Friday, December 24, 2010
Posted by Markys mom at 10:42 PM
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This is an ongoing story of our family as we struggle day to day. Marky has a very rare disease called retro-peritoneal fibrosis which simply means there's a fibrous coating of crud all over his organs. His prognosis is unknown, since the disease is so rare. We appreciate all who visit Marky's blog and thank you for your love and support.
2 comments:
I love those smiles! They say pictures are worth a thousand words...these pictures do demonstate that.
Love you guys,
Sarah
Cute! Love that little tongue sticking out!
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