I went to UW for
the third time in four days. I received
IV immunotherapy, obinutuzumab, and IT chemotherapy, cytarabine. Everything went okay, and the peanut butter
and jelly sandwiches were just as dried out as usual. Think a pumice stone for exfoliation.
I learned from
Amy, the nurse practitioner who did my IT chemotherapy, that I am scheduled to
move forward on the CAR T-cell therapy, with or without cancer in my CNS.
I might see 2022,
and the possibility of another drug or treatment to come online to keep me
alive a little later once I relapse from the CAR T-cell therapy.
That is what has been
happening since July of 2020.
I felt terrible yesterday
but took a large cocktail of drugs last night which helped. I was tired as all get out, then seemed to
catch a second wind and struggled to fall asleep.
The skin issue
seems to be turning the corner. It would
be nice to not awaken at night because I itch so much.
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