Share Your HG Story With Us!
We'd love to hear your story and share it with our community! Please take a moment to fill out our survey.
If you have any pictures you'd like to include, feel free to email them to us at story @ hyperemesis.org.
We appreciate your contribution to spreading awareness. Thank you for sharing your story with us!
Tiffany Shares #HERstory
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 and Maxwell on HG and Prematurity
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.
HG Impact: Sabrina
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.
HG Impact: choose your words carefully
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.
HG Impact: Sally
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.
HG Impact: Maria and Her Family
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.
HG Impact: Liz
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!
HG Impact: Shola
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.
Why we do what we do!
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.
Yasemin’s HG Truths
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.
