Sir Cliff Richard

Posted by peterj116 @peterj116, Dec 15, 2025

Another one has joined our unpopular club.

Sir Cliff Richard has revealed he has been treated for prostate cancer.

The 85-year-old singer said the cancer was discovered when he had a check-up for a recent tour, but that it had been caught early and had not spread.

"I was going to Australia and to New Zealand and the promoter said, 'Well we need your insurance, so you need to be checked up for something'. They found that I had... prostate cancer."

"But the good fortune was that it was not very old, and the other thing is that it had not metastasized. It hadn't moved, nothing into bones or anything like that. And the cancer's gone at the moment."

"I don't know whether it's going to come back. We really can't tell with those sort of things.

"But we need to, absolutely, I'm convinced, get there, get tested, get checked.

"I think we, as men, have got to start saying, we've got to be seen as human beings who may die of this thing."

Sir Cliff said he wants to work with the King to improve cancer screening for men, after the King spoke last week about his own cancer treatment and emphasised the importance of checks to catch cancer at an early stage.

Sir Cliff is known for decades of hits including The Young Ones, We Don't Talk Anymore and Summer Holiday.

The musician described the lack of a national screening programme as "absolutely ridiculous".

"We all deserve to have the same ability to have a test and then start the treatments really early," he said.

"It seems to me - I've only been for one year now in touch with cancer, but every time I've talked with anybody, this has come up, and so I think our government must listen to us."

Last month, the National Screening Committee – which advises governments across the UK – said a screening programme for prostate cancer for all men in the UK is not justified.

They say only men with specific genetic mutations that lead to more aggressive tumours should be eligible.
(sigh)

Interested in more discussions like this? Go to the Prostate Cancer Support Group.

Peter, Don’t you wish that WE were diagnosed at 85?!🫣
Phil

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Profile picture for heavyphil @heavyphil

Peter, Don’t you wish that WE were diagnosed at 85?!🫣
Phil

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@heavyphil I was. There's that ....

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Profile picture for heavyphil @heavyphil

Peter, Don’t you wish that WE were diagnosed at 85?!🫣
Phil

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@heavyphil It sounds like a better option, but the recovery from the surgeries would be harder. Sometimes I feel like an 85 year old now.

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Profile picture for stew80 @stew80

@heavyphil I was. There's that ....

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@stew80 Oops! Look at the bright side, Stew…you didn’t get diagnosed UNTIL you were 85…now imagine living with this from age 64 or even younger…
But it does suck at any age and I don’t make light of anyone having it.
Phil

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At my annual "wellness" checkups in 2024 and 2025, my primary care doc ordered PSA tests, because I was presenting with various urinary symptoms. Medicare paid in 2024 but did not pay in 2025.

Sometimes I go through a dispute process just to get a better understanding of how the system works, rather than just pay. (I think the testing company wanted $65).

I called the company that did the test. I called the doc's office. I visited the doc's office with a statement from the testing company that said they probably hadn't submitted the bill for it with the right code.

By the time I decided to call Medicare to dispute this with a person, I had an MRI result in hand, showing PI-RADs 5 "highly likely clinically significant cancer" in one large mass and several other places in my prostate. This meant nothing to the person I talked to, so it seemed. The Medicare rep agreed with me when I described my understanding of current Medicare policy as - they will pay for one PSA test per year as a screen.

Without missing a beat, she explained that the doc had not convinced them that this PSA test was "medically necessary" so they didn't have to pay. What do you think a test approved for use as a yearly screen is, I argued, medically unnecessary? I pointed out that this PSA test led me to get an MRI that showed I had "highly likely clinically significant cancer". Medicare, according to this rep, didn't have to pay.

I hung up. A few weeks later, I was about to pay the testing company when I discovered that they had decided I didn't owe them anything because Medicare coughed up the payment.

There is a lot of weirdness around testing.

Because the 2024 test was 3 and the 2025 test was 5 the primary care doc sent me to a urologist. I wasn't that interested in acting on what he called this "jump up" in PSA results and turned down his advice I get a biopsy. I agreed to repeat the test in a few months. The repeated PSA showed the level was increasing. I agreed to an MRI. Suddenly I was down the prostate cancer rabbit hole. Etc.

What caused me to delay looking into this was this controversy around PSA testing. I had heard that the US screening guideline committee in 2012 had recommended against routine PSA screening. I wondered: if the info they were getting from a test was any good, they wouldn't be recommending against it. Docs wouldn't be told: don't do it.

The problem is what to do when the result comes in. There's nothing wrong with the test. Its one of the best tests for any cancer that is available.

The problem is patients freak out when they find out they have "cancer", and doctors respond with treatments, and all the treatments have some toxicity. Not all of the detected cancers would have caused any problem to the patient during their lifetime, especially when compared to the toxic side effects of the treatments. Some of the detected cancers will kill.

Everyone involved is learning. I wish I had looked into this controversy over PSA testing and concluded it made sense to get tested every once in a while. But it took a diagnosis, cT3b "high risk" prostate cancer, to wake me up.

REPLY
Profile picture for climateguy @climateguy

At my annual "wellness" checkups in 2024 and 2025, my primary care doc ordered PSA tests, because I was presenting with various urinary symptoms. Medicare paid in 2024 but did not pay in 2025.

Sometimes I go through a dispute process just to get a better understanding of how the system works, rather than just pay. (I think the testing company wanted $65).

I called the company that did the test. I called the doc's office. I visited the doc's office with a statement from the testing company that said they probably hadn't submitted the bill for it with the right code.

By the time I decided to call Medicare to dispute this with a person, I had an MRI result in hand, showing PI-RADs 5 "highly likely clinically significant cancer" in one large mass and several other places in my prostate. This meant nothing to the person I talked to, so it seemed. The Medicare rep agreed with me when I described my understanding of current Medicare policy as - they will pay for one PSA test per year as a screen.

Without missing a beat, she explained that the doc had not convinced them that this PSA test was "medically necessary" so they didn't have to pay. What do you think a test approved for use as a yearly screen is, I argued, medically unnecessary? I pointed out that this PSA test led me to get an MRI that showed I had "highly likely clinically significant cancer". Medicare, according to this rep, didn't have to pay.

I hung up. A few weeks later, I was about to pay the testing company when I discovered that they had decided I didn't owe them anything because Medicare coughed up the payment.

There is a lot of weirdness around testing.

Because the 2024 test was 3 and the 2025 test was 5 the primary care doc sent me to a urologist. I wasn't that interested in acting on what he called this "jump up" in PSA results and turned down his advice I get a biopsy. I agreed to repeat the test in a few months. The repeated PSA showed the level was increasing. I agreed to an MRI. Suddenly I was down the prostate cancer rabbit hole. Etc.

What caused me to delay looking into this was this controversy around PSA testing. I had heard that the US screening guideline committee in 2012 had recommended against routine PSA screening. I wondered: if the info they were getting from a test was any good, they wouldn't be recommending against it. Docs wouldn't be told: don't do it.

The problem is what to do when the result comes in. There's nothing wrong with the test. Its one of the best tests for any cancer that is available.

The problem is patients freak out when they find out they have "cancer", and doctors respond with treatments, and all the treatments have some toxicity. Not all of the detected cancers would have caused any problem to the patient during their lifetime, especially when compared to the toxic side effects of the treatments. Some of the detected cancers will kill.

Everyone involved is learning. I wish I had looked into this controversy over PSA testing and concluded it made sense to get tested every once in a while. But it took a diagnosis, cT3b "high risk" prostate cancer, to wake me up.

Jump to this post

@climateguy Yeah, that 2012 recommendation ruined a lot of lives…gotta wonder how many lives will be ruined by our current Secretary of Health’s unscientifically based recs..,
Phil

REPLY
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