Our patients' stories

Expanding Surgical Capacity to Treat More Children Like Leo
Leo has needed surgeries for cardiac, urology and ear issues. CHOP’s new hospital will feature multiple advanced operating suites.

Pleomorphic Adenoma, Benign Salivary Gland Tumor: Zion’s Story
Zion’s salivary gland tumor was rare, but CHOP has a new program geared specifically for those types of problems.

High-risk Neuroblastoma: Donor-Funded Research Helps Lily Stay Optimistic
Although Lily’s beloved sports are on pause, her joy and optimism remain steadfast.

Siblings with Sickle Cell Disease: Donor-Funded Research Creates Hope
This disease affects so many aspects of their lives.

Waiting to Breathe Freely: CHOP Tackles Asthma Triggers in Homes
By investing in home repairs, CHOP and Philadelphia are improving asthma outcomes.

Fetal Surgery During a Pandemic: ‘I Trusted CHOP’
Not many people can say they underwent fetal surgery during a pandemic, but Jasmin did it to give her daughter a better chance at a healthy life.

Liver Transplant in the Midst of COVID-19: Keeping Briana Safe
As COVID-19 swept through Philadelphia, Briana’s biliary atresia worsened. She needed a liver transplant. CHOP safely performed the surgery. Now Briana’s future is bright.

Creating access to world-class orthopedic specialists for kids like Jackie
At 18 months old, Jackie needed hip surgery. CHOP’s new hospital will give families like hers easier access to CHOP’s world-class orthopedic experts.

Cate’s Story: Attaining a Genetic Diagnosis With the Help of the Epilepsy Neurogenetics Initiative
Learning a genetic diagnosis has enabled one family to connect and share their own wisdom and experience with families of children with the same diagnosis.

William’s Story: Gene Replacement Therapy for SMA Type 2
Untreated, children with SMA type 2 will never be able to walk. After receiving a one-time dose of gene therapy, William has gained strength and hit milestones his family previously didn't think possible.

Oliver’s Story: Prenatal and Postnatal Care of CDH and Giant Omphalocele
After an unexpected prenatal diagnosis, Olly’s parents found comfort with the experienced team at CHOP’s Center for Fetal Diagnosis and Treatment.

Lupus Nephritis: Emily's Story
When Emily experienced sudden fatigue, bruises and fevers, her family turned to CHOP. Within days, she was diagnosed with lupus nephritis and began treatment.

Maddie’s Story: Medical Management of Chronic Migraine
The Headache Program team have worked with Maddie to manage her migraine and minimize pain and disruption to her life.

Ava's Story: From Down Syndrome to College
When Mia's baby was born with Down syndrome, she worried about her daughter's future. Today, Ava, 19, is a student at Penn State.

Hyperinsulinism and Beckwith-Wiedemann Syndrome During the Pandemic: Dominic’s Story
With a dual diagnosis of two genetic conditions, Dominic’s family came from California to CHOP during the pandemic to ensure he got the specialized care he needed.

Bold Steps in the Field of Food Allergy
Advancing knowledge about why certain foods cause reactions, which patients respond to treatment and much more.

Donor Story: Kathy and Tim Donnelly
Appreciative of the care their son received, the Donnellys want to help extend the reach of CHOP’s expertise.
Multi-generational Philanthropy
The Sugermans’ children and grandchildren learn the power of philanthropy by selecting beneficiaries.

A Passion for Behavioral Health
A family tradition of charitable giving is carried on by three generation of women.

Seed funds for visionary programs
Bringing together the best minds to address complex and unsolved pediatric health conditions.