a bloody nose!!!
This was the
scene yesterday
as we were playing
catch with a
bouncy ball and
Mom threw a wild
toss!!!!
SOOORRRRYYYYY
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.
Posted by Markys mom at 6:34 PM
3 comments:
I found this blog through a friend's, and Marky hasn't been far from my mind since. But what exactly is the story behind his and his family's ordeal? Would you mind doing a recap post for us?
Hi! If you want to see the history of Markys ordeal, check out the blog archives located at the bottom right of the front page:)
See if that works....if not let me know---Im always happy
to talk about Marky!!!
Now you are a real, authentic soilder...blood on the battlefield!! Love you bunches, Aunt Dianne
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