Eli’s body was full of cancer. Now he’s full of life.
At age 2, Eli faced a cancer almost never seen in kids that age. Fortunately, his team at Doernbecher was ready to meet the challenge.
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.
December 21, 2021Read More
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.
November 17, 2021Read More