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.
Sunday, December 20, 2009
Mark is headed to surgery for his Bone Marrow Biopsy. This after a night of throwing up and discomfort.
Lynette was the parent-on-duty through the night. Lori and Diane are arranging the schedule for tonite and tomorrow but it is unlikely Lynette will stay away.