Disabled Trans Guy Escaping Abuse

Disabled trans guy escaping abuse

A photo taken of me (pale, androgynous guy in a tie dye hoodie) in the dark.
A photo of my black cat loafing in a gray fabric box. One eye has blue-grey cataracts, and the other has an extra eyelid, making the eye seem black.

Hi friends! I'll try to keep this short (long version under the cut), but I need help. I may be getting into a housing program soon, made the mistake of telling my parents, and today they've been manipulating me trying to get me to stay. There's a long history of abuse, neglect, transphobia, and ableism - mainly on my dad's part.

I have $24 in my bank account. I can't drive, can't work, and am severely disabled. My mom wants me to make her and my father into healthcare proxies. When I was younger, my dad threatened me with institutionalization and conservatorship. I'm scared for my safety.

I just need some help. I'll apply for assistance when I qualify. I'm gonna need an emotional support animal. I don't know if I'll get the apt yet but see the cut for an explanation.

Venmo: julesfairy

I don't know what goal to set so I'll update this post when I can. Reblogs help a lot, if anything for knowing I'm not alone.

Long version: I'm 23, mentally ill/disabled, have no income, $24 in my bank account, live with my abusive father, and my parents refuse to call me my name/pronouns/etc. I also just left a cult-like group and found out I have a shit ton of nerve damage all over my body. So I'm having a time!

Anyway. I mistakenly told them that I've applied for a housing program and may be getting into a 1 bedroom apartment. They do not want me to leave, and today lovebombed, gaslit, and otherwise manipulated me into staying.

WHY I'M MAKING THIS POST NOW:

They know I'm meeting with the case worker tomorrow.

I don't know how they're going to react once they realize I'm going through with this. I'm worried about my father's reaction specifically - In the past, he's threatened to kick me out, kill himself, throw me in the psych ward, or put me under conservatorship. My mom just told me she wants me to make her and my father my healthcare proxy.

If I get this apartment, I'm going to apply for SNAP and Temporary Assistance as soon as I qualify, and rely on food banks. But if anyone can spare some cash, that'd help a lot too. I just need some help, I'm desperate. I don't know if I can take another failed escape.

More Posts from Girlish-in-pain and Others

2 years ago

I think the biggest misconception abled people have about disabled people's pain is that it feels like normal pain everyone has felt before, and that you can get used to it and grow a tolerance like normal pain.

ITS NOT LIKE THAT

Here's an example, when I was 12 I got a daith piercing in my ear, It was the worst pain I had ever felt. I felt like someone was trying to crush my skull.

Then I became disabled, And that became the worst pain I ever felt. My joints felt like they were literally on fire almost constantly for over 3 years. It NEVER felt less painful.

Last year I had to get my daith repierced, it felt like a tiny pinch.

The constant chronic pain I feel has increased my tolerance for normal pain, but you cannot increase tolerance for chronic pain. It is always excruciating at worst, very uncomfortable at best, the pain never hurts less. You just learn how to accept it and strengthen your mind enough to think past the pain. YOU CANNOT GET USED TO CHRONIC PAIN. That's why we can't "push through it", or "toughen up". It's not normal pain, your brain is literally confused and forces you to feel pain because it thinks you're extremely injured.

Imagine burning your arm on something reeaaally hot, now imagine the burning sensation you feel is inside your muscles and joints and not on the surface on your skin, now imagine feeling that 24/7 and you can't get rid of it. That's what I'm dealing with man. Do you abled people get it now??

1 month ago

reblog if you think sign language should be taught as a language in schools.

2 years ago

🥄Spoon Stop! 🥄

Take a spoon or two to complete any tasks you need to finish soon. Reblog to give your mutuals a spoon

🥄Spoon Stop! 🥄
8 months ago

Just made an account on Medium so I could read this. Made it about 1/3 through and I'm absolutely hooked and excited to finish it!! But first, time for a nap.

For the longest time, I have had trouble understanding FND - specifically whether it's just a shitty diagnosis made up by the medical system to gaslight people or if it's a genuine medical condition. This essay is rly helpful and has already broadened my understanding. It's incredibly well written, particularly bc of the extremely thorough research it's a result of

Cadenza for Fractured Consciousness
Medium
A Personal History of the World’s Most Misunderstood Illness

I am one of the most medically examined people in North America. For over a decade, no one could explain why I lost my ability to walk, speak, and use my hands. Why the lightning-like headaches? Why the ringing in my ears? Test after test came back negative. Doctors thought I might have a genetic abnormality no one's ever seen before, or a condition so rare that it had previously escaped medical classification. Then I got accepted to the top undiagnosed disease research program in the world, and they told me the only diagnosis I was unprepared to hear: it was Functional Neurological Disorder (FND), a much-misunderstood condition which was once known as Conversion Disorder, and before that, as Hysteria. And that was only the beginning of things getting weird. The essay above is the product of three years of research into the history, neuroscience, and politics of FND. It touches on the many medical failures that define the history of the disorder, the pervasive sexism and lazy mind-body dualism that prevented scholars from seeing it clearly, and why - finally - a better understanding may be at hand, with revolutionary implications for how we understand human consciousness and the experience of having a body.

FND fucked my life up. This is my reply. Thanks for reading.


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2 years ago

When I go to the doctor, they hand me paperwork with a chart to locate my pain. I can’t pinpoint it. I “X” my whole body. My entire life.

— Glenis Redmond, from "I Stay Sick," The Listening Skin

1 year ago

Honesty, some of these genuinely changed my life once I started to really listen and incorporated them into it

collection of useful things tumblr has taught me:

even if you can't fall asleep, laying down with your eyes closed will still rest your body

you don't have to brush your teeth standing up

you don't have to do any chore standing up, from dishes to showering

you don't have to shower with the lights on

if you can't brush your teeth, flossing and a tongue scraper gets rid of plaque and bad breath

if you can't do that, mouthwash kills a lot of bacteria

eating "unhealthy" food is better than eating no food

you can make the same meal everyday for however long you still want it

some pills come in syrups or chewables if you can't swallow them

kids nutritional shakes can be a quick way to get fuel if you can't eat/don't have time

if walking hurts/exhausts you on a regular basis, canes and rollers are for you, no matter how young you are

we have free will—if doing something "out of the ordinary" makes life easier for you, do it

2 years ago

I love spoon theory bc you can literally explain it exactly the same way it was originally explained, with actual spoons.

But also I feel like the failing phone battery is more accurate lately.

Like, you charge it all night, but it only slow charges. It never gets to full battery anymore.

When it says full battery, it doesn't mean the same as everyone else's, because it'll be gone twice as fast.

You have to limit your app usage bc of the battery drain, and even when you aren't doing anything the percentage is slowly going down.

Keeping it plugged in full time to charge means you can use your apps longer, but since it's slow charging it'll eventually reach 0 even when plugged in.

Keeping it plugged in full time also means the battery gets reliant on being constantly plugged in.

Actual percentages are a lie.

That shit will turn off with 5-10% battery still showing and there's nothing you can do about it.

8 months ago

I don't have a scooter attachment or any motor attachment for my wheelchair, but I sometimes drive fast bc I am able to and I love it. I'm genuinely considering getting a "ringing bell" (idk I forgot the English word for it) and/or a "honking thing". Bc people walk sooo slow and I'm zooming ahead and most people are completely unaware of their surroundings

For the Danes or Danish speaking individuals, the words I'm thinking of are "ringeklokke og bĂĄthorn" :D


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24, they/them, nonbinary lesbian, disabled. Studying medicine, working on my internalised ableism, prioritising finding out what I like to do. I write, ish, or try to at least and that's something

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