Friday, January 1, 2010
Posted by Markys mom at 9:31 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:
you are very brave with all those needles coming out of your arm! hang in there! sonia hunt
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