Where to Start When You Learn Your Unborn Baby Has Spina Bifida
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For parents who find out their unborn baby has spina bifida, the biggest question is often “what do I do next?” Here’s advice on where to start.
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For parents who find out their unborn baby has spina bifida, the biggest question is often “what do I do next?” Here’s advice on where to start.
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The documentary features interviews with a Children's Hospital of Philadelphia expert and patients.
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On June 3, more than 2,000 patients and families returned for CHOP’s Fetal Surgery Family Reunion to celebrate their breakthroughs and how far they’ve come.
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As director, Magnusson leads a robust, multidisciplinary team that provides coordinated care and consultative services to patients with spina bifida and spinal cord defects.
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For families facing a prenatal diagnosis of clubfoot, our CFDT and orthopaedic experts meet with families to discuss findings, postnatal management, treatment options, and long-term prognosis.
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In January 2018, Dr. Adzick and the Kane family headed to Washington to advocate and raise awareness about birth defects, fetal surgery and more.
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A study of 183 children with spina bifida who had fetal surgery shows a clear-cut benefit in outcomes at 30 months, including ability to walk independently.
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Families, including patients treated while still in the womb, reunite with their doctors and nurses during an event hosted by the Center for Fetal Diagnosis & Treatment.
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At the 37th Annual News and Documentary Emmy® Awards, PBS was awarded an Outstanding Science and Technology Programming Emmy for "TWICE BORN: Stories from The Special Delivery Unit," featuring Children's Hospital of Philadelphia.
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In June, CHOP representatives joined the Rodriguez family for the Children’s Hospital Association’s Capitol Hill Advocacy Day in Washington, D.C.