◇ Xe/Ze/They ◇ Art Commissions Closed (opening again soon) ◇ Just a queer and disabled cyborg posting about queer disability stuff and sometimes art.
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my mum’s horse has finally noticed my presence despite the fact I’ve been living right next to his stable for the last week or so 😂. He’s been staring at me for the last half an hour wondering why there is a human so close to him that’s not feeding him 😂. He is also not a fan of my cat (which seems to be mutual lol)

#his name is cranky Franky by the way#he’s especially cranky today because mum had to put sunscreen on his nose and he tried to lick it off and failed lol
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Poe the Fire Mage
Commission for Mr Poe on Fur affinity! I really had fun with this one! The pose and the fire was a good challenge, and I got the chance to try out some new stuff with the linework on it as well! Thanks again Poe! [ID: A digital, cell-shaded illustration of a grey, anthropomorphic drake wearing red robes and a blue cape. He is shooting a blast of fire from his paws as he jumps back /End ID]
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My mum’s cattle dog is very timid. apparently I deeply traumatised her in November when I went to go feed her, I went down the ramp too fast and my wheelchair made a weird noise and She has not come near me since 😭 the only way I can get her to even look in my direction now is to use the How To Train Your Dragon approach and throw her some of her favourite treats while looking away.
today, she licked my hand before she bolted because I wasn’t expecting that and jumped in surprise, so… Progress?
#gif#she’s like this with a lot of people so I don’t take it personally#I tried getting out of my wheelchair but the wheelchair alone seems to scare her more#dogs#disability#dog#dogblr#wheelchair problems#wheelchair user
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I’ve finally moved (and have consistent-ish internet again) and been unpacking for 3 days and I feel like there’s more shit left than when I started.
I threw out so much, where is it all coming from? I feel like there’s a kobold or something summoning more boxes of junk every time I turn around. 😂
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Nintendo releasing a 1st party wheelchair basketball-meets-rocket league game and announcing it in the switch 2 direct was not on my bingo card but I’m hyped for it!
#hopefully the gimmick controls aren’t too obnoxious it looks like a fun concept#drag x drive#switch 2#disability#disabled#dragxdrive#nintendo switch#nintendo direct
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Trying to organise dates and times for moving stuff between 3 people (me, my partner and my mum) who all have raging time blindness issues, with the help of 2 other time-blind people (my sister and her partner) is a fun experience, 10/10 would recommend /sarcasm
#I love my family but we are all neurodivergent disasters#and as an -everything needs to be on a schedule- autistic this will be a very rough 2 weeks 😭#light-hearted vent
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I finally have a date for when I’m moving!
My partner and I were supposed to move into my parent’s farm long term in January, but mum told us at the last minute she still needed to clean out the old furniture she had stored in there and replace the flooring in the little granny flat we were going to stay in. It was supposed to take a week but the builder who was doing the flooring disappeared on her for 8 weeks 🤦 so we’ve just been in this awkward half packed state since last year lol.
It’s finally sorted though and going in this week, so we are officially moving in 2 weeks time!
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I’ve probably said this before, I don’t remember, but I’d be way more likely to put in the effort to use and stick to using my prosthetics if they didn’t have to be so damn boring.
Half my hometown already thinks I’m demonic for being queer, let me have fun with it and give me goat leg prosthetics! Or dragon legs, or legs with those digitigrade stilts built in.
But nooooo, it’s “not safe” and “not good for my spine” so instead I get stuck with legs that look mostly normal and can only wear a narrow range of shoes. Bah! Buzzkills…
#i’m only half joking#in all honesty the novelty would legitimately help 😂#amputee#disabled#prosthetics#queer#disability#double leg amputee#leg amputee
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Mirage is the second of the two characters I’m playing in a one-on-one Pathfinder 2e campaign my partner and I were planning. Mirage is a dragon-blooded merfolk ranger, and chitters is their “faithful” mount. Mirage doesn’t really fit the typical ranger archetype, they were a prince (though very far from the throne) cast out over a disagreement with their mother. The Queen disowned them, exiled them from the kingdom and only allowed them to take their mount Chitters before chasing them out of their kingdom. Like many nobility, mirage enjoyed hunting for sport, and was quite good at it, but they quickly learned that the hunting trips they went on, surrounded by royal attendants, are very different from living out in the wilderness and having to hunt enough to feed both you, and a very grumpy wyvern that was not particularly keen to be taken from his life of luxury. [ID: A digital, cell-shaded illustration of two characters. One, named chitters, is a light green-teal wyvern, standing on it’s back legs and using it’s wings as front legs. It’s tail ends in two articulated stingers and on it’s back is a saddle and attached to it’s horns are a pair of reins. Chitters is looking back at it’s rider, Mirage, annoyed. Mirage is a merfolk with the head and claws of a dragon. They have blue, slightly iridescent scales covering most of their body with a yellow underbelly and fins, both at the end of their tail and on either side of their head. they wear simple clothing made out of kelp, adorned with pearls. They are sitting side-saddle on chitters with one hand resting on the front of the saddle and the other holding a very large pearl which they are admiring. /End ID]
#cy cyborg draws#id in description#pathfinder#pf2e#ttrpg#dnd#pathfindercharacter#fantasy#dragon#furry
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My partner and I have been planning to do a one-on-one pathfinder 2e campaign, partially to test out some new homebrew mechanics he’s been wanting to trial before he uses them with our very chaotic group, but also to help me practice character dialogue that actually sounds different from character to character (which has been a bit of a reoccurring issue I’ve noticed in some of my comic scripts lately 😅). Because of that, I’m going to be playing two characters while he GMs, and this is my first one, Sarneir! They were inspired by Armanite demons in DnD 5e but mechanically, I’m playing them as a Nephilim/Centaur Champion! [ID: A digital, cell-shaded illustration of a demonic centaur-like creature. They have red scales all over their body, four split-toed hooves, a long, devil-like tail ending in a sharp, jaggered blade on their “horse half”, and on their more “human” half, they have two human-like arms with clawed fingers. Their head is long like a horse’s and covered in black spikes and horns, with large, black tusks protruding from their mouth. They are holding a bronze tower shield in one hand, and a kukri in the other. Their armour is a simple bronze breastplate with a red gem at it’s top where the shoulder straps attach, and a leather “skirt” made out of panels that sits right at the joint of their humanoid torso and horse-like body. /End ID]
#cy cyborg draws#id in description#pathfinder character#player character#pathfinder 2e#pathfinder#pf2e#ttrpg#dnd#centaur
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Kev
Kev is one of 6 main characters in the wheelchair basketball comic I’m working on. He’s is a retired wheelchair rugby player - hence why his chair looks so different to the other characters I’ve drawn so far - and when his wife (who’s art is coming soon) started a wheelchair basketball team, but was struggling to get the numbers to actually play, he signed up too. Personality wise, Kev is the team’s jokey uncle and is meant to be a direct foil to the more serious characters on the team, like Ruby. He’s already done the whole “serious athlete thing” and while he enjoys the game, at the end of the day, just there to have fun and support his wife, and remind the younger members to not get too wrapped up in it all. He’s a quad amputee (through the palms on his hands, above the knee on his legs) and is missing a good chunk of his tail too, making him a low-pointer on the court. Low point players are those who’s disabilities impact their ability to play more severally, and they usually play in more defensive and supportive rolls than high-point players. [ID: a digital illustration of a grey-ish green anthropomorphic crocodile in a red basketball singlet with the number 14 on it. He is a quad amputee, missing all of his fingers and both legs above the knee, and is sitting in a silver wheelchair rugby chair with red wheels, holding a basketball in his lap. The background is an abstract orange stained-glass pattern. /End ID]
#cy cyborg draws#id in description#wheelchair basketball#disability sports#furry#sfwfurry#furryart#crocodile#disabled#disability
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Why is physical media like DVD’s still region locked in 2025? I mean I know why (capitalism) but I thought we left that behind in the 2010’s?
I’ve been trying to buy as many of my comfort shows as possible as physical media, both because I can’t afford all the subscriptions anymore but also because where I’m moving has even worse internet than where I am now, so streaming might not actually be an option all the time. I’ve found most of them but Steven Universe is the only one left I’m struggling with. It’s apparently very difficult to get the physical dvd/bluerays in Australia. Apparently we just never got a physical release here. So I went to go buy it from an American seller because there were no other options I could find (if I wanted it in English) and noticed that there was a tiny warning at the bottom of the listing saying the disks were region locked and wouldn’t play on most Australian dvd players or PCs. I double checked and yeah, nothing I own can read it. Well my pc disk drive can technically do it, but there’s a limit to how many times I can change the region settings, and considering most of my DVD’s are region 4 (and this is region 1) it’s not really practical. That’s even more aggravating though because it means it has the capability built in and it’s artificially locked off…
And just…why? I want to access the show legally and give you money, why are you making it harder?? And yeah, there are ways around it, but man I just want to watch my silly kids show about gay space rocks while I do my work.
#this isn’t just about SU it’s just the one that’s frustrated me the most recently lol#even streaming SU the first time I watched it took a while because not many streaming sites here had the whole show#media
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Ruby
It’s been a while since I shared anything from my comics, so I did this between commissions!
Ruby is one of the 6 main characters in my wheelchair basketball comic I’m working on (and honestly, she’s one of my favourites)! She’s an Eastern Quoll who comes from a family of athletic high-achievers and Olympians, and is under a lot of pressure to live up to their expectations in a world that doesn’t see her as equal to her other athlete relatives.
Ruby is a high-pointer, meaning that, on paper at least, her disability has less impact on her ability to play - though not necessarily on her day-to-day life. This is an especially important distinction to make for Ruby in particular, as her disability (EDS) does impact her daily life and does impact how she plays, but not in a way that neatly fits into wheelchair basketball’s points-based classification system, which causes some…issues for her later in the series.
[Image Description: A digital illustration of a fluffy orange, anthropomorphic quoll woman with white spots on her head, shoulders and legs and a red basketball singlet, sitting in a red high-pointer’s basketball wheelchair. She is holding a basketball to her chest that is obscuring the number on her singlet, and snarling slightly. /End ID]
#Cy Cyborg Draws#id in description#Disabled#Disability#WheelchairSports#WheelchairBasketball#Furry#SFWFurry
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Please remember I am trans/nonbinary, my pronouns are xe/they.
I am starting to get genuinely annoyed with people’s shocked or doubtful reactions to hearing I want to have kids in the near-ish future. And I don’t mean strangers. Strangers say weird things to me all the time lol. I mean my family, my doctors, people who have known me for decades.
My mum in particular has made several comments now ranging from just genuine shock at the mention my partner and I are planning for kids during a conversation about plans for the future (I’ve literally talked about wanting kids to her since I was a kid) to outright saying during a casual conversation that “they (referring to doctors) probably wouldn’t let me carry to term”. Over Christmas my partner also told mum that we had some news we wanted to share in person, and her first reaction was “Cy’s not pregnant are they?” My partner said no and she responded with “oh thank god!”
My sister and dad have also made similar comments. Dad has brought up valid concerns (mainly about some genetic stuff that caused complications for my mum) sprinkled with the same ableism my mum always goes to. My sister I’m willing to give a bit more leniency, since she’s the only family member I talk about my transition with and she admitted recently she thought i was already medically transitioning and she thought that made you infertile so she just assumed kids were off the table. Neither of those things are true but her doubts at least aren’t tied to my disability, just bad info.
But it’s the doctors (and other healthcare professionals) that are the most frustrating. It’s not one or two. It’s nearly every doctor. Every nurse. Every medical technician. If the subject comes up, they all have something to say about it.
I don’t want to go into pregnancy blind, I know I would be at higher risk than the average pregnant person and I want to know what those risks are before I agree to them. I want to know what recourses are available. I want to know how me being in a wheelchair will change the process of things like giving birth. I want make sure the local hospital is equip to deal with that and I won’t be having to educate people while I’m in labour or if I’m better off going somewhere else.
But every doctor I’ve tried to discuss the subject with has shut the topic down and hand waved it with “we’ll cross that bridge if we get to it”. Like it’s something I’d obviously want to avoid that I probably don’t need to worry about. Even trying to get my contraceptive replaced, get a fertility test done or even getting a damn pap smear has been a nightmare. why am I fighting to get a Pap smear??? I’m nearly 30 and still haven’t been able to get one because several doctors seem to be under the impression I’m not sexually active, even when I bring my partner into the appointment. If they say it out loud (half the time they dance around the subject) and I correct them, they are genuinely shocked, then tell me we’ll worry about that later. Nurses and other healthcare providers are no better. There’s been several occasions where I haven’t been asked the mandatory “could I be pregnant” question when going for X-rays or CT scans (and I know they were supposed to ask because if I ask to see the paperwork, it’s always there and they’ve just checked “no” without asking), or if I am asked at intake, they say something to the effect of “I know the answer is probably no, but is there any chance you could be pregnant?”
Though I take back what I said earlier, there’s one comment from strangers on this front that pisses me off, and it’s “be thankful you don’t have to deal with being pestered about having kids”.
No, I won’t be thankful when my reproductive health is ignored, my family are telling me constantly they think I shouldn’t have kids or expressing surprise that I’m even “allowed to” and I can’t even get any answers about what it would look like if I DO get pregnant. My heart goes out to the people who are harassed and pressured into having kids, and to the people whose health is ignored for the sake of them being able to have a baby. Both my mother and sister have dealt with that, my mum almost died because they didn’t want to do anything that would prevent her from having more kids she didn’t want after my younger sister was born. But BOTH things are terrible and shouldn’t be happening!
Im not unreasonable, if someone brought up a decent, genuine concern to me that wasn’t just “can someone in a wheelchair even look after a kid” or “I didn’t think someone like you even has sex�� I would reconsider. If it was found I would be likely to experience serious complications for myself or the baby, I would reconsider. If I found out I wasn’t going to have the needed supports to raise a kid, I would reconsider. But everyone assumes that’s what I want. If I were infertile, or any of these things were true, I’d reconsider, but I’d be upset about it! I’ve always wanted to be a parent and if that was something that wasn’t actually possible, I would be sad about it.
But my family members talk to me about it in the same way they did when I was 10 and didn’t know where babies came from, doctors are shocked at the idea I’m even sexually active let alone thinking about children. I’m genuinely worried the people in my life other than my partner would treat any fertility issues like a good thing, or be shocked that I’d be upset if kids weren’t actually on the table anymore.
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17th- and 18th-century tiles decorated with representations of disabled people. From Barcelona, Catalonia. Museu d'Història de Barcelona: 1, 2, 3, 4, 5.
This tiles are "rajoles d'ofici" (meaning "job tiles" in Catalan language), a typical kind of decorated tiles that were very common in Catalonia between the 16th and 19th centuries, and which have become one of the most iconic examples of Catalan folk art. "Job tiles" are called this way because very often they represented people working, but they also represent people taking part in festivities, hobbies, or many other activities from daily life, as well as animals and workplaces. Thousands of these tiles have been preserved, and thanks to them we can see snippets of life a few centuries ago. (You can find more information and examples of these tiles in this previous post.)
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I swear Centrelink’s goal is to just be the most time-wasting government organisation 🤦
I went into the office in person 3 weeks ago to report income from my commissions, which is how I was told to declare the income last time I asked about it.
I explained how the income had been acquired (custom artwork via the internet) and why there was no abn attached (if you’re self employed, you’re supposed to have your own, if you have a normal job, whoever pays you should have one). After explaining it they said I don’t really fit in any category they have, so go home and they’ll call me when they know what to do, but it’s on my file that I tried to report so I won’t get into trouble at least.
A week later, they call and said that I need to register as self-employed, but an abn won’t be needed (yet). All they need is a profit and loss statement and a form. Easy, I did the same form for my partner’s door dash income and it’s pretty simple, and there aren’t exactly a lot of profits or losses for 3 digital-only commissions so that’s also simple. However, they told me on the profit and loss form to include things like electricity and internet costs as losses. I don’t exactly know how to calculate that so I decide to go to a tax agent for help, since what I submit to Centrelink needs to match what I will submit to the ATO later anyway, at least roughly, so it’s easier to do that now and get the more accurate numbers.
It takes a week to get in, the tax agent chats with me for 5 minutes and says she’s not entirely sure why Centrelink is asking me to do this, in the ATO’s eyes I don’t qualify to be a business yet and I wouldn’t qualify by centrelink’s definition yet either. I can register now if I really want to but it won’t be worth it until I’m making a more regular income. She also said she can give me a profit and loss statement but once again, it’s not really worth it and she’d have to charge me more than what I’ve made in total, so she highly suggests I don’t do that, and go back to Centrelink. Also they gave me the wrong form because of course 🙃.
I’m getting really confused at this point, and hear my explanations to each person getting more and more jumbled (which happens when I’m overwhelmed) so I wait until my support worker is there to go back in, since she’s helped me with Centrelink before and is getting good at understanding me when I get overwhelmed lol.
We go in, relay what the tax agent said and showed them the documents from the ATO that backup what I’m saying said to the person at Centrelink. The worker sighs, apologises and says that I was right the first time, I didn’t need to do any of this and the income should have just been reported when I came in last time. She confirmed that with her supervisor just to be sure and then wrote me a note with a big offical stamp on it to give to any other Centrelink worker who tries to say this is incorrect in the future, because it will happen again due to some vague wording in the rules they have to follow 🤦 she’s left a note in my file about it but people don’t always check so the paper note is a backup.
It took 3 week but I finally declared my commission income once it was all sorted out and hopefully the next time I go back it will be simpler…
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I am begging the FDA to require that companies CANNOT just put "spices" as an ingredient but have to label the spices.
"Spices" can mean "this has some oregano and black pepper in it" or it can mean "this has cumin cayenne and paprika and if you eat this you will be sick in bed in pain for a week" for me.
Seriously, this is an allergy issue and a huge oversight on the part of corporations.
Require detailed labeling of spices used in packaged foods NOW.
#I legitimately never know what is safe to eat or not because my allergies (onion mainly) are almost always included in that “spices”#that or vegetable extract#I was puffing up seemingly at random and having breathing troubles for years#also a lot of companies won’t disclose it at all even on their websites because of secret recipes and shit#food allergies
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