A Rare Genetic Diagnosis Gives Arturo’s Family Answers—and Hope
Stanford Children’s experts combine advanced genetic testing and rare-disease expertise to guide care for MED13-related disorder.
Posts By
Ada Preda
From Hawaiʻi to Stanford Children’s: Henaʻi’s Journey to a Brighter Future
Henaʻi received a lifesaving procedure and specialized care at Stanford Children’s after being diagnosed with tetralogy of Fallot.
An IBD Journey to Remission: Leo’s Journey Back to Childhood
Child with very early onset IBD achieves remission with the help of Stanford Medicine Children’s Health IBD experts.
Rivers’ Journey With Celiac Disease: From Diagnosis to Resilience
Child with celiac disease embraces a healthier, happier life thanks to Stanford Medicine Children’s Health celiac disease experts.
Small Baby With PDA Thrives After Having a Constellation of Symptoms at Just 6 Days Old
How Stanford Medicine Children’s Health turned challenges into triumphs for a newborn with heart defects.
