With help from a new FDA-approved oral immunotherapy (OIT) treatment, Noah can now experience life without fear of adverse reactions from peanut protein.

Michael, 5, is meeting all his developmental milestones after surgeries for a severe heart defect. He was closely monitored by the Cardiac Kids Developmental Follow-up Program at CHOP.

A combination of surgical procedures corrected Phoebe’s macrodactyly, an uncommon condition that causes irregular growth in a child's fingers or toes.

After Jack was diagnosed with cancer, his family was impressed how everyone at CHOP, from the check-in team to the world-class doctors, made them feel special.

Hannah is determined not to let having chronic intestinal pseudo-obstruction – or the colostomy pouch she must wear — keep her from a future in nursing.

A rare, fast-growing cancer was clogging the drainage system in Lucas’ body. After a short, intense round of treatment, he’s set to play soccer in the fall.

Chemotherapy damaged the bone tissue in Michael’s legs, requiring surgery and the use of a wheelchair for several months.

Five-year-old Mia has spent a great amount of time isolated because of her weakened immune system. Now she can’t wait to ride roller coasters.

After Nicholas, 14, received a diagnosis of Hodgkin lymphoma, his care team supported the entire family’s well being in every possible way.

When Thomas was 2 and being treated for leukemia, he was terrified. When the cancer returned, he faced it bravely.

Lauren, who was named Miss Wheelchair New York 2020, is participating in research at CHOP for a rare form of epilepsy

Emma’s bone marrow wasn’t producing what her body needed to fight infections. A bone marrow transplant transformed her life.

Caleb depends on electricity to run his ventilator, suction machine and feeding tube. CHOP’s Medical Legal Partnership helped his family keep the utilities on so now Caleb can focus on other things — like preparing for kindergarten.

Addison’s peanut allergy has improved greatly thanks to a promising new treatment at CHOP. The 12-year-old has shown her thanks by raising money to help more kids like her.

Facing a tough diagnosis together, CHOP doctors offer Dakota hope and support, while she helps them learn more about her rare mitochondrial disease.

Born with a severe heart defect, Hudson experienced a harrowing journey before he had a heart transplant at Children's Hospital of Philadelphia.

In just two years of life, Lincoln has spent more than 5 months in the hospital overcoming premature birth, brain injury, multiple surgeries and near-death experiences.

When Izahd had hand surgery for brachial plexus, his family was consistently impressed by the care their son received at Children’s Hospital of Philadelphia. Each stage in their journey inspired them to give back.

Children's Hospital of Philadelphia (CHOP) doctors unraveled the clues to find the answer to Autumn’s severe stomach pain caused by recurrent pancreatitis: bile duct surgery to treat a choledochal cyst.

Adam’s hyperinsulinism/hyperammonemia wasn’t well controlled until he came from Chicago to CHOP. Now he’s participating in research to help find a better treatment for HA.