And yea, I already did all the standard things. CBT for insomnia helped somewhat. My insurance didn’t fully cover it either, unless I was willing to wait for 8 to 12 months.
And I recently met someone with slow moving metastatic cancer. Thanks to LLMs they will most likely live another 3 to 5 years extra since the Dutch conventional mainline treatment hasn’t been taken yet. But it is German doctors that helped them and Belgian doctors that pointed out in a second opinion that a lot more can be done.
LLMs have a part to play. The false positives are awful, but I have seen an average of 5 out of 10 care when things become too complicated.
Except for trauma treatment. The Dutch healthcare system is amazing once they diagnose classic PTSD.
So it’s definitely not all bad but the trust I had when I was younger has been eroded quite a bit and LLMs can meaningfully step in, in my case at least.
[1] I know there are worse systems. But from what I have heard there are clearly better systems nowadays. It has slipped a lot
So 3 days out of 7 days I have guaranteed good sleep. The other 4 days are a toss up. But an average of 5 days of good sleep is much better than 3.5 days out of 7 days.
I told my mechanic the film flam is broken but he said it was the rim ram. He fixed it and we all went in with our lives.
But doctors insist on this God like status so it’s a “nightmare” when patients try to help themselves.
The dad was a retired neuroscientist who delayed cancer treatment against medical advice because he was certain he had been misdiagnosed based on his own research that he did with the help of A.I.
https://www.nytimes.com/2026/04/13/well/ai-chatbots-cancer.h...
There's a comment on the article from Ben Riley:
> I am very grateful to Teddy Rosenbluth for sharing my father's story with the world, her kindness and curiousity proved to be restorative in ways I didn't anticipate.
> The two words that everyone used to describe my dad: "intelligent" and "kind," and he was indeed both of those things. The sad irony here is that it was his human intelligence, combined with these strange new tools that purport to be a form of 'artificial' intelligence, that led to his ill-advised decision to forego the treatment he needed for his CLL. A doctor has already commented on this story with the observation that AI "confidently asserts erroneous conclusions," and we simply have no idea how often this is happening or the magnitude of the harm that results.
> Not a day goes by that I don't feel the pang of my father's absence. He might still be here if not for AI. I try not to think about that, but sometimes I can't help myself.
This is the real root issue.
At 75 years old, he was stubborn. Is that reasonable ? Yes, perfectly. Could he have been right since the beginning ? Certainly. Did he deny evidence ? Yes.
Zero doubt that he was intelligent, everything points toward that direction, but that doesn't make a person less stubborn, because accepting the evidence, is also accepting that you were wrong if you initially postured yourself as adversarial instead of cooperative.
He would have read Wikipedia, scientific papers, etc, even without AI.
He did not want to be convinced. It works both ways:
https://www.foxnews.com/health/woman-says-chatgpt-saved-her-...
or
https://www.today.com/health/mom-chatgpt-diagnosis-pain-rcna...
Nonetheless, someone very smart, just didn't want to move from his position.
Your comment is akin to saying "Karen from facebook who is a human pushed essential oils and ivermectin as a cure to cancer. Now doctor Y is suggesting chemo. Both are humans, humans cannot be trusted!"
The same issues that were present with search-engine self diagnosis are still present with LLMs. If you provide Google with an incomplete list of symptoms and can’t interpret the information you find correctly, you will likely get an incorrect diagnosis. The same is true for LLM output.
But AI's problem is that its completely full of shit, sometimes, and the people most qualified to evaluate whether its full of shit are the doctors, not the patients, but just like OP's original article, patients are left feeling like their second opinion from AI might be more trustworthy than their doctors opinion.
Examples of things normal people can verify
- procedural errors that Claude can capture like some blatantly high dosage (grams instead of milligrams)
- outdated treatment plan, maybe there’s a credible new treatment plan that’s been used for years but the doctors were not updated
- literally being injected homeopathic drugs (takes no smart person to flag this)
Let’s stop talking as if doctors have a divine right here. And let’s accept some agency.
Studies have found that newer reasoning AIs are about as good at diagnosing illness from a written description of symptoms as doctors are.
Granted, it cannot actually examine a patient, so we're not replacing doctors anytime soon. But your view is obsolete.
It may have some utility after diagnosis, but this test doesn’t demonstrate utility for patients.
The more training data, the more questions it can answer with a reasonable degree of probability of accuracy.
Throwing away a potentially useful analysis just because it’s probabilistic seems a bit like throwing the baby out with the bath water.
[0]: IF.
The clanker said I'd be fine, I just needed some rest and OTC meds.
The medical staff immediately turfed me to surgery because the same set of symptoms I told the clanker were enough to concern them that I needed emergency surgery.
Had I have listened to the clanker, I'd be dead because I did need emergency surgery. (Hell, I almost kicked the bucket because I waited for someone to wake up to give me a lift because.my insurance probably doesnt cover an ambulance ride.)
We need studies that quantify error rates from each source type, then we need to account for the fact that the artificial type will keep improving.
Pretty much the like most manager these days, so I understand the frustration of the GPs.
A con artist, a fraud
Like any domain, when you have questions or need a solution, you make research first, then you ask a specialist.
If you explain well the symptoms and context you can have proper advices and then decide on the path next:
Case A) It looks benign and advices / information that you collected seem reasonable, then you go your way.
Case B) You need second opinion of a specialist because the subject is too complex, or there are medications that you need approval.
At home you have the time to assess the options, pros and cons of each approaches, the possible questions to ask and then challenge the doctor.
Shared decision-making is an actual evidence-based model of care, and patients who arrive understanding their condition and carrying specific questions tend to get better attention and better outcomes.
Some doctors get annoyed, because they have big ego and choose to be patronizing, but it is exactly their job to answer such questions.
With LLMs, it's quite good, you get nuanced and rather useful answers.
Before LLMs, no matter the topic you searched for, the answer was the same: "you have cancer / an [obviously deadly] rare disease"
• The doctors are not affordable
• They are too busy for you (< 15 minutes)
• You may need to wait months to get an appointment
• They are not good (country-side is an example, and sometimes even country-level)So, you have something deeply bothering you, your only appointment is in 4 months. It would be insane not to take the time to explore different solutions and not to come informed about the topic.
If you express your prompt properly and do not rely on imagery, you can absolutely have top-tier advices.