Division of Nephrology Patient Stories

A seemingly routine illness led doctors to discover Peyton’s primary hyperoxaluria diagnosis. Alongside CHOP, she’s pushing through treatment to keep playing softball.

When 6-year-old Cora began experiencing blood in her urine, her family turned to Children’s Hospital of Philadelphia and found answers and a care team they could trust.

With expert guidance and support from the Glomerular Disease Clinic at Children’s Hospital of Philadelphia, Aviva’s rare kidney disease is under control.

Colton faced overwhelming odds from birth, but with resilience, family support, and CHOP’s dedicated care, he’s overcoming ARPKD and thriving through new initiatives.

After a year of being misdiagnosed, Alexander’s parents found answers and a team they could trust at CHOP to manage his condition and prevent recurrent kidney stones.

Isaiah was born with congenital nephrotic syndrome, the same genetic mutation that caused his older brother to die in infancy. Isaiah’s improved experience and outcome showcases how multiple departments at CHOP work together to ensure the best patient and family care. 

When Carolyn was 28 weeks pregnant with her third child and her doctor in New York discovered that her baby carried the gene for autosomal dominant polycystic kidney disease (ADPKD), she became dedicated to changing the historical lack of pediatric research on the rare disease.

After Molly qualified for a kidney transplant, a new organ from a living donor was identified thanks to CHOP’s involvement with the National Kidney Registry.

3 year old Nolan’s leg pain and swelling of his eyes and stomach led to a diagnosis of nephrotic syndrome, now managed by immunosuppression.

Innovative care for Chloe’s kidney stones is closer than ever at CHOP’s new hospital in King of Prussia.