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.
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.
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.
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.
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.
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.
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.
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.
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!
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.
