Congenital Heart Information Network
Mission:
C.H.I.N. is a national organization that provides reliable information, advocacy, support services, financial assistance and resources to families of children with congenital heart defects and acquired heart disease, and adults with congenital heart defects.
Results:
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CHDDad
11/30/12
TCHIN was the first organization that I was introduced to after giving birth to my first son who had a complex congenital heart defect called Hypo-Plastic Left HEart Sysndrome. TCHIN's website had all the information that I needed to help me through my journey and to connect with others in the same...
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StLouisBookworm
11/16/12
My daughter was born 17 years ago with Hypoplastic left heart syndrome, and there was very little information available. I clung to a copy of an article about a little boy who had the same thing because it made me feel we were not alone. I became involved with the Congenital Heart Information ...
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lyoung
11/13/12
My son was diagnosed with a heart defect, couple days after being born and a few hours before we left the hospital. I was told he'd need open heart surgery sometime in the first two years of life, or he wouldn't survive. I was told to see the cardiologist in his office in a week, that we'd be ...
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