It used to be that prosthetic limbs and style had little to do with one another. Prosthetic limbs have typically had as much style as
orthopedic shoes, sheathed in beige fabric to cover the metal and
plastic parts within. They lacked originality, they lacked flair and they certainly didn’t reflect the wearer’s personality. Now, that couldn’t further from the truth.
It isssss like truly this show. Like hiring and actual Deaf actor is pretty great. I hope this gets this dude more roles. Shout out WaWa he did a fucking great job.
“Warren Snipe: Be on the look out of Lauren Ridloff, Michael Spady, CJ Jones, Michele Banks, and me. There’s more to come!”
“ It’s a huge deal for the Black deaf community & for POC deaf talent in general. We’re not repped enough nor are we called for rolls often because we are not written into scripts. We’re far more likely to be overlooked or passed by than our white fellow actor/actresses. We are extremely talented in many areas and STILL have to fight to get a notice. “Hollywood” would people who just simply doesn’t fit the character. If the character called for a black deaf person, sometimes the ethnicity needed, would get changed to prevent backlash and etc. I’ve seen it firsthand. Right now, I know about 5 POC deaftalents making waves now.. but there are so many of us who can fit the bill. Know what I mean”
London-based student Lewis Hornby is a grandson on a mission. When he noticed that his dementia-afflicted grandmother was having trouble staying hydrated, he came up with Jelly Drops—bite-sized pods of edible water that look just like tasty treats.
Each of these colorful “candies” is made up of mostly water, with gelling agents and electrolytes making up just 10% of their composition. Available in a rainbow of colors and presented in packaging reminiscent of a box of chocolates, Jelly Drops are an easy and engaging way to avoid dehydration—a common problem for those suffering from degenerative neurological diseases.
“It is very easy for people with dementia to become dehydrated,” he explains. “Many no longer feel thirst, don’t know how to quench thirst, or don’t have the dexterity to drink.” With this in mind, Hornby set out to find a solution. In addition to seeking advice from psychologists and doctors, he opted to “experience” life with dementia himself through the use of virtual reality tools and a week in a care home.
Once he was familiar with what dementia patients need, he brainstormed what they want. “From my observations, people with dementia find eating much easier than drinking. Even still, it can be difficult to engage and encourage them to eat. I found the best way to overcome this is to offer them a treat! This format excites people with dementia, they instantly recognize it and know how to interact with it.”
Case in point? Hornby’s own grandmother’s reaction: “When first offered, grandma ate seven Jelly Drops in 10 minutes, the equivalent to a cup full of water—something that would usually take hours and require much more assistance.”
some things that horror movie culture has taught you are scary…. are just ableist
….clarify?
okay sure. psychosis? scarier to have than to know someone who has it. DID? im more a threat to myself than people around me. wheelchairs and psych meds? are tools that help people live more functional and flexible lives and are not judgments of the persons character and for sure are not scary things. and for real, intellectually disabled people are not threats, but movies love to make them villains because they act different and understand the world differently. and people with notable physical differences? people who’s bodies look different? people with scars, growths, amputations, etc? are literally just people. and seeing themselves painted like monsters on the big screen is absolutely sickening and damaging to how society will see them.
its not only bad writing but its extremely harmful to people who actually live with conditions that are misrepresented in media. when i found out i had DID, my mom freaked out because her only point of reference was Sybil. when i was younger and first went on psych meds, i thought it meant i was set on a track to be a bad person, because in so many movies and video games you find out the bad guy has medication in his bed side table for some sort of psych disorder. the worst thing a hallucination has ever made me do was wake my mom up at 3 AM to check my bathroom to see if the bugs i saw everywhere were real and the worst thing an “episode” of any sort has made me do is hurt myself. my ptsd doesnt make me kill people, my alters dont kidnap people, my autism doesnt make me so morally unaware that ill murder for senselessly, my ocd doesnt make me hurt people etc etc etc
literally the only “horror” is the ableism. and the only way you can write good horror about disability and mental illness is if the focus is on how society and the medical field treat us rather than focusing on how we are apparently so scary, threatening, and bad.
The new Venom movie has a scene with intense flashing lights (the lab entry scene) and I received no warnings and had to leave (just for that scene) as I am epileptic!!! PLEASE share this since I’ve seen NO warnings being shared and this is very important and can prevent people from having seizures etc during the film.
If you’re going to watch a terrible movie, at least stay safe doing it!
The app is called Be My Eyes and allows blind people to phone or message for help. The app seems to allow video and photos to be sent and the sighted person on the other end can send a message to the blind person, answering whatever inquiry they have.
[This is a set of screenshots about the app called Be My Eyes.
First photo: The overview page for the app. The top says “Be My Eyes- helping the blind.”
Second photo: The preview page on the app store. It shows two phones. The one on the left is titled “Volunteer” and says “Join the community and help it grow.” The one on the right is titled “Blind.” The phone under the title has “Call first available volunteer,” written in large font.
Third photo: More previews. Shows the messages between two people texting each other. The visually impaired person sent a picture of two cans of food, and is asking which one is beans. Another example shows the person sending a picture of their milk carton, and asking if it is expired.
Fourth photo: An iphone lock screen. A notification from the app says “a blind or visually impaired person is calling for help.”
Fifth photo: The profile page of a sighted user named Francis, who speaks English and Español. The top says there are 74,768 Blind and 1,033,846 Volunteers using the app.
Sixth photo: Text that says “Learn how to answer a call. When a blind or visually impaired person requests help, the app notifies multiple volunteers, and the first to respond is connected. The notification might look different whether your phone is locked or unlocked. Here you can try both scenarios.
Seventh photo: A notification from the app on an iphone home screen. The instructions say to pull the notification down or tap it to answer a call.
Eighth photo: The same notification on an iphone lock screen. The instructions say to tap it or slide it to answer the call.]
Please reblog the version of this post with image descriptions. It’s a service for blind folks, posted about in a format blind folks don’t have access to (without the descriptions).
Also, if you’re willing to download and use this app but you don’t go out of your way to add image descriptions to the images you share, please reevaluate that! Contact me if you need help adding image descriptions to things.
This app is actually very useful. The way sighted people are talking about it is not.
It’s ok to use mobility aids as much or as little as works for you.
You are the boss of your own body. You have done nothing wrong.
I support you. You are important.
Making shitty jokes or being an asshole about fat people who need mobility scooters is wrong.
Anyone who replies to this with something nasty about fat people who use mobility scooters will be blocked.
I don’t care if you’ve followed this blog for three years. Immediately blocked.
You are making people afraid to use the tools they need to be able to use, that exist to make life easier for them. That is NOT ok. You should be ashamed of your behavior.
Go do better.
And I won’t get thinner if I ‘‘get up and do something “
No I won’t.
I don’t care what your personal knowledge of biology is. I live in this body and know better than you what it can do.
Some light in the darkness that is Gaming news right now
gaming is SO IMPORTANT for so many disabled people (myself included). There’s not many hobbies that have the range of interactivity and engagement that gaming has, while still being something someone can do with little movement or motor control.
I’ve met a few people who were very disapproving of my gaming hobby (was literally told to “go read a book” in a snooty way by one of them) and it frustrates heck out of me that they can’t see how important and fun gaming can be. Gaming isn’t passive like a lot of other hobbies recommended for disabled folks. Gaming is something to get pumped about and something that you can get better at! You can improve your gaming skills and feel accomplished!
if it weren’t for video games I would be a much, much more unhappy and unfulfilled person.
This is why its SO important to make gaming accessible to disabled people.
This new ‘trend’ of strobing when hit [Destiny/Assassins’ Creed to name a few] is very detrimental to anyone with a seizure disorder that is effected by strobing. A lot of people with motor disorders often have visual disorders too.
Developers really need to make flashy visual effects optional or toggled on/off in menus; not left as a fixed point.
Gaming is SO important to help with my motor skills and comprehension skills and making it inaccessible to some audiences is really detrimental.
^^^Really important commentary
video games are sometimes the only thing that will help keep me sane.
I’m crying : ’ ). Videogames are important for all ages and degrees of abled people. My grandma definitely has kept a somewhat sharp mind since she plays golden sun and pokemon feverishly, though apparently she was stuck at the Sky Pillar in Ruby for two months (arthritis problems).
i just wish we could get more games that relied less on violence and fighting but Diablo fuckin rules and i’m so glad this person found a way to make it work for them.
we need to make sure all the disabled have the tools and support they need to live the lives they want to.
There is a charity called Able Gamers that helps people with varying disabilities and gives them the chance to play video games. They work both with caregivers, gamers themselves and video game developers (both indie and mainstream)to help make video games more accessible on a software level as well as through assistive technology like Ken here is using. I urge everyone to check them out and donate if possible or spread the word about their foundation!
L.J.'s Obsessions 