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Cake day: September 30th, 2023

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  • As someone chronically Ill, I feel this so hard.

    Every minute that I’m not at work I’m dedicating to making sure I’m likely to be well enough for work tomorrow.

    I don’t do anything after work without asking “how will this impact my health tomorrow?” and that includes things like not being able to sweep my own floor because I know I need to sweep at work and the nerve damage in my arms won’t let me sweep twice in one day without keeping me up all night in pain, and if I don’t get enough sleep, I’ll get a migraine and won’t be able to physically see anything.

    Most of my days off are spent in agony trying to restore myself and desperately trying to reset my house and home life so I can keep up with work, without overdoing it on Sunday and making myself sick for Monday.

    So yeah, on the one day a month where I wake up for work and I don’t throw up or almost shit myself, and my heart rate is doing what it’s supposed to do, and I can see and hear and feel my feet… The temptation to “call in healthy”, so I can actually have a day off to enjoy myself for the first time in over a month is really hard to ignore.

    I actually did that this week because Wednesday was my birthday, I went to work, it was a “bad workable day” (vs a “good workable day” or a “bad unworkable day”) and Thursday I woke up feeling really good, I only had a 2 hour shift and it was just admin so I took my first sick day in 6 months and used it to do all my linens and towel laundry. It felt like a proper day off because I was healthy enough to get stuff done for myself, without being in pain or having to stop to run to the bathroom or let my heart calm down, or give up on folding because I can’t feel my arms.

    I can’t do that every time I want or even need to though. My bank account is really good at forcing me to go to work, healthy, half dead, or heaving. Chronic illness is expensive, and some days trying to keep up with work feels like it costs my health more than not working. but sadly not working is not an option for me, because I’m capable of work, so I must. (and continue to push my gov for universal basic income)

    For context as to how working while disabled messes you up. I got hit by a truck on the way to work last year, I got to the office and used their first aid kit to patch myself up. Booked a doctors appointment, told my boss I’d be leaving early, then kept working until my appointment.

    My boss was fine with this, and then someone on reddit posted a photo of the crash and my boss saw, they realised when I said “I was hit by a truck” what I meant was “I was hit by a truck”

    When asked how I was feeling, and reporting “no different to usual” my boss sent me to the ER because they thought I had a concussion and was acting confused. ER checked me out, dislocated shoulder and wrist, soft tissue damage here and there, but otherwise nothing major or serious or nothing I don’t already deal with on a daily basis. I went back to finish my shift and my boss asked what I was doing working after I’d been hit by a truck.

    I feel exactly the same level of pain today as I do every other day. If I take today off because this level of pain is apparently unworkable, it’s a slippery slope, eventually I’m going to have to come back to work despite being in this exact same level of pain. This is my baseline, now I can truly compare it to being hit by a truck.

    I used to be on a pension, I wanted to work because I wanted purpose in the neo-liberal hell scape of my society. but my mental health was too shot because of this deep rooted idea that I deserved rest just for being in any level of pain that was out of the ordinary, and subconsciously I would talk myself out of doing anything because I deeply believed I shouldn’t have to.

    But I don’t have that luxury, my ordinary will always be “hit by a truck” level, so right now I either learn how to consistently work through it, or drop dead broke and homeless.


  • In Australia Google maps has issues with routing cyclists on 80km busy truck transit roads that have no bike lanes, footpaths or shoulders. You’ll regularly get stuck behind lost uber eats cyclists whose map took them through a motor vehicle only underpass.

    The other day google maps decided to reroute me from a quiet, wide street with no bike lane that was otherwise perfectly safe, and tried to send me through a nightsoil alley, down a heritage stock run that was paved with cobblestones and crossed over a storm drain 4 times in a zig zag.

    Yeah, “safer” because there’s no cars I guess, but not suitable for bikes at all.


  • I have galactorrhea, pumping rooms aren’t a natural maternal family matter, for me, it’s a medical procedure.

    Privacy is a lactating person’s choice, and right. public feeding is a choice that I agree needs to be destigmatised. Personally I’m not comfortable with public pumping, because I see my breast milk as medical not nutritional, so I choose privacy for myself.

    It’s also difficult, it’s stressful, it’s uncomfortable. Having comfort, focus, peace and quiet, it’s important.

    I don’t even have a uterus, so getting my leaky chest out in public is even further from being socially acceptable. I’ve lost count of how many times I’ve had mastitis because I have not been able to expell in a timely manner. Partly that was because I was embarrassed by my condition and didn’t stand up for myself and my need for access to a pumping room at work, and part of it was because my employers didn’t understand my need for a private room, they pointed out that it’s never been a problem for mothers in our office to whip a tit out when baby was hungry, and/or that my need was different because the reason I I had breast milk at all was different.

    No one gets to expect me to be comfortable with nudity. My breast milk, my choice if I have privacy or not.

    I used to do it in the bathroom because I didn’t have anywhere else, but that was a gamble, do I let myself get an infection because I’m letting my ducts clog, or do I risk an infection by pumping milk in the toilets.


  • DillyDaily@lemmy.worldtoMemes@lemmy.mlZen Z
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    1 month ago

    Accessibility.

    We will never get rid of the analogue clocks from our school, we’re an adult education and alternative model highschool qualifications centre.

    We primarily teach adults with no to low English, adults and teens with disabilities, and adults and teens refered via corrections services.

    There is a significant level of illiteracy within numeracy, and for some of our students, it’s not a failing of the education system, it’s just a fact of life given their specific circumstances (eg, acquired brain injuries are common among our students)

    Some students can learn to tell time on an analogue clock even if they didn’t know before.

    But even my students who will never in their life be able to fully and independently remember and recall their numbers can tell the time with an analogue clock.

    I tell my students “we will take lunch at 12pm, so if you look at the clock and the arms look like this /imitates a clock/ we will go to lunch”

    And now I avoid 40 questions of “when’s lunch?” because you don’t need to tell time to see time with an analogue clock, they can physically watch the hands move, getting closer to the shape they recognise as lunch time.

    And my other students can just read the time, from the clock, and not feel infantalised by having a disability friendly task clock like they’ve done at other centres I work at - they’ve had a digital clock for students who can tell time, and a task clock as the accessible clock. But a well designed face on an analogue clock can do both.

    I myself have time blindness due to a neurological/CRD issue, so analogue clocks, and analogue timers are an accessibility tool for me as well, as the teacher.


  • At the end of the day, alcoholism, depression, and obesity, they are unhealthy states of being.

    They are not something people choose, and while there are treatments, it’s not something everyone can control.

    That doesn’t mean we should simply accept this state of being. People living with depression deserve better, people living with alcoholism deserve better than for us to say “it’s out of their control, they can’t help it, so we shouldn’t judge, let them be” when what they need is better support and better treatment options.

    Likewise, obese people deserve better than “eat less, move more, fatty!” but they also deserve more than “all bodies are beautiful, just let us be”

    I say this as someone who was a fat kid, and a fat teen, and a fat adult. I had a BMI of 50 for a most of my life. In my mid 30s, I got it down to 28, and still going.

    So I say all of this is as someone else who was fat, obese, and morbidly obese. Obesity should be viewed the same way we view depression and anxiety, though depression and anxiety also need some better PR.

    Being obese may not not always be a choice, but the the ultimate end goal of how we view obesity as a state of being is to find ways we can all manage our weight. Because obesity is not healthy, for those who can’t easily control their weight, life sucks, they are patients in need of treatment, not morally failing people, but also not “perfect plus sized activists who are healthy at every size”

    Because while bodies and sizes vary and we can do healthy things at every size. Obesity is inherently unhealthy. Obviously being bullied won’t solve anything, but neither will society politely ignoring how hard it is to live a full life while suffering from obesity.

    Being black isn’t an inherent health issue. It genuinely is just a different state of being. 99% of problems unique to black people are social issues, not medical issues… So the comparison between obesity and substance abuse issues is more helpful than trying to compare being obese to being BIPOC.



  • Yup, thyroid, adrenals, and gonads have been checked, both with blood work and untrasound.

    I have dysautonomia due to a brain stem herniation, and temperature regulation is effected by that, but it’s just been so weird that the way this symptom effects me was decades of not feeling the cold, then suddenly now I’m not feeling the heat.

    I know which one I’d choose if I got to pick… and it’s the one where I don’t need to go to a wound nurse for frost nip in February.


  • I was a year round shorts guy, genuinely didn’t feel the cold. Last year I suddenly became a year round thermal stockings, skivee, thermal gloves, jumper and woollen pants guy.

    I can’t get warm. It’s like I’m catching up on 30+ years of never feeling the cold by feeling the cold all the time.


  • I never really understood at what point a language evolves enough to be an entirely new language.

    Old English feels so far removed from even middle English, let alone modern English.

    We have “new” and “old” to differentiate them, but with how many Latin words alone entered English between Old English and Modern English, It’s something I’ve never found a comprehensive answer to.

    I guess, what is it about proto-indo European that we acknowledge as a distinct language from the hundreds of thousands of languages that evolved from it, other than time scale and global impact.


  • Well not if you strip it from all context and the nuance of OPs specific word choice.

    Because I could tell a story about my Turkish co-worker that ends like:

    “my co-worker of specific race is doing dodgy shit and it’s so harmful for the whole community that he’s doing this, especially with how much anti-ethnic group hate is going around, he’s giving everyone a bad name and I’m worried his behaviour as an individual aashole who happens to be race is going to start a spree of hate crimes against others who aren’t doing anything wrong, because most people aren’t, my co-worker is”

    And I would argue that this story is fundamentally different from just leaving it as “my Turkish co-worker is doing dodgy stuff”.


  • Yes and no, if you scambait hard enough your number can eventually be added to a blacklist for larger scam organisations that bought your data for use in multiple scam attempts.

    In my experience that has really cut down on the calls.

    In 2020 the department of human services accidentally posted my personal phone number on a list of support services for people experiencing housing or food insecurity. This number was then circulated by every major news source in my state. I couldn’t change my number at the time because I had no legal ID (still don’t… Can’t figure out how to get ID without ID, but I have a new number now at least) at first I didn’t really notice the ratio of spam calls to genuine calls for the wrong number (ie, people calling my number because they needed housing/food) . I just remember getting 40+ calls a day at many stages.

    But as the actual number for the food relief service was circulated, I eventually stopped getting genuine calls and I was getting 3-5 scam calls every single day.

    After a year of scam baiting, I was getting 2 a week.

    Now, I’ll do something online that requires sharing my current number, within a few hours I get a scam call because my data has been sold, but I bait the heck out of that first call and I usually don’t receive any further calls which suggest my number was blacklisted by a larger scam organisation, and I won’t be hassled until my data is sold again as a new item.

    It’s hard to avoid getting your number on scam lists when the largest health insurance company, and the second largest telecommunications company in my country both had major data breaches where millions of customers identifying information was accessed and sold to scammers…






  • The female condom has two rigid rings, one in the sealed end that sits under the cervix, and one at the open end.

    The ring at the open end is designed to hold the condom open and give the penetrating partner a nice big safe target to make sure the penis/toy/whatever goes inside the condom and not accidentally between the condom and the vaginal wall. This ring also provides some minor protection to parts of the vulva due to its size.

    The internal ring is much smaller by comparison, and is not that much larger than a diva cup. The internal ring of a female condom is a similar size to a “soft cup” menstrual cup, it’s a little bit smaller than a contraceptive diaphragm.


  • DillyDaily@lemmy.worldtoAntiwork@lemmy.mlThat's all it is.
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    4 months ago

    Exactly! I have a genetic illness that caused congenital deformities and injuries and disability later in life, starting around my teens thanks to puberty.

    From an early age my relationship with work was distorted because I found myself trapped in the gap between two pathways. I was obviously capable of work, with the right treatment and support I had a lot of potential. But I was disabled, and I required expensive supports and medical intervention, and under the public healthcare system there reaches a point of disability and limitations in capacity that you are written off by the system. Shoved in a residential group home, given a pension below the poverty line, and expected not to try. (genuinely, we’re expected not to try, if someone on a disability pension works a job, they can loose their pension, which is many cases is also tied to housing and access to medical services)

    I’d flip between the two systems, I’d have a great few months with regular access to treatment, I’d get a job plan from the dole office, I’d sit through work readiness courses, I’d be getting healthier and looking forward to working and being a good little contributor to society. Then I’d hit a waiting list for my medical care, my health would slip, I’d be re-assessed by the welfare department and deemed too disabled to work, my job plan would be shredded and I’d get a pension support plan. Then I’d get to the top of the wait list, resume treatment, and get back to getting to work.

    I didn’t start a “real job” until I was 24, it was a call centre gig and I near killed myself trying to do it.

    It wasn’t even hard. It was a true 9-5 (no overtime, no bullshit) and you mentally didn’t need to bring any of it home with you. It was easy for me, but my body decided it was too much. My health suffered and it took years to fully recover, with me barely pulling myself together here and there for gig work in between being bounced on and off the disability pension system.

    The whole endeavour was far more expensive to tax payers than a system like UBI. Processing my case 70 times because the disability support, and employment support eligibility requirements are so strict and the lines between streams so black and white took a lot of administrative resources.

    I’ve been in my current industry for 10 years this November. I work part time, 12-20 hours a week depending on my health. I’m highly successful in my field because I’m working within my body and mind’s means and playing to my strengths. I’m a whole person with a life outside work and I bring that range of experiences to my job, enriching what I bring to my organisation - which is good, because my job is a mutual exchange between me and my employer, it’s not exploitive towards me the worker, which further prevents burn out for me.

    But we exist within the capitalist system of funding and our wages are set by the department of health and human services. I make $34,000AUD a year and it’s not enough to survive.

    But if I work any harder my body will not survive.

    I’m asking to do what I can do for my community, while living a safe existence… Not being forced to choose between litteraly breaking my back working for someone else’s greedy profit, or starving in a tent (though realistically, a lot of people are doing both)


  • Yeah, nah, Tamworth. We have our own branches of country music down here mate.

    Blak Country is a seriously cool branch to explore if you’re curious about how Australia has interpreted US country music into a localised sub-genre. Swap your mouth organs for a gum leaf and add some yidaki riffs for extra bass.