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We came across this inspiring blog post from the Pediatric Congenital Heart Association. Five mothers give truthful answers about what it is like to have a child with a congenital heart disease. It’s not always easy, but these mothers share their struggles and give advice for others in similar positions.
We hope you enjoy this Q&A as much as we did!
The Todd and Karen Wanek Family Program for Hypoplastic Left Heart Syndrome (HLHS) is a collaborative network of specialists bonded by the vision of delaying or preventing heart failure for individuals affected by congenital heart defects including HLHS. The specialized team is addressing the various aspects of these defects by using research and clinical strategies ranging from basic science to diagnostic imaging to regenerative therapies.
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