Much happening in cancer center these days. Turns out while I was slowly poisoning my body, ruining my feet and hands and greatly diminishing my hearing and eyesight....a tumor was being born and growing in the area I had surgery.
My surgeon recommended starting radiation RIGHT NOW, but the radiologist connected to my care team wanted to do multiple scans. So you know how this works....you wait for an appointment, then you wait for results, then you wait for a follow-up consult appointment because the one they scheduled for you was made in an alternte location 30 minutes after your scans were happening....and that location was almost 45 minutes away. So you had to wait for another day. That day came and since the radiologist knew you wanted to have your radiation done in the place you live, he pretty much just sent you packing. The one thing he did do was suggest I get a DVD of those scans to take to the new radiation place.
The next day I walked in to the local facility only to find the other radiologist had not sent a referral so I walked in cold and plunked down my movie and made an appointment. And I waited. By the time I finally got an appointment with the new radiation doctor it had been 9 weeks since my final chemo treament. He did his exam, ordered scans and embarked on a 2 weeks planning session on how best to treat me. He did show me the pictures on the DVD (still don't know why I couldn't have seen those prior). All that was on my mind was after all this time had passed how much had that tumor grown while be unbothered by any kind of treatment. Quite a lot it turns out.
To date, I have had 7 radiation treatments and they are kicking my tail. Because of the size and aggressive nature of my tumor (which I have named Tilly) my treatment level is pretty high. Having to be somewhere every day is intense because the whole act of getting ready to go somewhere takes me forever. It takes me forever because my feet still don't work and neither do my hands.
On top of this I am doing every 3 weeks immunotherapy....and surprise surprise both radiation and Keytruda make neuropathy worse.
I am still hopeful and optimistic that I can squeeze out a few more years. I have 2 little dogs that count on me and I'd like to fulfill the committment I've made to them. It is hard being in this place right now, because of neuropathy I can no longer do the things I'm used to doing to fill my time. I can't sew, draw, crochet, knit or cross-stitch. I can barely type. So that leaves TV and I've watched so much of that I have a hard time finding things I haven't seen.
I rarely go anywhere for reasons mentioned above, so it's me and the dogs on the daily and I think they are bored with me but for now they are stuck with me.
Meanwhile I continue to ask these questions.
Why after all these years is cancer still "a thing" and why suddenly does it seem worse than ever?
Why do they put laundry rooms so far away from the actual source of dirty clothes?
Why do people turn up their noses at adopting black dogs? (Particularly shelter dogs)
Why do people in Arkansas not know how to merge?
Why do so-called Christian people refuse to forgive and move on?
Why do so many people want to take your story and make it all about them?
Where does a cancer patient go to have their toenail issues dealt with?
Who holds the answers to all these things that leave me wondering?
So that's what's new with this Pussycat. She's not purring and cuddling up to anyone...she's got her claws out and is hissy and pissy a whole lot of the time.
But she's alive, still fighting, still trying to move out of this chapter into a better one.
Happy Thanksgiving! Don't be a turkey!
And this year Shop Small - they need it more than big box stores or Amazon.


