A Wavy Line to Wellness: Liam’s Journey
Two rare diseases lead to an unexpected genetic diagnosis of primary ciliary dyskinesia for a little boy at Children’s Hospital of Philadelphia.
No matter your child's specific needs, our team of pediatric pulmonology and sleep experts is here to provide the best possible care.
Two rare diseases lead to an unexpected genetic diagnosis of primary ciliary dyskinesia for a little boy at Children’s Hospital of Philadelphia.
Ada, 6, was healthy when she was born. She hit her early milestones with ease. As soon as Ada turned one, however, her health suddenly took a turn for the worse.
After being diagnosed with a rare type of tumor in her airway, Peyton came to CHOP for surgery that successfully saved part of her right lung.
Bennett’s breathing easy after the tumor blocking his lung was removed not with surgery, but with cutting-edge techniques, treatments and trial medication.
Born at 26 weeks, Leila’s lungs failed to develop. Specialty care during her CHOP stay and after helped her breathe on her own and her family cope.
CHOP’s diagnosis and treatment of a rare lung disease solved a medical mystery for Jacob. Shared care with his Virginia pulmonologist is keeping him healthy.
From Chicago to Philadelphia: Parents of ailing teen go the distance for CHOP pulmonologist’s unique expertise.
Lucy was born with small lungs and critical breathing challenges. The care she received at CHOP prepared her to go home with minimal breathing support.
While doctors at CHOP helped Ethan’s premature lungs develop, other staff helped his family manage the stress of having a sick newborn.
From Day 1, June was breathing too rapidly. The Rare Lung Diseases Center diagnosed her condition: pulmonary interstitial glycogenosis. June was lucky; her mild case resolved on its own.