how do you use tumblr /ɟe̞ː˧.ä˧.jɔ˩.ji˥.mi˧.kä˥.o̞ː˧/ jay-ah-yaw-yi-mi-ka-oh • Yoruba • Queer • Autistic • NSFW • 2000 • they/she/iel• I like stories, snakes, spiders, the Oxford comma, and short swords. Fuck respectability. If I'm wrong, call me out. WIP@the-prince-is-not-a-woman @cobab-fan-project
Call me J, J Sanguine, or J Ayọ̀-Yímiká. The 2000 in my bio is my birth year.
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Ọ̀ràn Ìfẹ̌ is a short (?) story about a lonely homemaker and mother who didn't really intend to be either of those things falling for her best friend who didn't intend to fall back. I'll be updating every 3 days unless I finish the story or give up. It's on hiatus. Devlog posts are tagged matters of love.
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I just watched an incredible Indian film about grief and the rural queer experience called Sabar Bonda (Cactus Pears)
If you are in the UK you should see it too!
Find UK showtimes here
Q&A with the director Rohan Kanawade was great too. I’m so glad he ignored the conventions others expected of a queer narrative and just focused on the authentic story he wanted to tell. Watch this film!!!
[ID: a digital drawing of a black girl in profile from the neck up. Her hair is in many small braids, each ending in round yellow beads with green stems that resemble oranges. She has an orange-coloured over the ear hearing aid and a large earring shaped like an orange. end ID]
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Every single one of the 599 refugees the US admitted last month was a white South African, according to data the State Department’s Bureau of Population released Friday.
In fact, so was every other refugee admitted this year. Since October 1, 2025, the US has accepted 6,668 refugees. Of those, 6,665 were white South Africans. Three—admitted last November—were from Afghanistan. No other refugees were admitted.
And this is only half the story. They are also revoking the legal status of existing immigrants granted protected status due to fleeing dangerous conditions in their home countries… and let’s look at which countries they are:
Since Inauguration Day, more than 1.5 million immigrants have either lost or will lose their temporary legal status, including their work au
this disability pride month, i want to actually open up a bit about my disabilities and… well… call them what they are. because the truth is, due to toxic ex-friends and my own internalized ableism, i never felt like i could call myself disabled.
i felt like, compared to others, i wasn't disabled enough. i can function, albeit with great exhaustion, on my own. i'm not entirely dependent on others. i'm not professionally diagnosed due to the amount of money it would cost, not having insurance, and also living in a us state with a piss poor healthcare system (even by our country's shit standards). and most of my disabilities are invisible.
but, they still impact my life greatly. and this year, i'm proud to call myself disabled. 🫶
the most "obvious" disability i have? visual impairment.
i've worn glasses since i was a young child because i have myopia and astigmatism. these are my only true diagnoses, so you can't fake claim me (sarcasm). anyway. i cannot see things clearly if they're more than an arm's length away from me, and even fine details up close get lost. likewise, lights in dark environments are horrific to look at and decipher, both with and without my glasses.
then, from what little family medical history i do know and my experiences, endometriosis and lupus. my monthly cycle is… or was (shoutout opill i love you opill; i haven't had a proper period in over a year, just breakthrough bleeds)… horrible. disabling pain, heavy bleeding, and full body cramps. my iron levels would plummet into anemic territory day one, and by day seven i'd look like i belonged in an emergency room. on top of this, my body always just… seemed to be attacking itself.
every small thing would trigger a feverish sensation and fatigue. my face would get so much redder so much quicker than others' when i was out in the florida heat (which is a 24/7 ordeal), and i didn't actually learn about the lupus until my cousin was being tested like… last year! that, and my partner has seen my face get red and noticed that distinctive butterfly mark appear when my body feels exerted doing the most simple things.
and that? that was triggered by long covid. or exacerbated to the point i noticed it, because everything has truly been worse since then. i've talked a bit about my long covid before, but to briefly touch on how that's impacted me:
i can barely wear sports bras, let alone a binder, because the moment my chest feels compressed i literally cannot breathe. likewise, i have a lot of trouble breathing normally now.
the memory/brain fog is so bad that i've genuinely been scared that i'm enterting early onset dementia territory, especially since that also! runs in my family!
i have random, intense chest pains where i've actually been woken out of my sleep thinking that was it for me; those started in the past year and have mostly settled with the removal of major stressors in my life, but i still experience twinges and aches
one time my body decided to have a random, one-off allergic reaction to peanut butter (something i have eaten for 20+ years just fine) and i was probably tiptoeing the line between normal reaction and the beginning stages of anaphylaxis. it hasn't happened again, yet, but this shows how it's impacted the lupus as my body is so much more sensitive to things in general… like i also developed skeeter syndrome, so i like physically cannot go outside during summer evenings now.
post-exposure, i had a solid month+ of daily migraines ranging anywhere from 5/10 to 9/10 on the pain scale. if you've known me, you'll remember that i had to pause my uni studies (and later pay the difference because they refused to pause my aid allocation and accommodate me) because i literally could not get out of bed most days. these migraines happen semi-frequently still.
i'm not sure how this happened, but ever since that initial exposure, i've become hearing impaired. i've seen some studies about it, but i notice i have both sensorineural hearing loss and auditory processing disorder. the latter feels much more prominent, as if there's any sort of background noise no matter how small, i have so much trouble listening to people. it's gotten me in a lot of trouble with people.
and these, my friends, are just the physical disabilities!
my brain is a complex soup that has seen some shit and developed some shit. i'm honestly getting tired just typing this post, so i'm gonna rapid fire:
complex posttraumatic stress disorder: pretty self explanatory, but my life has not been… great. definitely privileged compared to others, but the types of people i've been raised by and the circumstances i've been put in by them and by simply existing as who i am have deeply wounded me.
depersonalization-derealization disorder: see above; i think it's a combination of cptsd and some sort of anxiety issue. i tend to have a fairly equal? presentation of depersonalization (feeling detached from myself) and derealization (feeling detached from my environment).
autism spectrum disorder - also pretty self explanatory, so i won't go into detail (also because i've just talked about my autism a lot)… but i will always make it a note to tell the story that my support needs were so obvious as a child that i was pulled aside by several teachers and school professionals throughout elementary and middle school and recommended an assessment. my parents never allowed it because i wasn't a "drooling [r-slur]" like autistic folk are "supposed" to be ^_^
attention deficit hyperactivity disorder - my partner pointed this one out after they got their diagnosis, and we're like the exact same person. i've noticed that i have a predominantly inattentive presentation, or what used to be labeled as "add."
bipolar 2 - this one i'm honestly scared to talk about, because of how people stigmatize people with personality disorders, even those who are allies that i've seen so much lateral ableism/sanism from… but. bipolar 2 is prominent on both sides of my family. it's been diagnosed in close proximity to me. and the behaviors of diagnosed individuals, i see in myself. the intense depressive episodes followed by unexplained periods of expansive mood, irritability, and inflated self-esteem. the constant lack of sleep during these periods that throws a wrench in my plans as my chronic fatigue from other disabilities fights for the energy it needs. racing thoughts and impulsive behaviors (especially now that i have my own income) and intensive suicidality. it's… a lot! i can't predict my own state of mind and it's scary. but i'm not a scary person. nobody with a pd is inherently scary or evil. we're just… dealing with a lot. and i hope that me talking about this doesn't change how people see me :(
I cannot recommend bringing your heritage and culture into how you view media enough.
It is important to consider the culture of the person who created the piece, absolutely; but the different perspectives offered by the viewers is fascinating in and of itself and does not always detract from the message.
As an example, when I was younger, I watched Schindler's List. This movie is famously shot in black and white except for one section, concerning a little girl in a red coat. The camera follows her until her eventual death.
I am Turtle Island Indigenous and I was always taught that the only color spirits could see was red, because it is the color of life and blood.
So the second the girl in the red jacket came on screen, something inside me chilled with fear.
The only color in the movie was that red. At some point, I, the viewer, had died.
I remember sobbing at the sight of the burning human piles that were shown, convinced I was buried in there somewhere. The reason I had only seen red on the girl was that my death was recent. I was the ash in the air mistaken for snow. I had died before her and had followed her, helplessly, until she followed me.
The message I got for that was maybe not what the creator had intended: that there was no "being clever enough" or "good enough" or "kind enough" that would shield or protect you from such a massive tidal wave of evil.
You are not exempt from tragedy, that red jacket whispered. You are not special.
When I told some of my white friends about my experience with viewing Schindler's List, some were shocked and the rest just out-and-out mocked me for my "media illiteracy".
"it was just a filming trick to make you feel something," I remember one saying, which terrified me. How had he not felt anything even before she showed up?
However, when I repeated my viewing to a college class, they were fascinated. The implications of what I had seen and felt made the film all the more terrifying and solemn. It encouraged a lot of people to try to ask themselves what media meant from a cultural perspective, where they hadn't done that before.
I genuinely am starting to hate the "I love when female characters are allowed to be feminine and girly and powerful at the same time" take, because that's literally all of them and that's literally all they ever seem to be.
"Women could only be powerful if they were portrayed as butches 🙄" Girl where. From Wonder Woman to Elsa. Where is this Butches Epidemic in mainstream media. WHERE.
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Genuinely though it is so frustrating that nonbinary rights and exorsexism are not treated seriously at all, even from within the queer community. It sucks that there's not even an option for an X gender marker in so many countries, including in more progressive queer-friendly ones. It sucks that if enben want to get gender affirming care that we're advised to lie about our gender (or lack thereof) in favour of a more binary trans identity lest we jump through a million extra hoops on top of the million already in place for binary trans people to prove we're serious in order to get the care we want/need. It sucks that in most cases we're still forced into some kind of binary and I wish that the issues we deal with were acknowledged more.
Hey there, my name is Sera, you might be familiar with my past work behind the scenes such as the Mass Effect trilogy, Dragon Age, Silent Hills & many more. If you have cherished my work, please pay attention.
I'm an agoraphobic Kanienʼkehá:ka (Mohawk) mixed lesbian who has fought for several years a worsening health condition that is currently killing me. I've spent years exhausting any means to get help, enduring extreme pain. I share as much as I can without undermining my privacy and safety (due to stalking by my abusive family.) More in the link below ❤
If you have been following me for a while, you are familiar with my struggle and saw me talking about it throughout the years. A warm thank you to @transmechanicus & @mightyjoke , the kind souls who made this possible. I would be lost without you.
(Updated fundraiser for currency and geographical reasons as of April 2025. Original was paused at 20.8k & kept up for transparency. New goal takes it into account.)
Whether you donate or not, know that you are loved.
(Hey everyone ! This is the new updated fundraiser which is ran by Jo & Erika f… Joanna Monteis needs your support for Help Sera Access Life
happy disability pride month and once again, FUCK lazy subtitles. fuck the [speaks foreign language] instead of actually transcribing the words, fuck shortening sentences and changing whats been said for no reason, fuck censoring swearing in captions but not in audio and fuck anyone who says youre being 'too sensitive' for being upset about a lack of accessibility
And that’s a wrap! Thank you for tuning in to this year’s pride comic! A very special thank you to my sister who did beta (black fill) for many of the panels.
Hope you and your loved ones had a wonderful pride! 🏳️🌈 And keep making yuri!
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MRI machines and cooling units and AC and IT systems in hospitals are breaking due to the heat. Lab equipment is failing. Some cancer treatments cannot be done due to machine failures. A&E overcrowding is worse due to heat related health issues and sheer amount of people is making the heat in hospitals worse (and the AC! Is breaking!) Patients with appointments are being advised to bring in "a lot" of water with them to be able to safely attend. Fans cannot be used in hospitals. Norwich has no functuoning MRI scanners right now. And the staff have to keep working through all of this, they are getting ill and sleep deprived which is compounding issues further. This is not normal 👍