We are glad to inform you of the arrival of our son. He was born weighing 7 pounds and 3 ounces. While we are most grateful to God, we are particularly very thankful and appreciative of all of the support the HER Foundation gave us.
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The HER Foundation educated me on the website and social media, and I used the HG Care app. When I was scared to take Zofran, they sent me the lastest research. HER understands, and I didn’t feel alone. One day, they will find a cure.
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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.
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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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Hospitalized with a central line, TPN feeding tubes, and multiple medications at 4 weeks, the damage had begun. Four specialists said her liver would fail if she continued her pregnancy, she terminated her much wanted IVF pregnancy.
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My name is Sally. I have three children: Rachel (born 1988), Timothy (born 1991), and Emilia (born 1997). I suffered from HG with all three pregnancies, before the HER Foundation began.
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Thankful! Thankful is what I am. My babies and I survived Hyperemesis Gravidarum only because of the amazing support we received from the HER Foundation.
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I’m pregnant with my second baby right now. My first pregnancy was a healthy, and I wasn’t expecting Hyperemesis Gravidarum (HG) at all!
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I felt depressed a lot because I was dealing with my sickness by myself, but I was able to find an online support system through the HER Foundation and meet other women experiencing the same difficulties. I did not feel alone.
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