Ron has prostate cancer 😟

Well, it’s Saturday, 4 days after his last infusion. He’s still crippled with pain, balance is off, not sleeping. If this infusion runs the same course as his last one, by tomorrow he’ll feel considerably better.

His Cycle has changed, so now he’s getting infusions Day one (last Tuesday) and day 15, so he skips next Tuesday. He’ll continue on that schedule apparently for several more weeks, though it does depend on his response, determined by the endless blood work he gets when he goes in.

He has 10 days of work scheduled starting next Monday that was work Sheri had lined up weeks ago and now can’t do, so he will. It’s not too taxing apparently, but even so, I’m worried about his ability to withstand the labor, especially knowing that some of those days after work he’s going to see Sheri in the hospital before he comes home so he won’t stagger in till 8.00pm or so, after leaving the house around 7.30am to start his work day.

It’s good that he wants to push through and not succumb to the cancer, the pain, the emotional and mental toll. We have a 75 year old friend who was diagnosed with prostate cancer within days of Ron’s diagnosis. Chip’s hasn't metastasized, he doesn’t require chemo, he’s getting radiation and his prognosis is good. Still, he’s deeply depressed, morose, going to see his chaplain several times a week, convinced he’s terminal no matter what the doctors say.

I’m grateful Ron’s outlook is so upbeat and positive. He’s a realist as am I, so he’s aware that the best his team can do is keep the cancer under control until they just can’t anymore, but he’s determined to wring as much fun and positivity and activity out of life as he can, for as long as he can.

Nonetheless I worry when he pushes himself as hard as he does.
 
He isn’t any better. His cancer team decided he needed to go to the ER to be evaluated. We’ve been there all day, just now getting ready to leave because they were back and forth on admitting him.

They gave him IV morphine and a muscle relaxer, did an MRI, xray, bloodwork, and can’t find any reason for his muscle and joint pain other than reaction to his cancer treatment. He also has a rash that popped up all over his torso and underarm are, wrapping around to his back. No explanation for that either other than reaction to treatment.

He felt better in the hospital after the meds kicked in. Was actually able to move his head from side to side and up and down a little, lift his arms a bit higher, sit and stand with somewhat less pain. We’re home now after a full day spent in the ER, with a muscle relaxer to take every 12 hours. He’s back in bed trying to sleep, feeling no better than when he left other than the slight relief he got in the hospital with the meds they gave him there.

He’s loaded up with pain pills and another dose of the muscle relaxer. We’ll see how he does when he gets back up.
 
Oh god, Ronni. The rash could absolutely be from the TX. But the other? Yeah, probably. It does sound like he needs better pain management. The one thing I've learned in my life is that we are not at all the same and our reactions can be a mystery when others don't bat an eye. He just might not be tolerating it as well as most. Although add in his daughter's challenges that could amplify his own physical reaction.

Do they know about the situation with his daughter?
 
PSA 11 at recent path test have to go back in three months to see if it had changed again (six monthly visits previously).

Am part of a cancer study, I suspect I am part of the cohort that looks at if doing nothing leads to a better outcome (don't really know). I am told that if it spreads (no sign in the last PET scan) the treatment will be hormone treatment only.

Quality of life is the watchword apparently. The cancer has absolutely no effect on my daily life at the moment (I am 79)
 
He isn’t any better. His cancer team decided he needed to go to the ER to be evaluated. We’ve been there all day, just now getting ready to leave because they were back and forth on admitting him.

They gave him IV morphine and a muscle relaxer, did an MRI, xray, bloodwork, and can’t find any reason for his muscle and joint pain other than reaction to his cancer treatment. He also has a rash that popped up all over his torso and underarm are, wrapping around to his back. No explanation for that either other than reaction to treatment.

He felt better in the hospital after the meds kicked in. Was actually able to move his head from side to side and up and down a little, lift his arms a bit higher, sit and stand with somewhat less pain. We’re home now after a full day spent in the ER, with a muscle relaxer to take every 12 hours. He’s back in bed trying to sleep, feeling no better than when he left other than the slight relief he got in the hospital with the meds they gave him there.

He’s loaded up with pain pills and another dose of the muscle relaxer. We’ll see how he does when he gets back up.
I'm so sorry to hear this, Ronni. I follow your updates, and I'm waiting for things to turn around for Ron. šŸ«‚
 
Ron is feeling somewhat better today! He started improving around the middle of the day yesterday. We don’t know if it was the latest cocktail of meds that his doctor in and he started taking yesterday morning, or if it’s the fact that he’s far enough out from his last infusion that his body is adjusting.

Either way it’s a huge relief! His pain has been reduced by half, which just makes it possible for him to move around a bit more easily and not be confined to bed.
 
Oh god, Ronni. The rash could absolutely be from the TX. But the other? Yeah, probably. It does sound like he needs better pain management. The one thing I've learned in my life is that we are not at all the same and our reactions can be a mystery when others don't bat an eye. He just might not be tolerating it as well as most. Although add in his daughter's challenges that could amplify his own physical reaction.

Do they know about the situation with his daughter?
Yea they do. They were in the same hospital, just different buildings and Ron would sometimes be able to go visit with her in between tests and bloodwork and such. His team would let him know if there was going to be enough time in between so he could go see her.
 
PSA 11 at recent path test have to go back in three months to see if it had changed again (six monthly visits previously).

Am part of a cancer study, I suspect I am part of the cohort that looks at if doing nothing leads to a better outcome (don't really know). I am told that if it spreads (no sign in the last PET scan) the treatment will be hormone treatment only.

Quality of life is the watchword apparently. The cancer has absolutely no effect on my daily life at the moment (I am 79)
This makes sense. They’ve caught your cancer early enough that active surveillance is your ā€œtreatmentā€ plan.

The QOL issue is big. I understood the term theoretically, but watching Ron go through what he has this past few weeks, particularly after this last treatment, made me realize how important it is. It didn’t take long for Ron to become emphatic about his future treatments, and that he’d choose a shorter life with good quality to it over an extended life with those treatments. I had to agree.
 
I am following you two as, Ron goes through the cancer treatments.
Hoping for the best results for Ron.

My husband starts radiation treatments next week.
He's been reading over & over the paperwork they 'gave' him.

We have been seeing doctors for his health various problems this year.
Our hope is that the doctors we see "might" stubble onto the reason for his other pains.

Don't mean to crowd out your worries,, just trying to let you know I'm slowly following you.

IF you think you"feel" a small old lady following you,, could be me!! Hugs ā˜ŗļø
 
I am following you two as, Ron goes through the cancer treatments.
Hoping for the best results for Ron.

My husband starts radiation treatments next week.
He's been reading over & over the paperwork they 'gave' him.

We have been seeing doctors for his health various problems this year.
Our hope is that the doctors we see "might" stubble onto the reason for his other pains.
https://www.seniorforums.com/attach...=104018&hash=7baf782baa0e8c83908fd2ce96ec1d56
Don't mean to crowd out your worries,, just trying to let you know I'm slowly following you.

IF you think you"feel" a small old lady following you,, could be me!! Hugs ā˜ŗļø
Thank you @Sliverfox šŸ™

A dear friend of ours was diagnosed with prostate cancer at the same time as Ron. His hasn’t metastasized, so though they’re both on daily hormone medication, other treatment plans differ based on the metastases or lack

Chip is getting radiation daily, 5 days a week, for a month. His prep is a bit annoying (full bladder empty rectum) but the treatment itself is essentially painless, and the side effects are minimal, mainly just fatigue.

Telling you that just to let you know that if your hubs is starting radiation there may be few side effects for him..and you..to worry about. ā¤ļø
 
Ron slumped again after that last update (post #136) One of the meds he was given was 3 days of steroids, and that must have accounted for his upswing because as soon as he finished them he was bad again.

We went to the cancer center Tuesday where he was supposed to get another infusion, but I insisted on a consult with his team instead. We told them he had no quality of life, spent most days in bed, he was in a lot of pain, and that there was no way he would continue with treatment if this was how he was going to feel.

They listened. They said let’s skip a week of infusions, give him steroids as that was what made him feel so much better, and provided he feels decent by the time his next Infusion comes around (this coming Tuesday) they’ll lower his dose to what he was tolerating well before they raised it.

That’s reasonable. He feels much better, so provided that holds till Tuesday, he’ll take a chance and get the lower dose infusion, and see. If it still knocks him out, we’re done with this clinical trial and will explore other treatments.
 
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