#but im ill physically and mentally

[himbos-hotline]

*watches all my fics get ignored* i love writing so much

[amanfromnewjersey]

I am going insane about these stoats

(my insta is @trisideseye and that's where I mostly post art. I'm purely posting here bc @quiddie is active on here and I need aabria to know, personally ,how fucked up I am about these stoats)

[firelordhotman]

we talk a lot about how mental and physical disabilities are different lived experiences and just having one doesnt mean you understand the other, BUT i dont see a lot of people talk about how they can still interact with and feed off of each other!! so heres a shoutout to:

medical trauma survivors

medical abuse survivors

people with endocrine disorders that affect their brain chemicals

people who are depressed due to the isolation of living in an inaccessible world

people who are anxious due to ableism in the world

people whose mental illnesses led to their physical condition worsening

suicide attempt/self harm survivors who retained lasting injuries, pain, or other illnesses

physical abuse survivors who retained lasting injuries, pain, or other illnesses

people with chronic illnesses induced by eating disorders

people with chronic illnesses induced by substance abuse

developmentally disabled people whose condition affects both their mental and physical motor skills

people whose psychiatric medical team doesnt understand their physical barriers

people whose physical medical team doesnt understand their mental barriers

people caught in the loop of their mental and physical conditions making each other worse

and everyone else who lives with me in the middle of the venn diagram of physical & mental disabilities. its hard when everyone seems to assume you can only be one or the other, especially on a website full of discourse yet entirely devoid of nuance. i love each and every one of you!

[naamahdarling]

You know what? You know what I think?

I think that if we lived as we were meant to, in larger intimate ("extended family") groups and with more shared labor and time to do it (UBI NOW) people like me would not feel so useless and burdensome because there would be people around to help and to do what neurodivergent people can't while making valuable space for the neurodivergent to do what they ARE good at.

The way we live right now, all right, the way we live right now forces units of two adults to be able to do EVERYTHING or PAY to have someone come do it for them. I have to do the housework. I have to do it! But I am having to do a million different things and most of them I am not good at. I suck at them.

I wouldn't feel like shit, okay, if I had more than one other person around who was not a child and who could do the things I can't, like do the yard and cook and do repairs and basic maintenance; and someone else to split everything else that I like but is too much for me. It would free me to do what I am good at and enjoy. Cleaning, as in the sink and toilet, the windows, the blinds. Taking out trash. Folding, hanging, and sorting laundry.

But because all the shit I can do often relies on other shit being done first, and I can't do or have trouble doing those things, the shit I can do often can't be done. And even the shit I can do, I can't do ALL of it. So I can't keep up, and things get very bad.

We aren't meant to live like this. We are not meant to live like this.

That thought hurts so much because being able to flee the birth family is integral to survival for so many people. I'm so afraid that living in larger family groups would create more opportunities for, say, queer kids to be isolated, rejected, bullied, and abused. But if we gave people enough money to survive, and stopped considering children the property of their parents with no system in place to help them escape bad situations except a system that is often just as bad, just different.

I'm aware that communes and collectives aren't all that successful and are kind of a joke. I don't mean that. I mean a fundamental shift to multigenerational families where taking in "strays" (which my family did) is also normalized so people escaping abuse into existing households was accepted, with these families centered in maybe a couple of different larger residences so not everyone has to buy and maintain their own fucking washing machine and vacuum cleaner, and so people can benefit from large group meals that yield leftovers, and so child and elder care can also be centralized.

Then disabled people and the neurodivergent and sick and injured people, and pregnant people, and grieving people, would not have to either labor through all those stressors or consign themselves to living off an unlivable pittance or being put under legal guardianship.

I'm not saying anything new. People live like this in other parts of the world and maybe it sucks and I am wrong. But I'm just really mad right now because I can either do laundry or clean the sink but not both, and I really think we could improve society somewhat by making it so I did not have to choose one without sacrificing the other.

[foxett]

Holy flip!! Fully colored suntan post?? Decently done grass??? Someone pinch me (day 10 suntan)

[ohgreat-moretapes]

Tim I noticed a lot of indigenous patches on your jacket, are you Native?

Idk what my dad was 'cause I never knew him, but yeah my mom is (or... Was.. I guess..) Muscogee, the tribe native to the part of Alabama I'm in.

If I remember correctly she came to Alabama from Oklahoma (where a lot of Natives were displaced to in the 1800s) to "get back to her roots."

But yknow, I was separated from her in childhood (which tbh is upsettingly common for Native families) and I was raised in a very white very Catholic asylum so I'm not as connected to the culture as I'd like to be.

-Tim

[fella-lovin-fella]

the thing about mental disorders is after you're diagnosed with more than 2 people stop taking you seriously

[cdmodule]

A few months ago I drew out some headcanons related to various disablities & other physical conditions and decided to finish them up now that It's disability pride month ( Even If not all are necessarily disablitles <3 )

[ First time doing Image descriptions so I'd appreciate feedback! ]

[transmascissues]

i’m going to be starting a job soon where it looks like almost all of my coworkers/bosses are going to be cis women and i am…terrified. especially since this is the job i’m going to have to get time off from for top surgery.

if there’s one thing i’ve learned over the almost ten years of my transition, it’s that a situation where i’m the only guy there is one where my gender is guaranteed to not be respected. it really feels like far too many cis women realize they’re alone with a trans man and just see it as an opportunity to act out some sort of power fantasy where they get to stick it to the big bad evil men by taking out their anger on the first man they see without the power to fight back. that or they decide you’re “just one of the girls” and will not hear otherwise, but honestly, given where i’m at in my physical transition, i have a feeling the former is more likely.

there was a time when i felt safer around cis women than around cis men, but now it’s just a different kind of threat.

[give-grian-rights]

We'll never have dream smp again you'll never get to be a mcyt during the lockdown

Every waking moment of my being was dedicated to dream smp. I was never more disconnected from people and more intertwined with thousands of others.

I'll never be a teenage mcyt people blorbo post about and I'll never go back

But that's just me talking without my meds ...

[ganondoodle]

so with echoes of wisdom .. i havent watched any of the trailers beyond the very first one and the thumbnails/screenshots and what others have said about it-

but with the world inside the rift being called "Welt des Nichts" aka "world of nothing/void" in german ('still' in english, for some reason) and demises title in french being "avatar of nothing" ... yeah my anxiety is shooting through the roof again

(hopefully you can be a little more forgiving for me being anxious/weird about it bc demise is my blorbo)

i had similar worries with totk, that werent proven true thankfully, but the darn book is making it all worse again with all those weird lore things the game doesnt even so much as hint at AND potential retcons- im in for a really rough time huh, not just stress in real life (more in tags.. its alot) but now about my specific hyperfixation from two things even (AND artblock still..)

weird as it may sound, i dont want demise to get more lore, partly bc i dont believe theyd do anything with him that i would like (given their track record) but much more importantly- the fact that he has this little lore about him is precisely one of the reasons why i fell in love with him, i tend to like characters that are neglected by the narrative, and his story being both so flat and already done meant i can be very creative with what i come up with for him without necessarily contradicting anything in canon (which is ... or was a big point of how i wrote destiny's story and lore, working with canon in a way that reframes it all without straight up ignoring it ... but i suppose i urgently need to let go of that and accept i spend alot of time working things that will go to waste :( ) AND not having to worry that there will be more stuff with him that would massively change not only what im writing but also potentially how i feel about him since the game he was briefly in was the oldest chronologically and ended with his death- i didnt expect them to mess with anything that far back and thought theyd just go forward and leave the timeline behind and wouldnt mess with it again, given how botw seemed to be a sort of 'fresh start' that seemingly regarded the past as the past that needs to rest and that the timeline was finally no longer a discussion if everythings unified through botw and one thing going forward

but i suppose i was very wrong with that .__.

right now the only thing that motivates me still is the left over determination and spite to work on my zelda comic, since i have never gotten this far and really want to get something done for once, but i cant lie that im feeling like i should pause all work on it too to wait and see waht the book and the new game will do .. either to determine if i still have the will to keep working on it after those things are out (my love for tloz has been taking alot of hits lately ..) or if i have to change stuff (mostly bc of my lore problem trying to not ignore it ..)

[little-tangerines]

kids are generally weird and religious kids are just plain scary honestly

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[raincamp]

the masculine urge to throw myself down a stairwell because i feel like nobody is paying attention to me

[jameswilsonsupremacy]

@irenespring commented on my post and said:

“Do you think if House and Wilson were together in canon, would there prank wars get more or less intense? Like they would obviously be closer and probably a bit sappier so less vicious? Or would a blatant domestic life offers a whole new frontier?”

My thoughts were Too Long for a comment so here’s my response for the silly hate crimes md fans!!

I ACTUALLY THINK ABOUT THIS A LOT!!! and it absolutely depends on the situation—aka, if Hilson is established already and have been in a committed relationship for a while, or if it’s new (in terms of romance).

I think that if they got together during the events of the canon episodes, it would be a bit of a transition. As in, I feel like they’d wait a bit before their next prank war as they’re still navigating what it means to be in a relationship. So House might lowkey let his guard down a little and let Wilson win parts of prank wars (though not the overall war, c’mon, he’d just let Wilson get ahead a little bit). He would like seeing Wilson’s silly grin and how excited he gets to tell House how ‘oh I TOTALLY got you, you should’ve seen your face!!’ and House orchestrated the whole thing but doesn’t tell him. (Wilson does the exact same thing and they don’t even realize it.)

If it’s canon but they’re already established & have been together for a long time.. those would be so ruthless. Arguably much more intense than what we see in canon, bc now House/Wilson have been vulnerable with each other where they Genuinely Know each others hard limits & boundaries (aka the Do Not Mess With subjects) and they know how far they could push. One may argue that they pushed each other in canon while knowing boundaries, but if hilson is established, then I think they’d rly have a talk about their boundaries and how to make it all work. And then they could hardcore attack each other in prank wars without even having to consider going too far.

but regardless, I feel the prank wars would stem to the pranks that House plays on his team as well. House tries to use Wilson as an advantage but so do the Ducklings and Wilson basically goes back & forth on who he helps.

I also think that Wilson would make some of the pranks more themed to their relationship because he is a silly romantic and the hospital Knows That. So is House, arguably more, but he pretends he isn’t. So I feel like Wilson would also have pranks where he’d try to embarrass House in front of the team—see what they can get away with before House almost kills a duckling (because they lovingly made fun of him & how he is literally a lost puppy with major heart eyes at Wilson) or until someone gets Cuddy to intervene.

[thedisablednaturalist]

Tw for weight loss mention

The whole exercise will cure your disability thing is a fucking joke. Yes exercise is beneficial for your health, but only if you aren't already on shaky foundations. You need to be on a treatment plan that WORKS before going into the maintenance phase. You wouldn't do regular maintenance on a broken item, you'd work on getting it up and running first. And maybe it would even need specialized maintenance afterwards if it's especially fragile.

I have fibromyalgia and acute degenerative disc disease. My immune system attacks my nerves and discs in my spine are slowly calcifying and causing the bones to constrict and damage my nerves (i think thats how it works). I have days where it feels like my body is on fire from nerve pain and days where it feels like my spine is about to rip from my back. And days where I have both (like today!). I get numbness in my hands and feet. I have horrible migraines. I can no longer walk unaided more than maybe 5 minutes without severe pain. I have something wrong with my knees and hips but the doctors don't know what yet.

You'd think I live an obviously seditary lifestyle correct?

Hell no.

I walk aided on average 6 miles a day over difficult terrain OUTSIDE of regular activity almost everyday. My legs are muscular and strong. I get my heart rate up and a good sweat, like all the gym rats swear on. I am often doing physical labor such as weeding, digging, sample collecting, pruning trees etc.

I'm not saying this to make other disabled people feel bad or prove that they can do anything if they just tried harder. This is an extremely painful lifestyle I've chosen that takes a lot of lifestyle management AND BOUNDARIES to keep up with the work. I also have an extremely forgiving boss who is also physically disabled and knows what I'm going through (deciding between your passion and your health and having to do so each and every day) No one should ever be expected to do what I do. I'm not even sure if I should be doing this myself.

This is to prove that exercise? Has not cured me. My muscles are strong but still hurt as if they're broken and I have to take more breaks than my coworker. I am constantly getting out of breath and I flare up regularly if I'm not careful. I am in excellent physical condition outside of my disabilities. I go to different doctors several times a month to get checked out.

I previously went through a diet program and lost a lot of weight (basically starving myself and got off my depression meds which cause weight gain but are also the only ones that work) and guess what? That didn't do shit either!!! I still felt horrible!!! I've since gained back the weight anyway after switching to focusing on adding more nutrient dense foods than taking stuff away from my diet (also muscle weighs more than fat, and fat helps cushion my aching joints and spine).

The muscle doesn't do shit for my disabilities outside of maybe some stability. Exercising everyday doesn't make the pain go away. Without my medications and aids and nutrition plans and steroid injections and spinal adjustments and physical therapy (that takes my fibro and spine into account) and alternative work methods I WOULD NOT BE ABLE TO DO WHAT I DO. Exercise alone is like trying to make a car run with no oil. Yes it'll go but it'll get more and more damaged till it can't and will need its entire engine replaced!

And yet I see new doctors and they look at me and the first thing out of their mouths is do I exercise? I should try doing a little every day :) and then i fucking blow their minds when I tell them about my job. No longer can they use that fucking cop out on me. I've been through this rodeo. Ive tried their suggestions. If you are in pain and nothing is helping? Exercise ain't going to do SHIT. You need to get to a point where you can move without severe pain first (if that's even possible). Then and only then should you consider implementing regular exercise if you can. Also weight loss talk is a red flag and a cop out. They made me lose 50+ lbs before they would look into the reasons behind my pain. Weight loss did nothing for me and exacerbated my pain.

I am living proof that all that shit is a lie and a cop out. That is the point of this post. I cannot believe people with serious medical conditions are being forced to put their bodies through extreme duress just to be believed. You are not disabled because of laziness or because you sit a lot. Plenty of people live seditary lifestyles and do not live in constant excruciating pain (they may develop disabilities later in life due to this however, and should be doing preventative exercises to maintain their health)

Please, share my story with doctors. Use me as an example. I am proof that "exercise first treat later" does not work. I should not have had to wait years to have my pain validated. I'd rather hundreds of fakers get (what? A blood test? An MRI?) than one chronically ill person get told to try yoga and go away by a doctor.

[crippleculture]

Hot take but part of disability acceptance needs to be accepting and normalizing greasy hair. People are too obsessed with being neat and well-groomed 24/7 it's kind of an issue. A lot of disabled people simply do not have the energy or ability to take showers or wash their hair on a regular basis and they shouldn't have to sequester themselves away because of it. You won't die because that disabled person you see at the grocery store has greasy hair, you'll be okay I promise.