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.
Sorry all of Marky's friends..... I messed up my blogging settings and all the sentences are running together ! My friend is going to try to fix in a few min.s ! I'm a computer dummy, incase you havent guessed already !
Posted by Markys mom at 9:05 AM
1 comments:
If you need any help, let me know.
Love you.
Karie
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