It Takes a Village: Rallying Support to Cure Food Allergies
Nine years ago, David and Kori Shaw moved to Palo Alto with their 3-year-old daughter, Keegan, and 1-year-old son, Carter. Along with the usual adjustments of relocating—new job for dad, new...
Food allergies are a peculiar disease. Unlike other life-threatening conditions, the people they affect are completely healthy unless they are exposed to the allergen. They and their families live a...
There was something wrong with Joshua Copen’s hearing. No matter how many times doctors told Iara Peng, Joshua’s mother, that her baby with Down syndrome had normal hearing, she knew they were wrong...
Tierra Bergh, a busy mom of five, still vividly recalls this moment from nine years ago: “Maleki woke up, looked at me, and asked why we were in the hospital.” Her son Maleki, then 3 years old, had...
Guest blogger: Sophie HeerinckxWednesday, February 18, 2015
You are Our Sunshine
This month, our very own Philip Sunshine, MD, emeritus professor of pediatrics, will be honored as a 2015 “Legend of Neonatology” at an awards gala in Orlando. Called “one of the originals” in...
Brittany Lothe, mother to a NICU graduate, and co-founder of Will’s Way Foundation Tuesday, November 18, 2014
A Mom’s Viewpoint: Where There’s a Will, There’s a Way
On the day of Will’s birth, 1s were running wild. He was born in the 1 o’clock hour, on the 1st month of the year, on the 11th day of the month. He weighed a mere 1 pound, 11 ounces. Will was born...
Everything about Elizabeth Rodriguez-Garcia’s pregnancy had been perfectly normal. She’d had morning sickness on occasion and felt a little tired some days, but at 25 weeks, the only real news she...
Wednesday, Oct. 8, represents a milestone in the history of pediatric heart transplantation. That’s because Lizzy Craze, 32, hasn’t needed replacement of the donor heart during the 30 years it’s been...
Child Life Specialists Help Patients Cope and Thrive
On a recent Tuesday, 9-year-old Sarah Grace sat on a hospital bed in a bright pink Minnie Mouse gown, waiting for a CT scan. This wasn’t Sarah Grace’s first scan, but it would be her first without...
‘Heal EB’ and Eddie and Jill Vedder help fund treatments for children with life-threatening skin disorder
In another step toward the possible development of a cure for Epidermolysis Bullosa (EB), a rare and life-threatening genetic skin disorder, the Southern California-based non-profit Heal EB, www...
