DHREAMS - Diaphragmatic Hernia Research & Exploration Advancing Molecular Science
About CDH
CDH

Support Groups/Personal Web Pages


Global CDH: A non-profit support group created by a family affected by CDH
www.globalCDH.org
Breath Of Hope:A nonprofit public charity formed in 2004 by families affected by CDH
www.breathofhopeinc.com
CHERUBS: Association of Congenital Diaphragmatic Hernia Research, Awareness and Support. A non-profit organization founded in 1995 to help families and medical care providers of children born with CDH
http://www.cdhsupport.org/
Kamryn Hope's Blog: A personal story of a family affected by CDH
http://thestuddardfamily.blogspot.com/
The Parker Reece Foundation, Inc: A non profit corporation created by a family affected CDH
http://www.theparkerreesefoundation.com/
In Side Out: A personal story of a family affected by CDH
http://kali-insideout.blogspot.com/2010/03/yoku.html
Leo's CaringBridge: A personal story of a family affected by CDH
http://www.caringbridge.org/visit/leoschaeffer/mystory
Finley Anabelle: A personal story of a family affected by CDH
http://finleyanabelle.wordpress.com/
Sofia's Story: A personal story of a family affected by CDH
http://www.sofiascdhstory.com/
Life After CDH: A personal story of a family affected by CDH
http://lifeaftercdh.blogspot.com/
Henry's Story: A personal story of a family affected by CDH
http://henrysstory.wordpress.com/
The views represented on the above sites are their own and do not necessarily represent the views of the DHREAMS study group
© 2009 - 2017 Columbia University. All Rights Reserved. Our website was not designed to address all the genetic, medical, or emotional issues that may occur in families with CDH. Our website is not intended to substitute for a consultation with a licensed health care professional.