Thursday, April 8, 2010
Posted by kendude at 2:40 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.
2 comments:
Hey Nettie,
It does my heart good to see those pictures of Marky at school! I am so happy for him! He is such a trooper! I think it's very cute that you got a call from him saying he missed you. I think I will experience a touch of that separation anxiety next week when Zoe goes back to school. She's been my little appendage for the last 3 weeks. She continues to improve every day and is starting to look like her old self. She says she is going to miss her purple eyes :) I wonder if Marky is going to miss his cheeks? Maybe it's just their badges of courage, a little reminder of what they have been through? Anyway, I'm just so grateful that we have both been recipients of God's love and experienced these miracles. I read your blog all the time and your family continues to be an inspiration to me. Thanks for checking in on Zoe!
Love, Tricia
What a delight to look at the side-by-side photos of Marky currently at the top of the blog! One is of a brave boy with tubes, patches and scars and the other of a happy boy busy at school. What a miracle Heavenly Father has worked on your behalf! Thanks for posting these photos Ken; from a wishing star to a rising star! :)
Post a Comment