Our patients' stories
Crohn’s Disease: David’s Story
David came to CHOP as a teen to manage his Crohn’s. His parents now co-chair the Family Research Council, which supports research at the IBD Center.
Cystic Fibrosis: Jessica’s Story
Jessica has lived with cystic fibrosis since she was a baby. The Cystic Fibrosis Center at CHOP prepared her to manage her disease as she transitioned to college.
Very Early Onset IBD and Eosinophilic Esophagitis: Thomas’ Story
Thomas does karate and loves Lego robotics. With medication and a careful diet, he’s living an active life with IBD.
Crohn’s Disease: Matthew’s Story
Matthew’s problem was a mystery until he came to Children’s Hospital. After a diagnosis of Crohn’s, nutrition treatment has Matthew, 3, eating normally and thriving.
Hyperhidrosis: Alexa’s Story
Since having surgery at CHOP to correct hyperhidrosis, a condition that caused her to have excessively sweaty hands, Alexa can pursue her love of acting with more confidence.
Hyperhidrosis: Daniel’s Story
Daniel plays baseball and basketball with confidence after surgery at CHOP corrected hyperhidrosis, a condition that caused his hands to sweat excessively.
Yoga for Cancer Coping: Quinn’s Story
Yoga classes offered by the Integrative Health Program at CHOP helped Quinn and her family cope with her cancer diagnosis.
Heterotaxy Syndrome: Julia’s Story
An innovative procedure corrected a problem in Julia’s circulatory system. Inspired by the nurses at CHOP, Julia is in school to become a nurse herself.
Arterial Ischemic Stroke: Bella’s Story
Bella suffered a stroke as a baby, and her road to recovery has included years of therapy with CHOP’s Pediatric Stroke Program. Now 8, she dreams of becoming an engineer.
Type 1 Diabetes: Mary Grace’s Story
Mary Grace was born with Down syndrome and was diagnosed with diabetes at age 4. She is now a happy and healthy 19-year-old thanks to CHOP’s care and support.
Crohn’s Disease: Carter’s Story
Carter was diagnosed with Crohn’s disease at age 5. With nutrition treatment, he’s growing again and back to playing his favorite game: basketball.
Type 1 Diabetes: Liam’s Story
Liam, 15, embraces his Type 1 diabetes. He is very open about his condition and shares his experiences to educate others.
Slipped Capital Femoral Epiphysis: Lisa’s Story
After surgery to align a displaced section of the top of her femur, Lisa is back to the thing she loves most, dancing.
Crohn’s Disease and Pancreatitis: Adina’s Story
Adina loves singing and musical theater. She’s able to enjoy them more fully now that treatment for Crohn’s disease has reduced her stomach pains and nausea.
Crohn’s Disease Second Opinion: Ty’s Story
Ty spent two years on a mostly liquid diet because of inflammatory bowel disease (IBD). Two days after surgery at CHOP, he ate a cheeseburger.
Type 1 Diabetes: Emily’s Story
Emily was diagnosed with Type 1 diabetes after a near-fatal incident as a baby. Now, she’s a happy and energetic 2-year-old.
Type 1 Diabetes: Ricky’s Story
Ricky was diagnosed with Type 1 diabetes at age 7. Now, he’s an exceptional lacrosse player, recruited to play for a Division 1 college team.
Inflammatory Bowel Disease (IBD): Makenzie’s Story
Makenzie suffered a terrifying illness when she was 7, a rapid decline in which she lost a quarter of her weight. With treatment at CHOP, she’s back to her healthy, happy self.
Crohn’s Disease: Lucy’s Story
Lucy plays lacrosse, loves to bake, and shocks people with her theatrical makeup skills. She’s back to enjoying life after being very sick with Crohn’s disease.
Congenital Hyperinsulinism: Odinn’s Story
Óðinn Orri Sævarsson was born with a potentially life-threatening disease rarely seen in Iceland, congenital hyperinsulinism (HI). Quick action and a team effort between Icelandic specialists and CHOP's International Patient Services got Óðinn to CHOP for treatment, where he was cured.