CDH Research Studies, Patient Stories, Patient & Family Support, Events and more - managed by CDH International
Stories of patients born with Congenital Diaphragmatic Hernia
Stories of surviving CDH patients already printed in our newsletter, "The Silver Lining" and our book, "Stories of Cherubs" ***Please do not post your stories here (we'll post them for you after they are published) but please feel free to add updates to your stories or comment on other stories by using the Reply button on story post.***
Stories of CDH patients lost that are already printed in our newsletter, "The Silver Lining" and our book, "Stories of Cherubs". ***Please do not post your stories here (we'll post them for you after they are published) but please feel free to add updates to your stories or comment on other stories by using the Reply button on story post.***
Talk to other affected patients and families.
Current research participation opportunities
Congenital Diaphragmatic Hernia Awareness Events
April 19 International Congenital Diaphragmatic Hernia Day of Awareness, Parades of Cherubs, Save the Cherubs Campaign, Fundraisers and more!
CHERUBS 2010 National Congenital Diaphragmatic Hernia Awareness Campaign. http://www.savethecherubs.org
Updates, services, information
Services and projects offered by CHERUBS to help CDH Families
Polls, helping us with printed materials, donation lists, new siblings, etc