
One Nice Bug Per Day

Origami Around
DEAR READER
I'd rather be in outer space 🛸
we're not kids anymore.
todays bird

★
let's talk about Bridgerton tea, my ask is open
Jules of Nature

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Aqua Utopia|海の底で記憶を紡ぐ
Today's Document

Kiana Khansmith

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#extradirty
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RMH
almost home
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@fintegral

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Just saw a post talking about "having a superiority complex over not watching Disney live action movies" and I was like damn, the bar for superiority is pretty low these days. Just the other day I saw an open single-serve slice of American cheese lying on the sidewalk and I didn't roll it up and shove it down my gullet without chewing like a hungry duck, I guess that makes me a genius who stands above the vulgar masses like a god
someone is putting up pictures of me around town and they all say I’m ‘wanted’. which is nice
this lifetime is very bizarre and then youre not even supposed to also be bizarre. Ok
Vinyl records are circular because it's an efficient use of space: the grooves that encode the music are laid out in a spiral on the disc, so that the needle only has to move as far as the disc's radius to read the entire thing. Before this clever idea was thought of, the grooves were instead laid out in a straight line, and every LP was a narrow rectangle more than a thousand feet long. To flip an album to side b at least two people were needed, one at each end, coordinating via shouted instructions.

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I wasn’t going to derail the disability pride month post for people with peanut allergies but in relation to that topic
I have never seen another allergy that has been so viscerally hated and mocked by people working in education like nut allergies. I’ve seen fellow teachers cringe that their classroom was the “nut free” classroom that year. Support staff that are trained and willfully don’t follow cross contamination protocol in the lunchroom because it’s too “tedious” or “time-consuming”. Full preschools + childcare centers that refuse to accommodate nut allergies. Schools where the only free lunch is a PB&J. Before/after school programs and summer programs whose food curriculum has nuts and doesn’t provide an alternative activity.
Allergy discrimination is so so insidious and prevalent. It’s happening behind their back and it is everything from the exposure joke to possibly causing someone to go into anaphylaxis from willful ignorance.
Also other parents in the classroom are guilty too. The “not my child not my problem” brain rot means that those lunchboxes are like bombs for airborne exposure allergies
A 22-year-old woman said Lufthansa staffers were not sympathetic to her condition when she tried to explain her life-threatening peanut alle
I was not downplaying this. The stigma is real, and people are 100% willing to let people with allergies die.
This woman was laughed at for asking for allergy accommodations at multiple points in her trip, and was denied to the point that she was practically told she’d be refused care in the event of anaphylaxis.
I work in healthcare. I cannot get my coworkers to consistently change their gloves after handling a PBJ. They literally do not think of it, and I don’t understand why. I also don’t know how to make it stick in their brains that this is a thing they need to do.
I grew up in the early 2000s with severe allergies to not just peanuts, but ALL nuts as well as beef, pork, shelfish, seeds, kiwi, and some food dyes. The resistance that my family faced from educators in the early 2000s is frankly bananas, not to mention the shit other parents and kids got up to.
When my mom tried to enroll me in preschool, the school principal refused any basic accommodations like asking everyone to wash their hands after lunch before re-entering the classroom, not bringing straight up peanuts to snack time, etc. There was no such thing as a nut free classroom at the time. The principal told my mom and me (I was 4 at the time and definitely in the room when this happened) “if she’s so sick, she belongs in a bubble, not at school.” THE FUCKING PRINCIPAL! My mom had to threaten legal action under the ADA to get them to comply.
Look, I was on a 504 accommodation plan under the ADA for the entirety of my formative education (elementary thru high school). That’s all 12 years!!! And yet I have had teachers hand me items I’m allergic to as a “reward”. I have had other kids intentionally try to send me into anaphylaxis. One girl in 3rd grade asked me why I “wasn’t dead yet” when she had put on a lotion with almonds in it and then held my hand. I’ve had other parents write letters to the school saying what a terrible inconvenience it was to them to not be able to send their kiddo to school with PB&J, demanding I be Removed to a special education only class if my “needs” were such a “burden” to others. During elementary school “parties” held in the classroom on holidays and for student birthdays, I was always sent to sit out in the hallway or go to the library, because even though parents were only supposed to bring safe foods into the room (they had a list of all my allergies) they never once got it right. Administrators fought me tooth and nail for the right to carry my epi pen and other meds on my person at all times. Why they thought I would start dealing benadryl on the playground, I do not know. At lunch, I was always sat at a specific segregated table labeled the “Nut Free Table” alone because who the fuck is going to sit there with the literally segregated outcast? But ONCE notably I was sat on one side of a line of blue masking tape down the table top with the rest of my class on the other. One side was the NUTS side!!! As if allergens would respect that tape barrier. (Spoiler alert: they do NOT!)
Literally from preschool to my senior year of high school, I was “the peanut kid”. Other parents gave my mom books about how to “cure your child’s food allergies from HOME” by micro dosing with things they are allergic to (please never ever ever even attempt anything like a food challenge with a known allergen outside of the care and supervision of a medical professional, holy shit that’s so dangerous). My mom joined the PTA in my last year of high school so that I could maybe participate in all the senior-focused events like pool parties and breakfast at school on the first Friday of the month. The number of times another parent either (a) decided it wasn’t worth it to care or (b) intentionally brought peanut products to an event to spite either me or my mom??? I literally could not count. It happened constantly.
College was better, but I still occasionally had people BALK when I asked them to please not eat a Nature Valley bar with whole nuts in it right the fuck next to me in lecture, thanks. Work parties and catered lunches were always impossible. A few conferences I went to as an undergrad were SUPPOSED to be nut-free, but always fucked up the catering. At one, they set up snack tables by every exit of the conference auditorium so that when people left after the talk, they all congregated around the exits and opened macadamia nut cookies and granola bars. When I had subsequently had a massive allergic reaction and needed help getting home (I’d walked) after taking like 200mg of benadryl, the staff offered me a stack of napkins and a lukewarm apology.
Food allergy is a disability which touches literally every aspect of a person’s life. Everytime I share with someone new about what it was like growing up with my allergies, they have never heard anything like it in their lives. They’re always like “holy shit, seriously??? People did that??? Kids tried to kill you??? Parents wanted you kicked out of the classroom????” Yeah, man. Yeah. My own brother (who doesn’t have any allergies at all) doesn’t understand why I don’t “eat more adventurously” and why I won’t travel internationally. So, saying it REALLY LOUDLY for people in the back:
FOOD ALLERGY IS A DISABILITY FOR WHICH EVERYONE SHOULD BE ABLE TO ACCESS ACCOMMODATIONS AND HAVE THEM TAKEN SERIOUSLY.
i do trust sonic... but now i'm a lil bit suspicious
howmst the fuck did you do this so fast
According to time stamp, the artist posted their art 8 minutes after op posted.
Work it grandma
OK I SAID WORK IT AND SHE REALLY DID
I think you mean, "Work it, GREAT grandma". And she does!
There is a graphic tablet for blind and visually impaired people?!?!!!
So, basically dotpad is a tablet with a screen made of physical dots (i'll call them beads for easier writing from here), and it can be connected to a device like an ipad (appparently). It then loads whatever picture is shown and converts it into black and white and THEN it displays the image by lifting some of the beads while the others stay down.
ID: The image shows a black electronic device with a tactile display on top, then a row of buttons and a Braille line on the bottom. /End ID
This is amazing? And so simple? Yet I would have never thought of it as a concept. And I have never heard of it? And there's ony limited information out there, like, i couldn't even find it on my usual online stores?
Can we please spread those news? Please?
This is Accessibility and so cool!!!

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Man I miss free the nipple. Its getting warmer and we don’t even have free the nipple anymore
feminism has backslid so hard in recent years people don't even know what free the nipple means anymore
To clarify for those who don't know, "free the nipple" isn't about going braless, it's about going topless
No shirt, no bra, completely bare torso, just like cis men are allowed to
It's about desexualizing breasts and "female presenting nipples" and not being criminalized for our bodies if we want to go topless because it's a million damn degrees out. This was a popular growing movement that was still widely known a decade ago!
And the fact that not wearing a bra is so discouraged and stigmatized that people think the movement was about being able to go braless under your shirt in public rather than about being able to not wear a shirt at all says a lot about how far we've backslid in the past decade
She was intersex and raised as a boy for most of her life in Kenya. Then the bleeding started.
When 18-year-old Roberto first experienced menstruation, she was terrified. Born intersex and raised as a boy, she had never been taught about periods, let alone how to manage one. Before that terrifying day, Roberto had spent her entire life in a quiet village in Kisii County. Her parents never disclosed anything about her intersex identity, partly because they did not fully understand it themselves, and partly due to the stigma surrounding differences in sex development. Roberto grew up playing football with boys, dressing like them, and following all the expectations of male childhood. Yet, as she entered adolescence, she began noticing subtle changes in her body that did not match those of her peers. She occasionally experienced discomfort, mood shifts, and physical traits she could not explain. With no information about intersex bodies or reproductive health, she simply brushed these feelings aside. Conversations about menstruation were reserved for girls, leaving Roberto completely unprepared for what was coming. “I thought I was bleeding to death, but I could not tell anyone, not even my mother,” she recalls. “I used an old T-shirt and hid it under my mattress.” It was only years later, after meeting a community health volunteer who worked with intersex and gender-diverse youth, that Roberto finally shared her experience. The volunteer explained what it meant to be intersex, helped her understand her body, and connected her to a safe support group. Through these conversations, Roberto slowly began embracing an identity that felt more aligned with who she truly was. She chose to use she/her pronouns because it was the first time she felt seen, understood, and comfortable in her own skin. “It felt like breathing freely for the first time,” she says. “Like I could finally be myself without fear.”
The hidden reality of intersex menstruators
Roberto’s experience reveals a little-known truth: intersex individuals who menstruate are often invisible in menstrual health policies, education, and aid programmes. While Kenya, and Africa more broadly, has made progress in addressing period poverty among girls and women, intersex people are left behind, navigating their cycles in silence and shame. When 23-year-old John first experienced menstruation, it was not a typical “coming-of-age” moment. Instead, it became a confusing and isolating chapter defined by stigma and secrecy. Growing up in South Nyanza, John lived in a household and a wider community that neither understood nor accepted their identity, let alone their menstrual health needs. “I bled in silence for years, and yet I could not talk to anyone,” they recount. “My mother kept asking why I was not ‘normal’, but I was too scared to explain something I did not even fully understand myself.” Intersex persons like Roberto and John are often excluded from the conversation about menstruation. “This is despite the fact that they suffer in silence,” says Margret Mogaka, a reproductive health advocate at the Kisii Teaching and Referral Hospital (KTRH). Although the Kenyan government launched the Menstrual Hygiene Management Policy in 2019 to promote menstrual equity, intersex individuals are not included. “Menstruation is still framed as a female-only issue,” says Mogaka. “This excludes not only trans men but also intersex people, many of whom menstruate and need the same support.” She adds that many public schools, clinics, and community programmes assume only girls need menstrual products or information. “This makes it nearly impossible for intersex menstruators to access sanitary pads or counseling without facing ridicule.” [...]
real C&L pros know you gotta take as many ladders as you can while also avoiding the chutes
gender to me is like a car i dont really want one and society would be much better if it was not structured around it. but i got one because it helps me get around and sometimes its fun to make it go fast
idk but when i discover new books and music i’m just excited to be alive again. yes a bit dramatic but that’s how i feel when i discover them

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Digital de-aging is bad not just because it always looks creepy as fuck no matter how much money they pour into it, but because it deprives me of getting to see the fucking black magic of a) the casting director somehow finding someone who looks unnervingly like the original actor despite not being related at all and b) the actors completely convincing me that they are, in fact, the same person at different times in their life.
And occasionally, the amusement of sticking a bad wig and some makeup on the original actor and just demanding we accept they're a teenager now.
ghost