“If I wasn’t pregnant, nurses and doctors would treat this like a real problem and not something I just need to nibble my way through,” says Kristina. Hyperemesis Gravidarum must be recognized and treated to improve outcomes.
Read More about Kristina’s HG RealityOn my first Mother’s Day, I commemorated my suffering of 271 days by photographing you, my child, with 1/4 of the medications I had to take to function at barely 50%. I love you kid: your bright eyes, gummy smile, and nonsensical chatter. Thank you for making me a mother.
Read More about Amrita’s Hyperemesis Gravidarum RealityHG robs women of the joy of a healthy pregnancy, and HG robs families of a mom, a sister, and wife. HG destroys society with the expense and burden of caring for someone.
Read More about Vanessa’s HG Reality and LossI knew nearly nothing about hyperemesis, even after my ER diagnosis. The HER website helped educate me about symptoms and how to approach medical professionals. HER helped alleviate some concerns about medications.
Read More about Hannah’s #HGrealityBefore discovering the HER Foundation, I felt alone and like something was wrong. After discovering a community and support, I knew I wasn’t alone. HER brings together HG sufferers and supports them.
Read More about Danielle’s HG JourneyHG isn’t the price to be paid for a healthy baby. It doesn’t have to happen in order for pregnancy to be viable, so it doesn’t have to be “worth it.”
Read More about Words That Trigger in the HG CommunityWe 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.
Read More about Queeneth Shares a Beautiful Message of ThanksThe 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.
Read More about Tala Shares #HERstoryMy 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.
Read More about Tiffany Shares #HERstoryCandace 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 More about Candace Renee and Maxwell on HG and Prematurity
