Awoke
to hic-quakes today 0530, shaking my body and my bed … very Exorcist. With the
cool mist vaporizer running full throttle the chemo mist was confusing me.
I
have not slept through the night since chemotherapy began 9 days ago, factor in
chemo fatigue … and chemotherapy is kicking my ass. I pray it is also kicking
cancer’s ass as relentlessly.
It’s
also about my own stupidity. Where did I ever get it into my head that by the
third day I would be feeling better? I had even briefly agreed to perform on
the 4th day before cancelling out by day 2.
My
oncologist assures me I am not unusual … some patients are up and about within
the week, others may take another week or two.
After
a quarter century of spouse caregiving, ‘dependency’ was never my future view …
and it is spinning my world off its axis.
I
must assume that cruising through brain radiation therapy addled my brain.
Retuning for saline drips and/or sugar water drips has been helpful and
restorative if only for a couple hours.
Plus
the chemo lounge is a world within a world or a dream within a dream. Our own
daughter even remarked how seeing another adult daughter watching over her Dad made her feel less alone ... it took her 16 years to find another like her, with a Mom in a wheelchair with MS
Skipped
today just to see how it might go. Started out OK but as usual without a saline
and or sugar water drip it deteriorated. Returning tomorrow, Friday, for a
booster for the weekend.
Plus I've developed a garden variety laryngitis which is only frustrating
everything.
Blood
work, vital signs, etc. are “excellent”
Just wanted to say that you are such an inspiration. I'll admit that it is your MS caregiving blog that drew me into your world, but I've read your both your blogs for so long that I feel like we are almost old friends. Hang in there and thanks so much for sharing your life with all of us here in internet land. Wishing you peace, restful sleep, and the energy to face the day.
ReplyDeleteThank you Theresa you're wishes are a Godsend!
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