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Dad is using a walker now. He is okay with that. He can get about the house better. Mom told me that Dad said, after he fell the other night and couldn’t get up, “I never thought I’d end up this way…”
Small victories are the epitome of cancer.
After the initial diagnosis the first came when they said Grade III instead of IV, then there was no spread, then he wasn’t terribly sick from chemo just a little and then…on and on and on it goes.
For every down side there was a small victory, albeit tiny, squinting hard to find it victory…because without those little bitty scraps…you have nothing to hope for…
Dad hasn’t been taking his Lasix or Potassium and is only taking his TJN’s(twin jet nebulizor treatments) prn (as needed). He feels his legs aren’t as edematous, and they aren’t and that the TJN’s were making him cough more.
Ethel, one of Dad’s chemo nurses called on Thursday and said that Dad had to have an IV treatment of some sort (mom couldn’t remember) to “make his bones stronger). I think it has something to do with an elevation in his serum Calcium level. His is 1 point higher than it should be. Anyway…the thing is, the centrifuge was down at the office where they drew his blood and they had to ship his blood over to the hospital for a read, so the lab was different and I’m not sure I agree with treating him without another blood draw first.
So….we are supposed to go to our hospital on Monday, mid morning and get his IV treatment of some sort.
We’ll see. I may have to make some phone calls first.
We left for Kearney about 7 am in order to get Dad’s radiation treatment done before his chemo appointment. This time he got in and out of the radiology department quickly. We left for the oncologists office immediately and upon arrival, Dad got his blood work done. As we waited in the room for the NP(nurse practitioner) to come in and examine Dad and ask the same damn questions he just answered for the radiology nurses I heard the lab wench say that the centrifuge was not cooperating.
Let me guess.
Yes, another delay.
The NP came in and asked all the same question her nurse just asked that resembled the questions that the radiology nurse just asked and guess what?
The answers were the same.
Then…we were told that Dad’s blood work would have to be taken over to the hospital and that we would have time for “breakfast” and to come back in 45 minutes.
We went to Micky D’s and Dad ate apple pies and and an egg, bacon McMuffin and coffee. Mom nibbled that stuff too. I got a diet Coke.
When we returned we waited for awhile and another while and yet more whiles. Finally, the good news: The blood work is okay!
Let the chemo begin!
Dad was premedicated with Prednisone and Benedryl for the last 24 hours in preparation for this chemo treatment as he has reacted the last 2 times. Did it work?
HE STILL REACTED. Breathing shutting down, flushing, coughing…just not as bad as the 2 previous times.
shit fire and hide the fucking matches
After an IV dose of Solu Medrol he was fine and fit as a fiddle and able to take the poison aka cure from hell Taxol.
Mom and I left to do a few errands when Dad relaxed and started to doze and she returned some pants at Walmart and I wandered around buying a new curling iron, forgetting the very important item…hair dye, getting Mark orange and black shorts and a new black shirt that says basketball, and piling a sack of some kind of freaky trail mix into my cart.
We brought Dad a chocolate shake from Sonic and waited for the chemo to be done. Finally around 4:30 he was free from IV lines and we were out the door. Dad felt great and off to the wild blue yonder we flew.
How come when Dad gets chemo I’M THE ONE EXHAUSTED!??
Tomorrow…the last radiation treatment and then we don’t have to go to Kearney for 2 whole weeks!
Today Dad and I saw about 3,000 snow geese east of Axtell. Most had their downy asses planted in a corn field but some were hovering above the land all in a long white row. I wish I’d brought my camera. There was a light dusting of snow last night and the geese sure blended in to the rough stalks of corn and plowed land.
We had to wait for Dad’s radiation treatment for over an hour today which is not the norm. The cancer center had extra patients as they were helping out another place where the machines were down. The waiting room was full of new people. No one we knew for once. Funny, now we are the “old timers” there. We know where the goodies are, how to make the coffee, how to use the new computer terminal and sign in. We know the look of the newly diagnosed, the silence they wear in their eyes, the weight of papers they carry inside their new “living with cancer” guidebook. We know who the workers are and the ambulance drivers and the radiation tech’s. We know that turtledove nest above the cancer center doorway and that once should never look up when entering. We know the men’s bathroom can “lock itself” when empty and that you have to use a butter knife to get it open. There are no keys.
It might feel strange not going to the treatments. Kind of like we are not doing enough. We will have 4 more chemo treatments though. Next one on Wednesday. Hopefully the pre treatment of Prednisone and Benedryl will stop the annoying allergic reaction dad has – not breathing.