A Mother’s Quest to Help Her Son Hear
A cochlear implant helps a child with single-sided deafness.
Clinical Trials, Ear, Nose, and Throat, Health, Hearing, UNC Children's, UNC Stories
Stories
Read stories about families who have battled through illnesses, doctors who have gone above the call of duty, and more — because their stories are your stories, too.
Challenges and Hope for Girls and Women with Turner Syndrome
This chromosomal condition causes short stature and a lack of ovarian development.
Children's Health, Endocrinology, Health, Pediatric Medicine, UNC Stories
Treatment Brings Hope to Children Facing Spinal Muscular Atrophy, a...
Neurologists can treat spinal muscular atrophy with a new and powerful drug.
Children's Health, Neurology, Pediatric Medicine, UNC Stories
UNC Doctors Come Together to Treat Infant with Rare Heart Condition
Georgia Mae Braddy is, without doubt, a fighter. At four months old, she has already undergone three major surgeries, one of which took place while she was still in utero.
One Couple’s Journey with Primary Progressive Aphasia
This neurocognitive disorder that interferes with language abilities has changed the lives of Russell Flowers and his wife, Mary Jo.
One Man’s Experience with Scoliosis, and a Surgical Solution
Correction surgery helped repair an 80-degree spinal curve.
AED Saves Teenager’s Life After Cardiac Arrest
An unexpected collapse highlights the importance of automated external defibrillators in public places.
Kenan Scholars Story: Henderson
UNC Health Care is committed to expanding the number of primary care physicians who serve in rural and underserved areas in North Carolina. To that end, the Kenan Primary Care Medical Scholars Program gives medical students an opportunity to complete a six-week summer internship at a rural health care clinic. Each student works with a…
Kenan Scholars Story: Surf City
Six-week internship gives medical students a chance to learn and serve in rural, underserved areas.
A Long Journey for a Child with Rare Pediatric Cancer
For Sebastian and his family, no distance was too great to find treatment.
Growing Up with a Rare Disease
Avery Dixon is like any 10-year-old—except she’s living with arthrogryposis multiplex congenita and its complications.