Posted on July 08, 2021
Liliana was diagnosed after birth with a rare condition that affects about 1 out of every 10,000 live births, with medical complexities mainly affecting her gastrointestinal system and brain. Now 5 years old, she’s making great strides, learning to walk and communicate.
Posted on July 07, 2021
Born prematurely at 31 weeks and diagnosed with a rare condition that affects babies’ eating and breathing, Saylor is now on the road to recovery with care from the Esophageal and Airway Treatment team at Johns Hopkins All Children’s.
Posted on June 18, 2021
How Ethan, 13, and his family fought through a frightening COVID-19 experience.
Posted on June 10, 2021
Ron and Maria Del Carmen couldn’t have imagined what would be required to keep their daughter alive and safe in her first two years of life — a journey that would lead them from Guatemala to Johns Hopkins All Children’s Hospital.
Posted on May 18, 2021
After learning their unborn baby had a heart condition, Bailey and James found the care they needed in the Johns Hopkins All Children’s Heart Institute. Now 10 years later, their son James continues to beat the odds on and off the field.
Posted on May 14, 2021
The first FDA-approved treatment for peanut allergy in children is helping to give kids like Ian and their families peace of mind.
Posted on May 07, 2021
Specialized therapies and expert guidance from the Center for Behavioral Health have helped 8-year-old Huntley to thrive. His story was the centerpiece of this year’s virtual A Night for All Children, a new signature event benefiting Johns Hopkins All Children’s.
Posted on April 21, 2021
Even before he was born, a neck mass threatened baby Cameron’s life. A skilled team of specialists at Johns Hopkins All Children’s kept him safe.
Posted on April 20, 2021
Inspired by Audrey Resop’s passion for making a difference for the hospital’s patients and families, many in the Resop family have followed in her footsteps. Johns Hopkins All Children’s celebrates Volunteer Appreciation Week April 18-24.
Posted on April 15, 2021
Marina was born premature and lifeless with her organs outside of her body in a sac. After 10 months in the neonatal intensive care unit, five weeks in a coma, three years on full life support and 25 surgeries, Marina is a healthy and happy 13-year-old who gives back by supporting and volunteering for Children's Miracle Network Hospitals.
Posted on March 24, 2021
The hospital recently welcomed Brea, the first full-time facility dog to work with the Child Life department. Brea provides comfort, support and serves as a friendly distraction for children during procedures and throughout their hospitalization.
Posted on March 11, 2021
Four-year-old Nico has completed more than six food challenges with the Food Allergy Clinic to see if and how he reacts to certain foods he might be allergic to. A better understanding of exactly what causes an allergic reaction for kids like Nico makes a big difference for families and children navigating complicated food allergies.
Posted on February 24, 2021
Jase is an effervescent 5-year-old who has a genetic condition called neurofibromatosis type 1. When he was about to turn 4, an MRI scan revealed a problem that would change his life dramatically.
Posted on February 23, 2021
Baba Wilhm, who has been a fetal sonographer for more than 40 years, uses her keen eye and deep understanding of both congenital heart disease and fetal physiology to pick up on signs of rare congenital anomalies that are often difficult to detect.
Posted on February 16, 2021
Olive was born with a heart defect, and after two surgeries to repair her heart — the first when she was 2 months old — the 4-year-old is charting her own course, with an epic soundtrack to match.
Posted on February 09, 2021
Baby Dream was just over a month old when she was diagnosed with serious conditions affecting her heart and her liver. After several months of multidisciplinary care that has included two surgeries, she is happy and thriving — breathing better, playing harder, and forming her first words.
Posted on December 22, 2020
Three years after going viral on her birthday when a hurricane interrupted at Johns Hopkins All Children’s, Willow turned 6 (and still loves Frozen).
Posted on December 18, 2020
In 2021, the organizers of two established fundraising events — VIP Auction and Charity Ball — will join forces to create a new event to support children who receive care at Johns Hopkins All Children’s Hospital.
Posted on December 17, 2020
As part of the hospital’s Pediatric RN Residency Program, Hannah Ryan learned from the team that had saved her life as a child and inspired her to pursue a career in nursing.
Posted on December 09, 2020
Five-month-old Lukas is on the road to a promising recovery with care from the multidisciplinary team in the Johns Hopkins All Children’s Heart Institute.
Posted on December 02, 2020
Throughout Dorothy Dunn’s life, service to others was a guiding principle. The long-time elementary school teacher’s dedication to children’s well-being will long outlive her, thanks to the legacy she built.
Posted on December 01, 2020
A talented young teen faces a life change after suffering bleeding in her brain. Learn more about 14-year-old Ashley’s inspiring story.
Posted on November 25, 2020
Once a neurosurgery patient, Nathan Jones, R.N., is now a pediatric intensive care unit nurse at Johns Hopkins All Children’s, the very same hospital where he had with a rare benign bone tumor removed in 2001. He shares his experience with patients in the PICU who may be feeling anxious, to help them feel more at ease.
Posted on November 24, 2020
8-year-old Kelsie was diagnosed as a newborn with cystic fibrosis. Johns Hopkins All Children’s Hospital has been a partner in Kelsie’s life ever since, with highly specialized care from the hospital’s Cystic Fibrosis Center.
Posted on November 18, 2020
Jimmy, who began having seizures about five years ago, is the first patient at Johns Hopkins All Children’s to be treated for epilepsy with this surgical procedure.