Coming Soon !!!!

Thanks to the assistance of  QuestionPro.com, our Congenital Diaphragmatic Hernia Research Survey programming is under way!   We will be able to receive and tally data by March 31, 2009. 

In the meantime, parents and adult survivors can participate by joining and filling out the information at http://www.cdhsupport.org/members 




CHERUBS Congenital Diaphragmatic Hernia Research Survey is the combined efforts of over 2700 CDH families and medical professionals.   It takes information on the medical, family and exposure histories of CDH patients and compares data to look for the cause, prevention and better treatement of Congenital Diaphragmatic Hernia.  Participation is voluntary, anonymous and free to all CDH families and medical staff.   Data can be tabulated live for research and reference purposes.  

You can view our last survey results by clicking here.