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Updates to Consumer Terms and Privacy Policy

(www.anthropic.com)
747 points porridgeraisin | 1 comments | 29 Aug 25 11:29 UTC | HN request time: 0s | source
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ljosifov ◴[29 Aug 25 14:41 UTC] No.45064773[source]▶
Excellent. What were they waiting for up to now?? I thought they already trained on my data. I assume they train, even hope that they train, even when they say they don't. People that want to be data privacy maximalists - fine, don't use their data. But there are people out there (myself) that are on the opposite end of the spectrum, and we are mostly ignored by the companies. Companies just assume people only ever want to deny them their data.

It annoys me greatly, that I have no tick box on Google to tell them "go and adapt models I use on my Gmail, Photos, Maps etc." I don't want Google to ever be mistaken where I live - I have told them 100 times already.

This idea that "no one wants to share their data" is just assumed, and permeates everything. Like soft-ball interviews that a popular science communicator did with DeepMind folks working in medicine: every question was prefixed by litany of caveats that were all about 1) assumed aversion of people to sharing their data 2) horrors and disasters that are to befall us should we share the data. I have not suffered any horrors. I'm not aware of any major disasters. I'm aware of major advances in medicine in my lifetime. Ultimately the process does involve controlled data collection and experimentation. Looks a good deal to me tbh. I go out of my way to tick all the NHS boxes too, to "use my data as you see fit". It's an uphill struggle. The defaults are always "deny everything". Tick boxes never go away, there is no master checkbox "use any and all of my data and never ask me again" to tick.

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12ian34 ◴[29 Aug 25 14:44 UTC] No.45064814[source]▶
not remotely worried about leaks, hacks, or sinister usage of your data?
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londons_explore ◴[29 Aug 25 14:51 UTC] No.45064920[source]▶
I would far prefer the service use my data to work better and take a few privacy risks.

People die all the time from cancer or car accidents. People very rarely die from data leaks.

Some countries like Sweden make people's private financial data public information - and yet their people seem happier than ever. Perhaps privacy isn't as important as we think for a good society.

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1. ljosifov ◴[29 Aug 25 16:40 UTC] No.45066321[source]▶
In the past I have found obstacles to data sharing codified in the UK law frustrating. I'm reasonably sure some people will have died because of this, that would not have died otherwise. If they could communicate with the NHS, similarly (email, whatsapp) to how they communicate in their private and professional lives.

Within the UK NHS and UK private hospital care, these are my personal experiences.

1) Can't email my GP to pass information back-and-forth. GP withholds their email contact, I can't email them e.g. pictures of scans, or lab work reports. In theory they should have those already on their side. In practice they rarely do. The exchange of information goes sms->web link->web form->submit - for one single turn. There will be multiple turns. Most people just give up.

2) MRI scan private hospital made me jump 10 hops before sending me link, so I can download my MRI scans videos and pictures. Most people would have given up. There were several forks in the process where in retrospect could have delayed data DL even more.

3) Blood tests scheduling can't tell me back that scheduled blood test for a date failed. Apparently it's between too much to impossible for them to have my email address on record, and email me back that the test was scheduled, or the scheduling failed. And that I should re-run the process.

4) I would like to volunteer my data to benefit R&D in the NHS. I'm a user of medicinal services. I'm cognisant that all those are helping, but the process of establishing them relied on people unknown to me sharing very sensitive personal information. If it wasn't for those unknown to me people, I would be way worse off. I'd like to do the same, and be able to tell UK NHS "here are, my lab works reports, 100 GB of my DNA paid for by myself, my medical histories - take them all in, use them as you please."

In all cases vague mutterings of "data protection... GDPR..." have been relayed back as "reasons". I take it's mostly B/S. Yes there are obstacles, but the staff could work around if they wanted to. However there is a kernel of truth - it's easier for them to not try to share, it's less work and less risk, so the laws are used as a cover leaf. (in the worst case - an alibi for laziness.)