In this video you’ll join the Delaney family on their journey, learn about the large team involved in the separation surgery, and see how Abby and Erin are doing today.
In this video, clinicians and patient families talk about the diagnosis and treatment of cleft lip and palate, the most common congenital facial anomaly.
In this video, clinicians and patient families talk about the diagnosis and treatment of craniofacial conditions, including craniosynostosis, hemifacial microsomia, and other syndromes.
CHOP brings specialty and surgical services to families in our Specialty Care and Ambulatory Surgery Centers. The centers allow families access to the services of renowned Children's Hospital surgeons without a trip to the city.
An update on Abby and Erin Delaney, who were born conjoined and separated at Children's Hospital of Philadelphia (CHOP). Now now 2½ years old, they are making amazing strides in their growth and development.
AdoptCleft is a support group for parents wanting to adopt cleft children, parents that have cleft children (biological or adopted), and others that can contribute or learn from the conversations.
ACPA is an international nonprofit medical society of healthcare professionals who treat and/or perform research on birth defects of the head and face.
Changing Faces provides support and promotes respect for everyone with a visible difference. Helpful resources include advice for meeting new people when you have a visible difference.
March of Dimes is an international organization that works to prevent birth defects, premature birth, and infant mortality and to support expectant and new parents.
Philly Phaces provides peer support, advocacy, and resources to help Philadelphia-area children facing appearance differences from craniofacial abnormalities and cleft lip and palate.