help me solve an argument
what color is this ↑
red
blue
green
i don't know
i don't care
other
see results
Cosmic Funnies

gracie abrams

Product Placement
No title available

Game Changer & Make Some Noise

shark vs the universe
Interview Vampire Daily
hello vonnie

Jar Jar Binks Fan Club
No title available
Doug Jones

blake kathryn

PR's Tumblrdome
art blog(derogatory)
macklin celebrini has autism
EXPECTATIONS
Xuebing Du
KIROKAZE
Keni
untitled
seen from India
seen from Spain

seen from United States
seen from United States
seen from Lebanon
seen from Türkiye
seen from Ecuador
seen from India

seen from Kyrgyzstan

seen from United States
seen from Singapore

seen from United States
seen from Singapore
seen from Algeria
seen from India
seen from Czechia
seen from Portugal
seen from Poland

seen from Japan

seen from United States
@gay-ratcore
help me solve an argument
what color is this ↑
red
blue
green
i don't know
i don't care
other
see results
Trying to keep this short, but I have several surgeries coming up, and a PET scan which will tell me if i have cancer. They're thinking i have lymphoma. Below is some of the paperwork from my oncologist with personal info redacted. I need s lot of help to ensure I can have surgery and be prepared for chemo if thats my next step, bc if it is, I won't have much time to prepare.
PP--V--kofi--$C--gfm
$529/$2,000
No updates aside from the fact that my surgeon didn't wanna do the biopsy now that I have a PET scan scheduled. She said the PET scan will be more definitive than the biopsy, as biopsies are often negative with lymphoma anyways. This is all still urgent and progress has stopped.
incredibly bizarre and confusing seeing ppl call themselves "chuds" all the sudden b/c like
thats what we call neo nazis and shitty conservative bros? or at least its what we used to call them? why are ppl calling themselves "chuds" affectionately now
what is happening
yall know chud means fascist right like please tell me yall know that
im hoping this is a case of "younger folks on the internet adopting Silly Word b/c its Silly and not realizing it actually means something"
so here's me educating! you're calling yourselves fascists! thats what you're doing! maybe don't do that and use your head before you start using every goofy word you see!
let me be agonizingly clear
when you call yourself and your friends "chuds"
YOU
ARE
CALLING
YOURSELF
A
NAZI
Wikipedia screenshots for those unwilling or unable to look it up to verify. Article link here(link). Transcriptions are in alt text.
A reminder: "TND" is a Nazi dogwhistle, originating from the phrase "total (n slur) death."
being sick & miserable objectively sucks, but it has become significantly easier to cope with since learning that “sickness behavior” is a well documented part of the body’s immune response
feeling not only physically but also emotionally like fucking garbage is unfortunately an extremely effective way to force your body to prioritize fighting infection & keeping you alive. i don’t have to like it, but knowing why i get weepy & pathetic when sick does help at least a little
i just found out that this is not common knowledge and am reblogging so more people know
YOUR BODY DOES THIS ON PURPOSE
YOU ARE NOT A BAD PERSON BECAUSE OR "WEAK" WHEN YOU ARE SICK IF YOU CAN"T CARRY ON AS NORMAL
Rereading this on my sick days 🙏🏽
Why do I feel like I should print this out, frame it, and hang it in my office?
If your business can only be reached and all info about it only be accessed via Facebook or Instagram, know that it isn’t reachable or accessible AT ALL.
The whole metaverse can no longer be properly viewed without an account and I am definitely not making one just to see your contact info or opening hours.
Get a fucking WEBSITE. It can be just a static landing page with the relevant information. But get off the metaverse!
Totally normal for a legitimate for-profit company to refuse to reclaim or stop running their products even after they're no longer being paid to do so. I'm sure it's very normal to just keep running your service for free when your contract's been terminated. Spending money to continue running cameras that supposedly no one is looking at is definitely not an indicator they are just run by the federal government to spy on everyone and only a wacko conspiracy theorist would think so.
old sparkledogs and cat ocs in the files of old computers. wings extended forever in flight, tears frozen on their face from an event in a backstory long forgotten
the drawings made of others characters, in folders on a forgotten friend's computer, forever visiting, immortalized in drawings of silly inside jokes and gift-giving between amateurly-drawn colorful animals
a colorful cast, lined up in a row in a half-finished microsoft paint bitmap–smiling faces filled only most-of-the-way with the fill bucket tool. the comic text says "happy birthday!!!" the drawing was never finished, the gift was never sent. its they've been their birthday for 13 years in their eyes and they've never stopped smiling
colors paint-bucket-filled into downloaded free bases–folders of which still sit unused, waiting to spark new ideas, in a long-forgotten folder. most of them the well-known default colors until their artist realized how to use the custom color button
forever in a looping animation, only a third of the way finished–the artist wanted to animate like they saw online, those four frames probably took them weeks of frustration before the project was dropped–but their character is still running, for the rest of time, at 3 frames per second
the story behind this drawing, btw
Drug arrives years after pandemic’s peak, but could still offer protection to vulnerable populations.
An antiviral pill has, for the first time, been shown to prevent COVID-19 in people exposed to the SARS-CoV-2 virus at home, according to trial results published today in the New England Journal of Medicine1. The drug could be a lifeline for those who still face real danger from the virus, such as care-home residents or transplant recipients on immune-suppressing medication.
There are good things happening in the world.
You can read about it here without a paywall.
Households exposed to COVID-19 now have an oral drug specifically cleared to prevent infection after contact with a sick person. The FDA listed Xocova, the brand name for ensitrelvir, as a 2026 novel drug approval for post-exposure prophylaxis of COVID-19 following contact with an infected individual. The decision fills a gap that has persisted since the pandemic’s early years: until now, no oral antiviral carried an FDA-approved indication for prevention rather than treatment.
zero patience for "irreversible damage" rhetoric because like... parents are allowed to do all kinds of other irreversible body modification to their kids and nobody gives a fuck. you can pierce your kid's ears, you can sign them up for a sport that will injure them for life, you can provide or withhold medical care like vaccines according to whatever whims you like. i've mentioned this before but my mom forced me to get laser hair removal done on my legs when i was a teenager because my body wasn't mine, the way i chose to upkeep it was a reflection on her. "irreversible damage" is very much part and parcel of the broader belief that parents own their children's bodies.
This Re: Societal dismissal of the threat covid presents to everyone. In less than five years, long covid has become the most common chronic illness in children, surpassing asthma. Somehow HRT is "irreversible damage" but giving millions of kids a poorly understood chronic illness is just "back to normal"
(P.S. Wear a respirator. Don't catch or spread covid.)
Have had trouble sleeping because I need to get more pain medicine. Hoping to raise $25 today but I really need as much help as I can get. Please help a disabled trans woman who takes care of @rickybabyboy
Edit: added $25 to the goal, Ricky has 2 days of food left
$85/$105 raised
Venmo: AGIEF
Paypal: [email protected]
Ko-fi:
Support wizdev
Rare white woman win free my girl she ain’t do nothin wrong
She was just doing the coke that gives you the executive function to torch a misogynist
Seeing the article saying she did it because "he made a joke about scones." Like no she did it he made a joke about how she should be enslaved to a man
Here’s the thing: authors know when they get a rec on an older story. There’s a telltale uptick of kudos (with a 10-15% comment rate if you’re lucky) in your digest email.
The thing is, there’s no way to know where these people are coming from. In the before, when fandom was more in the corners we all knew about, you could search LJ or a message board or whatever social bookmarking site we were using. You could join the community and participate.
You could get a little dopamine hit by seeing someone tell their friends why they loved your story.
Anymore, those recs are hidden in discords, or in tiktoks or instagram slideshows that you can’t search for. They’re inaccessible, not discoverable unless you’re already there. You may never know why 27 people left kudos on an old story of yours, what they liked and found in your writing. You just get the thumbs up and a kinda lonely feeling, cause these could be your people. You could like them, maybe. You could be friends.
But you’ll never find out why they stopped by, or what people are saying about you behind your back, and that’s sad.
So thank you to the people who still do public rec lists on this webbed site. You are my sunshine, and I’m appreciative of all of you.
If you are recced a fic and enjoyed it, leave a comment telling the author where you came from! We like to know!
Nuke canada now
Did y'all know that 70% of all mining operations in latin america and the caribbean involve a canadian transnational mining corporation?
Anyway, when I was in college I was constantly going to marches and protests against canadian and saudi mining projects in the Santurbán páramo, one of the most important ecosystems in Colombia in terms of biodiversity, and the source of drinking water of 30+ municipalities in my state, including the city I live in. Ultimately these mining proposals lost their license due to environmental regulations.
But now that our new far-right president elect is looking to suck up to imperial core powers once again, canadian mining corporation Aris mining is interested in re-starting mining projects in Santurbán. Which, would inevitably give cyanide poisoning not only to my city's drinking water, but 30+ other municipalities and indigenous communities.
The imperial core will see one of latin america's veins and go "is anyone gonna cut that open?" and not wait for an answer
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 don’t have food allergies, but I do have food intolerances, which can kill slower, via manutrition and dehydration.
I can’t digest legumes or alliums. Period. End of. It isn’t an immune response, it’s a poison response. Those are not foods, to my body. Those are poisons.
Alliums include: garlic, onions, shallots, spring onions, chives
Legumes: peas, beans, soy
These are some of the most common foods in the world. They are in every ethnicity’s cuisine. They are in everything.
I too have had people say I should kill myself rather than live with the inability to have garlic and onions. I have had the “we should all stop eating meat” crowd tell me that I’m “throwing a tantrum” and that they’d rather have me die of malnutrition than let me eat the only protein I can digest. I was punished over and over and eventually kicked out of a homeless shelter for having “too many dietary restrictions”, even after getting a doctor’s note from the doctor that diagnosed me.
IBS is not uncommon, it’s so common that a lot of people assume common adverse reactions to FODMAP foods are normal when they are signs of IBS–and it’s a continuum. Some people, like me, absolutely cannot eat what their triggers are, but there are other FODMAPS they’re fine with. Some people have milder responses to FODMAPs. Some people, like my mom, basically can’t eat ANYTHING triggering or they are violently and dangerously ill for sometimes weeks on end. And sorry to talk about gross body stuff, but diarrhea can kill you, particularly if you do not have ready access to sanitary toilets and water and the ability to lay down (I was homeless on the street when I was diagnosed with IBS, I did in fact almost die).
Imagine having food poisoning all the time.
I am not in any way saying it is as sudden in its lethality as anaphylaxis.
But it wears you down. It takes away hundreds of sources of nutrition. I struggle with things like vitamin D deficiency, iron deficiency, scurvy, and on and on. The list of triggers is as long as my arm and it’s mostly vegetables. It isn’t just one food that makes me sick, it’s hundreds. Whole chunks of the food pyramid are just poisonous.
The prejudice is the same. The danger of someone else poisoning you on purpose, out of spite, is the same. The inability to eat adventurously is the same. The inability to engage in the most basic of human social behaviours, sharing food, is the same.
Because to many people, we are both the same thing: A Picky Eater.
And being A Picky Eater is apparently a capital crime, as in the punishment is death.
You are cut off from a huge source of sensory play and enrichment. You are cut off from doing anything but cooking from absolute scratch. You are cut off from a huge piece of human social experience. You are cut off, as illustrated above, from education. These are not small things. These severely lower your quality of life every second of the day. They isolate you from having friends or meaningful social interaction or an education. They force you to pick between not eating at all and using up all your energy on cooking from scratch; guess which choice I usually end up picking when I’m too depressed!
All because other humans will not accommodate you.
Because food allergies and intolerances don’t HAVE to be a disability. It doesn’t have to be this way. Abled people MAKE it one, for no good reason than laziness and cruelty.
And dietary restrictions are seen as something of a luxury, I can tell you that right now. Hospitals, asylums, shelters, group homes, schools, charities, rehabs, and other institutions simply will not accommodate anyone with food allergies or intolerances in my experience–like at all. Period. They would rather you die. I actively dread the idea that I might end up in one again someday, because I know I’ll starve to death while being blamed for it and mocked the whole time.
I don’t even bother asking for accommodation anymore, I simply tell people I will not go out to eat with anyone, I will not accept food gifts from them, if they want me to come over they have to let me cook, and the isolation and depression are the price I have chosen to pay for my safety. But I can only do this because I’m no longer homeless and have the luxury of a kitchen and a private home. That is not a guarantee for many, and it wasn’t always for me.
People are extremely, extremely cruel about food. Extremely cruel. Food allergies and intolerances are my big example of the Social Model of Disability, because again, these don’t have to be disabilities. Abled people MAKE them so.
July 20/21, 2026 - Anger is spreading across Italy after state thugs in Bologna murdered Abderrahim Fakir, a 42-year old Moroccan man, during an arrest on Monday. Footage of the killing has gone viral on social media, with Fakir clearly begging for help as policemen suffocate him. Workers and youth chanted "police murderers" and "the whole world hates you" at police lines during demonstrations in the city, and clashed with riot police. [video]/[video]