Center for Fetal Diagnosis and Treatment Resources
Get the facts about congenital diaphragmatic hernia then share this infographic with your friends and family to help raise awareness of the condition.
Did you know that spina bifida is the most common permanently disabling birth defect in the U.S.? Learn more spina bifida facts and help spread the word.
Get the facts about twin-twin transfusion syndrome then share this infographic with your friends and family to help raise awareness of the condition.
Get the facts about fetal surgery then share this infographic with your friends and family to help raise awareness of the ways babies can be treated for serious and life-threatening conditions even before they’re born.
See step-by-step illustrations of the stages involved in fetal repair of spina bifida.
Hosts for Hospitals is a unique nonprofit program that provides accommodations in the homes of local families at minimal or no cost to families whose homes are far away.
The Ronald McDonald House serves as a "home-away-from-home" for families whose children are being treated at nearby hospitals. The Philadelphia Ronald McDonald House has rooms available for patient families as well as mothers undergoing fetal surgery or delivering in CHOP’s Special Delivery Unit.
The Ronald McDonald House serves as a "home-away-from-home" for families whose children are being treated at nearby hospitals. The Ronald McDonald House of Southern New Jersey has rooms available for patient families as well as mothers undergoing fetal surgery or delivering in CHOP’s Special Delivery Unit.
Kathleen Huggins equips breastfeeding mothers with all the information they need to overcome potential difficulties and nurse their babies successfully.
This book provides information on how to get started with breastfeeding, including tips for latching on, increasing your milk supply, breastfeeding in absentia, breast pumps and more.
This book offers a comprehensive introduction to breastfeeding — how to get ready before the baby arrives, how to involve fathers and siblings, the best diet and foods for mom, and more.
Working mothers, stay-at-home moms, single moms, and mothers of multiples will all benefit from this book’s range of nursing advice, stories, and information.
If you or your loved one continue to have difficulty with a perinatal or postpartum mood and anxiety disorder, it may be helpful to contact a mental health professional for additional support.
These guided videos and audio recordings can help create a more peaceful and restful state of mind for parents, caregivers, and adolescent/young adult patients.
Directions, Maps & Parking
Use these maps to see the layout of the entire Main Campus, including floor maps of the Main Hospital, Wood Center, Seashore House and Buerger Center.
Parking at Children's Hospital of Philadelphia is available in three parking garages. Find parking for Main Hospital, Buerger, and Wood and Seashore buildings.
The Connelly Resource Center is located on the 8th floor of the Main Hospital. Inside, families will find a family and children's library, a learning center and a hospitality area for free services such as laundry, business needs, naps, learning or relaxing.
The Jill & Mark Fishman Center for Families, located on the first floor of the Main Building, provides families with a welcoming space as well as assistance with housing, transportation and local resources.
Perinatal and Postpartum Mood and Anxiety Disorders
The U.S. Department of Health and Human Services provides a free booklet on depression during and after pregnancy for women, their families and friends.
The National Postpartum Depression Hotline is available to help individuals dealing with postpartum depression. Call 1-800-PPD-MOMS.
NWHIC, a service of the Office of Women’s Health in the U.S. Department of Health and Human Services (HHS), focuses on emerging women's health priorities to meet the needs of women and girls. Their website provides health and wellness information, reproductive health resources, and information about diseases and conditions including postpartum depression.
Provides support to families experiencing postpartum depression. Find information about perinatal mood and anxiety disorders, and get connected with the best local resources available.
The American Pregnancy Association is a national health organization that promotes reproductive and pregnancy wellness through education, support, advocacy and community awareness.
This book is for children ages 2-10 whose mother is on pregnancy bed rest. It will help children better understand, be less fearful and realize there is an end to the bed rest experience.
Women undergoing bed rest during pregnancy will benefit from the insight McCann gained as she successfully endured both an at-home as well as extended hospital bed rest.
About.com offers free online childbirth classes that include a comprehensive discussion of labor and birth from a certified childbirth educator and RN.
Medline Plus' Pregnancy website offers late-breaking news, health advice, pregnancy anatomy and physiology, prenatal nutrition, and much more.
Sidelines is a national nonprofit organization that provides support to women who are on bed rest during pregnancy.
This book includes information on how to prepare for labor; epidurals and other medications for labor; cesarean birth, breastfeeding and newborn care and much more.
Amy E. Tracy shares her experiences ─ and those of many others ─ to help you and your family not only survive but thrive during your pregnancy.
Baby and childcare experts, Dr. Bill and Martha Sears, tell you what to expect, month by month, from conception through birth in this comprehensive guide.
When Pregnancy Isn't Perfect is a companion, adviser and lifeline for the thousands of women who face the prospect of a problem pregnancy.
Support and Education Groups
Mama Care combines prenatal care, childbirth education and a support group into one program for healthy mothers giving birth in the Garbose Family Special Delivery Unit at Children’s Hospital of Philadelphia.
The CFDT parent support group offers a supportive setting to connect with peers and learn mindfulness techniques to promote anxiety and stress reduction.
Before Avery was born, doctors discovered she had spina bifida, and she underwent fetal surgery. Fast forward four years, and see Avery run, jump and play.
This spina bifida video series talks about how to deal with a spina bifida diagnosis for your unborn child, from prenatal diagnosis, to treatment options, delivery and follow-up care at Children's Hospital of Philadelphia.
In this video series, doctors and nurses from The Children’s Hospital of Philadelphia describe the diagnosis and treatment of different fetal lung anomalies.
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.
Connor has been in the spotlight since before he was born. Doctors closed a hole in his spine while he was still in his mother's womb. Follow his journey.
In this video, clinicians and patient families talk about the diagnosis and treatment of cleft lip and palate, the most common congenital facial anomaly.
Watch this video about CHOP's Special Delivery Unit, the first birthing unit of its kind for families expecting babies with a prenatally diagnosed birth defect.
Families who faced the diagnosis of a birth defect join clinicians in sharing what makes the Center for Fetal Diagnosis and Treatment the best place for prenatal diagnosis, fetal care and fetal surgery.
This video about fetal surgery for spina bifida explains spina bifida treatment options, the benefits of spina bifida surgery before birth and more.
Watch highlights from the 10th birthday celebration of the Garbose Family Special Delivery Unit at Children's Hospital of Philadelphia.
In this video series, doctors, nurses and parents talk about abdominal wall defects, including omphaloceles and gastroschisis, and how these conditions are diagnosed and treated at The Children's Hospital of Philadelphia.
In this video series, experts from the Center for Fetal Diagnosis and Treatment at CHOP present a complete overview of twin-twin transfusion syndrome (TTTS).
Watch this short video to learn more about the long-term, multidisciplinary care provided through CHOP's Pulmonary Hypoplasia Program.
In this video, CHOP experts explain the diagnosis, treatment options and follow-up care of babies with congenital diaphragmatic hernia (CDH), and the advancements in the field of CDH repair.
In this video series, CHOP experts explain lower urinary tract obstructions (LUTO), from diagnosis and possible prenatal treatment, to delivery and treatment after birth and follow-up care.
In this video, clinicians from Children's Hospital of Philadelphia explain the diagnosis and treatment of various types of teratomas, or fetal tumors.
A video with illustrations explains the intricate steps involved in performing spina bifida surgery before birth and the expert fetal surgery team involved.
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.
Breath of Hope raises awareness of congenital diaphragmatic hernia (CDH) by educating and supporting parents, family members, medical professionals, and anyone who wants to learn more about CDH.
CDH International is a global collective of hospitals, researchers, and charities working together to stop congenital diaphragmatic hernia with a focus on advancing CDH research and accrediting hospitals and charities.
CHERUBS is the family support division of CDH International, a nonprofit group that supports families and medical care providers of children with congenital diaphragmatic hernia.
Find comprehensive breastfeeding information, online forums and support groups, FAQs, conferences, an international online store, and more.
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.
Omphalocele Awareness/Mothers of Omphaloceles (MOOS) is an Internet support group for families of children with omphaloceles.
Peyton’s Promise helps raise awareness and money for ongoing congenital diaphragmatic hernia (CDH) research. It was founded by Debbie and Dustin Laricks, whose daughter Peyton was born with CDH.
The Spina Bifida Association is a comprehensive source of information and resources about spina bifida, the most common permanently disabling birth defect in the United States.
The TTTS Foundation's website offers information for families during and after pregnancy, research updates, a message board, and more.