Do most people really want to know how you're Really doing?
OK, I'm doing it again. Thought Hans brought up some good points about how most people who know you have cancer actually don't really want to know how you're doing...they want the heroic answer that makes them feel better.
He has some retorts to the question that probably do trigger people. It reminds me of my son-in-law, who when people asked how he was doing, would say with great intensely, "Great!" The catch was that you didn't know if he meant great in a positive way or meant it sarcastically. It would definitely would stop you for a second.
Anyway....another link to Hans column and a graph from it....
“The truth, I have come to believe, is that much of illness in modern society is performative. We have collectively agreed that sick people should remain inspirational because actual suffering makes everybody terribly uncomfortable. Nobody wants honest illness. People claim they admire bravery, but what they really admire is tidy suffering, suffering that smiles politely, expresses gratitude, posts optimistic updates on social media, and generally avoids introducing unpleasant realism into brunch conversations.”
The Curious Performance of Being Fine
https://open.substack.com/pub/nutmegphantasy/p/the-curious-performance-of-being-dbf
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@surftohealth88
Crap! I should have moved to Germany. I was laid off about 3 months after my RP. I got a nice severance but a lifetime comp would have been GREAT! haha
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3 ReactionsI believe in the "need to know" philosophy and respond with "So far so good" or adding "One day at a time is a pretty good pace and thanks for asking." In other words, if there is not a real "need to know" about my condition I keep it simple. For close friends or others going through similar cancers I am more detailed. "Hey, how about coffee and we can talk." This can lead to deeper, meaningful conversations for both of us. Sharing the good and not so good is a healthy stance benefiting myself and hopefully the other person in similar straits.
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2 Reactions@wheel1 Candidly, before diagnosis....I knew nothing about prostate cancer. I didn't know about incontinence or ED, let alone the variations of those side effect profiles with all the various treatment options.
I was clueless and oblivious....till I wasn't. I didn't even know where or exactly what the prostate did.
But, you're right. Knowledge of the breast cancer journey is well known even to most men. And, yes, perhaps it's the stigma of the reality of PCa treatment is what keeps it from being known beyond our small communicties.
@thig350 Oh yeah, you describe the whole emotional/physical roller coaster ride well.
I found that only a couple of my really good friends who are note PCA patients might politely listen to what is going on with me....but think I"m surely freaking them out at the same time.
@northoftheborder Oh yeah, don't go there! (my mom had dementia....so yeah, dementia wins for sure)
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1 Reaction@thmssllvn I agree...there is no replacement for this support group. Candidly, I've tried several forums and several online support group meetings.....this forum has been the bet of all for me.
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1 Reaction@turtbean Hah-made me laugh!!! Not sure this would work as a pick-up line in a bar either...
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1 Reaction@prowler6b Yes, and yes. It can be very isolating. But, just know that there are a lot of great poeple here who are super glad to listen and support.
You don't need me telling you this, but feel free to share here whatever your state of mind is.
@rwski79 I really like that approach...."need to know." That's how I've managed at work (only one person at work knows and its for that reason.
Someday, maybe I'll be the pubic education and advocacy guy....but right now, it's just my closest friends.
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1 Reaction@fritzo Colon cancer took my father before his dementia prevented him from recognising me and remembering helping to raise me. That's not a silver lining; just two nasty things.
p.s. Even if you have advanced/metastatic prostate cancer, keep getting those colonoscopies, everyone.
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