Today is the 15th anniversary of Emily's diagnosis and heart surgery. But I'm not going to look back today - I'm looking forward and feeling proud of how she's turned out, how hard she works and the person she is.
it is great to hear from you and that your girl is living a normal healthy life. our girl is healing quickly and progressing as planned. thank you for reaching out to a stranger in need and for your support. your friends- thayne and amber hurst
Originally this blog was all about my youngest child Emily, who was born with a rare congenital heart defect called ALCAPA. It began as a means of putting her story down on 'paper'. That part begins here but as often happens I went off on a tangent...............
1 comments:
it is great to hear from you and that your girl is living a normal healthy life. our girl is healing quickly and progressing as planned. thank you for reaching out to a stranger in need and for your support. your friends- thayne and amber hurst
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