The Children's Story Project features stories written by patients and families about how Children's Hospital has impacted their lives.
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Craig talks about what it's like to work at Children's and what's special about the Craniofacial Center.
Catherine talks about what it's like to work at Children's and what's special about the Craniofacial Center.
Daniel was born with part of his brain outside his skull. His face didn't look like other people's. At Seattle Children's, a team of craniofacial doctors and neurosurgeons sealed the opening to Daniel's brain to protect him from disease and injury. And as part of this very complicated procedure, they gave Daniel the face he should have been born with.
Cam talks about what it's like to work at Children's and what's special about the Craniofacial Center.
Carrie talks about what it's like to work at Children's and what's special about the Craniofacial Center.
Timothy talks about what it's like to work at Children's and what's special about the Craniofacial Center.
A National Institutes of Health (NIH) study led by Matthew Speltz, PhD, is following the mental development of 250 children with isolated craniosynostosis.
Children's leads the nation in caring for kids with craniosynostosis — from the delicate surgery needed to reshape a child's head to the research that will find new ways to treat and prevent this condition.
Dr. Michael Cunningham, medical director, Craniofacial Center, is honored with Children's Family Choice Award.
Jennifer talks about what it's like to work at Children's and what's special about the Craniofacial Center.
Marti talks about what it's like to work at Children's and what's special about the Craniofacial Center.
Craniofacial Center researchers are currently testing a new type of imaging system that promises to revolutionize the way we treat children and teens with craniofacial abnormalities.
Cassandra talks about what it's like to work at Children's and what's special about the Craniofacial Center.
Physician gathers the information needed to enhance a cleft palette and craniofacial service at his hospital in Ghana.
Dr. Cunningham talks about what it's like to work at Children's and what's special about the Craniofacial Center.
Bay talks about what it's like to work at Children's and what's special about the Craniofacial Center.
Kathrina has Marshall-Stickler syndrome, an extremely rare condition characterized by a flat face, enormous eyes and a skull too small for her developing brain. Watch her journey to have a surgery that could help solve some of her problems.
Follow craniofacial patient Brenna Johnston in her quest for a new face in the Seattle Times three-piece article.
Vivid images from 3-D scans give Children's doctors a powerful diagnostic tool.