Hello! My name is Moth or Cowboy, either works. I am a disabled being mainly just trying to advocate for my disability aids, but also use this as a place to rant and talk about my experience with being disabled
More info below
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@byte-sized-supports
Hello! My name is Moth or Cowboy, either works. I am a disabled being mainly just trying to advocate for my disability aids, but also use this as a place to rant and talk about my experience with being disabled
More info below
I hate how expensive gear can be sometimes
I make all my gear for Byte and the others but I really struggle with patches so I am probably gonna bite the bullet and buy some custom ones soon, I picked some out but itâs around 30 dollars sigh
Thatâs not bad for custom patches especially six but I have about 77 dollars to my name atm- I really wanna get them before a convention Iâm gonna be at next month though so I gotta decide if itâs worth the easy to read text soon so they can be made and get to me in time
ironically enough, bringing a plushie to a public setting as an adult requires a tremendous level of emotional development, and attempting to shame an adult for having a plushie in public requires a significant amount of immaturity. this applies to a surprising number of things.
Harbor is the no at recent addition to my team, being a secondary outing aid and sensory aid mainly, but helps with many things
This is a post on info, frequently asked questions, and boundaries I have with Harbor
My body has been particularly unreliable the last few days đ
I have projects I wanna work on and to open commissions (unrelated to my plush content, thatâs just how I get money) but Iâve been struggling to do a whole lot even eat or play games so unfortunately Iâm not sure when Iâm getting to them
This may also is slightly slowing down content on all my platforms, logically Iâm gonna be most active here till my body decides to function right again since I donât have to plan out posts here I can just rant
I've seen people say that plushies helping you with pain management is still just emotional support and I'm like Damn. Didn't realize Tylenol was an emotional support pill.
Also, genuinely, calling mental health meds emotional support pills from now on.
Anyway, I have a migraine and it's making me mildly dumb, and the only thing helping distract me from the pain are Mio's different fur textures. Genuinely reduces the pain so much because my brain gets distracted from pain focusing. Especially one spot with like four textures you can touch at once. Sensory input is good.
Trying to argue that people ridiculing and othering those who use stuffed animals as an aid is not ableist because itâs not a âmedically recognized aidâ is not a good argument btw
Much of the ableism towards folks that need/use plushies to help them function, in whatever way that is, is rooted in society's hate for those that are neurodivergent. And even if thatâs not it, trying to claim someoneâs disability aid is incorrect and that they donât need it when it has zero effect on you is the same point people make towards other aids. Where exactly do you draw the line between the âcorrectâ aids and the ânot correctâ ones?
Just because a aid is not â medically recognizedâ (though can be added to accommodations, btw, I know folks that have their plush in accommodation lists) does not mean you still canât be ableist towards that person for it. My friend who needs to wear headphones everywhere because of sensory issues has been mocked and made fun of for them, would you not call that ableism too just because itâs not technically a recognized medical device? What about fidget toys? What about communication cards? I could keep going on the list of tools that arenât technically medical devices but many folks see as aids (yes these all can be added to accommodations as well btw)
Despite if you like it or not I and others have dealt with ableist remarks and harassment because we are using a âchildishâ aid and an aid many people have decided is not a proper aid just because they wouldnât use it themselves. I have been told Iâm faking my disability multiple times because I use plushies to help me handle my symptoms. Others have dealt with a lot worse. Please realize ableism is not just towards medical devices, you can be ridiculed for how you act, speak, look like, dress, and more. Ableism is so much more than just hating medical devices and runs deep in so many things.
(this is not directed at anyone, I just wanted to share this because I had this point given to me in my comments the other day and needed to post this somewhere so maybe I can help some people with the same point understand where Iâm coming from)
PLEASE COMMISSION ME đđ»đđ»đđ»
I put love and care into every single order, even while I'm on vacation!
I can draw ANYTHING!! animals, humans, humanoids, plushies, toys, robots, bugs, objects â anything!!!! you can order through my ko-fi or message me here if you have any questions! i promise i'm very friendly!
deadline: two weeks, or up to 20 days at most. if you need your commission by a specific date (for example, as a gift), just let me know and i'll do my best to have it finished by then!
please share this post if you can't order but would still like to help! thank you <3333
disabled ppl we need to start lying to nosy people okay? you tell me i'm too young to need a cane and i will tell you point blank that maybe you should tell that to the guy who ran me over. you don't get an explanation of my health issues you get lies and depending on how much of an asshole i want to be that lie will be anything from a humble car crash to a 1 billion lions attack. mind yr business.
"i could never live like that" well maybe you'll have to because this happened overnight. yeah you heard me i was the most able bodied man in the world but then one morning bam i woke up disabled. yeah you could have that too. there's no cure either you'll just wake up one morning and now you have to live like me
"what happened" well have you ever seen looney tunes? yeah an anvil landed on me and squished me flat.
nah, when people ask "what happened?" you just gotta stare out into the distance with that haunted look in your eye and go: "that damned seagull..." and just walk away with no explanation
I was once joking around with some other disabled folks about this topic and come up with âI got into a fight with my chinchilla and Guinea pig and they went for the jointsâ and one day I really wanna use that just to see the reaction
Harpy is my longest standing service plush, being my first and still being used to this day. They are mainly a at home aid currently and are not posted very often
This is a post on info, frequently asked questions, and boundaries I have with Harpy
Meta glasses make me scared.
I am legally blind without my glasses, I need them to see. I fear that with the rise of meta glasses, I could lose access to places.
I shouldn't have to prove why I need my glasses, I would be severely disabled without them.
I also don't like how a medical aid such as glasses are being used that way, glasses are a medical aid, a tool. They should not be used for recording
my submission for the @byte-sized-supports contest on tiktok!
july is disability pride month. it is also summer in the northern hemisphere, and this summer we have seen record breaking hot temperatures across the globe. it might be apt to remember that disabled people are a population vulnerable to extreme weather, and significantly more at risk of death or health issues during a heatwave. "the global mortality rate of people with disabilities in natural disasters is up to four times higher than people without disabilities." (source). disability may increase the relative risk of a heatwave more than old age, socioeconomic status, and being outdoors (source). even in the places most affected by the rising heat, disabled people are barely included in action plans for public safety, if at all (source). global warming is a an issue that affects a wide range of people, but let's not forget it is also a disability rights issue
I support researched self diagnosis btw
Whether you are striving for a diagnosis and do have the means
Whether youâre striving for a diagnosis but donât have the means
Whether a diagnosis isnât something youâre striving for
Or whether a diagnosis isnât a priority right now
I understand how difficult it can be to get diagnosed with certain things, especially if youâre a person of color or a minor.
Byte is my main outing and everyday life service plush, what I would count as my âmainâ I suppose as a lot of my presence online is based around them and they are used the most often
This is a post on info, frequently asked questions, and boundaries I have with Byte
Alright Iâm finally gonna lock in and do things like my plush intro posts and stuff, but I am probably gonna rewrite my intro and maybe my info posts, so as I get those done Iâll try to space out my posting so itâs not all at once but if I donât do good at that sorry lol
i dont WANT pride months to be over,
on the other hand...