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7 years ago
Our son Magnus was born November 19, 2009 with a serious congenital heart defect, HLHS. I set up this blog to keep our family and friends updated on his condition, and to connect with other families dealing with HLHS.
Wish I knew the words that could make this all better, but they don't exist. Know that Magnus has lots of friends and family who are wishing him well. We're sending love, hugs, kisses, and wishes for a speedy recovery.
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