Dejà Vu All Over Again, Back to a Pink Room

Here's Steve in a photo from last week, waiting for his blood draw.

Well, after a few weeks of doing well, Steve started feeling pretty rotten, very fatigued, blacking out and a handful of other strange symptoms. We ended up going every other day for tests and blood and plasma transfusions last week. His kidney function was dropping, his blood pressure sometimes extremely low. Then Sunday night it became really bad and Monday we went to the clinic.

He couldn't walk without passing out (he had to come down the stairs at his house sliding step by step on his bottom), so transport was by wheel chair. The clinic was extremely crowded after the holiday week-end. Steve looked like he was about to slip out of the wheelchair in the waiting room, so I begged a bed or at least a recliner in the infusion area. He was shivering and shaking and his feet were burning painfully. As cold as he was, he couldn't stand even a sheet touching his feet.

They began drawing blood and blood and more blood for tests. Long story short, Dr. Agura put Steve back in the hospital. There were no beds on the BMT floor, so they put him in the ICU in the main hospital. It was quite a shock after the caring and knowledgeable staff at the BMT. Transplant patients are so specialized in their care and treatment and the nurses in the ICU didn't have a clue. Plus family access in the main hospital was much more restricted and I kept tangling with the staff. I didn't leave until the middle of the night after being sure they weren't going to do Steve any harm. If they were running a popularity contest with those nurses, I would not have won any points.

After a night there, they managed to find a bed in the BMT ICU for Steve. Then in the middle of the night on Wednesday, they moved him off the BMT ICU into the main wing. Someone needed the ICU more than he did. All the nurses told him how good it was to see him again. Not that Steve loves going back to the hospital, but at least they inspire confidence that they will take care of him.

Early tests show he has a bacterial infection and EBV (Epstein-Barre Virus). EBV causes mononucleosis amongst other things. Steve is being treated for these and they say he will be in hospital for about a week. They have no idea what caused the foot pain but it is gone. He is in room 428 and can have visitors. He is feeling better now.

The good news is there are still no leukemia cells showing up in Steve's "storebought" blood. Bless the donor!

Here is a photo of Steve last Thursday at the clinic as Maria drew blood. Wearing a hat for warmth inside and sun protection outside. He is still quite bald, but a few moustache hairs are coming in. Still waiting for eyebrows and that mop of hair he normally has.