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.
Tuesday, December 22, 2009
Well, it looks like things have taken another turn. Mark woke up today with a high fever, so they will be doing a full exploratory surgery of his abdomen in about an hour. They will biopsy many different tissues for analysis. The surgery is to last 3 to 4 hours. Mark will then be moved to ICU and will not be able to have visitors to keep a very sterile environment. We will post more as we find out.
Our love and prayers are with all of you! We pray the doctors can soon get some answers and get you well Marky! We love you soooo much!
ReplyDeleteMarky had three little doggy friends come in to visit him before his surgery this morning. The Children's hospital is such a blessing. When asked by Ken today what was the one thing he missed the most and wanted to see when he got home, He replied was his little brother Sammy.
ReplyDeleteOur prayers are with you Marky and our Little Jeans family.
We love you Marky!!!! We hope you Get well soon :)- megan, jade and kids!
ReplyDeleteIf you get hungry, Marky, those dogs make a great soup.
ReplyDeleteWe love you too Marky, Lynette and James. We continue to pray for your peace and comfort. Stay strong Marky you are a champ!!!
ReplyDeletePlease let us know if there is anything you need.
Lots of love-
The Morris Family