CHERUBS Information for Grieving Parents of children born with CDH

 

Losing a child is the hardest thing anyone can go through.  You're not alone, there are 100's of other grieving CDH families that know exactly what you have been through and what you are going through.  Here, you can talk, cry, and remember your cherub.

 

Learn about Congenital Diaphragmatic Hernia and browse our frequently asked questions list   Suggestions on preparing for the funeral, how to handle family and friends, etc   Inspirational articles and poems    Our annual CDH Research Survey Results, CDH Research Library, current CDH research studies, and our petitions for better medical care   Free membership for families and medical professionals of CDH patients   Frequently asked questions about CHERUBS   Order some of our fundraising items, shop, or make a donation on-line at our secure e-store   Download our Information Packet, Parent Reference Guide, newsletters, and other materials in PDF format

Ideas on where to look for local support   Need someone to talk to?  Our On-Call Parents are ready to lend an ear   Bulletin boards, listservs, chats, ICQ network, and links.  Come meet other members, ask questions, and give and receive support   Meet our wonderful members by reading their stories, browsing our on-line photo album, or visiting their personal web sites   Contact your state or international Representative for information on local resources   Our Quarterly newsletter   Links to other support groups as well as to personal homepages of members

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