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In 2008 640 new families affected by Congenital Diaphragmatic Hernia joined our CHERUBS family.
640 new members.
We are so honored and humbled to be able to help so many families and to provide so much support, information, awareness and research. That is what CHERUBS is here for and what we are all about. Helping ALL CDH families as much as possible.
Mom of Shane (1/28/93-9/11/99) LCDH x6 and multiple complications and birth defects.
Founder and President of CDH International.
Executive Director of:
CDH International USA
CDH International UK
CDH International Canada
CDH International Switzerland
CDH International Netherlands
CDH International Singapore
CDH International Hong Kong
Messages may be answered by CDHi Team.
640 new members?!?! WOW!! I am saddened that these families heard the words "CDH"......but so very glad that they were able to find CHERUBS! I am so proud to be a member of CHERUBS and so proud of all that CHERUBS is!
It breaks my heart that all these families have been affected by this horrible birth defect.
NO family should ever have to walk this CDH Journey alone.
CHERUBS is here for these families and I feel blessed to be apart of such a wonderful organization.
Stephanie (Shelby's Mom LCDH 7-10-06)- ECMO 7 days- 2 DH repairs- hital hernia repair- Cliff Lip repair- Nissen and Mickey button. Shelby is eating and drinking by mouth now!!! THIS IS FANTASTIC!!!!! Mom to Lexi 8- Morgan 6 and Taylor 5. Blessed to have our little butterfly and our beautiful girls. [url]www.youtube.com/cdhsupport[/url] - Shelby's Journey [img]http://i258.photobucket.com/albums/hh257/gracebutterfly/CDHAwarenessRibbonShelbysmall.jpg[/img]
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