Just in case you want to understand more about the various leukocyte cell types circulating in the bloodstream and their specific functions:
So basically everything is going as expected. I have been warned that the worst side effects are yet to come. But they should last about a week, maximum. I still haven't had any nausea yet, nor any overt indication of mucositis. But my stomach is definitly unsettled. For the past three mornings I've had some strong discomfort with what feels like eosophageal acid reflux [post transplant note: this is the one mucositis lesion in my eosophageal pasageway I got from the chemo]. The nurses gave me some antacid liquid I can take when this occurs. It does not have an instantaneous effect and takes a while to kick in. But eventually it seems to do the trick.
For food, more often I'm turning towards the pudding and pasturized yogurt with a litle fruit in it. Jergen suggested the pear & apple baby food for when it get's really bad. I think I probably will do that.
Also. . . This morning the nurse removed my neck catheter. The upside is that it will be much better for me to take a shower without having to worry about keeping it dry. On the other hand, I'm going to now have to get stuck daily with needles for the blood tests and/or medication they might need to administer.
And thing to last note. . . . . daily tablet medication. . . they dropped my three steroid anti-nausea steroid medications and have added twice-daily Trimethoprim (Bactrim) wide-spectrum prophylaxis antibiotic as an added measure of infection defense.
Yuko and Judy bought some non-alcohol champagne for me to share with some of the fellow patients in the Ackermann ward during New Year. I hope your New Year will be a step-up compared with my scenario.
See you tomorrow!