Cherubs The Assoc of Congenital Diaphragmatic Hernia Research
Mission:
No one knows what life is like with a child born with Congenital Diaphragmatic Hernia like theother parents who have walked this path. It is a very emotional, stressful, and physically demanding time. Just knowing you are not alone can make allthe difference in the world. CHERUBS wasfounded so that no family has to go down this path alone. Noone knows what life is like with a child born with CongenitalDiaphragmatic Hernia like theother parents who have walked this path. It is a very emotional,stressful, and physically demanding time. Just knowing you are notalone can make allthe difference in the world. CHERUBS wasfounded so that no family has to go down this path alone.
Results:
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I was only 10yrs old when I first learned about CDH. My family was super excited about another baby coming into our family. I was hoping for another sister and my brother was hoping for a brother. I knew something was wrong, when the tech ask my dad to take us out of the room. I had no idea what...
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Melanie P.
04/04/13
I'm a co-rep in the uk for cherubs. My son was born in 2001 with left sided CDH. Cherubs helped us a great deal. We never felt alone with our cherubs family x...
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charleys mummy in uk x
04/04/13
I've been a volunteer Rep for Cherubs for over 12 mths now. My daughter is a CDH "survivor" despite her surviving Cdh she has endured many struggles and continues to do so. The reason I volunteer for this wonderful Unique charity is because they supported us not only during our pregnancy but have ...
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