CHERUBS - The Association of Congenital Diaphragmatic Hernia Research Awareness and Support
Bookmark and Share           Forums  |  Join For Free



CHERUBS - The Association of Congenital
Diaphragmatic Hernia Research, Awareness and Support
.

Non-profit organization raising global CDH awareness, supporting all babies & families affected by CDH and
promoting
research into the causes, prevention & best treatments of CDH since 1995.
CHERUBS - The Association of Congenital Diaphragmatic Hernia Research Awareness and Support
CHERUBS Homepage
What is Congenital Diaphragmatic Hernia?
CHERUBS CDH Charity
Congenital Diaphragmatic Hernia Research
Congenital Diaphragmatic Hernia Awareness
Congenital Diaphragmatic Hernia Support
Congenital Diaphragmatic Hernia & CHERUBS News
CDH Conference, Fundraisers, Get-Togethers and More
Shop for CDH Awareness Gear
Make a Tax-Deductible Donation to CHERUBS

CDH Support Forums Goodshop & Goodsearch for CHERUBSCDH Awareness ShopJoin the Angel ClubCDH HOPE Totebag ProjectCongenital Diaphragmatic Hernia Research BillCongenital Diaphragmatic Hernia Awareness
Pregnant with a baby diagnosed with CDH?Raising a special needs child born with CDH?Grieving the loss of a child born with CDH?
CHERUBS - The Association of Congenital Diaphragmatic Hernia Research, Awareness and Support



CHERUBS - The Association of Congenital Diaphragmatic Hernia Research, Awareness and Support



CHERUBS H.O.P.E Totebag Project
(Helping Other Parents Expecting)


Project Mission:   To assist families expecting babies born with Congenital Diaphragmatic Hernia by providing them with much needed free information and support items through a community project in which all CDH families can participate and honor their children while helping new families affected by Congenital Diaphragmatic Hernia.

Congenital Diaphragmatic HerniaCongenital Diaphragmatic Hernia (CDH) is a devastating birth defect that affects 1 in every 2500 babies.   CDH occurs when the diaphragm fails to fully form, allowing abdominal organs into the chest cavity and preventing lung growth.  The cause is not known.  

50% of babies diagnosed with CDH do not survive.   Of those that do survive, sometimes long hospitalizations and other issues occur.  It is incredibly important for CDH families to have accurate information of all the treatments for Congenital Diaphragmatic Hernia so that parents can make informed decisions for the babies' care.  Items included are a CDH Awareness Ribbon totebag, personal care items for baby and information for the parents and family.   Our CDH Baby Book is over 200 pages of valuable CDH information and advice.

Over 100 new and expectant CDH parents join CHERUBS each year.   This project was created for them, to help them through the first few weeks and months in dealing with Congenital Diaphragmatic Hernia.  Our totebags are put together by volunteers through donations.





CHERUBS - The Association of Congenital Diaphragmatic Hernia Research, Awareness and Support

Home  |  What is CDH?  |  About Us  |  Research  |  Awareness  |  Support  |  News  |  Events  |  Shop  |  Donate
  |  Contact Login Help
.
Copyright © 1995-2011.  CHERUBS.  All rights reserved.  Graphics & text created by CHERUBS may be used freely but we ask for a link back to our site.
CHERUBS is an IRS recognized public 501(c)III non-profit organization founded in 1995.
.
CHERUBS - The Association of Congenital Diaphragmatic Hernia Research Awareness and Support
Mailing Address:  3650  Rogers Rd. #290, Wake Forest, NC 27587, USA
Office:  S. Main St, Wake Forest, NC 27587, USA
Telephone:  919-610-0129    Fax:  815-425-9155    Login Help  /  General Info