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How likely is treatment of aggressive prostate cancer with metastasis to bones in an 82-year-old man who has stage 4 dementia? To me, hospice seems more likely than lifesaving measures.
It certainly seems like your post here was taken straight from the recent headlines about former President Biden, Fawnby. Only he doesn't have stage 4 dementia.
Why would it even be suggested that an elderly person with advnaced dementia take treatment for cancer? At 82 years old with dementia it sure seems to me like unnecessary cruelty.
My ex has lived with Stage 4 aggressive, hormone-based prostate cancer for 5 years now. He is relatively healthy and active and is enjoying his grandchildren, travel and social activities.
I would not put him thru the chemo needed to maybe cure him. Just going under could speed up his Dementia. He deserves to live peacefully with whatever time he has left. I say Hospice.
All I know is the pain from bone cancer is the most excruciating I've ever felt in my life. And cancer treatment can ruin the quality of one's life. With his level of dementia at play, hospice seems like the best bet. However, I'm quite certain this condition has been known about for awhile now.....WE are just hearing of it. There must be plans already in place for treatment, one way or another. God bless and help him.
Are you now qualified to make a dementia diagnosis? Former President Biden's doctors have never made any statement about him suffering from dementia.
When he did the debate he may have had a UTI or some other kind of infection. Who knows? Since you are not one of his doctors, you really shouldn't be talking about his "level of dementia" at all.
Are you wanting to check what the AIM of the treatment is?
My LO was dx at stage 3 or 4. Initially, hormonal treatment aim was to slow progression. Later, chemo & radiotheraphy aim was to attempt to shrink bone massess.
These were discussed frankly but not bluntly. I don't think we really considered the term *palliative treatment* until near the end.. yet that is what it really was the whole time.
I have mixed feelings. Did it all buy more time? Improve quality of life?
Or did the side effects hasten the end?
Did the hormonal treatment cause the brain fog? Or did the cancer cause it?
Was the pnumonia & infection storm that hit after the first chemo session worth it? Could that have happened at any infection anyway?
Was the intense bone pain triggered by the first radiotherpy session due to the treatment? Or by the bone mets & just a coinsidence?
What I saw was heartbreaking. But I was merely someone to hold a hand - the decision to take these not-so invasive & invasive treatments was not mine. I respected the decision to try.
Each person can react differently to treatment too.
But I know that experience left a deep impression on me.
Depends on the type of treatment, and the overall mental strength of the patient.
In 2010, I met a famous rock guitarist at a Battered Women's fund raising concert. I'd been a fan for decades, and was doing video. Afterward, I was backstage packing my stuff, when he asked me to talk privately. He asked me not to publish the video I took, since he was having a "bad night." He told me he just had prostate cancer treatment 2 days earlier, where they put "radioactive beads" into his prostate. He was clearly depressed, despite a great show. I told him my experience was it was curable, since several family and friends of mine had survived it. I pumped him up the best I could. I told him how important he was to so many people. He actually smiled and seemed better. I emphasized his cancer was found early, which was what would save him. I think he was scared to death, and who wouldn't be? He was in his mid 50s at that time, with a wife and no kids.
Six months later, I heard on the radio he had shot himself while fishing alone. It broke my heart. His treatment was not considered aggressive. He probably didn't have the right mindset, or his depression treated. Who knows?
My take is a man in their 80s would not tolerate aggressive cancer treatment. Both my late husband and best GF of 30 years had "aggressive" Stage 4 cancer treatments, and Brett (age 32) tolerated it, yet my GF (age 56) was violently ill and forced to stop. Both of them died within 1 year of their Stage 4 diagnosis.
The (alleged) "dementia" has nothing to do with it. Bone cancer is extremely painful, but is not the primary cancer. In the last decade, many new treatments have been developed. My Dad died at 50 after his heart attack in 1970, because cardiac bypass was not available yet. My sister (retired RN) had a triple bypass in 2018 at age 70, and has been fine since.
What prognosis does the oncologist give? Will your LO cooperate with the treatments? Does your LO have any other health issues (like, COPD, CHF, diabetes, etc)?
My father had prostate cancer and lived with it for a decade before bone metastasis. (No dementia)
After the bone tumors appeared, he underwent further radiation, chemo, hormone therapies as palliative treatments, but it took only a year and a half before he died.
One uncle-- not related to father-- was fully cured of prostate cancer decades ago, but had different initial treatments and of course everyone's situation is unique...
I would suggest hospice for the "patient in question" above. It was a blessing for my father, and greatly eased the pain during his final months.
Hospice would, in the opinion of this retired RN, would be a mercy. Bone cancer is dreadfully painful. Often enough medications cannot be given to relieve pain without entering a person into a comatose state. This is for whomever is POA to discuss with physicians. There are new and better cancer treatments, but the treatments themselves have repercussions to the heart, lungs, kidneys general health and well being of an octogenarian. I myself am in my second cancer in my lifetime (first being beaten 38 years ago). I have accepted a mastectomy and radiation, but refused the harvesting of lymph nodes for testing for chemo as chemo as this stage is not a fight I wish to make, having once already endured it, and is not a fight that would likely lead to a long term win, nor is my life now in ANY case long term.
These are all decisions we make as individuals. When there is stage four dementia at work, then the quality of life is already not very special. And there is already some trusted family member in charge to see that what is bad isn't made worse by worthless and senseless treatments of devastating illnesses. This POA will be aware of the person's wishes, and will consult with doctors about what can and cannot be done for best end of life care.
By proceeding, I agree that I understand the following disclosures:
I. How We Work in Washington.
Based on your preferences, we provide you with information about one or more of our contracted senior living providers ("Participating Communities") and provide your Senior Living Care Information to Participating Communities. The Participating Communities may contact you directly regarding their services.
APFM does not endorse or recommend any provider. It is your sole responsibility to select the appropriate care for yourself or your loved one. We work with both you and the Participating Communities in your search. We do not permit our Advisors to have an ownership interest in Participating Communities.
II. How We Are Paid.
We do not charge you any fee – we are paid by the Participating Communities. Some Participating Communities pay us a percentage of the first month's standard rate for the rent and care services you select. We invoice these fees after the senior moves in.
III. When We Tour.
APFM tours certain Participating Communities in Washington (typically more in metropolitan areas than in rural areas.) During the 12 month period prior to December 31, 2017, we toured 86.2% of Participating Communities with capacity for 20 or more residents.
IV. No Obligation or Commitment.
You have no obligation to use or to continue to use our services. Because you pay no fee to us, you will never need to ask for a refund.
V. Complaints.
Please contact our Family Feedback Line at (866) 584-7340 or ConsumerFeedback@aplaceformom.com to report any complaint. Consumers have many avenues to address a dispute with any referral service company, including the right to file a complaint with the Attorney General's office at: Consumer Protection Division, 800 5th Avenue, Ste. 2000, Seattle, 98104 or 800-551-4636.
VI. No Waiver of Your Rights.
APFM does not (and may not) require or even ask consumers seeking senior housing or care services in Washington State to sign waivers of liability for losses of personal property or injury or to sign waivers of any rights established under law.
I agree that:
A.
I authorize A Place For Mom ("APFM") to collect certain personal and contact detail information, as well as relevant health care information about me or from me about the senior family member or relative I am assisting ("Senior Living Care Information").
B.
APFM may provide information to me electronically. My electronic signature on agreements and documents has the same effect as if I signed them in ink.
C.
APFM may send all communications to me electronically via e-mail or by access to an APFM web site.
D.
If I want a paper copy, I can print a copy of the Disclosures or download the Disclosures for my records.
E.
This E-Sign Acknowledgement and Authorization applies to these Disclosures and all future Disclosures related to APFM's services, unless I revoke my authorization. You may revoke this authorization in writing at any time (except where we have already disclosed information before receiving your revocation.) This authorization will expire after one year.
F.
You consent to APFM's reaching out to you using a phone system than can auto-dial numbers (we miss rotary phones, too!), but this consent is not required to use our service.
Why would it even be suggested that an elderly person with advnaced dementia take treatment for cancer? At 82 years old with dementia it sure seems to me like unnecessary cruelty.
Are you now qualified to make a dementia diagnosis? Former President Biden's doctors have never made any statement about him suffering from dementia.
When he did the debate he may have had a UTI or some other kind of infection. Who knows? Since you are not one of his doctors, you really shouldn't be talking about his "level of dementia" at all.
My LO was dx at stage 3 or 4.
Initially, hormonal treatment aim was to slow progression. Later, chemo & radiotheraphy aim was to attempt to shrink bone massess.
These were discussed frankly but not bluntly. I don't think we really considered the term *palliative treatment* until near the end.. yet that is what it really was the whole time.
I have mixed feelings. Did it all buy more time? Improve quality of life?
Or did the side effects hasten the end?
Did the hormonal treatment cause the brain fog? Or did the cancer cause it?
Was the pnumonia & infection storm that hit after the first chemo session worth it? Could that have happened at any infection anyway?
Was the intense bone pain triggered by the first radiotherpy session due to the treatment? Or by the bone mets & just a coinsidence?
What I saw was heartbreaking. But I was merely someone to hold a hand - the decision to take these not-so invasive & invasive treatments was not mine. I respected the decision to try.
Each person can react differently to treatment too.
But I know that experience left a deep impression on me.
I assumed stage 4 Prostate Ca, on top of existing Dementia.
I re-read it now as NEW Prostate Ca, with current stage 4 Dementia.
Very different stages of health, independance, prognosis.
Hopefully I was wrong the first time 😞
In 2010, I met a famous rock guitarist at a Battered Women's fund raising concert. I'd been a fan for decades, and was doing video. Afterward, I was backstage packing my stuff, when he asked me to talk privately. He asked me not to publish the video I took, since he was having a "bad night." He told me he just had prostate cancer treatment 2 days earlier, where they put "radioactive beads" into his prostate. He was clearly depressed, despite a great show. I told him my experience was it was curable, since several family and friends of mine had survived it. I pumped him up the best I could. I told him how important he was to so many people. He actually smiled and seemed better. I emphasized his cancer was found early, which was what would save him. I think he was scared to death, and who wouldn't be? He was in his mid 50s at that time, with a wife and no kids.
Six months later, I heard on the radio he had shot himself while fishing alone. It broke my heart. His treatment was not considered aggressive. He probably didn't have the right mindset, or his depression treated. Who knows?
My take is a man in their 80s would not tolerate aggressive cancer treatment. Both my late husband and best GF of 30 years had "aggressive" Stage 4 cancer treatments, and Brett (age 32) tolerated it, yet my GF (age 56) was violently ill and forced to stop. Both of them died within 1 year of their Stage 4 diagnosis.
The (alleged) "dementia" has nothing to do with it. Bone cancer is extremely painful, but is not the primary cancer. In the last decade, many new treatments have been developed. My Dad died at 50 after his heart attack in 1970, because cardiac bypass was not available yet. My sister (retired RN) had a triple bypass in 2018 at age 70, and has been fine since.
After the bone tumors appeared, he underwent further radiation, chemo, hormone therapies as palliative treatments, but it took only a year and a half before he died.
One uncle-- not related to father-- was fully cured of prostate cancer decades ago, but had different initial treatments and of course everyone's situation is unique...
I would suggest hospice for the "patient in question" above. It was a blessing for my father, and greatly eased the pain during his final months.
These are all decisions we make as individuals. When there is stage four dementia at work, then the quality of life is already not very special. And there is already some trusted family member in charge to see that what is bad isn't made worse by worthless and senseless treatments of devastating illnesses. This POA will be aware of the person's wishes, and will consult with doctors about what can and cannot be done for best end of life care.
It was his decision; it was as Alva said senseless and as his caregiver, it was torture for me as well.