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Born with pyruvate dehydrogenase complex deficiency (PDCD), a rare and severe metabolic disorder, Carleigh is a fighter. Once unable to walk or communicate, she now greets each day with a smile.
After a rare autoimmune reaction left 2-year-old Lydia Grace unable to walk, Niswonger Children’s Hospital helped her return to her fearless self.
Compassionate emergency care at Niswonger Children’s Hospital helped Trenton return to football practice after a car accident.
Meet Boone and learn how care at Niswonger Children’s Hospital and ongoing therapy helped him grow from a tiny preemie into a joyful, thriving toddler.
Meet Emilee and learn how NICU care at Niswonger Children’s Hospital supported her and her family from a premature birth to milestones they once could only hope for.
Meet Caroline, Adah and Stetson and learn how care at Niswonger Children’s Hospital supported the triplets and their family through their NICU journey.
Read Jack’s story and see how pediatric orthopedic care at Niswonger Children’s Hospital helped this busy 2-year-old get back to playtime.
Meet Averie and learn how pediatric therapy at Niswonger Children’s Hospital helps her build strength, reach new milestones and let her big personality shine.
Meet Emberlyn and learn how cancer care at Niswonger Children’s Hospital gave her family hope and support throughout treatment and beyond.
Meet Eden and learn how her experience at Niswonger Children’s Hospital inspired her to give back and bring comfort to other children.
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Aiden was one of the statistics you see in the news. Born addicted to drugs his mother took while pregnant, he spent the beginning of his life in the NICU of Niswonger Children’s in a special unit for babies suffering from drug withdrawal.

Born via emergency C-section, he was brought to the Neonatal Intensive Care Unit (NICU) at Niswonger Children’s Hospital to be treated for infection and air outside of his lungs.

Finley has come a long way since he arrived three-and-a-half months early at only 12 inches long and so small that his dad’s wedding ring could fit around his wrist.

Kim didn’t expect to go into labor three months before her due date, which meant she would spend the rest of her pregnancy in the hospital. Of course, she didn’t expect her babies to be born two months early weighing less than 3 pounds, and she certainly didn’t expect to have a hysterectomy following a C-section.

7-year-old Beckett’s active life changed one night on a family camping trip. As Beckett leaned toward the campfire to roast a marshmallow, his chair tipped, propelling his body into the blazing fire pit. He ended up at Niswonger Children’s Hospital with third-degree burns on his knees and palm.

Bubbly, friendly Cleo is a true performer. She loves making people laugh and performing in pageants. But those were put on hold last year when she was diagnosed with type 1 diabetes a week before she turned five.

Raena has practiced karate since she was four, but late last summer, Raena had to put up her bō so she could concentrate on her health. A week before her 13th birthday, Raena’s parents, Michael and Crystal, noticed she had no energy, and she was diagnosed with leukemia.

At 2 years old, a terrifying seizure landed Gracie and her family in a series of specialist appointments looking for answers. She was diagnosed with neurofibromatosis, a genetic condition she inherited from her mother which causes tumors to grow in the body.

Since the day he was born, Edgar never got sick beyond an occasional cold. Then, a few weeks before his sixth birthday, he developed a nasty cough. His mother, Leonor, took him to Niswonger Children’s Hospital Emergency Department.

At just eight months old, Waylon was brought unresponsive to the Niswonger Children’s Hospital emergency department. He had suffered a severe traumatic brain injury from being violently shaken.

She was born with neonatal abstinence syndrome (NAS), addicted to five substances, including meth and cocaine. She received no prenatal care and after birth, spent 10 days in the neonatal intensive care unit before being released.

Ridge loves playing outdoors, chasing animals on his family’s farm and… breakdancing. But three years ago, when a stubborn fever slowed him down, his mother, Shea, knew something wasn’t right.

Avianca’s first symptoms were large, “angry purple” bruises, which she calls “purpuras.” They looked alarming enough that Avianca’s parents, Frik and Elizabeth, took her to urgent care, where they were immediately sent to Niswonger Children’s Hospital.

In January 2017, 5-year-old Ellee's journey started with excruciating leg pain and a visit to Niswonger Children’s Hospital’s emergency room. Within a few hours, she was admitted and diagnosed with acute lymphoblastic leukemia, then flown to Memphis two days later.

Named after her great grandmother, Arimina (Air-ah-mine-ah) is a little girl who is as special — and as strong — as her name, which means “soldier.” Born with Down syndrome and now diagnosed with acute lymphoblastic leukemia, Arimina and her family have bravely faced some tough times.