I swear my terminal ileum just wants me to suffer.
Why don't you just perf or obstruct so I can actually get you dealt with and not just have to be borderline delirious in pain and the side effects of it.
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@the-trauma-dumpyard
I swear my terminal ileum just wants me to suffer.
Why don't you just perf or obstruct so I can actually get you dealt with and not just have to be borderline delirious in pain and the side effects of it.

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I thought pride month meant that people knew not to be bigoted arseholes on main.
Anyway, I was just fucking hatecrimed again living in uni accommodation because someone took the pride pins of my door FOR THE THIRD TIME.
And of course all the stress and dysphoria from it is making me want to relapse with self harm.
How do I explain that I'm not replying because it's not that it's too much loving sentiment, it's the fact that you say that WHILST ACTIVELY MISDENDERING ME, that caused me to freak out and not respond?
And I mean both my parents know it's a knife edge of walking away again because I've already done it once when they were constantly deadnaming and misgendering me and I really only still talk to and see them because they're not deadnaming me still.
IDK where else to vent about this.
I have chronic pain, chronic pain I have no known cause for, chronic pain which is barely managed by medication.
I've been SH clean since like 2024. But the thing is I still get really bad compulsions, especially when my pain is flaring up.
It's REALLY FUCKING ANNOYING because I want to basically control the pain I feel by SH but also don't like the pain so it's basically a paradox loop of me not taking my pain flair med and also wanting to burn and deeply scratch myself so I can basically have so control over where I have pain/injuries.
AND, AND because my nerves and sensation is FUCKED from constant pain and trauma the deeper stuff that scars I don't feel pain from, and honestly they're annoying to heal, but the more surface stuff I have compulsions about don't scar enough to in my mind make it worth it.
I am so fucking sick and tired of people minimising ARFID and other eating disorders that aren't AN or BN.
Because people I know think it's just me "being picky" and not eating a few things based of smell or another sensory characteristics.
Where it's actually fucking starving myself because the place I'm staying is catered and the one safe breakfast food I had currently isn't there and I know I'll either throw up or freak out if I try to eat anything else.
Like no I can't just "eat something else" because there's nothing fucking else for me to eat. I want to be able to comfortably eat more than 5 foods all of which clinically don't have great nutritional value besides the meal replacement drink.

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LMAO
Guess who's probs gonna fail an end of year prac exam with an 80% pass grade because my legs have been spastic (like grade V spastic) for the last 3 days and I haven't had the mental energy to do the academic consideration forms for them because like no mental energy and also it's chronic stuff and for my uni they're shitty with chronic illness
The good thing is it's only like 20 min and I've done the thing I'm being assessed on irl a bunch so at least I've got that going for me if I can get my legs to co-operate with me long enough.
EDIT: I passed, they haven't released marks so I don't know by how much but I know I passed.
shout out to “gross” disabled people.
people who can’t shower/bathe people who can’t shave people who can’t wash their clothes people who need help going to the bathroom people who have nasty habits (biting nails, picking nose, etc) people who can’t brush their teeth people who can’t go to the doctor people who can’t clean their room people who can’t make their beds people who vomit a lot people who wet the bed people who constantly have diarrhea people who’s physical deformities are seen as repulsive
and every other kind of person I missed that deserves to be here too.
you are people, first and foremost. your thoughts deserve to be heard, discussed, acknowledged, no matter what. you are not lesser. you are just another person. you should never be ignored for what you can/can’t do. you deserve care.
to abled people: check yourself. make sure you listen. and you can reblog, just don’t derail. maybe don’t add on, either.
happy July everyone
my favorite part of this post is seeing people in the notes whose hearts have been touched. if you don’t mind, I’d like to share a few.
keep in mind: this is nowhere near everyone. Some responses were too short, some were too long - I heavily advise you to go look in the notes yourself. And I’m sure many people reblogged this with just sorting tags or nothing at all, and that’s wonderful.
I made this post for myself, mostly. while I don’t do everything on the aforementioned list, I do apply to quite a few - but, ultimately, it was for me. I never expected it to boom like this.
And yet, it did. And that is a wonderful, wonderful thing. This post has helped people, even in small ways, something I never imagined. It’s wonderful.
so here, let me add a few more I missed. some taken from notes, some of my own.
people who pee in a bag people who can’t brush their hair people who can’t wash the dishes people with stomas and catheters people who are gassy people who have constipation issues people with chronic hives/red bumpy skin/MRSA people with heavy birthmarks people with bugs in their homes/car/etc people with constant runny/bloody noses people who can’t do certain things from depression people who need help getting out of bed people who eat in bed and have crumbs in there people who can’t clean their sheets people who can’t make their bed people with shower chairs
and even more that I had to have missed. Again, please add on.
So for this July, every one after, and all the months in between, just remember: You are loved. You are not alone. The notes both below and above prove that. I promise I am not lying. You are a wonderful, beautiful person, no matter what you can/can’t do, and no matter what you look like. You deserve to be heard and listened to. Your voice and opinion matters.
It will never cease to irk me when people look at devices and tools made for disability and call it a "scam" just because it doesn't work for them.
Of course, kinesiology tape doesn't work on you if you don't have connective tissue or soft tissue damage. Your body doesn't need help holding itself together. Mines does.
"Posture braces are a scam, you should just exercise more." Okay, what if you can't? What if no matter how much you exercise, your body will always need extra support.
"Foam rollers don't actually do anything, just do exercise." Again, see the above.
"Neck traction devices? Pft, stop being lazy and exercise." Again. See. The. Above. Also, speaking as someone with a severe neck injury, sometimes you need those devices to exercise. And yes, sometimes moving half an inch is considered exercise depending on the nature of your injury and limitations. My current goal in physical therapy is to hold my neck up on my own for longer than ten seconds while lying on my back. It's taken me a year of intensive work to manage it. The traction devices have been a part of this, as recommended by my physical therapist.
"Balance boards, omg what are you, a baby who can't walk?" IN SOME CASES, FUCKING YES.
Like I get it, I get it. You've seen the infomercials and they look goofy, or you just plain cannot think of a situation where you personally might ever need some sort of assistance with your body. But good news! Disability is the only minority group you can become a part of at any moment through sheer bad luck, age, illness or a genetic ticking time bomb hiding in your DNA. May the odds be ever in your favor, and if not, may you encounter kinder people than yourself.
Please use what you find useful. Just because YOU may not find something useful doesn't mean someone else won't. Also in turn, if something works for you and it an "odd" but SAFE way to use it keep on doing it.
Fuck, I wear docs to work when most people are baffled why I do because they're 8 hour shifts on your feet. Why? Because they support my ankles more and are sturdy shoes. They're also the only work approved shoes I have that fit my AFOs but meh, no one at work really knows I have AFOs.
Is it like bad or not that I just want to change my last name?
So for context I'm trans non-binary and at some point am going to legally change my name. To a ridiculously long version of my name I use because sue me my legal dead name is long af and I love the length to be able to gauge how much trouble I'm in by how much of it is yelled.
I get along well with my parents (they've some what apologised and are better than they were a year ago) but they're also the main reason I have so much repressed trauma it's physically harming my body so...
I also just see them as people I'm biologically related to with no real deep emotional connection to them and all having a surname that is the name of a major district area SUCKS.
Actually comment your opinions because I want to know what people think btw.
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Why is chronic illnesses so fucking draining and exhausting to explain to people.
Like yeah, I should be doing a uni assignment I have due in a few days right now but I'm not because I'm in too much pain to right now. Because walking the 20 meters from my room to the shared kitchen is too much and I'm in too much pain to even concentrate.
And also jesus fuck family members are unbearable at times. Like you look at me with so much pity and concern but where was this when I was fucking twelve and telling you I was in pain. No, I've tried that, no (insert thing) won't work, yes I'm on this many medications and need this many mobility aids and supports now. Primarily because it's this bad because you didn't believe me when I was a litteral fucking child under your care where I felt I had I had to HIDE TAKING FUCKING PANADOL FOR PAIN THAT DIDN'T EVEN WORK HALF THE TIME.
Oh for fuck’s sake, people calling out racist writing in fanfic isn’t “censorship”. I say this as a fic writer but some of you need to get off your high fucking horse.
Truly some of the most irritating culture has sprung up around fanwork and fanfic in specific like… no, making something for free does not in fact make it sacrosanct or immune to criticism! Your right to “do whatever you want forever” or say “fandom is for fun” stops the second you’re being bigoted and making fan spaces unsafe for marginalized people!
"fandom is for fun" except for poc who have to deal with rampant racism and white people unable to acknowledge let alone take accountability for their racism
Can someone please give me advice on dealing with chronic pain, that's way worse than usual.
Like, the pain in my leg is WORSE than any migraine I've had as also worse than what is possibly trigeminal neuralgia.
Like I can't walk on it without spasms and shaking, I'm limping way more than usual. And like it's spread, my entire leg below my knee feels like it's on fire and I can barely move my ankle or knee when I walk.
IDK should I go to an urgent care clinic or the hospital. At this point I'm just gonna wait until I can get a gp appointment, maybe they might actually believe me that I'm in pain this time.
I hate this part of being sick with a stomach thing. Like I'm so hungry, but also can't stomach solid or puree food so 🫤🫤🫤 you just drink miso soup to stop the hunger, get a tiny amount of caloric intake and not make you nauseous at the same time.
Why, why do parents not tell you that you need to do something i.e. put the washing machine on a drum clean cycle.
Then get mad, to the point of calling you a useless idiot, at you when you didn't know you needed to because they didn't bloody tell you to or how to.

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Does anyone have advice for leaving an abusive environment as an 18 year old with around 3000 bucks who is also planning on leaving in like a month. And is also going no contact with the abusers (parents).
I also am a part time mobility aid user. (Crutches and cane).
Is it weird that even though I desperately want and to an extent need to leave I still don't want to because I don't want to hurt my parents.