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Cake day: December 7th, 2023

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  • Russ@bitforged.spacetoAsk Lemmy@lemmy.worldWhat scares you?
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    1 month ago

    That is awful, Celiac’s (and really any autoimmune disease) is no joke. I see a lot of parallels reflected in their post and I truly hate that for them so much - constantly struggling to find foods that you can tolerate, having numerous surgeries, seeing a million different doctors, being in and out of the hospital all the time to the point that its a second home, lab test after lab test that only result in more questions than answers, symptoms and other issues spiraling up due to complications of going through the condition - you name it.

    I feel for them, every day feels like you’ve got the curse of Sisyphus. I feel like there has to be a solution for people like them and I, and its unfortunate that there is just so much about the body and its various systems that we don’t understand. I constantly struggle with the idea that we’ve come so far with the sciences, and yet it feels like in matters of human physiology like the GI, immune, and nervous system we’ve barely scratched the surface.



  • Russ@bitforged.spacetoAsk Lemmy@lemmy.worldWhat scares you?
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    1 month ago

    I’ve had health issues since I was a kid (all stemming from developing Crohn’s Disease symptoms before I was even a teenager), and a lot of them still haven’t been resolved (in part of reasons such as developing new conditions due to medications I took to treat another condition). One of the worst things I fear is that if I randomly end up leaving this world in a way that incurs an autopsy, the results will end with something like “Damn, this man had issues. If his doctors had known about X then he could’ve lived a much better life, the treatment is simple”.

    I go through so much, and I’ve done countless research to try to track down possibilities that my doctors hadn’t considered (some of my research has in fact lead to me finding out new things that my doctors didn’t account for, even as of this year) - and I always have this terrifying doubt of “What if I had just chosen a different doctor, the next one on the list might’ve had this idea years ago and prevented some of this”. That line of thinking of “Could’ve, should’ve, would’ve” doesn’t help of course (as my friend likes to tell me “What if the sky were green?”) but that doesn’t stop me from thinking about it more often than I’d like to.



  • I personally use Sleep as Android which comes with a bunch of options to help ensure you’ve actually woken up. I utilize the “captcha” option in which when I go to turn off the alarm, it displays a screen full of sheep and all of them but one are sleeping - you have to click the one that is “awake” in order to dismiss the alarm. I guess the process wakes up my brain just enough so that I don’t go back to sleep, whereas with a regular alarm that has just a simple dismiss button I’ll absolutely either hit dismiss or one of the volume buttons to turn off the alarm before I’ve fully woken up.

    I also have it set to buzz on my watch for 90 seconds before playing a sound on my phone (which escalates in volume) - I’ve not had a problem waking up with this in the years that I’ve been using it.

    There are other options too, such as answering math questions, scanning a QR code, pressing your phone to an NFC tag, heavily shaking the phone, one called “Say cheese!” that makes you smile as hard as you can and uses the camera to detect it, and one that you have to “laugh out loud”.



  • Fucking Crohn’s Disease sucks. All of my “adventures” with it have been painful, but the one that takes the cake:

    A couple of years ago, my GI wanted me to do a pill endoscopy test, which is where they basically have you swallow a pill that has a camera embedded in it, and it takes pictures while it traverses your insides. You’re supposed to naturally “pass” it like anything else you eat, but in my case I did not, and it got stuck. My GI did not believe me, and it just kept getting worse and worse. To put a timeframe on things, this happened in early February of that year.

    I had ER trip after ER trip throughout that year, they determined that it wasn’t going to pass on its own and needed to be surgically removed, but since it was not “life threatening” they couldn’t just wheel me into an OR immediately and have it done, it had to be scheduled. Took forever to find a surgeon to schedule me under. One of the times that I was in the hospital due to this, the doctor on my “care” team wanted me to do what she called a “supreme bowel cleanse” to see if that would dislodge it. I was hesitant to do it, but I was pretty much willing to do anything at that point to end this nightmare, and only because she promised me that if it didn’t work, they’d take me into surgery and do it the old fashioned way. That ordeal was terrible, I’ve had Crohn’s since before I was a teenager, I’m very used to doing colonoscopy prep - this was far worse than that, the pain was unbearable and the amount of bowel cleanse that they gave me must’ve been right at the border of their ethical limits (or at least, I imagine that has to be a thing, right?) and plot twist she did not hold up her end of the bargain when the pill still did not pass, instead she gave me a few days worth of pain meds and discharged me the next day.

    My condition continued to get worse and worse, yet my operation wasn’t scheduled till early July. The hospital that the surgeon worked for agreed to pre-admit me into their care 2 months in advanced because it got to the point where I could barely even hold down regular water and I had to be put on IV nutrition with a PICC line and all.

    Fast forward to the operation day, they ended up having to do two surgeries in one go, the first being to remove the pill, and the second was to try to fix the damage that had been revealed on the camera. The moment I woke up from the operation I was screaming in pain, and begging them to put me back under (which they could not do). They kept giving me pain meds and I’d end up passing out eventually from the pain, wake back up, and the whole ordeal would start again. Eventually they put me on one of those self-administered pain med pumps where I could click a button every so often and it would give me some pain medication through my IV.

    I didn’t end up going home until the very beginning of September (first week I believe), and I had arrived there sometime in the middle of May. I will never do one of those pill endoscopy tests ever again. I also switched GIs since my current one at that time had refused to listen to me when I told her something was wrong at the beginning of the “experience”.


  • In my first year of high school, we actually went out to the massive Toyota truck factory in San Antonio, Texas as a field trip! Definitely the best field trip of all time (at least, for my area), I can’t actually remember the purpose of the trip (if it was tied to a lesson plan at the time, or if we just did it because it was cool).

    I remember being really amazed at the automatic robots that whirred around the facility. Sadly I do not have any pictures of the trip (and even if I’d had the means to do so, that was so long ago that I definitely wouldn’t still have copies anyways) however there is an article here from a team that took a tour, they even cover the “Stop, Point, Look” policy that they made us follow while we were in the manufacturing plant.

    At the time, I believe their “Tacoma” model of pickup trucks were only assembled in that plant (at least, in the US) - this doesn’t seem to actually be the case anymore, but I heavily recall them mentioning some model of truck that was only made there.






  • My desktop PC runs a dual boot of Arch Linux and Windows 11 (for the few things that don’t work with Linux cough Destiny 2 cough - damn it Bungie, and VR stuff). My MacBook runs a dual boot of Fedora 40 and whatever is the latest version of macOS that can run on it (its an older Intel model, Apple dropped support for it a couple of years ago - I think its running Big Sur? I hardly ever boot into macOS).

    And then my Steam Deck (its effectively just another x86 PC afterall) of course uses SteamOS.

    What about you, OP?




  • You’re thinking of install-time permissions, which technically does still exist, but pretty much most of the permissions you’d actually care about are runtime (or special) permissions - the application must request these from the user.

    There are three main types of permissions on Android:

    • Install-time, these are permissions granted to an application upon installation
      • In this group is also signature-level permissions, which are only granted to applications that are signed by the same party as the OS itself (usually your OEM)
    • Runtime permissions (also known as “Dangerous permissions” within Android internally), which are permissions that the application must request from the user. The system draws the permissions dialog, not the application itself. Permission can also be granted one-time only, or permanently (unless the user revokes the permission)
    • Special permissions, which also need to be requested by the application - except for these the system will not draw a permissions dialog, instead the application must send the user to the “Special App Access” menu within system settings, and the user must turn on the permission there. The best way I can describe these types of permissions is, “permission that the user really must think about before granting” - such as giving an app the ability to bypass DND rules, drawing over other apps, installing APKs from unknown sources, accessing all device files, etc. IIRC, Google also requires that developers provide justification for requesting these permissions when submitting to the Google Play Store as well.

    Runtime permissions were introduced in Android 6.0, which was released in 2015, I am not sure when the special permission system was implemented however.


  • Russ@bitforged.spacetoAsklemmy@lemmy.ml*Permanently Deleted*
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    4 months ago

    Hate? No, I do not hate Google. I still use a Pixel phone (and photos/assistant on it), my Gmail is still my primary email (I also self-host a few other domains but those are primarily used for automation and a few other one-off things), I subscribe to YouTube Premium, I still utilize my Stadia controller as my primary game controller, I use a Google TV set top box, etc.

    I don’t use Search (I use Kagi instead), I don’t use Chrome (Firefox), I don’t really utilize Gemini all that much (I just run ollama for the few times I want to use an LLM).

    Really I just use their products that work well for me, and don’t use the ones that don’t. There’s no love/hate about it.




  • Exactly the same for me too haha, I’ve beat the ender dragon with friends before on shared worlds, but I’ve never beaten it in my own single player world.

    I generally have really short bursts of playing MC these days, and by the time I play again a new update has come out so I usually just completely reset to new world features and such. I know that they generate in unexplored chunks and that you can go prune chunks and whatnot, but rather than spend time doing that I’d rather just spend the time playing. Hell, these days I don’t even usually get to the stage of getting Netherite gear.