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Patient Story
In Their Own Words: Shriners Children’s Patients Share Their Experiences
https://www.shrinerschildrens.org/en/News-and-Media/Patient-Stories/2023/08/In-Their-Own-WordsThree patients have penned heartfelt reflections on their medical journeys and what Shriners Children’s means to them.
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Patient Story
When Healing Becomes a Calling: Bianca’s Story
https://www.shrinerschildrens.org/en/News-and-Media/Patient-Stories/2025/09/Bianca-Congenital-Hip-Dysplasia-CareFrom patient to caregiver: Bianca’s inspiring journey of hope and resilience.
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Pediatric Care
Fracture, Sports Injury and Other Specialty Clinics
https://www.shrinerschildrens.org/en/Locations/Philadelphia/Our-Care/Specialty-ClinicsThe walk-in fracture clinic and other specialty clinics at Shriners Children’s Philadelphia are designed with convenience in mind for busy families and children.
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Patient Story
From Patient to Future Surgeon? Justin's Story
https://www.shrinerschildrens.org/en/News-and-Media/Patient-Stories/2025/09/Justin-Scoliosis-CareWhen he was 13, Justin began to develop severe pain in his back. It progressed steadily to the point where he could barely finish a day of school.
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Specialty Clinics
https://www.shrinerschildrens.org/en/Locations/Salt-Lake-City/Our-Care/Specialty-ClinicsShriners Children's Salt Lake City holds specialty clinics for a number of the pediatric conditions we treat
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Specialty Clinics
https://www.shrinerschildrens.org/en/Locations/Portland/Patients-and-Families/Specialty-ClinicsShriners Children's Portland Specialty Clinics, providing customized care and care plans for your child.
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Condition
Muscular Dystrophy
https://www.shrinerschildrens.org/en/Pediatric-Care/Muscular-DystrophyAt Shriners Children's, our unique team of specialists provides the highest quality neuromuscular care for your child with muscular dystrophy.
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Patient Story
A Genetic Discovery of Hope
https://www.shrinerschildrens.org/en/News-and-Media/Patient-Stories/2025/03/Jeffrey-Orthopedic-CareJeffrey is a Shriners Children's Philadelphia patient who shares the same rare genetic condition, SCA29, with his mother, Theresa.
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Patient Story
Rare Disease Day 2023: Keira and Hannea's Journeys at Shriners Children's
https://www.shrinerschildrens.org/en/News-and-Media/Patient-Stories/2023/02/Rare-Disease-DayRead the stories of Keira and Hannea, who both found their homes away from home at Shriners Children's Philadelphia while receiving care for their rare medical conditions.
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Patient Story
VBT Friends Forever
https://www.shrinerschildrens.org/en/News-and-Media/Patient-Stories/2022/12/VBT-Friends-ForeverTwo patients become friends after getting the same surgery done on the same day at the hospital with the same surgeon.
Patient Information
Providers & Research
