Congenital Diaphragmatic Hernia
Who to Contact
CHERUBS - The Association of Congenital Diaphragmatic Hernia Research Advocacy, and Support
3650 Rogers Rd. #290
Wake Forest, NC 27587, USA
CHERUBS offers a support group for families and medical care providers of children born with Congenital Diaphragmatic Hernias. Site features stories, links, photos, FAQs, and more.
We are proud to serve over 3000 families in 38 countries and all 50 states affected by CDH since our creation. Through our dozens of free ground-breaking services and the friendships made within our member community, CHERUBS has positively affected the lives of 1000's of CDH families and inspired many new CDH charities and project who have followed in our footsteps. We will continue to lead until Congenital Diaphragmatic Hernia is no more. We are devoted to finding the cause, prevention and best treatments for CDH.
Where to Go to Chat with Others
The Association of Congenital Diaphragmatic Hernia Research, Advocacy, and Support
This mailing list is for grieving families of children born with Congential Diaphragmatic Hernia. All subscriptions must be pre-approved to assure that only grieving parents are members. This action protects these families privacy in sharing their emotions and opinions without the risk of being viewed by medical professionals or parents of survivors. CHERUBS- The Association of Congenital Diaphragmatic Hernia Research, Advocacy, and Support. Listserv for grieving parents.
- Breath of Hope
This group is for those who had a child with CDH (Congenital Diaphragmatic Hernia). This listserv as of 2/2004 is for both survivors families and those who have had nonsurvivors - but then we are all survivors.
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