N/IICU Services at King of Prussia Campus
The Newborn/Infant Intensive Care Unit (N/IICU) at CHOP's Middleman Family Pavilion in King of Prussia, Pa., is a Level III unit that provides specialized care.
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N/IICU Services at Philadelphia Campus
The Harriet and Ronald Lassin Newborn/Infant Intensive Care Unit (N/IICU) located on our Philadelphia Campus is one of the biggest and best in the world.
The Plastic Bronchitis Foundation
The Plastic Bronchitis Foundation provides information about plastic bronchitis, research into treatments, family support services and more. The group also helps raise awareness of plastic bronchitis, funds research into the disease and assists patients and their families with treatment-related travel expenses.
Lymphangiomatosis and Gorham's Disease Alliance
The mission of the LGD Alliance is to improve the care of patients with lymphangiomatosis and Gorham's disease by promoting research that will identify effective treatments and ultimately a cure. On this site, you’ll find patient resources including patient support services, patient registry, a physician directory and more. You'll also find access to disease information, research resources and latest news and events.
La Leche League International
Find comprehensive breastfeeding information, online forums and support groups, FAQs, conferences, an international online store, and more.
Normal Lymphatic Anatomy and Flow Video
Watch this video of lymphatic flow and drainage from the Jill and Mark Fishman Center for Lymphatic Disorders at CHOP.
Holding Your Baby in Intensive Care
Read common questions parents have once they're able to hold their baby in intensive care.
New Diagnostic Procedures and Interventions for Patients with Systemic Lymphatic Disease
View this presentation from Christopher Smith, MD, PhD, with the Lymphatic Education & Research Network.
Management of Infants with Lymphatic Disorders Clinical Pathway — Inpatient
This pathway is to be used for infants from birth to 1 year of age, admitted to an intensive care unit, with concern for lymphatic flow disorders without history of surgical/traumatic chylothorax, congenital heart disease, or isolated lymphatic mass.
Cornelia de Lange Syndrome Foundation Inc.
The Cornelia de Lange Syndrome Foundation is a nonprofit organization providing families and caregivers with a wealth of support, services, education and information about Cornelia de Lange syndrome (CdLS).