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.
Thursday, December 17, 2009
Please join us in a special fast for Mark and his family. Thank you!
Thank you so much for making this blog. It has been a great way to keep up with Jeanes' without calling them everyday (which I'm sure they are getting plenty of that). We love Marky and know he's a fighter so our prayers and fasting will not stop as we know he will not stop fighting...LOVE YOU GUYS!!!!!
We love you all so much and know the Lord will bless you all. You are in all of our thoughts and prayers every minute of the day. Marky we love you. Thanks for the blog updates!
Thank you so much for making this blog. It has been a great way to keep up with Jeanes' without calling them everyday (which I'm sure they are getting plenty of that). We love Marky and know he's a fighter so our prayers and fasting will not stop as we know he will not stop fighting...LOVE YOU GUYS!!!!!
ReplyDeleteWe love you all so much and know the Lord will bless you all. You are in all of our thoughts and prayers every minute of the day. Marky we love you. Thanks for the blog updates!
ReplyDelete