hey man it's me. your old friend. qing dynasty portrayal of the mexican flag.
pollo👍
I like how the snake is also a chicken.
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@ecopunkacademia
hey man it's me. your old friend. qing dynasty portrayal of the mexican flag.
pollo👍
I like how the snake is also a chicken.
LG Chocolate (2006)
Is anyone else constantly bothered by the fact that all of a child's medical care is required to go through their parents? That they must rely on these people to decide when they do or don't need medical care?
No matter how injured. If a parent doesn't deem it necessary to see a doctor, it doesn't happen. Teachers can suggest a doctor visit, but unless it's a very acute injury (and even then), it's ultimately up to the parents.
You can be 13. Twisted, maybe broken ankle. You teacher lets you sit out in PE. She's concerned, and tells you to rest when you go home, and see a doctor. You get home, ur parents fill a bath and add some Epsom salts, and then laugh at you for using it moms old colorguard stick as a cane. Take some ibuprofen they say. It's just a little sprain, ur a kid.
You go to school the next day, go to ur office assistant time. Office calls ur mom to come get you, because you're clearly in too much pain for school. Your mom laughs when she gets you, says you just were so determined not to miss school. Scolds you for making the office ladies worry.
You never see a doctor for the injury.
Your parents come into the exam room at every visit. This does not stop with age, except for gynecologist. But your parents are on the medical release forms. They fill them out for you, with you. You do not get to take them off.
You never get to tell s doctor about the ankle. Even though it never quote healed right, and it hurts every day.
Then your 18. In college. Still on your parents insurance, and have no car. The on campus clinic only does std testing. You fall down some stairs. Same injury. You call your parents, crying from the pain. You are using a mop as a cane. They console you and say to have a bath, take some meds, and let them know how it feels in a few days. You end up borrowing your roommates rolling chair to get around for the weekend.
By Monday, you can walk again. You walk miles to class every day. You ask to see a doctor, but your parents won't drive the hour to come take you, and you don't have the insurance card. You are still at their mercy for medical care. The ankle tries to heal again. This time worse than before. The tendons click with every step.
Now you're in your twenties. Finally have your own healthcare. You see a doctor. You get to mention the ankle! They say it's been too long to really even know what was damaged. That you have arthritis now. It healed wrong but it can no longer be fixed.
I'm 32 now. My ankle tells me the weather. I wear boots to keep it stable. What could have been a funny story about a fall and a cast has become a lifetime injury. Because children do not have access to medical care without a parents approval.
Hula’s Bar & Lei Stand, Honolulu HI 📸 : Ted Sahl, c. 1985
(guy who's not getting anything done voice) I need to learn every skill and all information
australian sour patch kids have gluten in them i am truly at my fucking limit im crashing out im waging war against wheat idgaf anymore
oh is that one of those things where ableist companies put in traces of common allergens so they can just avoid the cost of making it safe
WHAT
A trend we predicted in 2016 continues.
US based but it’s similar reasons in other countries. and of course many companies have international locations. idk if that’s why it’s happening with sour patch kids but this is a thing
I cannot even explain how ANGRY I am at this.
My nephew is very allergic to eggs, peanuts, tree nuts, and sesame. Last year my sister discovered all hot dogs and hamburger buns now contain sesame. Not "may contain", but listed in the ingredients. This year basically every brand of sliced bread also now contains sesame, making it very difficult to find bread items he can eat.
They're just adding it to their products, so they can just list it as an ingredient and not bother with worrying about cross contamination. And they aren't even bothering with telling anyone. Capitalism is going to kill us all.
"Which brings us back to Kellogg’s. Back in 2016, the company found a way around the added burden and expense of complying with the FSMA: they simply began adding trace amounts of peanut flour to their cracker products. Doing so allowed them to list peanuts as an ingredient of the product, freeing them from having to prevent cross-contact.
At the time, Kellogg’s notified Food Allergy Research and Education (FARE) about the impending change and left it to them to warn the allergic community. In this case, Pearson’s didn’t even bother as near as we can tell."
I wonder if that’s part of the reason behind my seeing an upswing in products adding corn starch or corn flour to things that didn’t have those before? <- rhetorical question, because I’m certain that’s what’s going on.
The Lancaster News Journal, Pennsylvania, July 4, 1915
this is come alive in the heat Cas
maarten inghels
@sherbertilluminated there's a line somewhere in Ursula Vernon's Digger that goes something like "it is difficult to be metaphysical around the truly geologically minded"
500 years from now there’s gonna be some film historian who’s entire career is built off of searching for a copy of goncharov
and they're never gonna find it cuz they fucking took it off poob
remember how instead of "global warming" we started saying "climate change" because of too many smartasses who refuse to understand averages being like "if global warming why snow in April?", "if global warming why mild summer?"
But now it's simply fucking hot and they still deny it somehow
spiralling over climate change... literally help lol
https://www.bbc.co.uk/news/science-environment-58874831
this helps im so glad i'm marrying you
clickable link
there are places in the world today that are experiencing 40°C for the first time in recorded history. of course there's no way to know whether chucking billionaires into volcanos will appease the sun god but i feel we're doing the scientific method a disservice if we don't at least try
A lot of you on here sure don’t like the idea of making any kind of sacrifice for the benefit of others huh
Some of you act like doing minor inconvenient acts of kindness is equivalent to donating a kidney as if it’s not those acts that form our communities and make the world go around.
Return your grocery cart. If you’re able-bodied offer your seat to someone who is not. Help your friend move. Drive your sister to the airport. Make sure drunk people have a safe ride or walk home. Pet-sit for your coworker. Participate in a meal train. Volunteer in your area. That’s what friendship and community is about.
not gonna lie i increasingly just find myself thinking... what are single disabled people supposed to do? basically everything assumes that either a) you have never been independent and are fully reliant on caregivers, whether this is parents or a paid carer that you are somehow funding, or b) you have a partner who can look after you, drive you to appointments, pick you up after you've had sedation, advocate for you, be your proxy, do the housework when you're sick, push your wheelchair, be your companion when travelling (e.g. handle the luggage if you're using a wheelchair), etc
and like. first of all even for people with partners that's assuming they're abled themselves and can handle all that. you can't assume that. secondly: what about people who are single, who live alone, who will probably always do so
"get someone to keep an eye on you when you start this new medication" who. "don't over exert yourself" nobody else is going to do the tasks. "this can be a walker or a transit wheelchair so your partner can push you when you get tired" my what
like it's not a coincidence that amatonormativity discussions started / developed in care contexts because it is so often the assumption that intimate partners will fill these needs. but I feel like this is often discussed in the context of "and this is too much to ask and puts too much unpaid labour on the unqualified partner" which is not untrue and needs discussing but like. also. what about people are single, independent adults who are neither emotionally nor geographically close to their siblings etc and are not Disabled Enough to have a paid carer (a group that grows as resources shrink). like are they just fucked then. they're on their own. punishment for failing to be enough of an adult to couple up.
a few years ago i was having a procedure for which i was going to have partial sedation, so they wouldn't let me leave the hospital alone afterwards. even though i would just be getting a taxi from outside the door back to my house
i had to ask my housemate to come to the hospital in a taxi, leave the taxi waiting outside, come inside to fetch me (they wouldn't even let me go from the ward to the taxi even though i could point to my phone and the texts saying that my housemate was outside), and then go back to our house with me. fortunately it was a weekend, so she didn't have to take time off work to do this, but they went on about how she'd have to keep an eye on me for the next day or so
bear in mind that i barely knew my housemate when we moved in together. we had mutual friends but it was an arrangement of convenience
these days i do have nearby friends who own a car, so would potentially be able to pick me up in a situation like this. but they don't live with me. so they wouldn't be able to keep an eye on me overnight as my housemate was assumed to be willing to do. my flat only has one bed in it. like. i don't know. it just seems to be completely beyond their comprehension that somebody could live solo and not just have someone who will look after them?? and this was for a small routine procedure that lots of non-disabled people have, so not even assuming high care needs! hospitals just can't comprehend that single adults exist!
That reminds me of the time I was giving blood and (in addition to my usual fainting shenanigans) there was a concern that the phlebotomist had given me nerve damage.
Trying to get the blood people to understand that I had driven there and that no, I didn't have a partner to come fetch me and monitor me was a flipping task and a half.
It took me over an hour to get out of the centre and I had to promise to call 111 (the non-emergency medical line) if anything happened.... Not sure what they would have been able to do for a tweaked nerve over the phone, or indeed what having a partner there would have achieved...