Of course it goes without saying that I am hopelessly dependent on the ingot
occasionally subtle

#extradirty
wallacepolsom
YOU ARE THE REASON
Cosmic Funnies

blake kathryn
Cosimo Galluzzi
Lint Roller? I Barely Know Her
Monterey Bay Aquarium
Noah Kahan
Stranger Things
let's talk about Bridgerton tea, my ask is open

gracie abrams
🪼

shark vs the universe

izzy's playlists!
Aqua Utopia|海の底で記憶を紡ぐ

pixel skylines
Sweet Seals For You, Always
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@sammyofthesea
Of course it goes without saying that I am hopelessly dependent on the ingot

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Hi I'm 1 years old and learning to read through your posts. Cigarette.
very good job using your words! will someone get this toddling bitch a smoke
how manual wheelchair users move (explainer for non-users)
frequently when i’m out and about with someone walking, they can’t anticipate what path i will take and therefore they’re in my way pretty frequently. this is fine! i can politely ask them to step to the side. but it makes me think about how little non-wheelchair users understand the way wheelchair users move. as someone who used to walk everywhere, it was an adjustment period for me to figure out how to navigate the world in a chair. here are some things that didn’t occur to me so that you don’t cut off your friend right as they’re building momentum to go up a ramp 😆
for context, i use an active manual chair. the world is very different in a power chair. even among active manual chair users, there is a huge diversity in physicality and strategies for getting around. this is a general guide that i think will apply to most manual wheelchair users. i’m starting super basic and getting more complicated as i go.
———
1. manual wheelchairs are a momentum game. it is very easy to maintain speed and direction. but speeding up, slowing down, or turning, is hard. one thing this affects is if we’re on a wavy sidewalk or other twisty-turny walkway, that is a pain in the ass and i am taking as straight a path as i can.
2. wheelchair users also have to pay attention to the slope and condition of the pavement, so our path somewhere will be different than yours, even if we’re taking the same route to the same place. for example, i usually have to go down slopes straight, not diagonally, to avoid tipping over sideways. one area this affects is crosswalks. many intersections have one curb cut for both roads you could cross, which means i will go down curb cuts to a crosswalk as if i am aiming for the middle of the intersection.
your path in orange, mine in blue. to you it seems indirect, but to me it’s the path of least resistance.
i also will be building speed in the second half of the crosswalk. this is a much easier way to tackle a ramp. if i approach with momentum, i won’t have to drag myself up the slope once i get to it.
3. building momentum and maintaining it is only half of the job. the other half is stopping. manual wheelchairs cannot stop on a dime if they’re moving with any kind of speed. if i tried to stop immediately when going downhill, i would fly out of the chair. so don’t walk right into the path of a wheelchair in motion and then stop! i will have to turn to the side very quickly and hope i don’t tip. i can’t tell you how often parents pushing strollers will stop their stroller directly in my path and then get offended when i am alarmed and turn sharply to avoid hitting their child. from their perspective, i was being careless and going “too fast.” in reality, normal walking speed takes a few feet to slow down from and stop.
4. in terms of slope. see this street in san francisco?
i can’t go down this street, it’s way too steep. i would give myself friction burns on my palms trying to control my speed. if i was in a situation where there was no avoiding this street, like in an emergency, i would be breaking my straight-slope rule and zig-zagging in the middle of the road.
this would require several zig-zags back and forth, more than the four that i drew. i also could not go up this road other than with this method. up or down, i risk tipping over sideways if i’m not careful.
4. in a similar vein, consider terrain. slopes with grass or carpet take huge amounts of energy to get up. this grassy hill isn’t insurmountable, but it would take me like thirty minutes to get up there. honestly i would probably go backwards, because it’s easier to pull yourself up a slope than push yourself.
other types of terrain can be completely immobilizing, though. this decorative gravel pathway is beautiful, and inaccessible to me. my casters (front wheels) simply will not go through that.
5. in terms of walkways and obstacles. if there’s a deep gap in the pavement lined up the way i’m going, and it’s, say, an inch wide, that is an obstacle for me. my casters are one inch wide, and my back wheels are an inch and a half. i’ll get stuck in it like a train on a track.
i have to straddle this, even if it means being too close to the middle of the sidewalk and preventing us from walking side by side.
similarly, if a crack is greater than an inch high, i’m gonna wheelie over it. at two inches, i have to. a wheelie may require a change in speed, either faster or slower depending on the person.
i have 4 inch casters, so a lip as little as 2 inches will stop me in my tracks. a lip as little as one inch, hit with any speed, can knock my casters out of square. casters can get knocked out of alignment pretty easily depending on the chair. i’d rather not have to pull out an allen wrench and a level, so i’m gonna wheelie.
this happened when i hit about a 1.5” lip on a pavement crack when i was going downhill at maybe 3mph.
6. putting it all together. see how diagonal this crack is?
this is another situation where i have to go straight relative to the slope. because that crack is wide, it will probably also require a wheelie. if i tried to approach that straight relative to the sidewalk, my left caster would get up the slope, i’d wheelie, then my right caster would land in the crack. i have to go this way.
(also lol at the trash can blocking the curb cut)
these are just a few things to keep in mind when walking about with a wheelchair user! ofc the best strategy always is just to listen when someone asks you to move out of their way 😆 but i think being able to anticipate movement a little better will help it seem less random. feel free to ask any questions!
Ice cold takes from a Transgender Woman:
Men are not inherently Evil
Everyone has the capacity for evil
Transgender Men are men
Transgender Women are women
Excluding Cisgender Men from your spaces requires Transgender Men to out themselves if they want to engage (Same for Women)
Anyone can be Non-Binary, there is no "look" or requirement
Non-binary masculine presenting people should be welcome in queer spaces, many are just treated as men and predators
Non-binary feminine presenting people should be welcome in queer spaces without being seen as "Woman-Lite"
Edited the wording on the first point because too many terfs keep thinking I'm their friend.
This gives me hope in the world again
DuckDuckGo, Signal, and NordVPN all stated they may stop serving Canada if Bill C-22 passes.
Here is a petition against Bill C-22, which I believe can be signed by both citizens and residents of Canada (it will tell you when you fill it out).
Bill C-22 requires digital service providers to retain metadata on Canadians for up to a year and disclose it to authorities, who can request it without an individual being under suspicion or investigation. Even with planned adjustments to the bill to require encryption, this still represents a massive security issue. It also represents a huge privacy concern and raises concerns over Canadian protections from unreasonable search and seizure.
Please reblog to spread the word.

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Today in australia they started senate hearings on the bill the government hopes will make enough disabled people die or disappear to make us all less irritatingly expensive for them. We had two weeks to submit feedback on over 400 pages of complicated legal terms. They don't care what we have to say and they don’t care that this will kill people and disenfranchise disabled people across the country.
There are 760,000 Australians on the National Disability Insurance Scheme, the system that - if they feel like it and your personalised plan says you get to have it - provides funding for everything from personal hygiene care to support workers to therapies to assistive technology. It's already very hard for disabled people to get on the NDIS, regardless of your disability. It's near impossible to access most support and equipment without being on the NDIS. And the government has announced that they want that number to drop to 600,000 in four years. 160,000 of us cut off the Scheme - and countless more denied access. This will cause deaths. People will die and people will suffer because there is no safety net. The NDIS is the only option for most of us. Even private health insurance doesn't cover most of these things. Nobody will swoop in to save us.
The bill wants to give the (non disabled!) NDIS minister basically unlimited power to cut our funding. They're already planning what they'd do with that power. What rights they'll strip from us. What dignity and freedom they'll remove to make their budget look better.
The bill wants to force people to try every treatment out there before they're allowed to be on the NDIS. Including if the treatment is literally impossible to access. There’s a lot of us living in regional areas or out bush who can't just pop to the capital cities for specialists. This will especially hurt disabled First Nations people in regional and remote communities, who already experience limited access to healthcare. Oh, and it includes chemical restraint, too. The government has directly refused to exclude chemical restraint from the required process, calling it "trialling medication".
If you're australian and worried, the ABC did a good breakdown of the proposed changes.
I know australia stuff doesn't really pop up on the radar on this site, but I want everyone to know what's going on. What we're fighting for here. Your australian disabled friends might be NDIS participants fearing for their life, rights, and freedom. They might not be a participant and afraid these changes mean they never will have access. We deserve better. The government built a system with no backup plan, and now they want hundreds of thousands of disabled people to pay the price for their bad planning.
Sorry we're too expensive to have rights, I guess.
Quick guys how do I establish contact with a male I find attractive
i cant fucking believe you guys
A “where are they now” kind of reflection on this post that was made 12 years ago and has 70,000 notes for some reason:
- I really appreciate that truejaku not only mentions one-ler, my cannibal once-ler ask blog, but also includes context, allowing this post to be enjoyed by those outside of my circle. I believe their contribution is surely the defining factor in the success of this post, which truly gets funnier the less you know me.
- I like pennydreadfuljournal telling me to show him how well I boil an egg. This may seem to some like a “haha random xd tumblr humor” moment. But it’s actually something very relevant and personal to me, because 12 years ago I was really into boiling eggs.
pedestrians don't seem to realize how exhausting using a wheelchair is, both manual and powered. i had to wheel around a hospital today with several ramps i had to go up and down multiple times, and even with my smoov i ended up with shoulder and chest pain and deep exhaustion.
people look at wheelchair users and think "well you're sitting down all the time that doesn't take effort" no actually it does. pushing a manual chair takes a lot of fucking effort, especially without a power assist. repetitive stress injuries are a huge problem manual chair users encounter all the time. going up hills and ramps is so deeply fatiguing.
this doesn't just apply to manual chair users btw. power chair usage can also be really exhausting, especially for people with complex seating needs. going over bumps and cracks can trigger many symptoms such as spasticity, pressure sores are common, even just sitting upright can be exhausting for many people.
basically don't assume using a wheelchair takes 0 effort, it really really does. getting to "sit down all the time" doesn't mean it's easy.
im gonna need you able bodied motherfuckers to stop comparing the extreme pain and exhaustion that comes with using a manual chair to being in a car for 8 hours. not even remotely the same thing.
I’m more than a little concerned at seeing recommended tumblr communities with names like “queer teens” or “nonbinary teens” and advertising themselves as a space for teenagers as young as 13 to make friends with each other. I don’t wanna sound like anyone’s dad here, but this is… not safe. Anyone can join those communities, they’re not private unless you make it private. You can’t trust that everyone in there is actually a teenager, so please don’t advertise your age or other people’s ages like that in online spaces. You can absolutely make private communities or discord servers with trusted friends, but not public communities that anyone can join, especially if those communities are specifically targeted at marginalised— and therefore vulnerable— teenagers.
Meanwhile this was what various medical professionals in that reddit thread had to say about it.
They do not, in fact, love it.
The proof that chiropractic is an utterly failed medical profession is not that adjustments can cause harm, but that the profession has responded by ignoring and denying the harm, rather than studying it.
All medical treatments (other than complete placebos) have some risk of harm, but for real treatments given by real professionals, the harms are tracked, measured and warned about. If the harms are too severe, the treatment is no longer used.
One of my colleagues was a chiropractor. After a while he began to suspect that a lot of his patients actually just had muscle tears, not spinal issues. He bought an ultrasound machine, learned how to use it and how to read ultrasound, and found that to be the case. Between that and the constant pressure from management to get customers (because lbr, they're not patients, they're customers), he got sick and tired of it and bailed to become a sonographer full time.
And before people pipe up with "but my chiro is good, they have me do exercises and so on!" that's just regular ass physiotherapy. See a physiotherapist. A lot of people who sing the praises of chiros because they saved them from chronic pain would have gotten the same benefits from seeing an actual licensed physio, who can prescribe the same or even better exercises because they have an actual fucking education.
The amount of fucking charts I've seen where a patient went to a chiropractor and now needs a surgery is fucking insane. All I do is medical charts, day in and day out doing medical code. I've gone over hundreds of patients whole year of appointments. Unless the chiropractor is also a physical therapist, that patient is going to get worse and need surgery with very few exceptions. It doesn't matter when they mention seeing a chiropractor, by the end of the year they need surgery for issues that started after *shock and awe* a chiropractor appointment! I've seen patients needing multiple surgeries to be functional after chiropractors. I've seen patients lose their ability to walk because of chiropractors. And all the way up till they need surgery, through the issues piling up and needing more pain meds, the patients insist it's helping because the want so badly for it to be helping. I wish it did

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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!
isn't it insane though how schizophrenic people are viewed as violent and dangerous by the majority of society when in reality schizophrenic people are nearly 14 times more likely to be on the receiving end of violence than to be the perpetrators...
schizophrenic person: makes a post trying to raise awareness about the disproportionate abuse and harmful stereotypes schizophrenic people face
yall: "yeah im not gonna reblog this they used the word ins*ne which is so problematic ://"
What the fuck happens that changes these stats to such a massive degree?
1) schizophrenia hardly ever causes people to be violent so schizophrenic people aren’t more likely to be violent than anyone else
2) schizophrenic people’s autonomy is often taken away from them because of their schizophrenia. because the authorities and mental healthcare providers often automatically assume schizophrenic people to be violent, they’re more likely to immediately react to schizophrenic people's symptoms with violence, without even knowing for sure said schizophrenic person was going to be violent. all of this causes schizophrenic people to be more likely of being victims of violence and abuse. schizophrenic people also have a harder time getting out of abusive households because of the risk of their autonomy being taken away. if a schizophrenic person’s relative or partner is abusive, often the schizophrenic person has no way out of the situation, both because our disconnect from reality can result in us being easier to manipulate, and because the system is built in a way that it takes away our autonomy because of our condition.
also schizophrenic people and psychotic people in general, please do a lot of research before picking a provider for your own sake, and if they try to treat your psychosis in a way that you think is harmful then don’t hesitate to switch providers. your safety and wellbeing should be a priority over everything else.
can y'all please reblog this version instead
I need to add that if you're in any kind of healthcare, you need to listen to your schizophrenic patients! You should believe them when they talk about their life. Your assumption should not be "anything bad this person says is a delusion." You have a duty to care for your patient, not protect your patient's abusers.
Accidentally the most dramatic camera work ever seen in the commons today.
before someone screenshots this and posts it elsewhere this is me
PREV TRUTH NUKE
We need to start seriously treating the concepts of "obesity" and "weight loss" as a dangerous pseudoscience and I'm not kidding.
It's some shit that everyone thinks they can understand based on vibes but science just doesn't work that way. Real scientists have proved time and time again that it doesn't work how people assume. Many medical conditions where it's assumed weight is a "cause", something to blame the patient for, it's often actually a symptom.
Body size is based on so many individual possibilities. genetics, upbringing, wealth, what type of food you eat, what type of work you do, where you live, etc etc etc. it is impossible to control for all of these.
I was a child born to fat, impoverished, labourer parents, and I grew up doing farm labour, gaining muscle - I will never ever be thin. It's just how my body developed. And no matter how much weight I were to hypothetically lose, doctors would still push me to lose more. Family would push me to lose more. Society would push me to lose more. It will never ever ever be enough. You will never be thin enough, there is no bmi low enough to satisfy them, there is no "progress" that won't just make them pity or shame you even more. Your personal circumstances aren't important to a pseudo-scientific practice, the variables don't matter that much, it must be a one-size-fits-all solution.
Every weight loss pill, every low calorie shake or meal replacement, every weight watchers frozen meal, it all contributes to the pseudo-scientific cult of thinness. Every ad that says you're not good enough, it pushes you to drop your critical thinking skills. We have created a world where people think shitting themselves into thinness using potions with untested ingredients is healthier than having some fat on their bodies. But it's not! That's absurd! You're sending your body into a constant state of gastric shock!! And one day, when you get bored of eating tasteless nutrient paste and decide to eat something with some flavour in it, your body will react with a starvation response and store every little bit of fat that it can, because it's so used to being fucking starved. Which sends people into a panic response, buying up more pills and trying to crash-diet and lose their meagre protective layers.
Your body stores fat because that's your reserve energy. Fat is protective. I thank my body every day for storing so much energy for me, fuck knows I need it! That's your blubber!! You are a large mammal. Your body is designed to keep energy in reserve so you can sleep and stay warm and keep your brain alive. You should research the human metabolic process. You should research the cow metabolic process. You should research bear metabolic process. YOU NEED FAT!
And just like so many other pseudosciences, fatphobia and all that it entails is deeply rooted in racism and specifically antiblackness. It is not a mistake that the ozempic-chic era is coinciding with one of the biggest waves of open, globalised white supremacy we've seen in decades. Whiteness needs to perform & police whiteness constantly, maintaining appearances is THE way to stay part of the ingroup.
You must commit to removing yourself from that ingroup. Do not allow it a single toe in the door. A pseudoscience, no matter how comforting and easy to digest it may be, is not your friend. It is feeding you lie upon lie upon lie.

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I'm gonna say it, I do think that even the laziest person imaginable should have a roof over their head, food in their stomach, and access to healthcare
a lot of people are reblogging this saying that most "lazy" people are actually just disabled or that the concept of laziness itself is a product of our society's obsession with productivity. this is all true, but it is not my point.
even if someone WAS just lazy and simply didn't want to do anything but lie on the couch and watch tv, they should still have these things. it's irrelevant whether some people aren't actually lazy because everyone, including hypothetical lazy people, should have their basic needs met.
if we have the resources to do it, there is no defense of letting people die because they don't want to work, and much less because they can't.
I don't want lazy people to have basic necessities because they "actually" deserve them because they ARE working or CAN'T work. I want lazy people to have basic necessities because they are people, and we shouldn't leave them to die when we have the resources not to.