Our patients' stories

Glucose Transporter Type 1 Deficiency: Dominic’s Story
Dominic’s life can be broken into two parts: before and after he started the ketogenic diet. Today, he’s a happy and healthy first grader.

Janessa and Matt’s Story: A Path of Healing
The CHOP care team helped Janessa and Matt prepare for the loss of one daughter, while finding joy in welcoming another.
Mitochondrial Disease: the D'Aria Family
The D’Aria family lost their daughter, Giuliana, to a serious form of mitochondrial disease. Their story highlights the importance of funding research.
Crohn's Disease: Morgan's Story
When Morgan was 11, her weight dropped to just 50 pounds due to complications from Crohn’s disease. Now 14, she’s excelling in high school.

Atrioventricular Canal Defect: Henry’s Story
After cardiac surgery at Children’s Hospital of Philadelphia to repair a defect in his heart, Henry has more energy than ever.

Biliary Atresia and Liver Transplant: Haley's Story
Haley had a life-saving liver transplant when she was 4. Now 15, she’s an active teenager who players lacrosse and enjoys cheerleading.

Hemophagocytic Lymphohistiocytosis: Luca’s Story
After receiving treatment for hemophagocytic lymphohistiocytosis (HLH) at Children’s Hospital of Philadelphia, Luca is on the road to recovery.

Tetralogy of Fallot (TOF): Alissa’s Story
When Alissa was a baby, she underwent heart surgery at Children’s Hospital of Philadelphia to treat tetralogy of Fallot (TOF), a congenital heart defect.

Using Meditation and Diet to Treat ADHD Symptoms: Anna’s Story
Anna, 6, has been able to control her ADHD by changing her diet and embracing meditation instead of using medication to treat her symptoms.

Fetal Surgery for Spina Bifida: Mason’s Story
A spina bifida diagnosis led Baylee and Louis to make the trip from their home in Florida to Children’s Hospital of Philadelphia for fetal surgery.

Sickle Cell Disease: Caylin’s Story
Now 12, Caylin’s regular visits to CHOP for sickle cell disease treatment have inspired her love for comparing numbers, gathering data and experimenting.

Coarctation of the Aorta with Aortic Arch Hypoplasia: Jude’s Story
Jude, 2, was born with coarctation of the aorta with aortic arch hypoplasia. Procedures at Children’s Hospital of Philadelphia helped save his life.

Yoga for Cancer Coping: Lucas’ Story
As Lucas undergoes chemotherapy, he uses yoga to stay calm, offered as part of the Integrative Health Program at Children’s Hospital of Philadelphia.

Spinal Muscular Atrophy Treatment: Claire’s Story
With a breakthrough drug for spinal muscular atrophy treatment and ongoing therapy at Children’s Hospital of Philadelphia, Claire is reaching new milestones.

Crohn’s Disease: Ella’s Story
After years of pain and stilted growth due to her then-undiagnosed Crohn's disease, Ella is now receiving treatment, and growing taller and stronger.

Specialized Treatment for Amplified Musculoskeletal Pain Syndrome: Sebastian’s Story
After six months of debilitating pain and countless doctor visits, Sebastian is now thriving — thanks to expert care from the AMPS team at Children's Hospital of Philadelphia.

Celiac Disease: Mikayla’s Story
Mikayla, 16, is a competitive gymnast and coaches younger children. Diagnosed with celiac disease in eighth grade, she has adapted to her new diet.

Prenatal Testing for Cystic Fibrosis: Shane’s Story
Genetic testing showed a 1 in 4 chance that Jessica and Greg’s son would have cystic fibrosis. A sweat test after he was born confirmed the diagnosis.

Crohn’s Disease: Zachary’s Story
Nutritional therapy proved to be the key to treating Zachary’s Crohn’s disease and eventual remission. Now 18, he’s looking ahead to college symptom-free.

Mariella's Congenital Cystic Adenomatoid Malformation (CCAM) Story
Before Mariella was born, doctors found a life-threatening cyst: a congenital cystic adenomatoid malformation. Her family turned to CHOP for lifesaving care.