CHERUBS Research Database Goes Live

After 20 years, CHERUBS is proud to announce that our CDH Research Database is now live!


You can view it at

This database is the compilation of family input medical information.  It is the only database of it's kind and compliments the research databases of the CDH Study Group and DHREAMS.   Our fully HIPAA compliant, real time research database will not only allow families and researchers instant access to CDH information and statistics, but it will allow us to work on joint research projects with several leading Congenital Diaphragmatic Hernia Research centers.   We would like to thank DHREAMS, Dr. David Kays and the CDH Study Group for all their support of this project over many years and we look forward to working with them, and many others, to help fight CDH. 

You can participate by becoming a member of the charity at

Join the Angel Club and make a monthly or annual donation in honor or in memory of your cherub.

Donation Amount Options
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2017 - News from CHERUBS

PRESS RELEASE: New Organization Leads the Way in CDH Research

For immediate release

New Organization Leads the Way in CDH Research

20 year old charity expands to raise survival rates for birth defect.


Finish up the CDH Survey - Get a FREE Hat!

The CDH Research Survey went live on April 1st but in order to take full advantage of all research opportunities, we need ALL families to fill out the complete CDH Research Survey.  


Have you registered for the 2017 CDH Conference in July in SLC?

Make sure to register to attend the largest annual CDH event and the first conference in the midwest in several years!