To those affected by a heart defect:

Haven’s Heart: Back online!

December 7, 2009 at 10:22 pm by Mom & Dad

Sorry for the delay!  The site should be fully functional now (mostly).  For those of you who have been awaiting new content, we promise a new video will be available for Haven’s birthday.  We will also be adding information to the new links that you see on the bottom left and right sides of the screen.  Stay tuned…  Thanks again for your patience and your vigilance.  It’s nice to know that people are still looking in on Haven now and again.

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This site contains the story of Haven Leigh and serves as a source of hope and encouragement to anyone who has or knows a child born with HLHS, a congenital heart defect, or other terminal illness. Here, we show the rewards of nurturing and supporting a special child while celebrating her memory by sharing her story with others.

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Please come back soon for the new version of Haven's Heart.net!!!