Wednesday, December 15, 2010
Posted by Markys mom at 7:43 PM
Subscribe to:
Post Comments (Atom)
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:
And look at pretty Nettie . . . all those trials & still smiling!
Post a Comment