Category: nsclc

  • February 8, 2023 – It Was a Good Run

    After almost seven years of living with his diagnosis, M is gone.

    I thought we were ready. We weren’t.

  • October 29, 2022 – The Word Hospice Carries a Lot of Baggage.

    Because hospice comes with so much baggage I struggled with how to discuss it with M. Then I was lucky in that Dr. M had the new doctor in the clinic suggest it. I’m pretty sure Dr. M was motivated by never wanting to have to deal with M again, but however we got here, I’ll take it.

    We met with the paperwork person Thursday, the nurse came Friday morning, they delivered a portable oxygen concentrater Friday afternoon, then today the pharmacy delivered the emergency pain comfort kit. M said if he’d known this would be the care level he’d have signed on months ago.

    He’s still the healthiest sick person I know but we’re definitely seeing progression in pain levels, the struggle to keep weight on, and weaknesses. It’s good to know the support system is now in place if / when things get worse.

  • September 29, 2022 – Amazingly, We’re Still Out Here

    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.

  • March 14, 2021 – Just Out Here, in Isolation

    Next Saturday, Shot #2

    The Saturday after that? Lowe’s, in a mask. M has been a model in lockdown.

    Then, during the week after that he has a CT scan & Dr K.

    We’re almost at five full years!

  • July 3, 2020 – Better is Better than Nothing

    So M is nowhere near 100% <–understatement. But, he is decidedly better than he was on my last post.  He’s napping at the moment, he’s definitely more easily fatigued.

    I don’t think it was Covid-19.  Though that is continually a fear.  M has a lot of co-morbidities.

    He’s scheduled to go see Dr. K at the end of July, and Dr. L at the beginning of August.  I won’t go to the Dr. K appointment, there’s nothing to be gained by doing so – there’s no testing and Dr. K never seems to have anything worthwhile to discuss when there’s been no testing.  I’ll definitely go to the Dr. L appointment, the idea that all this weirdness recently could be a new tumor is not lost on me.

  • June 20, 2020 – Something Just Isn’t Right

    Last Monday, M woke up really nauseous.  This has happened a few times here and there over this journey but something felt different this time.  I’m not sure what made if feel that way.  He was really weak, cold & clammy, no fever…  Dr. Google says heart attack.  M swears he doesn’t have chest pains.  Well, dear reader, we all know you don’t have to have chest pain to be having a heart attack.

    I had to go to work.  I was scared but, as I’ve said before, I can’t stay home every time M is sick.  As an extra added stressor, due to some poor career choices in the past eight months, I have no available time off.

    M never replied to my texts after lunch and I was getting concerned, but he did answer my call on the way home.  Sounded weak as all hell.  Tuesday, a small bit better, then a small improvement each day.  Yesterday, Friday, he ate more than he’s eaten all week.  This morning?  Boom, back to how he was Monday.

    Again, I don’t know what is making this feel different, but it does seem so.  Nausea, weak, occasionally sweating & clammy, and he can’t sit for 30 seconds without nodding off.  I got him to eat a little chicken noodle soup this evening and he fell asleep between spoonfuls.

    I’ve told M my concerns.  I’ve been pooh-pooh’d.  And there it is.  He’s an adult and I’m not his mother.  He’ll let it get out of control bad before he’ll agree to be seen by a dr.  It has been 15 years since his first heart attack.  That one gave warning signs for at least a month that he refused to acknowledge.

    Something just isn’t right.

    (edited in July to note – the Dr. L appointment that was to happen in May?  Postponed.  M did not want to go into a hospital in the midst of the pandemic)

  • June 11, 2020 – So Far, So Good

    M’s CT scan had no changes to the cancer.  However, it also shows extensive emphysema so add another top 10 killer to M’s health record.

    We cancelled his MRI.  We really didn’t need to, but M wanted to.  We’re rescheduled for July.

    He’s getting weaker.  I just sort of really been noticing this last week.  I know he’s lost a bit more weight, I don’t know how much, I’m trying not to nag.

    Still keeping him mostly out of stores and the public.  Masks if he needs to go.  I try to be careful coming home from work / errands to wash my hands and change my clothes immediately.

    We’re at four years and one month.  The man has nine lives, there is no doubt.

  • March 14, 2020 – I Sense a Bumpy Ride Ahead

    Covid-19

    Coronavirus

    Whatever the name… it seems like it isn’t going to be kind to folks like M. He has a CT scan scheduled Monday and then Thursday he gets the results from Dr. K. It will be good to have a baseline of where he’s at…

    (Edited in July to add, no CT scan changes – I realized I hadn’t said that in the next couple posts)

  • December 22, 2019 – We Made It

    Back when M was diagnosed in May of 2016, I didn’t think he’d see our 22nd anniversary that December, let alone our 25th in 2019! But, amazingly, here we are!

    We took a beach vacation for our anniversary. In normal life I don’t see M all day, every day. It was eye opening as I didn’t really grasp his strength level or muscle mass. Stairs were the roughest obstacle for him though the airport almost did him in as well. It’s hard to know how he’s really doing as he often won’t tell me without a lot of pushing on my part but under that setting there wasn’t any way to hide the reality.

    CT coming up in March and MRI in May. I have my suspicion that not all news will be good but that may just be fear influencing my predictions. Unless something changes I likely won’t update until then. As they say, “no news is good news.”

    The drooping in his face I saw in April seemed to go away

  • July 14, 2019 – Nothing to See Here

    M’s MRI was clear and his CT scan had no changes. Dr. L says he doesn’t need to see him again for a year unless we notice any neurological changes. Dr. K will see him in October but there won’t be a CT Scan at that time. So for now? Life is going on as normal…

    M is out mowing. He does most of his normal activities and is maintaining his weight. So for now, there probably won’t be many updates here!