Our team recently had the opportunity to attend the CREOG/APGO conference. We aimed to raise awareness and share valuable insights about Hyperemesis Gravidarum (HG) with obstetricians (OBs), residents, program directors,…
National Geographic mentioned the HER Foundation and its board members, Kimber MacGibbon, RN, Dr. Marlena Fejzo, and Dr. Aimee Brecht-Doscher, in their article, “We finally know the cause of severe…
November 17th is Prematurity Awareness Day. Hyperemesis Gravidarum (HG) is one of the leading causes of prematurity and results in babies that are small for gestational age and growth restricted.…
Celebrate Giving Tuesday with Us! Here at HER, we are ready for a BIG day in the nonprofit world: Giving Tuesday, November 28, 2023. Giving Tuesday is the largest giving…
November is Prematurity Awareness Month. Hyperemesis Gravidarum (HG) is one of the leading causes of prematurity and results in babies that are small for gestational age and growth restricted. Support…
Join the #HERDanceParty! Dance, Invite, and Donate to improve HG care through research and education.
May 15th is International HG Awareness Day and HG Reality. You can help the HER Foundation raise awareness and educate about your HG Reality!
The HER Foundation has accomplished a lot in 2022! We are thankful for the support of our donors and community and want to share the highlights that made this HER’s best year yet! This is what 22 years of Helping Generations survive Hyperemesis Gravidarum (HG) looks like.
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.
