Carsie Blanton doing a rework of "Come Out Ye Black and Tans".
(The Black and Tans were the military forces who were the foot soldiers in the British Government's brutal occupation of Ireland.)
RMH

Origami Around
Aqua Utopia|海の底で記憶を紡ぐ
Peter Solarz
I'd rather be in outer space 🛸
TVSTRANGERTHINGS

Love Begins
let's talk about Bridgerton tea, my ask is open
AnasAbdin
will byers stan first human second
Game of Thrones Daily

Janaina Medeiros
noise dept.
YOU ARE THE REASON

❣ Chile in a Photography ❣
Xuebing Du
taylor price
"I'm Dorothy Gale from Kansas"

JBB: An Artblog!
seen from Poland

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@snowdrop-yoongi
Carsie Blanton doing a rework of "Come Out Ye Black and Tans".
(The Black and Tans were the military forces who were the foot soldiers in the British Government's brutal occupation of Ireland.)

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getting kicked off love island for just swimming in the pool and not talking to anyone
getting kicked off love island for just swimming in the pool and not talking to anyone
The office was created a year ago and seemingly named for a far right European plan to expel minorities and immigrants from Western nations.
I promise you things will get so much better when you start processing people’s behavior as information rather than a verdict on your self-worth. If someone doesn’t text back, suddenly pulls away, whatever it may be, the solution isn’t to put on a tap dance for them and try to regain their approval. It’s not to crash out on them and try to force them to react a certain way. It’s just to take a step back, take a deep breath, and assess what this tells you. What’s this saying about them? What’s this saying about you??

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I don’t think healthy people every really get chronic illness.
I have a friend I know from when we were both 6. She is the only person living nearby and so she saw me go from walking through limping to wheelchair on a daily basis. I keep her updated on my health even tho we rarely hang out anymore. She was gonna come over yesterday and I had to cancel. She asked if I can’t hang out later that day. When I said i won’t feel better later, that if I feel that bad in the morning later will only get worse she got annoyed and “joked” that I’m just finding excuses. And I was surprised, she knows all about me being disabled after all? So, a bit taken aback, I told her it’s a normal thing for me.
“But you got the diagnosis now, aren’t you better?? I thought you’ll get better now”
She was honestly surprised and it made me realize a thing. They don’t get it. They don’t get that getting diagnosed only equals benefits like welfare or parking spot for us, and sometimes better pain meds but that is just like pushing luck. That it’s a forever thing. That that one day we felt good a week ago was just a bright spot and doesn’t mean we won’t need our aids anymore, cause chronic illness is not linear and will make a great comeback in next four hours, and the next good day is planned on when we’re 70. Cause when abled people are sick, they get better. And our illness is just an excuse for them. And when we say we will never get better they think we’re being dramatic and pessimistic. And I don’t think they’ll ever get it, cause to get it you need to live it. And I want my friends to stay healthy and not go through hell.
This is definitely okay to reblog and abled people are encouraged to reblog cause maybe it’ll help others understand
Hello it’s me Lexa and this post is relevant again as I just had the Legit Same Talk with someone and I exhausted my number of fucks to give
MARIE ANTOINETTE (2006) dir.: Sofia Coppola
So funny story actually. One of my friends was hooking up with this girl, they were friends with benefits. She needed a date for some work party so he agreed to go with her. Turns out her dad owns like 3 dental practices and she worked as the business manager for one of them.
Anyway my friend had some not so nice teeth and during dinner the father of his fwb was like “you work where you work, you sleep with him and his teeth look like that? Get him an appointment.”and then bounced. So his fwb made him an appointment at the practice she managed and my friend ended up needing like 3k worth of dental work and his friend with benefits just gave it to him for free.
So that is the story of how my friend not only got sex, but dental out of the friends with benefits deal.
Seeing people I know and like using AI is making me understand the protagonists of those old time sci fi dystopia's.
"Oh I don't normally use AI, I just wanted it to plan my trip"
You lived on this planet for decades, you know what you like, there are hundreds of websites where you can type into any search engine " things to do in [area]" and have at least a hundred different options.
"Oh I only use it so I can figure out what to make during the week with what I have"
The most popular website as you type in "recipes" into google have sections where you click dinner- quick and easy and those usually rely on staples + 1 or 2 items. I found 30 recipes on chicken alone.
"I had a writing idea, so I typed a few sentences into Chat GPT and I was able to write 20 pages with it."
Youdidn'twriteit.Youdidn'twriteit.youdidn'twriteit.youdidn'twriteit.YOUDIDN'TWRITEIT.YOUDIDN'TWRITEIT.YOUDIDN'TWRITEIT.

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what the fuck
ohhhh you elfsturbating 😧😲
I translated the Ea-Nasir complaint into vulcan and engraved it in on a cooper plate
The tumblrest sentence I have ever seen
hello! I'm sorry to bother you but Ive been searching for texts and references about self harm from an antipsych perspective and I wondered if you knew any. I have checked your book recs and resources, as well as self-harm-harm-reduction's and library-cards but I haven't found much. thanks anyway, no trouble if not!
Well I can't help you with that, since I as stated in my pinned post do not collect such resources.
Not all of these are explicitly antipsych, but may be of interest to you:
Chandler, A. (2016). Self-injury, medicine and society: Authentic bodies. Springer.
Chaney, S. (2011). Self-control, selfishness and mutilation: How ‘medical’ is self-injury anyway?. Medical History, 55(3), 375-382.
Chaney, S. (2017). Psyche on the skin: A history of self-harm. Reaktion Books.
Gilman, S. L. (2013). From psychiatric symptom to diagnostic category: Self-harm from the Victorians to DSM-5. History of Psychiatry, 24(2), 148-165.
Millard, C. (2013). Making the cut: The production of ‘self-harm’ in post-1945 Anglo-Saxon psychiatry. History of the Human Sciences, 26(2), 126-150.
Millard, C. (2015). A history of self-harm in Britain: A genealogy of cutting and overdosing. Palgrave Macmillan.
Also see this essay [link] [1] for a more antipsych perspective of self-harm.
[1] pasleciel. (2024, October 25). Measure once, cut twice: In defense of self-harm.
Amazing, I gathered some resources for this anon as well and I'm pretty sure we have none in common! Can't believe I didn't see that the author of the antipsych FAQ I linked has written an article about self harm :) Excited to look into these, thank you for sharing!
Couple of tumblr posts to start things off. Caden's blog is a great place to find resources about a variety of antipsych topics
hello fellow grad student 🫡 do you know of any articles/books that talk about bodily autonomy/self harm/self mutilation ? i've read some int
hello, you mentioned a while ago that you disagreed with a lot of the premises in A History of Self-Harm in Britain: A Genealogy Of Cutting
This is a great starting point for learning about antipsych perspectives/frameworks/etc
03/2025 - for a prison abolitionist, psych abolitionist, pro-drug, communist perspective.
"Cutting The Risk." Practical guide for self harm risk reduction. Some of the language and approach is more prescriptivist than I prefer ("don't do it this way because it increases your risk of [whatever]" instead of "if you do it this way your risk of [whatever] increases" which i really do feel is important) but theres a lot of good technical information, and it is generally nonjudgmental:
Nonjudgmental zine by and for people who have self harmed or currently self harm:
Some useful technical first aid advice, but some of it feels iffy- "one pill over the prescribed amount" does not generally, maybe almost ever, constitute an overdose & I don't think that's a useful thing to tell people. For non-substance-related first aid advice though, this seems a generally good overview:
And having said that, for some actual good substance related harm reduction advice and technical information, National Harm Reduction Coalition's "Getting Off Right" guide is an amazing resource, written by and for people who inject drugs:
This training guide outlines the process of developing and managing an Overdose Prevention and Education Program.
And NEXT distro's resource library is invaluable:
Harm reduction advice for eating disorders:
i have a handful of anonymous asks in my inbox right now asking about harm reduction as applied to eating disorders that their loved ones ar
This article looks potentially relevant/interesting but it's paywalled & all I could read was the abstract. If you have access through a school or something, though, it might be worth a read
I believe @doyoulovethewayzeylily has some posts about harm reduction in the context of self harm but ive already hit the max number of links I can add. Hope some of this is helpful!
I can only find a few offhand
people should not be shaming you
it's okay that you don't have a better answer right now
Amity told girls that they're not broken and paid the price
@estrogen-chalk-blood talks about this sometimes
Big thanks to y'all for helping anon out!
It is still very slow going but I am able to read and comprehend nonfiction now! I was told the cognitive decline was part of the schizophrenia not a side effect of the meds.
I have only gone down 40mg on my antipsychotic but it has made a difference in my cognitive ability. I can see the light through the cracks now.
I had a very similar experience reducing my own antipsychotics, despite also having been told that the meds were harmless and the cognitive impairments I was experiencing were inherent to having schizophrenia. It's actually a notable problem in schizophrenia related research that taking antipsychotics is such an obligate part of the treatment that we barely have any studies on schizophrenia where all the schizophrenics involved weren't also on antipsychotics. Thus separating schizophrenia itself from the effects of being on antipsychotics hasn't really been done. Though I remember reading that if we look at the few statistics available from countries where access to antipsychotics is very limited, schizophrenics have significantly better long term outcomes in those places.
A very irritating thing about being disabled while also having a mental illness is that everybody and their dog will assume the mental illness was caused by the disability. People seem to think that being disabled must be a miserable enough life to cause mental illness. By doing this they write off any other causes and factors in mental health, and they act like mental illness is inevitable for disabled people and therefore normal and expected.
it also absolutely ignores the ways disability actually can lead to mental illness and very little of that is inherent to the disability. Some disabilities like ABI/TBI may bring on mental health symptoms and susceptibility, but many don't just make someone mentally ill. But how someone is consistently treated by the people around them, the people they encounter, and society at large, absolutely fosters an environment for mental health issues to grow. For people with disability that changes over time or who acquire their disability suddenly, the changes to their life can be very hard to handle and they may not have access to support that understands what they're experiencing. For people whose disability has been since birth, the constant battle of butting up against ableism and inaccessibility and the life goals nobody will support them with is incredibly emotionally exhausting. But when people think disability is miserable and mental illness inevitable, they never think of it like that. They don't think of the fact the mental health problems are still coming from the same stresses and lack of support that might cause them in any abled person. As soon as they don't recognise someone's life it's like they stop being able to understand the same ways we all need support when things are hard. Instead, it's treated like it sucks but it was always going to happen. That, or it's ignored, because they think you can only have one thing going on and being disabled is the only thing they see. It's not inevitable. We deserve support, not assumptions and ignorance.

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Its disability pride month so if I see any one of you use the word “psychotic” as a synonym for “evil” you owe me $1000000000000
The thing with disability is that your brain and the people around you will tell you that it's not okay to do things that will make your life easier. But it is in fact okay, good even, to do things that will make your life easier
Getting a pedal bin for my kitchen because trying to use a regular one with one hand was awful was what inspired this post, and you have no idea how much better this one small thing has made my life since. Anyway do that thing to make your life easier that you've been thinking about, it's completely worth it and you deserve it