Each day it gets harder and harder to get out of bed in the morning.
Last night, I got mad at Nick. I maybe can’t say mad…more like frustrated.
I work all day ….. and come home to a mess. Granted he rinses his dishes…and puts them on the counter…..right above the dishwasher. Recycles…go on the counter closest to the basement door instead of walking 3 more feet and opening a door to throw them. A big plastic jug, I took the screw cover off, put on the counter and put the jug NEXT to it. He put the lid back on and moved it further away from the basement door. (I did that one as a test. He failed)
I’m exhausted when I get home. Then I hear “I’m helping out as much as I can!”…no luv…..you are making more work for me. I don’t say this out loud but I feel guilt.
When we moved? I got yelled at SO many times to put the boxes where they were to STAY because he didn’t want to move them twice. So it’s OK to move things 3 times now?? *throws hands up in confusion*
I know it sounds petty but seriously……he wants me to do nothing but cuddle on the couch when I get home from work……..which I am more than willing to do….but AFTER I clean up his messes.
Which…..really? Should I have to clean up? He spent the morning in the garage yesterday. So he did have the energy to take care of these few things. The few things that would have saved me close to 45 minutes last night.
I’ll shut up now.
It’s Administrative Professionals Day today.
And see’s ya laters taters!!
This just made me chuckle…
They put Nick on a new regime of Chemo a couple months back. Every Friday…..or so I thought.
Now, they are going to do Chemo 3 weeks on, one week off. The Scan 10 days ago shows that the Cancer has not shrunk…….but it has not grown. I may have told y’all this already but I am seriously brain fried lately with all that we had to do for the benefit. I’m glad that is behind us so Nick and I can go back to normal…..whatever the hell THAT is.
He’s put on some weight. Not much but I do think every pound helps. He got as high as 117lbs but is now hovering around 114-115lbs.
He just sleeps when he crashes. So he’s changed his chemo to Fridays. He’s hopped up on Steroids and Anti Nausea meds from Friday to Sunday night. Which means we can actually DO something on the weekends instead of me sitting there watching him sleep. Maybe we can have SOME semblance of a life. Not what I expected when he and I married….but we are together…for as long as God wills.
Megann really hopes he makes it to her wedding. Sept 10th she and Trav will tie the knot. I hope he does too. I hope he makes it longer, too. After Christmas would be nice. We are trying to live every day like it’s his last….which can be heartbreaking. Sometimes we just sit on the futon, me holding him…and soon I hear his gentle snoring signalling that he’s crashed again. I just hold him…and stroke what is left of his hair. It’s coming out in handfuls of 8-10 strands every time I run my fingers thru it…..so then I stop. He wants to shave his head. I won’t let him…..funny thing is his hair is thinning equally. It’s not leaving huge bald spots like *gasp* in the movies cause we all know how real THAT can be….*
He’s getting very bored sitting home…..alone….every day. I don’t blame him. He doesn’t have enough energy for housework. Putting the dishes away out of the dishwasher taxes his strength. Even carrying in the bag with 3 lightweight sleeping bags and a blanket in it….did him in.
And it’s hard not to step in and do it for him. He needs to feel needed and useful. So I do my best to let that happen.
And it’s heartbreaking…….
Well I spose I should get back at this!!
Hope everyone is doing well.
We are finally going to try a trip more than 2 hours from home.
Nick wants to go to his sisters. 5plus hours of driving. I’m thinkin’ we may go half way and stay at a friends house over night. Then go the rest of the way the next morning.
He started crashing last night.
So we’ll see.
I do wish………for a day, an hour…..someone else would take over worrying about Nick. And let me be me again.
I would like to be ‘us’ for a day. For an hour. Without this cancer thing hanging over our heads. The benefit was a good success and we really enjoyed seeing SO many of our friends there! It was wonderful. Ask me sometime about the ONLY people who did any bitching. Betcha got that figured out already, don’tcha?? His child keeps putting in his cards “We are counting on you to beat this cancer.” It upsets Nick but apparently that doesn’t matter. Or they wouldn’t do this. It sets him up to fail. So it frustrates him because what more can he do?
Nick is at Chemo right now. Then he’s off to Jefferson for the car show/swap meet. He feels pretty good when he’s hopped up on steroids and anti nausea meds. That usually lasts 2 days. But his crashes are not nearly as bad as they were. He’ll be home later Saturday then we are off to STARSHIP at Black River Falls. 9pm concert…..it will be interesting to see if he actually makes it thru the whole thing without snoring. I’ll just hold him upright.
CT Scan last Thursday says the tumors have not shrunk…..but they have not grown either. So maybe, even tho the Chemo has been so sporadic, it’s still working…? And by working, I mean holding off the inevitable and giving him the time he would like to have…..because of where the tumors are….being cured is NOT an option.
And we both hate being reminded of that all the time. It’s hard enough as it is….
I read this. Then I read it again. And it was pretty uplifting today.
Yesterday, a dear friend of mine lost his best friend. When he told me Finn was gone, I got this lump in my throat, and my eyes started to leak.
I don’t think I had the honor of meeting Finn. But I did hear stories and saw photos of a handsome best friend of my friend. Finn was a gorgeous dog. Sleek and what a coat on him.
And I thought back to the day, that still seems like yesterday, when I held Bear as he slipped from this world to the next one.
The pain is real.
And they are not ‘just a dog’
They are here for us when no one else is.