Just something I really want to share on here because it’s important.
Dear game developers:
Make your games more accessible by
Allowing Button remapping
Supporting multiple kinds of controllers
Supporting multiple types of inputs for when solving puzzles or clues
Match the color and or pattern puzzle
Follow the sound and controller vibration to find the mcguffin
Allow for zooming in and out if you’re doing any kind of “pattern alignment” puzzle.
Subtitles on everything, for fuck’s sake
If your motion/camera thing’s instructions start with “stand up and….”, rethink your design.
Allow for adjusting the field of view
Aim assist.
If someone is struggling with a puzzle or task, start offering tool tips and hints on screen
Remember that the goal is not to have the player play the game like you would. The goal is for the gamer to have fun and experience the game and art you’ve spent so much time and energy to create in a way that brings them joy.
Removing and avoiding harmful tropes around disability - physical or otherwise.
i love when i see another cane user/ disabled person in public and we make that eye contact of solidarity
like yes!! you are like me!! i am like you!!
So many people wouldn’t have asthma in the first place if it wasn’t for these corporations…Shifting blame from actual culprits to people with asthma (and people who can’t help but use plastic straws at that) is peak capitalism.
I saw a post saying that stimulants for ADHD are life saving medications because they reduce car crashes and while stimulants are very important for people with ADHD they just... aren't life saving.
some medications you will die without. stimulants for ADHD are not on that list.
when other disabled people talk about life saving medication we don't just mean "very important" we mean "life saving"
I would die of organ failure caused by inflammation from lupus if I didn't have my biologic. diabetics would die of diabetic ketoacidosis without insulin. people with asthma would suffocate to death without their inhalers. that is what it means to have a life saving medication.
you can emphasize the importance of a medication without comparing it to truly life saving medications. it just comes across really insensitive when you compare lower risk of car crashes to guaranteed death without a medication
like, the shortage of stimulants is absolutely detrimental to people with ADHD but it's not comparable to a shortage of a life saving medication. without a stimulant people with ADHD would still live, without insulin diabetics would die. when stimulant prices are inflated and people can't access them it is hard but it does not equate to death. when people with life threatening autoimmune diseases can't afford their medication it does equate to death.
if you want to talk about the importance of stimulants for people with ADHD and the negative effects of the shortage that's great! but refer to the medication correctly- it's life changing, it's not life saving
This is an archive link of a previous post I made on January 23, 2025, so I can grab the link for citation and inclusion in thesis appendices. If the link doesn't display the text or you aren't a member of the community in which it was posted, this is what it said:
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I'm running a survey for my graduate thesis at Delta State University about how social friction is perceived in interactions between disabled and able-bodied people. The survey probably takes about 15-20 minutes to complete, and I'm looking for respondents from individuals 18 or older who identify as disabled or partially-disabled. If you've already completed the survey, you don't need to do it again. As an incentive for participation, there's an optional raffle that you can participate in for the chance to win an Amazon gift card. Both the survey and the raffle are open to individuals outside the US!
"Let Me Get That For You": Analyzing Frictional Situations in a Disability Context (via Google Forms)
Thank you everyone who has participated in the survey so far, and special thanks to the people who helped identify places where the survey could be improved!
This research survey has received approval (IRB number 2025-037) from Delta State's Institutional Review Board.
As a part time user of crutches (specifically smartcrutches, hence the below image), I've found a couple small products have been able to improve the quality of my experience when using them out n about n decided i might as well make a post with them on :) i might add more as i try out other things in the future and such also
The first thing is a small storage bag to attach to your crutch, you can get ones made specifically for crutches, and smart crutch even has their own branded one for the sizing of their crutches, but I got a bag intended for use on bicycles and found that it fit quite well for a fraction of the price, and likely would also do so on normal forearm crutches. I can't put too much stuff in the bag for regular usage as it would throw off my balance but it's great to have my phone and some change in to be within easy reach.
The second thing is new ferrules, specifically I got flexyfeet's ferrules which are available in a variety of sizes to fit pretty much any crutch or cane, they have shock absorption and their flexibility also means I get a lot more grip and feel safer walking with them than I did with my previously very worn down standard ferrules.
This is that giraffe bottle i was talking about in case anyone else with complex needs wants it. It's pretty cool and I'm definitely keeping it in mind for when I eventually DO need to transition to something that doesn't need to be picked up at all.
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