#disabled in need

[cpunkwitch]

Please help me pay off my visa

I have $4 in my account right now, ice been needing to use my visa for so much this year and now that I don't have a job I can't pay it off like I was

I have so many options to check out in my store and I would really appreciate it if I could get help paying off some of my debt through it

Every little bit seriously helps

I'm not getting any income from anything until after Xmas

I would really appreciate it if you could go to my store and help out

Reblogs, sharing, donations, buying and commissions are all very very helpful

[evilartist37]

My mom’s a bitch and wants to buy herself a tv but not my sister’s fucking epipens.

So, uh, anyone want to commission me?

I also have a ko-fi.

[myownjadedpieceofmind]

I could really use some help.

In any way possible. Car insurance is due, electric bill is due, I haven't been able to get supplements I need that my insurance doesn't cover, and I've still not been approved for benefits.

I can't be without a car, because then I won't be able to make it to my appointments. I can't be without electricity because the little bit of food I do have will go bad without the electricity to keep the freezer and fridge running.

My website is live, tons of handmade pieces ready to ship out. I am always taking custom orders, which the holiday season is coming up, so there isn't a better time to get in on the list.

What I'm saying is.. life is kicking me while I'm down, but I'm trying like mad to earn my way, even with all the disabilities that I am learning to navigate around. My case with social security should be being approved any day now that my doctor sent in the residual functional capacity evaluation that social security asked for. I just gotta make it a little while longer.

If you can help, anything at all- even just $5. .. I would greatly appreciate it.

Cashapp: $6od3ss

Venmo: @ jaded-ink

Or, shop my website : Jaded Ink Designs

[2003-playground]

Can we stop using "still lives with their parents" or "unemployed" or "doesn't have a drivers license" or "didn't graduate high school" as an insult or evidence that someone is a bad person? Struggling with independence or meeting milestones is not a moral failing.

[disabledavocado]

maybe harsh take. but. shitting on people who can't care about selves. who live with parents. who rely on partners in 'basic' tasks. (yes even body care tasks). who got chores done for them. who don't work. is ableist. even if clarify 'this specific person isn't disabled.' it still perpetuates stigma. it still ableist.

say exactly what wrong. have they overstepped someone's boundaries? have they pressured someone into care? have they manipulated abused etc.? something else? point wrong behavior. n critique this behavior.

'they're 30 n live with parents' not bad behavior. 'their parent cut their nails' not bad behavior. 'they don't work' not bad behavior.

'but they're abled!' 1) you don't know for sure. can't know for sure. undiagnosed n invisible disabilities exist. not every undiagnosed individual able to take care of self. recognize undiagnosed n invisible disabilities existence not only when they look 'nice' for you. 2) it still contributes to stigma around needing care. disabled people often not seen as disabled. even if visibly disabled. every individual presumed abled because ableism. so disabled individuals will be shitted on because need care. because presumed abled.

to destigmatize needing care. have to destigmatize getting care. even if not see as 'reasonable' n 'justified.' can't destigmatize needing care if say 'getting care depending on others living with parents etc. is bad but disabled is exception.' because still stigmatize process of getting cared.

people don't need allowance n approval of society to get care.

(not say not call out bad behavior. ask call out bad behavior specifically. not stigmatized neutral things).

[sag-dab-sar]

Medical devices should not require an iOS or Android app to work. It took me twelve fucking minutes to set up and get my phone to connect to my migraine treatment device, 12 minutes during a horrendous migraine and I had to fight with my phone to get it to work instead of pressing a fucking button on the device. It might need a small controller to change strength but thats not fucking difficult to add.

Relying on a phone is bullshit: what if I'm out of battery? what if bluetooth is broken or something? what if I'm in too much pain to get the treatment app to work defeating the purpose? What if I'm paranoid about privacy so chose a non iOS/Android phone? What if I have issues with smartphones so use a classic cell phone? I know people that require that.

Requiring a disabled person to have iOS/Android in order for treatment to work is an unnecessary and borderline discriminatory practice.

Edit: After seeing all the personal anecdotes in comments reblogs and tags, I've come to a new conclusion— it is discriminatory.

[salt-baby]

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

[bean-spring]

Hot take and not to be a killjoy or the shipping police but people treating Viktor or Jinx's aroace headcanons as if they were canon is not the revolutionary take people think it is.

Headcanons are always all right but we have to acknowledge that they are somehow damaging when they apply to stereotypes. It might not be the case for everyone but most of the time people unconsciously assume that disability/mental illness=asexuality. These headcanons erase the freedom of attraction from people who are already seen as unable to have sexual/romantic experiences/desires, when it's completely untrue and harmful.

You can headcanon Viktor and Jinx as aroace, but I have seen people changing their minds once Viktor is no longer disabled (s2 with all of his other forms) and Jinx is no longer as mentally ill (alternate universe Powder). And it speaks wonders of how people see these characters.

"I never thought about Jinx being able to feel romantic/sexual attraction until s2!" To believe she's actually only capable of that when she's not "damaged" is incredibly disturbing. Especially since Jinx has always had a bit of a flirty personality too.

"I've always seen Viktor as asexual, I don't know why!" That's fine. You can headcanon him as ace. But I believe there is a reason behind it, most of the time, if for some inexplicable reason the "vibes" of the disabled character are making you think he's ace.

I say all of this being aroaspec myself, by the way. Headcanon all you want but going to people's posts commenting how "it's weird for you that they have romantic/sexual plots when they're clearly aroace" is not a win at all. It's a headcanon, after all, and it should be treated as such, and that's fine. But it also is damaging to spread stereotypes like these.

Of course the disabled character is asexual. Of course the mentally ill character is aromantic. It's not as revolutionary as you might think, tbh.

Fandom is not activism and it's all right to have any headcanons you want BUT some of them are filled with damaging stuff and perhaps we should look into ourselves more before treating these assumptions as something canon.

[nightmaretour]

Anyway, people with brain damage I love you. People who have had strokes I love you, especially if you're told you were "too young" to have one. People who acquired your brain damage by less common means such as infection, lack of oxygen at birth or degenerative disease, I love you. People with moderate and severe brain damage, I love you. People who lost their sight or hearing or ability to speak because of their brain damage, I love you. People who have paralysis from their brain damage, I love you. People with amnesia and severe cognitive issues from their brain damage, I love you. People with rare and unusual symptoms from their brain damage, I love you.

You are not a punchline, you haven't lost your humanity, your thoughts and opinions are as valuable as anyone else's. We deserve respect.

[ID: a dark red banner with the words "This post is about physical disabilities, do not derail." in grey font. Either side of it is a lighter grey wheelchair user symbol with the user leaning forward with the arms raised and back, giving the appearance of wheeling fast. End ID.]

[bisexualseraphim]

You know what, fuck it. Let’s show some love for the “unpleasant” autistics.

For the autistics who are always accused of being angry or moody when all they’re doing is sitting there.

For the autistics who take everything literally and respond sincerely.

For the autistics who come across as “blunt” or “rude” for being honest.

For the autistics who are called “control freaks” for needing a sense of order and routine.

For the autistics who get told to shut up for infodumping about uncomfortable topics.

For the autistics who find it too exhausting to mask and pretend to be sunny and friendly.

“Unpleasant” autistics, I love you.

[cpunkwitch]

I just paid my visa and this is what I have left. I still owe my visa, my parents are charging me rent, I need to save *something* and I don't get paid again till the week after next.

Before anyone points it out yes it's edited, I did that on purpose to avoid giving away information like my card numbers and account name. (Plus the charge on my visa won't change yet since I *just* paid it so I made that edit to show the difference it *should* be now)

I take art commissions, if my commission prices are high for you I take paid doodle Requests, I do tarot readings, I sell hand woven pride bracelets, I sell prints of my art both fanwork and original and I offer plenty more over on my store.

I need to pay for meds, aids, rent, food and plenty of other things. I should have gone clothing shopping for actual summer clothing but I have not been able to. I have gotten heat stroke at least 3 times and I'm still recovering from a nasty sunburn that's probably scaring my shoulder. I would have liked to get new shorts for work because my uniform is entirely black and there's days I have to walk to work in the sun but I don't have the money for clothing.

Seriously anything is a huge help right now and greatly appreciated.

I physically cannot handle a second part time job and even if I could it's really hard to find work that will actually take people in let alone a place I can work in healthily and accommodated with accessibility.

I prioritize peoples orders over my own projects, so you can be assured I will be focused on your commission/order/request.

My Kofi is free to check out below, you can also find my work on @spirits-art, @shutterbuged and cassderolo on Instagram

Again anything helps. Thank you /g

[uncanny-tranny]

[longlostdiaries]

I don't know who needs to hear this but:

-"it only hurts a little" is still pain

-"I can ignore it" is still pain

-"I can cope with/manage it" is still pain

-"it's bearable" is still pain

-"I can push through it" is still pain

-"it doesn't hurt that much" is still pain

-"it doesn't stop me from doing x" is still pain

You don't need to be in agonizing pain to be in pain.

[lightning-system]

As a medium/lower support needs autistic who works with young higher support needs autistic:

We all matter. We all have the same diagnosis. We all deserve to be treated with dignity and respect.

But we are not the same.

I can mask and might be seen as 'odd' or 'weird' in public. The students I work with are seen as 'dangerous' and 'practically little kids'.

I can go to university and work with accommodations. The students I work with likely will never live independently and a few might find jobs that support them but still pay them less than an abled worker.

I have full control of my finances. The students I work with aren't allowed to make independent financial decisions, even if capable.

If I say 'no,' I'm making a choice. The students I work with can't say 'no' without being labeled as defiant and difficult.

I can feed myself, bathe myself, and take care of myself with extreme challenges. The students I work with are unable to take care of themselves without high levels of support/one on one support.

I had an IEP in high school but was mainstreamed in classes. The students I work with take separate classes and some rarely get to interact with their abled peers.

Our experiences are fundamentally different. Higher support needs autistics will experience a specific type of ableism I never will, and can never fully understand.

Lower support needs autistics need to stop saying we understand what higher support needs autistics are going through and then present autism as only being disabling because of society/lack of acceptance because that is dangerous. We need to stop saying every autistic person is capable of everything if given the right support because that leaves out huge parts of our community who will never be able to do certain things, regardless of support.

We are worthy of existence regardless of our abilities.

Autism is a spectrum. It is not the same for every autistic person. Autism acceptance and advocacy has to come with accepting, acknowledging, and listening to our higher support needs peers.

[schizoaffectively]

You are well within your right to be angry about the help you didn't get and should have gotten.

You are well within your right to be angry about having your needs neglected.

You are well within your right to be angry.

[lastoneout]

I keep thinking about all of the disabled activists and people before me who stranded themselves on the 4th floor of buildings for weeks and crawled up stairs and fought with airline staff and schools and doctors and refused to stop existing in the face of injustice and bigotry no matter how big and scary and hopeless it seemed. Every time I get angry and scared the protests that lead to the creation of the ADA pop up again and remind me that disabled people are so much fucking stronger than anyone has ever given us credit for, and I can't help but be proud of that. And I know not all disabled people feel like we should take pride in our disabilities and have flags or whatever, but I think not just living, but thriving, in spite of a world that wants us dead and gone, in the face of both illness and persecution, and how we've not only bought ourselves forward, but uplifted the disabled people around us, secured more equal futures for everyone who will come after, and truly changed the way so many abled people have seen us for the better is something to be damn fucking proud of.

We have always been here and we always will be, there will never be a world without disabled people because being disabled is not bad, it's a natural part of the human experience and yeah it sucks some times but even when it sucks we have fought to build beautiful, unique, happy lives with people, both like us and not, and that should be celebrated.

The first sign of human civilization is the healed femur. The body of the profoundly disabled person who would have needed help to even just eat being carefully laid to rest after decades of a full, happy life. The medicinal plants showing even before we were entirely human we were doing what we could to not just survive, but alleviate suffering while we're at it. Above everything, evolution selected not the baby who can walk and eat and be quiet, but the one that can ask for help.

Disabled people are not just angry cockroach motherfuckers who refuse to die, we are proof of humanity's HUMANITY. Proof that natural selection selected a species that takes care of each other. From healed femurs and medicinal plants to vaccines and IVs and insulin to now, we are driven to help one another, we are at our strongest when we don't leave our most vulnerable behind. And I am living proof of that. My mother is living proof of that. Every disabled and chronically and/or mentally ill person I know is living proof of that.

And I don't know about the rest of you, but will carry that shred of humanity's true nature inside me like it's my fucking soul. I am scared and angry and hurt, but I have a lifetime's experience being scared and angry, and I can shake off the kind of pain that would make Atlas crumble to dust like it's nothing but a stiff fucking breeze. Disabled people have always been here, turning fear and anger and pain into joy and beauty and connection, and I'm not going to let everyone who came before me down. I'm not going to give up. Not now, not ever.

It's okay if you're disabled and you've hit your limit, you're too scared and tired and hurt, I won't blame you. But I won't abandon you, either. I might not be able to right all of the wrongs in the world, but I'll be strong, I'll carry all of you with me, I will not give up.

As I've said before, society hates a cripple who won't die, so we must spite them and live anyway.

Please, live anyway. I know if anyone can, it's us.