C.H.I.N. is a national organization that provides reliable
information, support services, financial assistance and
resources to families of children with congenital heart defects
and acquired heart disease, adults with congenital heart
defects, and the professionals who work with them.
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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you of changes to this website. We never share email
addresses with other organizations. Please read our
privacy statement for
complete details.
Community
Read about our members in the Portrait
Gallery,and find information
about our online discussion groups
for patient/family support and professional communications.
Resources
Visit our Resource Room, which
presents informational materials for families created especially
for publication on our site. Here you can also find
Support Groups in your community,
read book reviews, and learn about
becoming a member of our organization.
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 Copyright �1996
- 2009 C.H.I.N. all rights reserved TX4-390-685
Please read our Privacy Statement
