It was International Women’s Day 2023 when I found out the gender of my third child – a girl. We already had two daughters, a 3-year-old and a 21-month-old. We…
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When the Doctor Becomes the Patient Severe hyperemesis gravidarum (HG) requiring hospitalization typically occurs in up to 3% of pregnancies. But sadly, there is still a lack of knowledge regarding…
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In May 2018, my husband and I finally received a positive pregnancy test result. We were thrilled and decided to wait until Mother’s Day to tell our parents. However, my…
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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.
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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!
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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.
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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.
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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.
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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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