So…this seems to have turned into more of a weekly update
now that I’m home. Went to the clinic
again today. I had my first of 4 spinal
chemo treatments early this morning (Doc has ordered 4 rounds post-transplant
as a preventative measure). Same anesthesiologist
(Dr. Morris) who did all of my first spinal chemo treatments did my appointment
today. He is amazing and I barely felt a
thing (just the numbing medication that he used at the very beginning of the
procedure and when he finally pulled out the needle at the very end. All in all, not a big deal.
I also met with Dr. Nash (my transplant doc) this
morning. He continues to be pleased with
my progress. He is now pretty sure that
my rash on my arms is not GVHD and he isn’t sure if it’s a medication reaction
or something else (excema possibly?) and he mentioned today that he is thinking
about referring me to a dermatologist to get it looked at by a specialist. We’ll see what happens next week.
Super interesting/fun news…when they did the labs on my bone
marrow from the last biopsy they also did a chimerism test. “Chimera” is a mythical creature that is a
hybrid of different animals (for those who are interested…go google “Chimera” for
cool pictures of the mythical creature :) Hematology/Oncology docs use this
term to refer to the measurement of “how much of my blood is mine & how
much is my donors”. The nurses have been
telling me since the biopsy that the first time they draw chimerism labs that
people are usually between 50-80% donor blood cells and not to expect much
higher than that. Well, my donor cells
are apparently over-achievers because my first chimerism results came back as
100% XY cells meaning that all of my bone marrow is “brother-blood” now! J
Pretty cool!
Here at home I’m surrounded by “sickies” (as my brother
calls them). Both John and Scotty are
sick (poor guys) and I’m not allowed to be around either of them. This is Scotty’s first cold (not bad for
being 8 months old) and I’m afraid that he’s already shared his germs with his
daddy. Thankfully we have 1 extra bedroom and John is sleeping in it
(downstairs) until he feels better and can return to the master bedroom with
me. Good thing my mom is here helping
out because I’m not allowed to care for Scotty or for John because of my
compromised immune system. She has been
an amazing help! I’m praying that I
don’t catch whatever the boys have… I don’t want to end back up in the
hospital!!!
-Chellie
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