Gary got home last night, so Casey is in the hospital alone right now. I will be going out to him on Tuesday. I will get the apartment and have it all ready for when he is discharged from the hospital. You never know exactly what day that will be and when you are 1500 miles away you need to plan in advance for the what ifs. Stevie is at home and doing well. She is a bit tired from all of the stuff they took from her and her back is healing. Most of the swelling has gone down. Gary and Casey had a nice Thanksgiving dinner in the hospital. Casey's counts are at 0.0 and he is having stomach issues, so he is very tired. He still has the blood clot, which they are trying to dissolve with medication. He will have to take it easy and take medicine for the next 6 months. He has very low platelet count and no immune system, so medication is the only option. At least with the port pulled out, the amount of pain has eased a bit. He does still have some pain, but it is manageable. Gary says all he does is works and sleeps. It really is hard to imagine how hard a swim coach works when they are not on deck unless you live with one (or sit with one in a hospital daily). The doctors want him to walk at least 3 times a day. So Casey, this is your mother, "you need to step away from the computer and go for a walk".
The doctor's tell him to expect his counts to start rebounding around day 21. We are at day 12. This is his 3rd transplant, but each one has been different. We really don't know what to expect, so we just keep praying.
Stevie says hi.
Gary's Thanksgiving Dinner
Casey's Thanksgiving Dinner
Casey and Caroline face timing on Stevie's phone. Gary says I need an I Phone. This is the happiest he has seen Casey all week. Caroline definitely recognizes him.