Welcome!

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.

–VISIT THE BLOG TO VIEW A VIDEO OF HAVEN–

The site has a new layout:

Click BLOG (at left) to revisit Haven’s story and read our latest updates.

Click PICTURES (at left) to see those big blue eyes again.

Coming Soon:

The links in the bottom left and upper right will soon contain information and encouragement to those affected by HLHS.  Stay tuned…

THANKS FOR YOUR LOVE AND SUPPORT!