read More
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 has been making HG history since 2000. In honor of Women’s History Month, we introduce the four women who have been with HER since the beginning.
Read More
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.
Read More
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 More
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…
Read MoreThe 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…
Read More21 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…
Read More