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“C” is also for Coping

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Things I have learned about coping with cancer this week:

  • Keep a large supply of tissues on hand all the time, everywhere, within reach. And premium tissues–the soft, thick kind–are worth it. The industrial, near-unto-sandpaper variety, not so much. (Ow.)
  • On a related note, switching to waterproof mascara for a while = good idea.
  • No matter how desperate I feel my need for information is, some things–which, furthermore, may not even be relevant to my case–I’m not emotionally stable enough to handle right now. After terrifying myself multiple times in the last few days, I’ve placed a moratorium on me Googling certain search terms until after I’ve met with the Emory oncologist.
  • Little things can be surprisingly life-affirming.
    • Applying sunscreen religiously every day is a necessity for me because of my Lupus/MCTD. But I’m also fanatical about it because exposure to sunlight’s UV rays is the single largest cause of signs of aging in skin, i.e., wrinkles. I’m vain. I want to still look pretty when I’m 94+. Sunscreen means I plan to make it to 94+.
    • Matthew took me shoe-shopping. A pair of new shoes means I fully intend to be sporting fashionable footwear next month, and the month after that, and the one after that and that and that. Shiny, life-affirming footwear:
  • While maintaining as much of my everyday routine for as long as I can is a good thing–my routine grounds me, helps me focus on something other than my terror and uncertainty–however, I’ve discovered and need to keep in mind that autopilot isn’t so auto right now.

    Yesterday, as I was getting ready for work, I almost put a half-full drink carton in the glasses cupboard instead of back in the ‘fridge, applied concealer with my eyeliner brush and accidentally dragged my concealer brush through a dollop of sunscreen, dropped my (hot) curling iron, and started getting into the wrong car in the garage. o_O

  • Which leads to: use more than one method to keep track of medication schedules.

    Holy crap I’m taking so many pills! And each has its own special dosage timetable and instructions: Once a day, twice a day, every six hours, with food, with a full glass of water, yadda yadda blargh. Hell, the prednisone is dizzingly confounding all by itself: two pills twice a day for three days, one pill twice a day for three days, one pill daily for three days. *thud*

    So, yeah, my day-per-week pill container just isn’t going to cut it. I’ve started keeping a log on my calendar to indicate when I’ve taken what and setting reminder alarms on my phone to remind me when I need to pop something.

Originally published at EugieFoster.com. You can comment here or there.

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On October 4th, 2013 03:18 pm (UTC), queenoftheskies commented:
::HUGS:: Keeping good thoughts for you!
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On October 4th, 2013 05:57 pm (UTC), threeoutside commented:
Moar ***hugs***!!!
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On October 7th, 2013 05:33 pm (UTC), whitecrow0 commented:
My mother-in-law was on a dizzying array of medications before she passed away. My father-in-law and sister-in-law kept track of them with an Excel spreadsheet, so they could double-check dosage instructions, "do not take with" (certain meds or foods), side effects to watch for or that she reported (especially if they were really bad), etc. Just a thought if something like that would work for you.
Also I've been a bad LJ-er for ... a long time so I'm just now learning this. I will have to read back to discover more detail. I'm sure you are still figuring out how to cope with this. My thoughts are with you.
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