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… our patient stories. Previous Next News & Articles June 23, 2026 Phoenix Children’s Names Jayson Argyle Senior Vice President of Community Hospitals News & Articles May 27, 2026 Phoenix …
Condition
Facioscapulohumeral Muscular Dystrophy in Children What is FSHD in children? Facioscapulohumeral muscular dystrophy (FSHD) is a rare genetic muscle disease that affects the muscles of your child’s face, shoulders, upper arms, and lower legs. These muscles weaken and shrink
Condition
Imperforate Anus in Children What is imperforate anus in children? Imperforate anus is a problem that your child is born with. It happens when your child has a blocked or missing anus. The final part of the digestive tract is the rectum. The rectum collects and compacts the solid
Conditions We Treat
Epidermolysis bullosa (EB) is a rare genetic skin disease most often present at birth with blisters or areas of missing skin on the body caused by minor trauma to the skin. While we have no cure for EB yet, supportive care is critical and includes wound dressings, infection
Doctor
Neil R. Friedman, MBChB
Director, Clinical Transformation; Diane and Bruce Halle Endowed Chair in Pediatric Neurosciences
Specialties
Article
Bodhi's Story
A first birthday is a time of joy and celebration, but for Greg and Colleen, it marked the beginning of a journey they never anticipated. In 2018, just before their son, Bodhi, turned one, he experienced his first seizure. Alarmed and worried, Greg and Colleen rushed him to
