CHD According to Me: Life Lessons from Family Members Living with CHD

In their own words family members offer their perspective on living with a congenital heart defect (CHD). Read perspectives from a mom regarding parenting a child with CHD, a dad regarding the desire to “fix” CHD, and a sibling reinforcing the need for open, honest communication. The mission of the Congenital Heart Public Health Consortium (CHPHC) is to prevent CHDs and improve outcomes for affected children and adults. Even with a public health approach the impact of CHDs on individuals and their families is central to the activities and outcomes of the CHPHC.

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