Hiii, I Thought I'd Make A Post Where I Write Some Stuff About Myself:) My Handle Used To Be "trapped-in-a-burning-body"

Hiii, I thought I'd make a post where I write some stuff about myself:) my handle used to be "trapped-in-a-burning-body"

So, intro facts:

▪︎ Danish

▪︎ 24 years old

▪︎ Nobinary lesbian

▪︎ My pronouns: they/them

▪︎ Disabled, lived with chronic pain for most of my life

▪︎ Studying medicine

I'm navigating going to uni while attempting to have a personal life and respect my body's boundaries. It's challenging on the best days, impossible on the worst. I've just learned how to bind books, and I've made a few too many already. I'm trying and failing to watch less netflix AND I've just started watching anime, which is very exciting. I love reading, mostly random medical books or fantasy, and I write poetry, mostly about being disabled.

I would love to connect with more people on here, so feel free to dm me:D

More Posts from Girlish-in-pain and Others

6 years ago

Denmark: we present you, Vikings

Europe, crying: yes

7 months ago

hey if you're not a mobility aid user, and you want a simple way to make public spaces more accessible to those of us who are, i have a tip for you:

push in your chairs when you get up from tables.

when people don't push in their chairs, people with bulky aids like wheelchairs and rollators can't get through. also a lot of people who use canes have wider gaits than able bodied people, and having a chair in the middle of their walking path is a real obstruction. while some of us are able to push chairs out of our way, a lot of us are not, and wind up boxed in/out because somebody didn't push in their chair.

so if you want to do something simple that can make a big difference in terms of like. navigating an outdoor food court or a cafe or what have you. push in your chairs.

4 years ago

sometimes I’m hardcore and numb and can deal with being in pain for the rest of my life and other times I cry at just a slight thought in that direction and I wish I could be strong all of the time for everyone around me but sometimes I’m just REALLY really overwhelmed by the moment I’m experiencing and that is compounded a million times over by the fact that this is the rest of my life 

3 years ago

ICELAND ICELAND ICELAND ICELAND

1 year ago

I recently started using a cane everyday and so my previously invisible disability is suddenly visible. I also started medschool. It's been a while since I was properly social so I have questions...

People don't walk next to me. And if they accidentally do, they leave to walk next to someone else even if that means squeezing in three people on the sidewalk. No one talks to me if it's not to ask me "what's wrong". I have really tried to make an effort and talk to people but I don't know what to do.

Can it have something to do with my disability and my cane? Like they're scared to say the wrong thing? Or maybe it's because they've sensed the autism?;)


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1 year ago

yes, doctors suck, but also "the medical ethics and patient interaction training doctors receive reinforces ableism" and "the hyper competitive medical school application process roots out the poor, the disabled, and those who would diversify the field" and "anti-establishment sentiment gets applications rejected and promotions requests denied, weeding out the doctors on our side" and "the gruesome nature of the job and the complete lack of mental health support for medical practitioners breeds apathy towards patients" and "insurance companies often define treatment solely on a cost-analysis basis" and "doctors take on such overwhelming student loan debt they have no choice but to pursue high paying jobs at the expense of their morals" are all also true

none of this absolves doctors of the truly horrendous things they say and do to patients, but it's important to acknowledge that rather than every doctor being coincidentally a bad person, there is something specific about this field and career path that gives rise to such high prevalence of ableist attitudes

and I WILL elaborate happily

2 years ago

It’s the not knowing when it’ll stop. The unpredictability. Wondering “will this ever get any better?” It’s the people close to you just accepting that this is how you are now. It’s the 24/7 nature of it all. It’s the not having a choice. It’s the not having a break from it. It’s the people around you thinking you chose this. As if you enjoy it. As if you actually chose this life. Nobody would ever choose this. It’s the having to play symptoms down. It’s having to pretend it isn’t as bad as what it is. It’s having people judge you, even the people closest to you. It’s having to live with symptoms that most people wouldn’t know how to even begin to cope with. It’s a lack of self confidence and self purpose. It’s staying hopeful when it doesn’t seem like there’s anything to be hopeful for. It’s a lot of things.

You might not feel it, but you’re one of the strongest people EVER. You put up an invisible fight daily. You do all that you can. You often survive second to second, minute to minute, hour to hour. You get through the day. You do your best no matter what obstacles are in your way. And it’s important to remember that even on the really bad days that you’re amazing. You’re strong. You’re tough. You’re fabulous. Lots of love xxxxxx

2 years ago

you do not deserve your pain

you did nothing to deserve your pain

4 years ago

me, every second of my life: but is it meaningful? but is it meaningful? but is it meaningful?

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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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