Thursday, January 14, 2010
Posted by Markys mom at 9:56 AM
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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.
3 comments:
marky, you look so much better and you even have a little smile on your face. that made me smile. You are such a brave boy! Sonia Hunt
I love seeing Marky in the standing position after seeing him only in the laying position for so long! How Great! Love ya Marky!
Larsen's
Amen. Marky, it's totally awesome to see you on your feet again! Now we can tell a bit better how tall you're getting. :) Love you Marky!
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