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.
Im working on trying to figure out how to
enlarge these pics...... be patient w/ me.
I called my blog expert, Jana Harris, to fix
it. ! She's a life saver.
Posted by Markys mom at 4:51 PM
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