People who like squirrels should get degus. Degus are not propely squirrels, but close cousins, and they are brilliant pets. Their intelligence is outstanding.
Honestly to me it seems that the objectively unprecedented migration levels in the UK of the last decade (caused explicitly by government policy) are better suited to be called "extreme" or "far" than the demands to roll them back
I use Windows 10 with a relatively obscure firewall software with a per-process/per-service whitelist, and try to not be stupid on the Internet. I also do regular backups. This should cover most of the risk model applicable to me. Has worked so far.
I know this is a popular "well actually" to do, but it is not always useful in a conversation. Yes, all cancers are different, but yes, cancer is also one thing: unchecked, harmful division of cells.
Bacteria are also all different, but still they are "one thing", and despite their diversity, antibiotics exist that can deal with many species of them at once. It is reasonable to talk about bacteria and antibacterial medications, it is also reasonable to talk about cancer and cancer treatment. I truly hope cancer will meet its "penicillin" one day (yes I know this is unlikely).
It seems relevant here because the question was “How will this potentially help me if I get cancer?” and the answer is “Not at all unless you get a particular form of cancer that this applies to”.
> Bacteria are also all different, but still they are "one thing", and despite their diversity, antibiotics exist that can deal with many species of them at once.
Except people don’t ask “what if I get bacteria” the way they ask about cancer. If the story was about a new antibiotic that only affected 20% of common infectious bacteria strains and someone asked “in laypersons terms, how will this help me if I get a bacterial infection”, it would be appropriate to clarify that it only applies to some bacteria.
> Except people don’t ask “what if I get bacteria” the way they ask about cancer.
Yeah, but doctors also don't tell people "you have bacteria" or claim "we found a cure for bacteria". The lack of nuance on average is largely due to a lack of nuance from experts. The media treats cancer as one big thing and bacteria and viruses as separate things. Thus the average joe inherits 'treating cancer as one big thing' from the media.
I agree with you about the media. Cancer is often presented as a monolithic thing by the media. I don’t agree at all about experts. Doctors and scientists who research cancers do not lack nuance.
Oncologists are actually way more specific than even that. Because there are many forms of breast cancer and different treatments depending on the type.
But yeah, oncologists aren’t telling people “you have cancer” the way they might say “you have MRSA”.
Yeah, it's WAY more specific. We got a genetic breakdown, multiple pamphlets on the drugs being used, what they are targeting, and why they work (along with the risks).
Honestly, I think people probably get false impressions because cancer usually hits old people and old people are, frankly, often not reliable narrators.
I understand where you are coming from here, but I think it is helpful for people to overtly grasp that there are very different cancers, very different treatments, and indeed very different outcomes.
Without this understanding it becomes a quick jump from "we're spending all this money on cancer" to "we've made no progress"
An example of the nuance plays out in the common cancers (like breast and prostrate). These have between 90 and 100% 5 year survival rates. Others (like the one in this article, pancreatic) have very poor survivability.
As you note, it's very unlikely that we'll "cure cancer". But we already "cure" (for some definition of cure) some cancers. Progress is slow, methodical, and incremental. It can feel like a lost cause when viewed from afar, but up close very real progress is being made. And that's an important message to pass along.
The other part that is simply missing is that cancer, very unfortunately, evolves and mutates. That's how you go from a cancer that responds to treatment to one that is treatment resistant.
Like you said, for a lot of common cancers we have multiple treatments. It's usually not just one magic drug, but rather the doctors working with the most effective treatments down to the least effective treatments.
Depressing: evolution has discovered a universal cure for cancer, and it's reproduction. You make a whole new human without the bad bits. Other humans have to evaluate which bits are bad.
Which is why we got ecchemo.. where the cancer affected pathways get seperated from the regular ciculatory system via shunt and then get fed the chemo seperately and get a little wash before reconnection to the full circulation. It would be even more ideal if you had the whole navel setup in two entirely seperated systems.. sorry, a man can dream..
> We have penicilin that works against all human cells.
Penicillin works against bacteria, in particular gram-positive bacteria; to a lesser extent gram-negative bacteria too (this depends on the cell membrane structure of bacteria; there are other penicillin derivatives that are also more effective on gram-negative bacteria than penicillin is, but by and large the main target will be gram-positive bacteria). It does not work against human cells. If your comparison is about drugs in general, then of course cytotoxic drugs will have an effect; simplest example I can remember off-hand is colchicin. Of course it should work against cancer cells and non-cancer cells, unless there are some mutations where colchicin could no longer bind to, but that seems very very rare, due to the natural target of colchicin involved in cellular division.
It was an analogy. Just like penicillin kills a broad variety of bacteria we also know substances that kill a broad variety of cancer cells. Arsenic, for instance, and shotgun bullets. The problem is they usually select for all cells or all human cells, not cancer cells more specifically.
Cancer cells, by definition, are not a uniform mass. It will depend on the cancer type, which in turn is defined by the properties those cells have. And mutations happen all the time, often more in cancer cells when their repair systems also have mutations, e. g. are less efficient. By that definition alone, there can never be a wonder-cure for all cancer types. At best you can find some proteins more important (p53 for instance) and while more than 50% of cancer cells have some form of mutation in p53, others simply don't. By that definition there will never be a penicillin-equivalent to all cancer types.
The correct way to read the sentence is “all cancers do not have the same causal mechanism” but people don’t talk like that because it’s off putting. Language is fluid and it’s generally on the reader to infer meaning from context. If we can do so reasonably, we do it, and we don’t need to then write additional posts chiding people over an interpretation that’s highly unlikely to be the intended one. I don’t mean to be pushy about this, btw. It’s just that pedantry can be valuable, but only if it isn’t abused.
You're simply wrong. Again, cancer is malignant by definition. And again, you seem to be confusing "cancer" with "tumor" -- your description applies to the latter, not the former.
You can label a slow-growing tumor as "not-cancer" if you want, for psychological reasons, I guess; "cancer" just sounds scarier. Some slow-growing "not-cancer" tumors are faster than others. It's a sliding scale, not a dichotomy.
Not the same thing, but I found a way to distribute markdown sources (with images) within the PDF files generated from these sources.
The trick is to generate the PDF normally, then zip this same PDF together with the sources again, with compression level 0, making sure that the PDF is the first file to go in the archive. (Easy to write a script that does this.)
The resulting file, when given the extension PDF, is readable as PDF, and when given the extension ZIP, is extractable as ZIP. So whoever wants the source can rename the file to .zip and extract the source. The instruction to do so can be in the PDF text itself.
Why it works: a) compression level 0 means that the input files are just copied into the stream, so the PDF reader will find the PDF header, decode the rest of the PDF, and ignore the trailing stuff. The trailing stuff contains the markdown sources and the zip directory, making the file a valid archive.
I suspect that tolerances in PDF readers and ZIP decompressors are being slightly abused here, but it works with all PDF readers and ZIP decompressors that I tried so far.
That seems like it would be incredibly fragile. As soon as the receiving party made a change that required re-saving the PDF -- like commenting, highlighting, changing default layouts, saving as a PDF/a, checking PDF/ua, etc. -- it might erase the attached files.
It's also very easy to use pdftk to embed or attach files in a PDF using the methods defined in the PDF standard. No renaming or special knowledge required of the audience.
I use "comment-driven development" by building out the skeleton manually, writing comments instead of code, and letting the agent fill the code in (and then repeat, until done). It is a "lower level" of AI usage, compared say to full-vibe mode, spec-driven development, whatever. But I feel that it's even easier to stay in the flow, because I do not get bored by boilerplate or mundane implementation details.
"Higher levels" of AI usage are exhausting and flow-free endeavours.
This sounds good except when you need to cross multiple files. I feel like a significant part of the value of AI is that it can just find things instantly instead of me having to navigate some menu or enter any commands. At least in my experience changing 1 thing requires traversing a large slice.
I guess to take it a step further you could just write everything in a single file with enough context to let the LLM figure out location but this is quite literally just a prompt.
I am on an enterprise environment. I had non stop issues with OneDrive, such as OneDrive process always pegged at 100% CPU, files not synching, files going cloud-only and inaccessible without Internet, and issues in git repos. I go out of my way to avoid OneDrive at any cost, including the cost of using a separate backup system for my files.
reply