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The Congenital Heart Defect Network
A social network for families who have a loved one affected by a congenital heart defect, or have been living with a CHD.
My daughter is 20 months old now and she already had two open-heart surgeries, the BT Shunt and Glenn. During her 2nd surgery, she developed Pleural Effusion and made her stayed in the hospital for seven weeks, she had diaphragm ligation, etc.…Continue
My name is Debbie and my son, Jayden, was born on June 17, 2011 with hypoplastic left heart syndrome and ventral septal defect. He has had one surgery about 1 month after he was born and had complications. He began to heal and got really sick…Continue