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#Actuallydisabled
frecklenog · 3 months
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i want you all to understand this.
insulin pens are very often used by diabetic children (or their parents, but they were very easy to use during the short time i was prescribed them when i was a child myself). they’re less cumbersome, produce less waste, and are far easier than pulling insulin from a vial with a single use syringe, as syringes are much more susceptible to air bubbles, which result in the diabetic not getting enough medication. i’m explaining this part because i know that some diabetic adults do also use them, and i’m sure that that’s true of diabetic adults in palestine with such scarce resources. when it’s life or death, you can’t really be picky.
the israeli occupation is now banning insulin pens from entering gaza.
lack of insulin results in diabetic ketoacidosis — essentially a very, very dangerous version of the effects of the keto diet. insulin is a key for the sugar from one’s food (both slow and fast acting, since all food has some carbohydrates, from nuts to potatoes to table sugar) to get from their bloodstream into their cells. without insulin, the body resorts to eating through its own fat stores rather than the sugar it cannot access and tries to flush the excess glucose that is in the blood through the urine. this results in weight loss, headaches, nausea, dehydration, blurred vision, abdominal pain, impaired mental faculties, and, if left untreated, will result in a coma, and eventually death within a matter of weeks. not “can.” it will kill you if not treated, and was largely considered a lethal diagnosis until insulin was discovered in the early 1900s and made readily available in 1922.
i’ve been in dka. admittedly, i was very young and have blocked much of it out. but i do remember that it fucking sucked. i couldn’t focus on anything, i was ravenous no matter how much i ate, and the room spinning to the point i felt like i was going to throw up became an increasingly regular occurrence. i was seven years old and wasting away like i was starved. i was dying. a few more days, and i likely would’ve gone into a coma and might not be here now.
to inflict that, willingly and knowingly, on innocent people, is nothing short of a crime against humanity, and violates the geneva conventions (item 2.a.ii. torture or inhumane treatment, including biological experiments and item 2.a.iii. willfully causing great suffering or serious injury to body or health). not that the israeli occupation cares, of course, as south african prosecutors have already extensively detailed their crimes in the icj, and this one in particular has already been committed near-countless times.
this entire occupation is a genocide, and this is only one more nail in that coffin. but, as a diabetic — as a human being who has been in that state and was lucky enough to have the resources to live almost another fifteen years (with the anniversary of my own diagnosis about halfway through next month), i can’t find the words to express my disgust and rage anymore. maybe it’s selfish to be so deeply impacted by this particular blow. i don’t know. but these people have done nothing wrong but be disabled in gaza, and as someone with the same disability, i know that no one deserves this, even if they have committed a crime (which, again, these civilians, largely children, have not). i will not fucking stand for it.
we need a ceasefire. we need an end to the occupation. we need a free palestine. now.
here’s a masterpost of how you can help.
EDIT: here’s a post on how to help diabetics in gaza specifically
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chronicbitchsyndrome · 7 months
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there's currently misinformation going around tumblr about what the SSI marriage penalty is, so this is my attempt to explain it in plain language.
when you marry someone who is not on SSI, and you are on SSI, their income is counted as your income. your SSI will be docked according to their income from then on. if their income outstrips your SSI (maximum SSI is $914 a month as of 2023), you will be ineligible for SSI from then on.
if two people on SSI get married, their maximum SSI benefits are reduced by 25%. they no longer get SSI as individuals, they get SSI as a couple, which is 25% less money than individuals are eligible for.
collectively, these two processes are known as the marriage penalty.
some news outlets are currently (September 2023) incorrectly reporting a bill as removing the marriage penalty. this is false. the bill is changing the savings cap for married couples on SSI. the savings cap is the amount of money you are allowed to save in your personal account before being kicked off SSI. this is different from the marriage penalty, and outlets referring to them as the same are conflating two different laws that apply to SSI recipients. please do not assume based on mis-worded news articles that you can get married without losing your income and health care if this bill passes. you may be putting yourself in danger by doing so.
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crippleculture · 7 months
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me: yeah i have about 8 or so disorders or conditions
someone who doesn't know what the word "comorbidity" means: wrow.... what are the chances of that....
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jemineye · 1 year
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i cant stress this enough, disabled people know their own limits. i fucking promise you. we are not being lazy or jerks because we won't do something YOU want us to do or something YOU THINK will make us feel better. it wont. stop.
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pots-plus-pans · 1 year
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destigmatize having a body/body parts that look “gross”
destigmatize having a reoccurring rash that you can’t control
destigmatize “strange looking” veins
destigmatize “gross” scarring
destigmatize having bodies that are broken and express that
destigmatize being disabled and having “atypical” physical manifestations of said disability
disabled bodies are beautiful
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rainbowchihuahuabunny · 6 months
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Every day I am brutally reminded in one way or another that this society isn't built with disabled people in mind
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hell-on-sticks · 10 months
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This disability pride month, I think it needs to be widely acknowledged that
a fundamental principle of disability justice is being able to recognise when someone might be more disabled than you.
[plain text: a fundamental principle of disability justice is being able to recognise when someone might be more disabled than you]
It's easy to point at ableds who will refuse to acknowledge others disabilities, not notice inaccessibility, or cringe away from catheterisation, stomas, hygiene problems and all the troubles that come with disability. It's simple to recognise that that's not okay.
But sometimes within the disabled community people don't do that well. And it's hard because there are of course many people fighting the internalised ableism that demands they downplay their disability. But the answer to that is not saying "nobody is more disabled than anyone else". This is not true. This has never been true.
You will not be able to work towards disability justice if you can't recognise that not all disabilities are equal. Even two people with the same disability - two people with SCIs, two people with autism, two people with EDS, etc. - may have wildly different levels of difficulty. And if you can't recognise that, you're being ableist. I'm sorry, I know that might be hard for some people, but you cannot have any kind of real understanding of disability if you cannot acknowledge when you are more or less disabled than another person.
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faesystem · 4 months
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As an ambulatory wheelchair user I have so many thoughts about how people draw/write disabled!Scar. This is sort of a guide/insight from a disabled person about writing/drawing disabled people.
Specifically in regards to wheelchair users.
Do not get me wrong, this fandom is genuinely probably the best group of people I have ever seen when it comes to drawing wheelchairs. I do not believe I have ever seen Scar fanart where he is in a completely unusable, horrible, hospital chair. It is so clear people have taken the time and energy to research into wheelchairs and I love it. I am in no way saying stop that.
I just think people could maybe put a little bit more consideration into him being disabled beyond visual appearance.
I saw a really amazing artwork of SL!Scar and he is in a sports chair. Which is really cool, in many ways, as it shows some thought being put into the setting. If I were in combat, I would in fact like to not be knocked from my chair or have my chair tipped over.
Yet, you have very limited mobility in a sports chair. It is, by design, made to prevent you from tipping over. Which means that you are incapable of going over bumps, really, let alone natural terrain.
Just in general, there really is not any wheelchair that exists in our world that would allow wheelchair users to exist in a setting like the life series.
So, I have some ideas:
- Horses. Hands down my biggest suggestion. Especially with Secret Life they fit in very well with the setting, everyone uses them, and it fits the bill perfectly for what he would need. Especially considering Scar is an archer, it makes a lot of sense for him to be on horseback. It suits him and his style of fighting so well.
- Some sort of redstone power chair. There are all sorts of ways you could design something like this. Perhaps with pistons that push down against the ground, allowing for jumps. Perhaps just a series of pistions functioning as like a bunch of little spider legs. There are a lot of things you can do with that, you can get very creative.
- For my Vex!Scar lovers, you could have magic be used as a mobility aid. Perhaps a magic wheelchair, or perhaps a magic exoskeleton.
And with all of the ideas, considering how they fit into the setting really changes everything. What are the strengths? What are the draw backs?
With horses, they are strong and fast and agile. But they are big, it is hard to fit into small spaces, and they can be killed.
With some sort of redstone chair, I feel as though it would make sense for it to be robust and strong. Depending on how it is constructed, something fast and agile or perhaps something a bit slower and more clunky. Is it loud? How would stealth work in something like that?
When it comes to any sort of magic you do not want it to fix the disability. It is a mobility aid like any other. Not perfect, not the same as not being disabled, just another tool with its own unique draw backs. Perhaps magic is draining or it takes concentration. Would he tire quicker than others? Would he require food quicker than others? Is it possible for him to lose focus on it in a stressful situation, leaving him stuck until he can calm himself down?
Other things to consider are really specifically the setting as well as what disability you are giving him.
I feel as though on Hermitcraft an option like a redstone chair just makes a lot of sense. Multiple redstone chairs, even, all constructed differently for different uses. Such as ones for building. How does long distance travel work with the chair and how you lore your setting? Is it something he can put in his inventory? Is it something he remains in when using an elytra? Does that have any draw backs, such as being slower or needing more rockets or being less coordinated in the air?
I feel as though in the life series a mix of vex magic and horses makes a lot of sense. The magic is good for small spaces and short trips and emergencies, but it is too tiring to travel across the map with and too much effort to maintain when he needs to concentrate on battles. That would be where the horse comes into play.
As for what disability, well, it truly depends. Most of my rambles here have been based upon paraplegia, because I often times see people making him an ambulatory wheelchair user just because they do not know what to do otherwise.
Not that making him an ambulatory wheelchair user is a bad thing by any means. I am one and I adore reading stories like that. It is just a bit clear that a lot of you are quite lost as to how to navigate hurdles disabled people face, so you make it so he can walk over those hurdles. Which, once again, I am not shaming you for! This post is just to show there are other options
But in the case of him being an ambulatory wheelchair user: why is he one?
Mobilities aids are disabling unless you need them. You cannot access spaces or you do not have hands free or any number of things. What to the Scar you are writing makes using mobility aids helpful instead of a hindrance? What times are they more trouble than help, and what cost is there for not using it?
A good example is if Scar can walk around short distances with minimal difficulty/drawback, but long distances are painful or physically not possible.
Look into different disabilities and consider it. A lot of people tend to default to chronic pain because that tends to be quite a common one across a lot of disabled people, but there are a lot more different reasons why.
It could also be that he is very slow because of his disabilities. I have muscle weakness sometimes because of my FND, and it is like moving through sludge whenever I try and move.
It could also be that the mobility aids are a preventative measure. He does not need to use his wheelchair, unless he has done too much walking and then his body refuses to support his weight. He does not need to use his wheelchair, but when he does not he is a lot more likely to dislocate something and then yeah he can't walk. He does not need to use his wheelchair, but he is a fall risk especially after a lot of walking or running. Him being in his wheelchair prevents him from falling! (And if he's a fall risk, maybe he's strapped in too!)
I just have so many thoughts and I wanted to share them.
I see so many of you putting in effort already and it warms my heart. It is why I feel comfortable enough to make this post, because clearly you all care a lot about representing disabled people well.
:]
If you have read this far thank you so much. Let me know what you think or if you have any questions.
Edit: I made a rough redstone wheelchair design. It is one of the few reblogs that has comments, if you filter for that you should be able to find it. If not, reply to the post and I can send you the link to it. :]
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defectivegembrain · 1 year
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"Autism wouldn't be a disability if society was different"
Full offense I didn't spend 18 years of life unable to take proper care of my hair because of society. People should've been more understanding, they shouldn't have stared and bullied me and treated me like the rest of me didn't matter, but they were right to be concerned. It was unhygienic.
There's never going to be a society with no difficult sensory input to tolerate, that's literally impossible. When I'm overloaded I can't function like usual. This could be improved with societal changes, but it'll always exist.
If everyone in society was accepting of my different social behaviour, I'd still miss cues and meanings that come naturally to most. That's disabling. Even if people are willing to explain, that's a disability accommodation. Accommodations don't make us not disabled.
We don't need a society where we're not disabled, we need a society where being disabled is accepted and accommodated as much as possible.
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switchcase · 1 year
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Right to repair for wheelchairs is legalized in Colorado, allowing wheelchair users to repair their chairs themselves.
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Feeling better after using an aid/accomodation/treatment does NOT mean you're better and should stop using it. That is the DEVIL talking.
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theygender · 2 years
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August 24, 2022
There's a new recall that I would like to spread awareness of: Great Value Shredded Hashbrowns have been recalled for possible contamination with listeria. Listeria can cause food poisoning and flu-like symptoms in healthy adults, but it more commonly affects infants, pregnant people, senior citizens, and the immunocompromised. In these groups it can also lead to more severe infections including sepsis, meningitis, and encephalitis, and symptoms of listeriosis can appear up to 2 months after a contaminated food item has been consumed. This recall currently only includes 64 oz bags with the following date codes and UPC, but if you're seeing this on any date other than the one listed above please make sure to check if the recall has been expanded:
Description: Great Value 64 oz Frozen Shredded Hashbrowns
UPC: 7874215557
Dates: 7/25/2023, 7/26/2023, 9/14/2023
This recall hasn't yet been reported by the FDA and at the moment this information is only being communicated by email to people that Walmart has records of having ordered Great Value Frozen Hashbrowns within the past 6 months, so if people wouldn't mind reblogging to spread awareness (especially among disability and parenting circles) I would greatly appreciate it. The current direction from the company is to discard affected bags and request a refund from the store, but I would caution against accepting any compensatory gift cards from the store in addition to your refund because they may try to claim it as a settlement if you need to sue for medical bills or damages later on
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pxppet · 1 year
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Mute people are humans worthy of respect.
Non-speaking people are humans worthy of respect.
Semi-speaking people are humans worthy of respect.
People with disorganized speech are humans worthy of respect.
Deaf people who don't speak are humans worthy of respect.
Autistic, disabled, mentally ill and all of it. We deserve to be treated like and thought of as real people with as much to offer as other humans. The lack of speech doesn't make us "useless" or "stupid" or "like talking to a lamp." Mute people of any kind have just as many thoughts and feelings and actions to offer as those who speak.
Life is still worthwhile and peace and happiness are attainable for us. We will find people who care to make the effort for us to be understood. You will feel yourself breathe softly again some day. You deserve it.
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crippleculture · 7 months
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Saying AI art is good cause it means disabled people can make art is an insult to disabled people, disabled people who can't hold a pencil can make art in so many different ways including mouth styluses and eye-tracking and theres alternative art forms and youre saying that's not as good or as valid as using a machine to steal other people's work and chop and screw it? Art is so much more than just making pretty drawings and disabled people of all types have been making art since the beginning of humanity.
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cosmiccripple · 2 months
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saw a post yesterday about a blind dog and the voice over said "just because he has a disability, doesn't mean he has limits" and...
the very definition of a disability is that it impacts your day to day life, as in limitations... (there's literally a term called activity limitation)
why are we being ableist to a fucking dog????? why's a disabled dog now your inspiration porn????
ableds confuse the shit out of me sometimes
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pots-plus-pans · 1 year
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normalize wearing sweats to places that they aren’t “appropriate” for
it takes too many spoons in the morning to get dressed and for me to wear clothes that bother me sensory-wise would just not be worth it
simply pulling on a tshirt and sweatpants is much easier for me than planning an outfit and then having to button/zip/whatever else
i’m not gonna spend spoons in the morning for that and most nights i’m too fatigued to plan out an outfit anyway
wearing sweats when “not acceptable” is fucking punk and we shouldn’t judge others on what they wear
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