Stories
Patient Stories
Finding his voice
Mason arrived 13 weeks early. At just two pounds, he was taken to OHSU Doernbecher's NICU — and the specialized care he received made all the difference.
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Patient Stories
Bringing visibility to a rare disease
Nevaeh was diagnosed with Alport Syndrome, a rare genetic disorder that causes kidney disease. Hear from Nevaeh about her experience at Doernbecher and her hopes for the future.
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Here for you
This holiday season, we celebrate you and the spirit of giving that makes a difference in people’s lives. We’ve gathered a few of the heartwarming, inspiring stories this past year made possible b...
Patient Stories
Where courage meets care
Penelope was born with a rare blood disorder. When complication after complication hit, her family turned to OHSU Doernbecher Children’s Hospital, who helped her family through a complex diagnosis.
Patient Stories
Powered up
Andrew was diagnosed with a brain tumor at 4. With care from OHSU Doernbecher Children's Hospital, Andrew is now a thriving fourth-grader who loves playing video games.
Patient Stories
Finding his voice
Mason arrived 13 weeks early. At just two pounds, he was taken to OHSU Doernbecher's NICU — and the specialized care he received made all the difference.
Patient Stories
Meet the Designers: Doernbecher Freestyle XVII
These remarkable young designers have each faced serious illness and now have the opportunity to inspire others and help kids at the same hospital that changed their lives. They are currently hard at ...
