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Phase three of the Management of Myelomeningocele Study (MOMS), known as “MOMS3,” is a study monitoring the health outcomes of participants ages15-24.
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Families who receive a diagnosis of the most severe forms of spina bifida need an amazing level of support and care coordination from prenatal diagnosis through delivery, treatment and discharge.
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In fetuses with open spinal dysraphism, the risk of talipes is increased with an MMC sac, and a larger sac may result in additional injury through mechanical stretching of the nerves.
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The birth of CHOP's 2,000th fetal surgery patient marks a record-breaking milestone for CHOP’s Richard D. Wood Jr. Center for Fetal Diagnosis and Treatment.
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Military families have not always had quick access to the experts who could help when facing a prenatal birth defect diagnosis … until now.
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New findings from the latest MOMS2 analysis show prenatal repair of the spinal column confers physical gains that extend into childhood.
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Here are some tips for keeping your children and family safe and healthy, both physically and mentally, during the ongoing COVID-19 pandemic.
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Taking care of your skin in the summer can be tricky, and for individuals with spina bifida, there are a few unique factors to pay special attention to.
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A high-fiber diet is crucial to a successful bowel regimen. See the benefits of a high-fiber diet and find recipes from the Spina Bifida Program's clinical dietitian.
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For 11 years, social worker Amanda Fonash has supported families in myriad ways.