Our pregnancy journey has been anything but easy. After years of battling infertility, multiple rounds of IVF, a heartbreaking miscarriage, and a failed transfer, we were finally blessed with our baby girl, Eden.
At just 11 weeks, we received devastating news—Eden had multiple abnormalities, including an omphalocele, cystic hygroma, and hypoplastic left heart syndrome (HLHS). From that moment on, our pregnancy was closely monitored. Midway through, the omphalocele and cystic hygroma resolved, allowing us to focus solely on her heart condition.
Due to PPROM, Eden arrived two months early on June 1st via emergency C-section. What I was told were Braxton Hicks contractions turned out to be the real thing. I felt immense pressure and told the medical team my body was telling me to push, though I knew she was breech and would require a C-section. I was only 32 weeks—our goal had been to make it to at least 34—but Eden had other plans.
I lost a significant amount of blood during delivery and nearly required a transfusion. I wasn’t able to see Eden for the first time until nine hours later. I knew we were facing a long and difficult road, but I never imagined it would end the way it did.
Being born prematurely only added to Eden’s already complex heart defect, as she needed to reach a certain weight to qualify for surgery. While we were aware of her HLHS prenatally, we did not learn until after her birth that she also had a congenital diaphragmatic hernia—adding a severe lung disorder on top of her heart condition.
Eden fought with everything she had. She met the milestones required to be considered for surgery, including the necessary weight, yet ultimately she was deemed not a surgical candidate due to the combined severity of her heart and lung conditions. Since surgery was not an option at our hospital, we sought second opinions from eight well-known children’s hospitals, desperately hoping someone would be willing to give her a chance. Every hospital declined. We were told her anatomy was too complex and her chances of survival were too low.
After 105 days, Eden went to her heavenly home. Throughout it all, we clung to our faith. She lived far longer than any medical professional believed she would, and every single moment with her was a miracle.
Eden’s life, though brief, is a testament to perseverance and faith—reminding us that miracles are not measured in the length of days, but in the purpose and love God weaves into each life, leaving an echo that continues to impact this world. Through her story, hearts have been opened to faith, lives have been changed, and systems have been transformed—from a soul coming to Christ, to a hospital implementing a dedicated cardiac NICU where one did not exist before. Eden has also woven together a new community of nurses and parents, and inspired the creation of a nonprofit in her honor—proof that even the shortest life can leave an enduring, world-changing legacy.
Our Story
Mission
At Edens Echo, our mission is to support families with children in the NICU by offering them spiritual and emotional guidance. We believe that every family deserves compassion during their most trying times. Our initiatives, including care packages and online Bible studies, are designed to build a supportive community that nurtures hope and healing.
We are committed to making a difference in the lives of families facing medical complexities. By providing resources and a listening ear, we strive to empower these families. Join us in our mission to extend love, support, and understanding to those who need it most.
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