Tuesday, December 13, 2011
Posted by Markys mom at 3:28 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.
1 comments:
Wow! Handsome boys! I can't believe they are so grown up! I didn't even recognize Scott for a second-- he's so good looking & changed from boy to man! And Marky looks SO great! Rosy cheeks & healthy! :) Sammy . . . cute as ever! I'm sure Santa didn't even have to ask if they had been good.
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