Skip to main content

Adjusting expectations, with bonus post, twisted theology (or, what not to say to someone with cancer)

Leland and I drove in our new car (Hyundai Ioniq 5 electric vehicle - yeah!) for my 3-month follow-up appointment in Pittsburgh on Thursday. My oncologist is on maternity leave, after having her 4th (!) baby. When the physician's assistant (a PSU grad, of course) and doctor said that the cancer looks "stable," my heart fell. They explained that from their perspective that is good news because Tagrisso is holding the cancer in check and it's not spreading. So they think it's working as it should.

I have read a lot about targeted therapy and Tagrisso and both Leland and I were under the impression that it would reduce (and maybe even eventually eliminate) the existing cancer cells. In the Tagrisso Facebook group there are lots of people who now have "no evidence of disease" (NED). That is what everyone with lung cancer is hoping for...but now I'm realizing that I have to adjust my expectations about what Tagrisso might do for me. Tagrisso doesn't kill cancer cells. I may never get to NED. So although the doctors said that stable is good, it didn't really feel like good news because I was expecting to hear the cancer was clearing out. It was a big reality check that the existing cancer cells may be there to stay and that stable is good. And it made me furious all over again that my doctor and pulmonologist in Germany never ordered an x-ray when I first saw them about shortness of breath in January and March 2022, respectively. The cancer kept slowly spreading until June 30, when I first started Tagrisso.

My Hillman Center doctors also noted that there's reduced inflammation, what seems like evidence of reduced scarring, and generally more dark (clear) areas in my lungs. I'm now only using O2 while walking to/from campus and for exercise, and recently reduced the O2 from 4 to 3 liters/minute. My goal is to get 13-15K steps per day. I don't feel out of breath climbing the steps in my house. I frequently do errands like grocery shopping without my portable. So that is all progress.

But if I'm honest (as Paul Hollywood would say), I am becoming more doubtful that I will be able to walk without O2 in the foreseeable future, much less hike, bike, or run. If I didn't still have shortness of breath on exertion, I would feel differently about the cancer cells hanging around. But I still can't do anything more strenuous than walking. As an experiment, I recently walked uphill from my house with no O2; my saturation dropped to low 80s in less than a minute (it's supposed to be at least 94%). Last night I dreamed that I was biking without O2 and was disappointed to wake up and realize that it was just that: a dream.


****
I posted yesterday morning in the Tagrisso FB group with a question about what Tag does and if it doesn't kill cancer cells, then why do some people achieve NED (no evidence of disease) status? Here was one response from a man whose last name happens to be "Lucky":

This kind of glib response and chalking it up to answered prayers makes me want to scream. What a twisted theology. So all those people who don't respond as well to Tagrisso or X treatment plan just need to get more people praying for them? Or God just chose not to answer their prayers?

I feel like writing Kate Bowler (professor, ordained minister, cancer patient, and author of No Cure for Being Human) about this exchange because I know she would share my outrage and maybe even rant about it in her podcast.

Comments

  1. Sorry to hear about the unhelpful FB comments, but glad to hear the cancer is not getting worse. There's a lot that doctors & scientists don't fully understand yet, about how diseases & medications interact with each person's specific immune state & our body's ability to respond. Your body is working hard to fight this off, and I'm glad the Tagrisso is helping. Your time frame just might be different than others. Happy to talk offline anytime, if you want more context. -MLS

    ReplyDelete
    Replies
    1. Thank you, Moriah. I wrote to an oncologist friend and was surprised to hear him say the same thing - that doctors/researchers still don't understand a lot about how targeted therapies work.

      Delete
    2. I agree with your friend Moriah. I am happy it’s not spreading but stable. Things can turn around fast and suddenly with cancer so your time is coming!!! You know you have a mighty prayer circle. Your outcome is going to be great. We have to trust & believe. I know that’s hard to do, but God loves you & is faithful. Your healing is coming soon! 🙏🏽

      Delete
    3. Thank you, Alisa. It was great to see you in DC!

      Delete
  2. Thanks for writing about these acronyms, its helpful to know what the lingo is for many others living with cancer. And the theology post, don't get me started...Ha!! Not that I know a blip of anything about anything. But the intersection between the physical and spiritual is something not to be formulistic about. If it were a formula, then where would faith reside? We say a thousand things a day in word and thought, and so easy to think God only hears our folded hands speech. Our breath is our prayer, and so sorry you were stung by that post. Peace. The Lord's love is the fountain of life and grace.

    ReplyDelete
    Replies
    1. Thank you, Brenda. Unfortunately illness and all forms of suffering seem to elicit really bad theology.

      Delete
  3. I can’t comment on the bad theology that a disease like this elicits. It’s all a struggle to make sense of the events of this world and the distribution of uncertainty and suffering. But I sure know that there are a whole lot of people who love you and who are following your efforts to regain your health and who have extraordinarily deep regard for you and your role in all of our lives. For what it’s worth I am very grateful for these blog postings. Thank you, Esther. And, courage! We are with you.

    ReplyDelete
    Replies
    1. Thank you, Kai. I appreciate your being a steadfast friend and champion!

      Delete
  4. Esther, hope that you are receiving good treatment from Hillman.
    David

    ReplyDelete
    Replies
    1. Thank you, David. Yes, they are top-notch. I am looking forward to seeing my regular oncologist again.

      Delete
  5. It is hard to believe someone in the same shoes would not think about the effect of those glib words! We will never comprehend the full will of God while here on this earth, but it is definitely not reduced to the number of your prayer circle. Sorry to see that, but not surprised. I don't really know the right or wrong things to say, but I am so thankful to be a part of this journey with you and to read the incredible strength and vulnerability you bring to these posts. Hope to get to see you soon! Henson

    ReplyDelete
    Replies
    1. Exactly (re: first sentence). Thank you, Henson. Maybe at some point I will make it to the Bahamas to see you!

      Delete
    2. This comment has been removed by the author.

      Delete

Post a Comment

Popular posts from this blog

Tipping point

Dr. El Khouray came in yesterday and determined that I'd reaching a tipping point, meaning the worst is behind me and I've continued to show improvement. This was really, really good news to hear. Proning continues to be very effective, so I've spent a couple hours each morning and afternoon on my stomach, in addition to sleeping on my stomach at night. In the afternoon I invariably fall asleep since there is nothing to do other than listen to an audio book! I'm able to move about the room more; yesterday I did something like 4 little loops with an occupational therapist.  Yesterday I was down to about 11-13 L oxygen/minute. The case manager told me that to go home I need to be at 6 L or less. Today I'm at 6 L and holding steady with my oxygen saturation rate. I haven't talked with a doctor yet today, but I think this means that Monday is still a realistic release date. Until today I had thought that Monday would be out of reach; I didn't want to set myself ...

Back in the hospital

Until about 1pm I had been doing pretty well. I even spent part of the morning off of oxygen during a student's comps exam on Zoom. Then out of nowhere I felt really short of breath; even on 6L (maximum) oxygen my saturation dipped into the 50s at one point. Leland had the brilliant idea of putting both cannulas (oxygen tubes) in my nose--one from the oxygen concentrator (6L) and one from the portable oxygen tank (5L). That helped stabilize my oxygen level until the ambulance came.  So I'm back in the ICU on high-flow oxygen. :( The doctors are investigating various possibilities, including pneumonia, some other kind of infection, side effects of Tagrisso (my cancer medication), or ??? I'm back on heparin (blood thinner), antibiotics, and steroids. My oxygen and heart rate are slowly starting to improve.  Just this morning I had called the Mt. Nittany physicians group to see if I could make an appointment with any of the 3 pulmonologists in their practice. No openings until...

transatlantic flight

The last time I took a transatlantic flight, I barely survived. I had to be carted off the plane by EMS personnel because I was too short of breath to walk even a few steps. Tomorrow I'm flying to England. Needless to say, I'm hoping this flight is uneventful. I'm relieved that my friend and colleague Carol is flying with me (we are presenting at the British Educational Research Association conference in Manchester). I wouldn't have felt comfortable making the trip by myself. I will bring a heavy backup battery for my portable oxygen concentrator because airlines stipulate that you need enough battery power to last 1.5 times the flight duration. I'm not looking forward to having to wear the concentrator tube plus my glasses and a mask (too much COVID still going around) for the 7- to 8-hour flight -- lots of tubes, bands, and apparatuses on my ears, nose, and face. I am grateful that my blood thinners are working and that my lungs have improved enough that I can o...