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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 ...

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