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Children's Story Project 

Children's Story Project

The Children's Story Project features stories written by patients and families about how Seattle Children's has impacted their lives.
Featured: Riley's story
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Sharing Expertise in Africa 

Sharing Expertise in Africa

Seattle Children’s team approach to treating craniofacial defects leads to an alliance with doctors in Africa that will improve how cleft lip and palate are treated in sub-Saharan nations.

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Q&A with Craig Birgfeld, MD 

Q-and-A with Craig Birgfeld, MD

Dr. Birgfeld talks about what it's like to work at Children's and what's special about the Craniofacial Center.

Read the full story 

 
Q&A with Catherine Rogers, MA, Craniofacial Family Liaison 

Q-and-A with Catherine Rogers, MA, Craniofacial Family Liaison

Catherine talks about what it's like to work at Children's and what's special about the Craniofacial Center.

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Daniel's Story: Craniofacial and Neurosurgery 

Daniel's Story: Craniofacial and Neurosurgery

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.

Watch the video 

 
Q&A with Cam Lanier, RD, Clinical Dietitian 

Q-and-A with Cam Lanier, RD, Clinical Dietitian

Cam talks about what it's like to work at Children's and what's special about the Craniofacial Center.

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Q&A with Carrie Heike, MD 

Q-and-A with Carrie Heike, MD

Dr. Heike talks about what it's like to work at Children's and what's special about the Craniofacial Center.

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Q&A with Timothy Cox, PhD 

Q-and-A with Timothy Cox, PhD

Dr. Cox talks about what it's like to work at Children's and what's special about the Craniofacial Center.

Read the full story 

 
Researching the Impact of Isolated Craniosynostosis 

Researching the Impact of Isolated Craniosynostosis

A National Institutes of Health (NIH) study led by Matthew Speltz, PhD, is following the mental development of 250 children with isolated craniosynostosis.

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Return to Form: Treating Craniosynostosis 

Return to Form: Treating 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.

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Part of the Team: Patient and Family Involvement Comes First at the Craniofacial Center 

Part of the Team: Patient and Family Involvement Comes First at the Craniofacial Center

Dr. Michael Cunningham, medical director of the Craniofacial Center, is honored with Children's Family Choice Award.

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Q&A with Jennifer MacKinnon, Patient Care Coordinator 

Q-and-A with Jennifer MacKinnon, Patient Care Coordinator

Jennifer talks about what it's like to work at Children's and what's special about the Craniofacial Center.

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Q&A with Marti Davis, Program Assistant 

Q-and-A with Marti Davis, Program Assistant

Marti talks about what it's like to work at Children's and what's special about the Craniofacial Center.

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3D Images Help Team Chart Mysteries of the Face 

3-D Images Help Team Chart Mysteries of the Face

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.

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Q&A with Cassandra Aspinall, Craniofacial Social Worker 

Q-and-A with Cassandra Aspinall, Craniofacial Social Worker

Cassandra talks about what it's like to work at Children's and what's special about the Craniofacial Center.

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Integrated Care Impresses Visiting Physician 

Integrated Care Impresses Visiting Physician

A physician gathers the information needed to enhance the cleft palate and craniofacial service at his hospital in Ghana.

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Q&A with Dr. Michael Cunningham, Craniofacial Center Director 

Q-and-A with Dr. Michael Cunningham, Craniofacial Center Director

Dr. Cunningham talks about what it's like to work at Children's and what's special about the Craniofacial Center.

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Q&A with Bay Sittler, Craniofacial Nurse Practitioner 

Q-and-A with Bay Sittler, Craniofacial Nurse Practitioner

Bay talks about what it's like to work at Children's and what's special about the Craniofacial Center.

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A Crown for Kathrina: A Children's Healthlink Special 

A Crown for Kathrina: A Children's Healthlink Special

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.

Watch the video: parts 12345, and 6 

 
The Seattle Times: The Girl in the Mirror 

The Girl in the Mirror

Follow craniofacial patient Brenna Johnston in her quest for a new face in this three-part article in The Seattle Times.

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Picture Perfect 

Picture Perfect

Vivid images from 3-D scans give Children's doctors a powerful diagnostic tool.

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For the first time 

For the First Time

Witness what happens when Seattle Children’s doctors give kids - and their families - a chance to experience life’s simple joys, including a 7-year-old boy undergoing facial reconstructive surgery to help him smile for the first time in his life.

Watch video 

 

Find a Doctor or Researcher

Find a Doctor or Researcher

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