New Option for Treacher Collins Syndrome

New Option for Treacher Collins Syndrome

Learn how a revolutionary surgery helped Hannah breathe without a tracheostomy for the first time.

Read Hannah’s story.

Doctors Create a Jaw for Little Girl Born Without One

Doctors Create a Jaw for Little Girl Born Without One

Using a process called distraction osteogenesis, our craniofacial team created a jaw for Lexi. Now she can breathe without a breathing tube. “Things like taking a bath were life-threatening before the surgery. Now she’s taking swim lessons,” says her mom.

Read Lexi’s story.

Predicting Learning Deficits in Kids with Craniosynostosis

Predicting Learning Deficits in Kids with Craniosynostosis

Learning deficits have never been an issue for Olivia. But some kids with single-suture craniosynostosis do have problems. Olivia took part in research at Seattle Children’s that could help better predict which children are at higher risk.

Read the full story.

A Family Approach to Craniofacial Care

A Family Approach to Craniofacial Care

Genesis is a fun-loving girl who was born with cleft lip and palate – the most common condition we treat at Seattle Children’s. Grayson’s family had a different challenge at their son’s birth:

Read how our Craniofacial team cared for these children and their whole family.

Lyla Gets Back in the Game After Orbital Fracture

Lyla Gets Back in the Game After Orbital Fracture

After a pop fly smashed Lyla’s eye socket, Seattle Children’s surgeons made a quick repair. The surgery protected her sight and let her return to the softball field that season.

Read Lyla’s story.

Boy Gets Smile for His 12th Birthday

Boy Gets Smile for His 12th Birthday

For his entire life, this playful Dallas boy who loves video games and LEGO bricks could not move his face muscles to smile. That changed in time for Christian’s 12th birthday, with help from facial reanimation surgeons at Seattle Children’s.

Read how Christian got his smile.

Beyond Face Value: Natalie Learns to Embrace Herself

Beyond Face Value: Natalie Learns to Embrace Herself

Through work with her care team, Natalie has gained confidence and self-acceptance. She has a powerful message for others: – “It’s OK to be different.”

Read Natalie’s story.

Family Shares Journey With Sagittal Craniosynostosis

Family Shares Journey with Sagittal Craniosynostosis

A family shares their journey through sagittal craniosynostosis treatment at Seattle Children’'s. They also have some tips for other families facing this challenge.

Watch the video.

Better Breathing and a Better Look for Kids with Apert Syndrome

Better Breathing and a Better Look for Kids with Apert Syndrome

A surgical approach developed at Seattle Children’s treats symptoms of Apert syndrome more effectively, including the “look” of the syndrome. As a result, children have the chance to have a more normal face and head.

Learn how this surgery helped James.

Craniofacial Microsomia: A Boy Transformed After Surgery

Craniofacial Microsomia: A Boy Transformed After Surgery

Being born with craniofacial microsomia gave Mavrick a jaw so small he had to use a feeding tube. This hockey player from Alaska considers each surgery at Seattle Children’s “one more step closer” to his goal of eating pizza.

Read how surgery and distraction osteogenesis helped Mavrick grow a bigger jaw. Watch the video.

Cleft Lip and Palate Surgery for Danielle

Cleft Lip and Palate Surgery for Danielle

Danielle Landis’ story started before birth, when she was diagnosed with cleft lip and palate during a pregnancy ultrasound. Using entries from months of blog posts and family photos, Danielle’s mother narrates a compelling slideshow.

Watch Danielle’s story.

A Smile to Match the Boy Inside

A Smile to Match the Boy Inside

A Yakima boy smiles for the first time, with help from facial reanimation surgeons at Seattle Children’s.

Watch Jhonatan get his smile.