Game Dev|Consultant|Mass Effect LE Community Council|
@TheGameAwards
Future Class|Accessibility Pro. Queer disabled Black superhero. she/her jay
@jayjustice
.net
Hi, I'm Jay Justice! I'm a game developer, writer, consultant & sensitivity reader available to work on books, comics, games & social media! I'm also a cosplayer, streamer, & TTRPG performer available for collaborations! I'd love to work with you!
👉🏿👈🏿
I saw a tweet that said "I miss the pre-panini days when we could send kids to school with cold symptoms, without having to see a doctor" and I just want to say, no?? can we leave those days behind? can we NOT have a culture where kids OR adults have to perform labor while sick??
So we're waiting for the elevator at Bangkok Pride, I saw an incredibly beautiful Thai lady & I said to her "Wow you look so beautiful, you look just like Miss Universe Thailand" and she said "I am Miss Universe Thailand, thank you!" and I realized it WAS her & nearly died LOL!?!
Of course, the response to this is 'but I can't stay home sick/with my sick kid! I gotta work to pay this rent!' can we please acknowledge that the government has GOT to do better by workers to legislate more paid time off so that they CAN stay home sick/with their sick children?
I just want to say that Miss Universe Thailand was incredibly sweet and kind, and I really appreciate the time she took to talk to me and my wife while we were hanging out at Bangkok Pride today! It was so nice to meet you!
@MUofficialTH
🫶🏿❤️
We need to ban school attendance rules that compel parents to send sick children to school where they can infect others, as well as rules which unfairly penalize chronically ill & disabled children who cannot attend as many days of in-person classes.
@JulieViolet2
this is an unedited cell phone picture lol! she really does look like this in real life 😭❤️
don't feel ugly though!! a beautiful flower growing next door does not make your garden any less lovely than it was before 🌻
#AmbulatoryWheelchairUsersExist
Some wheelchair users walk or stand. Doesn't mean they aren't disabled.
I am permanently disabled and use a cane or a mobility scooter 95% of the time.
I have a chronic illness, severe pain & damage all over my body even though I don't 'look sick'
@Imani_Barbarin
Thankfully it's a fake screenshot by a well known content creator who is always making fake tweets, but no one seems to have noticed this despite the fact that it's clearly watermarked with the link to his podcast and the location is a joke, which is what he always does on these.
Correct! Don't do this. Instead, hire a sensitivity reader, who has lived experiences that you do not, who can help edit your work to make it more authentic and less racist. I am a sensitivity reader for Black, queer, and disabled characters. Don't be racist. Pay a Black woman.
This is a 🧵about why it's so important to get medical help, even if you can't afford it. It is so hard to break the habit of ignoring our own pain, because poverty won't let us get help. Because we have to. The number one killer in the US isn't heart disease. It's capitalism.
Telling systematically oppressed ppl that we must be kind to our oppressors ignores the fact that their policies & practices will not change based on our kindness. Racism was not created because we weren't nice to them. Our kindness will not fix it. It's not on us. It's on them.
These are some of my favorite photos of the lovely Miss Universe Thailand Uttaradit 2023👑💫 If you'd like to see more of her fantastic looks & support her, her insta is @ wo.walan❤️and she is also on the official Miss Universe Thailand Uttaradit page on facebook/mut.uttaradit 🙏🏿
So excited to share the art I did for the Disability & The Witcher TTRPG with
@mustangsart
! The PDF is going to be 100% free to download and will be released in June! Stay tuned.
Looking for more work in TTRPGs. Hit me up!
#ttrpg
#Witcher
If you're a yt person who calls your Black female friend 'strong' & wondered why it upset her, here is why.
Being 'strong' is not a compliment when systemic racism gives us no choice. If we're not strong, we're dead.
Don't tell us we're strong. Help us so we don't have to be.
I'm very tired of being asked if I'm 'comfortable' going to restaurants or events. It's not a question of 'comfortable', it is an inability to survive being infected with covid due to being immunocompromised. It is already being chronically ill & disabled & not wanting to die.
Remote work risks wiping $800 billion from the value of office buildings in major cities worldwide by 2030 as the post-pandemic trend pushes up office vacancy rates and drives down rents, according to a new report
I'm in a crisis right now. My mobility scooter has completely ceased to function. I have to ship it 3000 miles away for repairs. Without it I cannot work, so my life has come to a standstill. If you'd like to help, donate or rt please:
#DisabilityCrowdFund
As a content creator who uses captions on the media I create & consume, they are mandatory, not optional. Some of my viewers say they've NEVER seen captions on stream before. Let's change that with a list of resources to make our content more accessible. Please reply to add more!
Racist yt man demanded to know why She-Hulk had 'negroid features' on a group photo of Marvel cosplayers where I was She-Hulk.🙄
6 years later, I am featured as She-Hulk on the variant cover of A-Force
#1
. My best revenge is becoming a limited edition collector's item. 💅🏿
They don't.
I'm immunocompromised.
When ppl say 'only people with underlying issues die'? That's me. I'm one of the ones for whom the vaccine isn't fully effective, who can't safely travel, whose death gets dismissed as inevitable. Whose life gets treated like it doesn't matter.
Update: I have a chance to move into a wheelchair accessible apartment if I can pay the $800 deposit by Monday 2/11 🙏 I appreciate any rts or support towards this goal. I'm selling merch at FarpointCon in Hunt Valley, MD this weekend as well, so stop by if you can!
I've just been evicted, while also struggling to get my benefits renewed and repair my mobility device. This is the worst time to move but I'm not being given a choice 😔 Trying to save up for a deposit asap
Agreed. I don't see how things can ever "go back to normal" without a vaccine. Which is 12-18 months away. A lot of people don't want to talk about that.
Where is the article about how white people can use their privilege to stop the violence against Asian Americans? Black people have always fought for & supported all victims of racism. When will white people be called upon to dismantle the white supremacy that is killing us?
I have several more medical follow-ups & neurological procedures and all of this is mandatory for my survival but costs more money than I am legally allowed to earn. The US government's mandate to permanently tie disability status to income limits is killing disabled people.
@Karnythia
I was a cosplay guest at
#UniversalFanCon
& the money earned there would have helped pay for my ♿️repairs, medical care & bills so this bad news has hit me pretty hard. Any donations or signal boosts are appreciated, thank you <3
Shout out to everyone who has ever told me 'you should just get a service dog' like its easy, inexpensive & simple.
#Disabled
folks who DO have service animals, please share how much it cost & how long it took so we can get an idea of what the process is really like?
#disability
I created my first
#DoraMilaje
costume within 10 days of the
#BlackPanther
trailer dropping last year. I was POSSESSED. A flurry of broadcloth, vinyl, plaster, craft foam & paint took over and I debuted her at
@blerdconDC
. Many more
#Wakanda
costumes to come!
#cosplay
Millions of people are living with the uncertainty of inadequate healthcare coupled with inescapable mandated poverty. Medical care shouldn't be a privilege. It should be free. Instead, it's denied to those who need it most & gatekept behind a paywall thousands of dollars high.
So Twitter has wrongfully deleted the original account of
@SaekoIzzy
, who worked so hard for YEARS building an audience and delivering such iconic cosplay looks & hilarious clap backs. If you're over 18, love anime, cosplay & smart sexy ladies, you need to follow her. Ijs.
I am disabled & have been dragging my wheelchair up & downstairs for years.
I am about to move into an accessible apartment.
Please help me do this by RTing or donating. Thank you!
All of this is why I avoided treatment for over 20 years, until it was clear that I had no choice. Regardless of your ability to pay, you deserve to live. Poverty is not a moral failing. Your life has value beyond measure. If you are in pain, please get help before it's too late.
Because I couldn't afford treatment, I didn't try after the first huge medical bill. I ignored migraines, vision & hearing loss, & periodic paralysis. I crowdfunded a wheelchair. I tried my best to survive.
And then I fell in love with someone who forced me to get an eye exam.
@OddsocksTango
I watch the Miss Universe pageants religiously and I loved Miss Universe Thailand's Q&A segments and all her outfits so much so I was seriously like 'wow you look JUST like her' like a total fool LMAO 😭🫠😂😭🤣 she was so nice, bless her fr 😭🙏🏿❤️
This has happened to me and many of my friends. Because able bodied people don't see wheelchair users as people. They see us as obstacles, issues, something to 'deal with' or 'fix'. It is dehumanizing & degrading. Don't ever touch a disabled person or their chair without consent.
Well, it finally happened. Someone grabbed my wheelchair and pushed me down the street — as I repeatedly asked them not to — because “I was in the way.” I would like for that to never happen again thx.
how about removing the poverty mandates on disabled people with SSI/SSDI if you really want to provide the key to equality, opportunity and independence?
Being a wheelchair user at bus station restrooms is always the worst because you're competing with every single abled woman that has a suitcase for the ONE wheelchair accessible toilet stall. They think they need the space for their damn luggage. Ableds, please stop doing this.
I am permanently
#disabled
& flying today.
I get out of my Lyft at the airport.
I begin to assemble my ♿.
The yoke is uneven. It gets stuck.
I struggle to remove it.
A man asks if I would like help.
I turn ready to say no, & see that he is a TSA employee in uniform.
@TSA
I am incredibly honored to announce my partnership with
@IntelGaming
as part of their initiative to support marginalized creators. I can't wait to use my new powerhouse PC, custom-built by
@PowerGPU
, to create more inclusive, diverse & accessible content. Thank you!
#sponsored
So fun little side note The color inspiration for Nubia's gold Eyeshadow came from
@thatjayjustice
. years ago she dressed as the character but with her own spin. She had this great striking gold eye makeup at the time an it really stood out to me.
I can't afford to replace it.
This is not okay. I'm not okay. I'm terrified that when I get off my flight, my ♿ won't work & there will be nothing I can do about it, because a
@TSA
agent couldn't wait 30 seconds to find out if it was okay to step on my mobility device. 😭
I'm Jay Justice. Cosplayer, writer, editor & consultant. I create programming for conventions, libraries & schools, & promote marginalized voices in comics, gaming & literature. For booking, contact me at ThatJayJustice
@gmail
.com. Here's a thread featuring my work!
#VisibleWomen
A friend who just saw
#Wandavision
asked if I was gonna do a
#MonicaRambeau
costume. I said 'I already have 3. She is my favorite superhero of all time. We finally got her in live-action, portrayed by the amazing
@TeyonahParris
. Girl what do you THINK?' FOREVER my
#CaptainMarvel
!
I have been permanently disabled and chronically ill since I was a child. I live with severe chronic pain in my entire body. I am also on SSDI, which means that I am not allowed to earn more than $15k a year or I lose my health insurance. This makes medical care unaffordable.
Star Trek 🤝 Cosplay
Infinite Diversity in Infinite Combinations
Someone once asked me why this cosplay version of Geordi has 4 pips. I said 'Because he's the Captain.'💁🏿♀️
Here's me as Captain Geordi La Forge for day 31 of
#ACosplayEveryDay
. Photos by
@DTJAAAAM
& Jason Colflesh.
The combination of extreme constant pain & the knowledge that healthcare is unattainable leads to not getting help until it is too late. It is a trap that has taken countless lives. People who deserved to live but were told that healthcare was only for the privileged. Not us.
Casual reminder that I will send free Home Chef, Hello Fresh & Marley Spoon meal boxes to anyone residing in the United States, no questions asked, if they DM me an email address. No catch. I just want to help as many people as I can. No one should have to go hungry. RTs are ok.
I love how well my P100 mask goes with my Tali hoodie.💜 I am always masked bc I'm immunocompromised, disabled & chronically ill, the pandemic isn't over and I am not trying to collect any more illnesses, thanks 😂 Extra protection from COVID feels very Quarian to me 😌😷
The crazy thing is, people don't have to 'get it' to simply allow disabled people to live?? without harassment?? Without demanding to know their medical history? You don't need to know why/how someone is disabled to be kind.
#AmbulatoryWheelchairUsersExist
The doctors say that if I had not gotten treatment when I did, I could have died. I have to be extremely diligent with my medication to prevent this. Medicare refused to cover it so I had to pay out of pocket. 1 month of the generic costs $260. That is over 1/3 of my SSDI check.
I just saw someone say that disabled people should be paid less than able-bodied people, that we don't deserve a living wage because 'a living wage varies from person to person', that if you're 'not high functioning' you don't need a living wage. Are we not alive?
#ableism
Because I couldn't afford treatment, I didn't try after the first huge medical bill. I ignored migraines, vision & hearing loss, & periodic paralysis. I crowdfunded a wheelchair. I tried my best to survive.
And then I fell in love with someone who forced me to get an eye exam.
One of the reasons plastic straws only on request doesn't work is that it enables gatekeeping & discrimination. Servers have interrogated myself and many other chronically ill disabled people to determine if we're 'disabled enough' to be allowed to drink water.
#StrawBan
#ableism
@thatjayjustice
And that is why we need to set a balance on this. Plastic straws are a necessary help to many with disabilities and the outright ban would rob people of this tool. I feel plastic straws should be available on request.
I'm so excited to watch
#SheHulkAttorneyAtLaw
!! She-Hulk has always been one of my favorite characters. I love cosplaying her. It was an amazing honor to get to be Jen for a Marvel Comics variant cover 🥹 I'm so ready to finally see Shulkie in the MCU!! 💚
#SheHulk
#cosplay
Because he is a
@TSA
agent I show him the issue.
He asks "can I step on this?" & before I can say "NO DON'T STEP ON IT" he stomps on the ♿ battery.
There is a loud crack.
I scream. I tell him what he has done & ask his name for the report I will be filing. HE RUNS AWAY FROM ME.
I have filed a written complaint with
@TSA
. I have been interviewed. I almost missed my flight to report this incident. They are checking the surveillance footage to find this man. There is a huge crack in my ♿ battery. It's probably not safe to use and could fail at any moment.
I moved in with my girlfriend. She immediately noticed how massive the fonts on my pc are & asked if I had ever considered glasses. I hadn't, because that involved going to the doctor and that was for rich people. She would not take no for an answer. So off to the doctor I went.
How to support me & my work:
1. Hire me as a sensitivity reader, editor, consultant or speaker. Request me as a convention
#cosplay
guest. Contact: thatjayjustice
@gmail
.com
2. Share or donate to my
#GoFundMe
to help me get medical care & a new wheelchair 💜
The neurology team discovered that I had over 4x the amount of pressure on my brain that you're supposed to have & did their best to relieve it. The cause is still unknown. I have been prescribed medication, but the optic nerve damage is permanent. My eyesight will not improve.
If you grab a wheelchair user from behind to 'help' without asking & they accidentally elbow you in the dick, you have no one to blame but yourself
#AskDontGrab
My Pride fit for
#BangkokPride2023
#DisabledAndCute
#BangkokPride
🥰🌈
Alt text : 3 second video, a Black person wearing a strapless rainbow dress & silver pointy flats, in an electric wheelchair waving a large rainbow clack fan in front of a "Love Has No Gender" sign at Pride.
The first doctor I saw was alarmed at the amount of nerve damage in my eyes and referred me to a colleague.
The second doctor I saw was very alarmed at the massive amount of swelling as well as nerve damage & asked how quickly I could get to a top neuro-ophthalmologist he knew.
I will probably get a lot of grief for saying this, but maybe mid pandemic with people dying of treatable non-covid causes because every ICU for 3 states around them is full, is not a good time to have mass gatherings & conventions. Please get vaccinated & be safe if you can.😢
Alabama man dies of cardiac event after 43 hospitals with full ICUs turned him away.
In his obituary, Ray Martin DeMonia’s family urged people to get vaccinated against COVID-19 to free up resources for non-COVID related emergencies.
Happy Birthday Avery Brooks! I didn't have time to change into my Starfleet uniform for this photo, but when he saw me he said 'Hello Nubia!' and knew EXACTLY which comic my cosplay was from! It was such a great experience🥰
I knew this would be expensive, but I was now being told that there was a very high risk for stroke, blindness, and/or death, so away we went. At the hospital for over 24 hours. My eyes were dilated twice because it wore off before they could finish all the tests. So many tests.