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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.

Please join our thriving organization! Become a part of our dynamic international community of health professionals, families, and individuals affected by Congenital Heart Defects and Childhood Onset Heart Disease.

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Disclaimer: The contents of this site are presented for informational purposes only, and should not be substituted for professional advice. Always consult your (child's) physicians with your questions and concerns.
Created and maintained by Mona Barmash and Uwe Baemayr for The Congenital Heart Information Network.
Exempt organization under Section 501(c)3.
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