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Cake day: September 30th, 2023

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  • DillyDaily@lemmy.worldtoLemmy Shitpost@lemmy.worldPills here!
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    6 months ago

    I mean, I’m anti-meds for treating exogenic issues when something can be done for those exogenic issues.

    If I’m sitting at home with the heater on and I start feeling warm and flushed, I wouldn’t take an ibuprofen (as an anti-pyretic) to bring my temperature down, I’ll turn the heater off.

    It’s the same for mental health, if the sole source of the stress/sorrow is external, medication is nothing more than a bandaid, which is better than nothing if the exogenic influence is outside your individual control (which it often is)… But we are at a point where the majority of people with mental health issues are experiencing a level of exogenic influence and there are enough of us that if we organised we could change the factors that are causing or worsening our mental health symptoms.

    So it bears talking about, is medication always appropriate?

    Medication is important, especially for endogenic conditions, and medication is life saving. But if you have exogenic depression and the meds aren’t working, the new prescription is protest.


  • This is what is breaking my mental health.

    Life is not guaranteed to be good, nature is cruel and has no rhyme or reason. People die and suffer in horrific ways every day because of nature.

    Why the fuck are we adding to that cruelty!?

    The chaos of the natural order of the universe sucks and you’ve got to learn to cope with that. But I’ve always found that side of life easy to accept because it is so inevitably universally unavailable.

    I was born with a genetic illness, it causes lifelong disability due to structural deformity, but can also just randomly cause fatal aneurysms in young people. That’s nature, that sucks, but hey, what are you going to do? Figure out how to do what you need to do to live and live it.

    But then I’m born into a country with no disability discrimination laws, and no right to access laws. Fortunately we had public healthcare and public disability services, and public welfare services, and when I was younger a disability act was finally brought in (though it’s often just lip service)

    Growing up I felt safe and secure knowing I had a good social support system…but the public disability services shut down and was replaced by an insurance model, the public healthcare has been functionally split to a semi public copay system and a private paid system, and the welfare pension is so far below the poverty line that people on a disability pension don’t earn enough money to meet the eligibility for public housing.

    (yes, You can be too poor, for public/social housing.)

    And it’s one thing for law and legislation to lag behind the needs of the people, it’s another thing altogether when an individual or small group of individuals in power systematically impose laws to remove the support and resources you used to have, for barely no more reason than “they want to”.

    I can’t help but feel that a significant portion of my suffering is the result of the few people in the local conservative government that shut down the public disability service providers because it was “costing too much” … Even though the insurance model they replaced it with costs the government more and supports less people than the previous system, and supports them less effectively.

    And how do you live with that?

    Like it’s one thing for nature to have cursed me to suffer, but a human being heard my story, and countless stories like mine, and still said “nah, fuck em” when it came to vote.

    We are living with psychopaths and sociopaths in complete control over our lives. The suffering is happening for a reason, and the reason is that those who are causing the suffering are enjoying the situation (because it gives them money, power, influence, or straight up sadism)

    How the fuck do you reconcile that and “learn to sit with your emotions” in one CBT session and in the very next session my therapist is going to teach me about “enforcing my boundaries”… How do I enforce my personal boundary to get the homophobic, transphobic, xenophobic and ableist government to stop abusing me? Oh, I don’t, I sit with that emotion.

    I can’t afford the pills they recommend.


  • I’m on board!

    I’m a big fan of the word cunt in all of its current uses it’s my preferred slang term for my own, though it’s rare to find someone who’s not taken aback by that in the bedroom.

    Would it be a grammatically consistent pronoun? “oh, someone left cunt wallet, I hope cunt come get it” or do we need a cunt/cunter situation? So cunt can collect cunter wallet.


  • The way the OP phrases it rules out trans men who have vaginas, trans women who have vaginas, and a bunch of cis women who’ve had certain pelvic traumas or cancers and therefore don’t have vaginas.

    What he’s trying to say is “if you were born with a vagina and you align with it” which is actually still funny because I was born with my vagina, I like my vagina, I’ll be happily keeping it even after all my surgeries…but if this OP saw my face he would put me in the “trans man” bucket because they lack nuance around identity.





  • I’m Australian and was always told the cover letter was unnecessary, especially if your CV has a bio.

    The cover letter was for additional information not covered by the resume - name dropping the manager at the company you know who inspired you to apply, explaining why it appears your changing industries, justifying “overqualifications”, mentioning a personal hobby that’s relevant to the industry and isn’t technical work experience.

    Basically the things you plan to bring up in the interview to wow them, you can introduce them while introducing yourself in a cover letter.

    But if your resume lines up with the position description, you don’t need a cover letter.

    Basically I was told a cover letter is necessary when you’re a burnt out nurse or teacher applying to be a cashier at kmart to avoid having your resume immediately thrown out.

    That said. I’ve literally never written one, even as a serial industry hopper. If there’s no email address to send my resume too, then the system is too auto for a cover letter and they don’t want to read it anyway, if there is an email address, just include a few lines of a short cover letter in the body text of the email before attaching your resume.


  • This, when I’ve got a new program or a program has updated I take my time to familiarise myself with it, it takes me more than five minutes because I’m visually impaired and have a learning disability, but it doesn’t take that long and I have fun exploring the program without pressure.

    But when a program updates the UI the morning I start work and I realise I’ve got 5 minutes to figure out where everything has moved? It’s overwhelming and unfortunately I have a “freeze” response to stress and it took me years of therapy to push through that gut instinct to freeze up and just stare at it feeling like it’s too much and I can’t.

    That said, I do still really struggle to find the button mid-meeting. I can vamp, but I can’t vamp while properly searching my screen because with my visual impairment that takes too much concentration, so the result is “okay I’m going to share my screen, but my UI has updated so everyone go refresh your coffees while I hunt down the screen share button” and some helpful person will try to explain where the button is, not understanding that my screen doesn’t look like there’s because I have adaptive software making things larger.

    Though a few times I’ve logged a ticket to IT saying “I’m sorry, I know the issues exists between keyboard and chair on this one, I can’t for the life of me find the print button” and they’ll remote into my machine and say “oh, that’s because you’re enlarged font has pushed half your toolbar off the screen entirely. You’re missing a bunch of features” and suddenly it made sense why I felt like my co-workers were more efficient in these programs. Unfortunately they couldn’t fix it so I still have to work around only being able to see half the screen of this program they suggested “returning everything to the original aspect ratio and getting better glasses”

    My boss seems to think our little 2 man IT department can fix Adobe’s bad adaptive UI.


  • I still feel like the nouns are in the wrong place when I read this.

    I’m reading it as “New York cows new York cows bully bully New York cows”

    When I want it to read “New York cows bully new York cows” which would be “Buffalo buffalo buffalo Buffalo buffalo” which isn’t enough buffalo.

    I have to inset my own “that” to be able to get my head around “Buffalo buffalo (that) Buffalo buffalo buffalo buffalo Buffalo buffalo”


  • This is the thing. Musk and everything his company does in terms of labour and marketing, and just their whole ethos is unethical as fuck, and I can’t stand that as a society we are celebrating Tesla.

    But self driving cars are not inherently bad or dangerous to persue as a technological advancement.

    Self driving cars will kill people, they’ll will hit pedestrians and crash into things.

    So do cars driven by humans.

    Human driven cars kill a lot of people.

    Self driving cars need to be safer than human driven cars to even consider letting them on the the road, but we can’t truly expect a 0% accident rate on self driving cars in the early days of the technology when we don’t expect that of the humanity driven cars.



  • Where does this this linguistically phenomenon come from?

    Is it a mistaken use of “an accident” with the preposition to reflect the personal involvement?

    Mistakes like “Could of” make sense to me because in my accent “could of” and “could’ve” are identically voiced.

    I can also completly understand where we get “alot” because alot is just the beginning of an acorn, minus a few hundred years of lazy pronunciation behind it (an oak corn =acorn)

    Google is telling me it’s because younger people will use “on accident” as an antonym for “on purpose”. That sounds feesible as an origin. Now I’m questioning if “by intent” is grammatically correct, I’ve been staring at words too long.



  • DillyDaily@lemmy.worldtoLemmy Shitpost@lemmy.worldOk boomer
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    9 months ago

    I genuinely can’t tell if you’re being facetious.

    I thought you were fully serious, but then I hit the line

    Even if prices in reality do not need to compensate, because margin is already big enough, it gives retail a free card to jack prices,

    And assumed you were just poking fun and the poor widdle corporations and their giant profit margins, but then you continued with your paragrap, and now I’m not sure again…



  • I mean, yes, but a 3.5mm to usb-c adapter is like $10, so that’s still not really an excuse.

    Most people use wireless headphones these days, and usb-c headphones are getting more common. (I’m hearing impaired, all headphones sound the same to me, but maybe an audiophile will tell me why usbc headphones suck compared to 3.5mm)

    When I bought my new pixel I went to the gym that afternoon and immediately realised I couldn’t use my headphones because I hadn’t been mindful of my missing headphone jack. Worked out in silence, and bought an adapter on the way home for my headphones. Problem solved.

    There’s tons of quiet things you can do on your phone if you’re bored and don’t have headphones.

    The only people who are allowed to have their phones on full volume plasting noises without headphones are visually impaired people, because otherwise they’d need to put their headphones in just to check what time it is on their phone.


  • It’s the microbial diet, so it’s got nothing to do with ethics, the mother was just following all the pseudo-science around which she foods are good for gut health.

    Kimchi is good for gut health (that part is not not pseudo-science, but it’s just good food, not a magic cure)

    Fish sauce is also fermented therefore arguably good for gut health, but regardless good Kinchela will contain fish sauce, so if the goal of your diet is just “eat all the fermented food that’s good for your gut”, it’s going to end up being lacto-pescatarian.

    Why the kid couldn’t eat dairy must be due to a second pseudo-science belief. Yoghurt is good for gut health so the mum must have had some other reason, something she read on Facebook like “cow hormones in the milk are bad for your human hormone levels” could explain cutting out the fairy without being ethically vegan.


  • Maybe it’s half of what you eat, but I’ve been “allergic” to nightshades my whole life and never felt lacking in options (I have a mast cell disorder, tomatos, potatoes etc cause anaphylaxis, it’s not a true allergy, but it functions like one)

    I can eat practically anything, it’s only like 20 plants I’m allergic to out of like 700 I have available to me. And if I travelled overseas I’d find more stuff I could safely eat there too.

    I just can’t eat much pre-made, packaged organic convenience foods. Most will contain potato starch, unmarked dextrose, “spices” (if it’s not specific in the ingredients list, often I avoid), etc

    Even desserts aren’t safe because e160c, paprika, is what most companies here used when they swapped out the red dye 40.

    So I cook from scratch, but I’ve never felt limited in my own kitchen because of the ingredients I have. (I am limited at restaurants, I usually order a black coffee and enjoy my dining friend’s company)

    I also don’t live in the America’s, so that helps. I can see why they would think nightshades are everything, all the best foods from the Americas start with tomato, or capsicums, and potato is a staple carb. Meanwhile my cultural diet is based on brassicas and oats.

    But at the end of the day, Beans and rice is nightshade free, it doesn’t take a genius to think of a non-nightshade vegetable to add to the mix to make a unique meal.


  • Another one to add to the list, Mast Cell Activation Disorders can have a huge variety of triggers, so much like IBS, individuals and may notice a connection between nightshades and their mast cell flare ups.

    One of the main treatments for MCAS is simply an elimination diet to identify riggers followed by avoiding triggers for the rest of your life.

    There are some MCAS patients who have to be entirely prescription formula fed because they have so many obscure dietary triggers.

    Unlike IBS which can be debilitating, but rarely life threatening, MCAS causes anaphylaxis, so it can appear like a real allergic reaction to food, and it functionally is, it’s just not a true IgG or IgE allergy to a specific protein chain.