Go in on Tuesday (2-5) for admitting tests, to be admitted
Tuesday evening. They will “plump” him up with fluids and start him on three
different Chemo Meds Wednesday morning. He will have daily Chemo for five to six
days. Then that will be followed by one to two days off, but still in the
hospital. He will then receive his own Stem Cells back and stay in the hospital
two to three more weeks. IF all goes well, and WE KNOW it will, he will get to
come back to The Tin Palace for a while and have daily blood test (of
course). From there we will see.
Liver biopsy was fine, just “fatty” At the time of the
biopsy his enzymes were down and today they are back up. Crazy don’t know why.
Maybe one of his diabetes meds, they don’t know.
They changed out his Big CVC for a smaller one and that
is looking fine ^ see above ^. I do the “flush” daily & changing of the
Caps No big deal as there are NO needles involved. I have not done the
demonstration of the Dressing Change as it has many steps and I don’t feel
confident with it YET. And hey they will be doing all that when he’s in the
hospital anyway.
Johnny is feeling pretty good about all this mentally and
emotionally. His spirits are high and he expects the best possible outcome. Physically
he does get tired and of course once the heavy chemo starts he may have side
effects - loss of hair, weight and appetite y’all know the usual. However one
of the meds can cause seizures so he will be put on an anti-seizure med for
that. And there is a probable chance of a skin rash Dr. Jones described it as “a
bad sunburn.
That’s it for now, I will update as news comes and the
internets around here allow. Please continue all your prayers. We are grateful
for all that y’all do.
xoxo
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