Diagnosed with FPIES, Isaiah could only safely eat five foods at his first birthday. Now 2 ½ years old, his diet has expanded to 35 foods and it's been more than a year since his last allergic reaction to food.

Josephine, 16, refuses to let Crohn's disease govern her life or impact her dream of playing division 1 field hockey in college.

With help from the Center for Celiac Disease, 8-year-old Justyna can maintain a busy schedule including acting, modeling and school.

Julianna is living a semi-independent life in Phoenixville, working as a barista and taking Zumba classes — and not letting Trisomy 21 hold her back.

Everett's parents followed their hunch and sought medical care at CHOP, where surgery to remove an extra valve in his urethra, as well as a cyst, saved his life.

Born at 29 weeks and weighing 1 lb 8 ounce, Joseph's mom credits his breakthrough recovery to the remarkable care he received at CHOP.

After years of struggling with severe asthmas and food allergies, 17-year-old Mena is finally breathing easier thanks for biologic therapy at CHOP.

Strong parent advocacy ensured Morgan’s diabetes was under control at school. Now Morgan is advocating for others.

Born with Poland syndrome, which caused his fingers to fuse together, Beau underwent surgery to give him the greatest possible function of his left hand.

Elijah needed a lifesaving surgery while he was still in his mother’s womb. Today, he's an active 6-year-old who loves basketball and T-ball, goes swimming, rides his bike, and rock climbs.

A unique program at CHOP allowed 7-year-old Isabella to attend school at the hospital while also getting radiation treatment for cancer.

Every day is a new adventure for Aidan, a 1-year-old with Down syndrome who embraces each new challenge with a smile on his face.

Diagnosed with severe allergic asthma, Lorenzo is no longer sitting on the sidelines. Thanks to biologic therapy at CHOP, he's back in the game.

Zach never let his spina bifida hold him back. He wants to make the world a better place and is raising money and awareness for the condition.

Bewildering symptoms, both physical and behavioral, brought Kayla to CHOP and led to a diagnosis of autoimmune encephalitis, a rare disease when a person’s immune system attacks their brain.

Born with a rare heart defect, Amelia received innovative, life-saving treatment at Children's Hospital of Philadelphia.

For years, Nora's family treated her severe asthma and food allergies as separate conditions, but a new biologic therapy at CHOP is improving both.

AJ’s life was relatively uncomplicated until age 14, when he began to experience unpredictable seizures and received a life-changing diagnosis of epilepsy. Thanks to the combination of a small, battery-powered device surgically implanted into his brain and an oral medication, he is now seizure-free.

Brayden struggled with severe constipation and encopresis for years before he got treatment to manage his condition at Children's Hospital of Philadelphia.

Kaitlyn lights up the room with her smile and emanates positivity, despite her battle with rhabdomyosarcoma.