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An Iowa family has recently celebrated a significant milestone for their remarkable son, Nash Keen.
Mollie and Randall Keen welcomed Nash on July 5, 2024. He entered the world a staggering 133 days ahead of schedule, born at just 21 weeks of gestation.
Nash has officially been recognized by Guinness World Records as the most premature baby to survive.
Earlier this month, Nash, affectionately nicknamed “Nash Potato,” turned 1 year old, and his survival story is a testament to resilience and hope.
At his birth in the University of Iowa Health Care Stead Family Children’s Hospital, Nash weighed a mere 285 grams, which is less than 10 ounces, and measured only 24 centimeters long. This information was provided in a press release from the hospital.
Two years before Nash’s birth, the Keens experienced the heartbreaking loss of their baby girl, McKinley, who passed away at 18 weeks of gestation. This tragic event deeply impacted the family.
Mollie Keen had been diagnosed with an incompetent cervix, a condition where the lower part of the cervix begins to open prematurely, typically during the second trimester. Additionally, she has polycystic ovary syndrome, a hormonal disorder that often complicates fertility efforts.
Just six months after their loss, the Keens discovered they were expecting again. During a 20-week ultrasound, Mollie expressed concerns regarding her health, prompting the doctors to examine her more closely. They found that she was already 2 centimeters dilated.
A few days later, labor began, and Mollie was placed on strict bed rest.
Reflecting on those anxious moments, Mollie said, “We were devastated. We thought we were going through the exact same situation, fearing we would lose this baby as well.”
The medical team at Stead Family Children’s Hospital specializes in providing life-saving care for infants born at 21 weeks gestation and beyond. Fortunately for Nash, his medical team managed to delay labor until just after he surpassed the critical 21-week mark.
Dr. Malinda Schaefer, the high-risk obstetrician who delivered Nash, stated, “We prioritize our patients’ best interests and strive to convey our uncertainty regarding outcomes for such extremely premature births.”
She emphasized that survival rates for infants born at this stage are generally low, and even for those who survive, there is a significant risk of long-term complications, even at just 22 weeks.
As soon as Nash was born, the team delivered essential medications to support his organ development and minimize the likelihood of complications.
Dr. Amy Stanford, a neonatologist who treated Nash, remarked on the size challenges associated with extreme prematurity, noting, “Sometimes, babies born at 21 weeks are simply too small for our tiniest breathing tubes and intravenous lines.”
After successfully placing a breathing tube, Nash’s heart rate stabilized, along with his oxygen levels, providing a glimmer of hope to his anxious parents.
Despite this encouraging moment, the reality remained stark; no baby born at such an early stage had ever survived before Nash. Prior to his birth, the record for the most premature infant to survive was held by Curtis Zy-Keith Means, born to Michelle Butler on July 5, 2020, at the University of Alabama at Birmingham Hospital, just 132 days early.
Dr. Patrick McNamara, division director of neonatology at Stead Family Children’s Hospital, conveyed the delicate balance between hope and reality for families facing such scenarios. He stated, “We never want parents to lose hope, but we must be realistic about the situation, as these decisions are challenging for everyone involved.”
At the one-month mark, the medical team began to feel a sense of cautious optimism about Nash’s fate. Dr. Stanford explained, “This was a pivotal moment, transforming our perspective from daily survival to pursuing long-term health goals for Nash.”
During Nash’s 198-day hospital stay, the healthcare team continuously monitored his heart function and brain health. In addition to numerous medications, Nash underwent surgery for a perforated bowel, an unfortunate condition with a high mortality rate.
Randall Keen commented on the care they received, stating, “They supported him through every step and provided us with clarity throughout this journey, ensuring we were well-informed regarding every decision.”
Finally, after over six months in the NICU, Nash came home in January 2025. The journey may have been laborious, but it laid the foundation for a new chapter in the family’s life. Nash will continue to be monitored for health issues, including a minor heart defect. He is currently undergoing oxygen weaning and is still reliant on a feeding tube and hearing aids.
While he has experienced some developmental delays, his mother reported that Nash is growing stronger and becoming increasingly interactive thanks to ongoing therapy sessions.
Dr. Stanford expressed her aspirations for Nash’s future, stating, “My ultimate hope is that by the time he turns five and begins kindergarten, no one will realize he was born so prematurely.”
Mollie Keen emphasized the importance of love and support in Nash’s life, saying, “I want him to know how deeply loved he is and the countless individuals who have cheered him on since day one.”
She added, “I wish for him to grow up healthy, happy, and confident in his identity, viewing his incredible story as a source of strength.”