. Please help us to continue our work here at CHERUBS to raise more CDH awareness, fund CDH research and to support families affected by CDH. In Honor / Memory of: Mailing Address To Send Acknowledgement To:   Our staff is strictly volunteer and all donations are tax-deductible.  . cdhsupport.org member section Everytime you search on-line, please use Goodsearch.com .   Sarah Elizabeth Rehm 11/22/98 - 11/24/98

. . CHERUBS- The Association of Congenital Diaphragmatic Hernia Research, Advocacy, and Support.    IN THE NEWS: CHERUBS Name Change  / 2008 CHERUBS International Member Conference  / Angel Ball  / Golf Tournament  / Congenital Diaphragmatic Hernia Awareness Activities  / CDH Research Site Begun  / Fall 2007 Silver Lining Issue  / New CDH Awareness Ribbon & Logos  / Member Blogs / "Stories of Cherubs" Book  /  Local Get-Togethers  / CHERUBS Family Photo Album / On-LIne Forum / Special Day Calendar / Member Photo Albums / CHERUBS UK Has Non-Profit Status! / 1000's of CHERUBS items for sale / Current CDH Research Studies / Donations Needed To Continue Our Work! / Volunteers Needed Worldwide / CDH Research Library Re-Opened / CHERUBS Timeline Purchase Tickets Now! 2008 Angel Ball Register Now! 2008 Member Conference Sign Up Now! 2008 Golf Tournament Events Across the U.S.! CDH Awareness Events   Welcome to our new web site!   We invite all CDH parents to join our free membership to access our on-line services.    Current members can log-in by following our temporary log-in instructions.  Log In Trouble?  E-Mail Us.  Not A Member?  Click Here to Join for Free!   CHERUBS was founded in 1995 to support families of children born with Congenital Diaphragmatic Hernia (CDH) and to research possible causes and better treatments for CDH.  Currently, CHERUBS is the world's largest CDH organization, with over 2300 members in 37 countries and all 50 states; including parents, grandparents, foster parents, pediatric surgeons, genetic counselors, pediatricians, nurses, ECMO directors, respiratory therapists, and epidemiologists.  CDH is a devastating birth defect, affecting 1 in every 2500 babies.  CHERUBS is an IRS approved 501(c)III non-profit organization located in North Carolina.  Membership for parents is free and our organization is run solely by volunteers and funded through donations from members and the public.   For more information on CHERUBS and CDH,  please feel free to browse our site by using the navigation bar at the top of our web site. For more information on CHERUBS and CDH,  please feel free to browse our site by using the navigation bar at the top of every page.

. Member Log In User Name:   Password:   Not A Member? CDH Parent or Medical Professional? Click Here to Join for Free! . .   Easter 2008, 8 years old

We have a lot going on at CHERUBS; our new web site, new volunteers, a charity ball & golf tournament being planned, lots of new items in our e-store including maternity wear, local get-togethers and a grieving parents get-together, our newsletter is out, we have a new Angels for Cherubs program, and much, much more!

DISCLAIMER:The information on all pages of this web site is for education only. It is not meant to be used in place of proper medical care and advice. CHERUBS does not encourage or discourage any medical treatments or procedures. Our purpose is to educate families and medical care providers so that they may make the best decisions for the patients' interests. You can not compare your child to other children born with CDH, they are all different. The opinions aired by members are not necessarily the views of all members, staff, or of CHERUBS.


 
 

In Honor / Memory of: Mailing Address To Send Donation Acknowledgement To:

   

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