Just in case there’s a single soul out there wondering – M is still plodding along! Amost six an a half years.
He didn’t have his last CT scan that was supposed to happen in October 2021. Dr. M retired before it was supposed to happen. Then, the doctor’s office screwed up the insurance authorization. They forgot to submit the paperwork at all until two days before it was scheduled so it had to be cancelled. They said they’d get a new date once the authorization came in and call us back. Well, we got the authorization letter from insurance and never heard back from the office.
That was it for M. He said he was done. Doesn’t want a new dr, doesn’t want the scan, done.
His choice.
Then, at the beginning of last month he had his MRI scheduled with Dr L. He got sick 1/2 way through (before the contrast) and refused to finish the test and said that was it, never having another. Dr. L wasn’t as pleasant as he has been previously. “Nothing of concern as much as can be seen without contrast.” No further follow-up appointments discussed.
So that’s where we are (or aren’t) as far as tests. M is done with it all.
The pain is increasing, I see it in him continuously, and then especially hard hitting in spasms – one of the worst spots is right over where the known lung tumor is. We can only assume it is growing but without tests it’s impossible to really know.
He won’t complain or tell the doctor just how bad it is… His original palliative care doctor, Dr. M, treated him as if he was a drug seeking junkie when he’d try to explain all the pains, rather than someone with metastatic lung cancer with chemo-induced peripheral neuropathy.
Honestly, it’s disgusting that a palliative care doctor should exhibit such a lack of empathy for his patients with a terminal illness.
It has been better since he’s been seeing Dr. Y, he feels like she listens to what he says, but he still puts up a “it’s not that bad” front. Unfortunately, she’s leaving, and Dr. M is the actual head of that department.
I’ve considered seeing about switching him to a different palliative group but the other option geographically is an hour away & M doesn’t like that. (Currently it’s 45 minutes to the doctor & Dr. Y was letting him have televisits except the yearly requirement to come in for the urine drug test.)
I also wonder if he’d be eligible for hospice but don’t want to (or know how to) have that conversation with him: “Well ya know, it’s looking like you might not make it six months, so…”
My apologies, I know that’s crude but it’s where I am.