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

Support Groups/Personal Web Pages


DHREAMS Research Study (Congenital Diaphragmatic Hernia)
www.facebook.com/pages/DHREAMS-Research-Study-Congenital-Diaphragmatic-Hernia/181478347688?ref=search
CDH International: A global initiative to stop congenital diaphragmatic hernia
cdhi.org/
CDH UK: The CDH Support Charity that consists of families, friends and medical professionals affected by Congenital Diaphragmatic Hernia (CDH)
www.cdhuk.org.uk/
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
www.cherubs-cdh.org/
Breath Of Hope:A nonprofit public charity formed in 2004 by families affected by CDH
www.breathofhopeinc.com
Kamryn Hope's Blog: A personal story of a family affected by CDH
thestuddardfamily.blogspot.com/
The Parker Reese Foundation, Inc: A non profit corporation created by a family affected CDH
theparkerreesefoundation.wordpress.com/
In Side Out: A personal story of a family affected by CDH
kali-insideout.blogspot.com/2010/03/yoku.html
Leo's CaringBridge: A personal story of a family affected by CDH
www.caringbridge.org/visit/leoschaeffer/mystory
Finley Anabelle: A personal story of a family affected by CDH
finleyanabelle.wordpress.com/
Henry's Story: A personal story of a family affected by CDH
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 - 2018 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.