Saturday, December 26, 2009
Posted by Markys mom at 5:39 PM
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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.
6 comments:
Ethan says "hi Marky ,hope santa brought you some fun stuff" .We miss ya and are praying for you.
love the Wilshers
xxxxx
Hi Marky! I am praying for you too and I want you and Jonah to come over and play as soon as you are better and the weather is nice!
Love,
(Jonah's Aunt) Heather
Hey Marky!!! We look at your blog everyday and talk about how awesome you are! We can't wait until it's summer again and we can all go swimming in Uncle Alan's pool! Love you little man!
Love,
Jenny, Bryant, Kaden and Lily
Marky is always in my thoughts and prayers. What a trooper! I hope you like the video of your class at school. Can you believe Santa left a message for you? That was awesome! LoL
You are an example to our family! Your sweet endurance has taught us to be less complaining and more grateful. Still praying for you!
Hi Marky, The high light of my day was watching you sleep this afternoon. You looked like a little angel. But sounded like a bear snoring. Only kidding. I enjoyed reading all the little cards and well wishes and visiting with your dad. He is a great guy and loves you very very much. Keep resting and get stronger. I miss teasing my little fruitcake.
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