[ID: screenshot of the box for adding an ALT ID. Text reads: image description, by adding an image description to your post, you are making it more accessible for screen reader users. end text, end id]
[image: a screenshot of the alt text in use, showing the id as white text on a black background. end id]
Not everyone who needs an image description uses a screen reader! I don't! (And can't, given my brain does not like processing sounds!)
I also can't read the bottom image! (And since when you click on the alt text box to view the image description and get exactly what is in the screen shot, I hope you can see why if I can't view the image, the alt id is exactly as inaccessible as the image.)
ALSO, when you click on the ALT TEXT to highlight it so you can copy-paste it into a word document in order to get plain text, as soon as you release your cursor, the site brings up the image as if you clicked on it rather than allowing you to copy paste the text! (Aka: you cannot copy-paste ALT TEXT so you can paste it into a format that is visually accessible, but also, I shouldn't have to keep a word doc open to copy paste image descriptions to make them accessible in the first place.)
My eyes do not like dark mode. It turns all those white letters into blurry halos of light, and then it makes it so I can't read anything else after because black text then turns to shadowy smears.
Like just. use PLAIN TEXT. Plain text. Nothing fancy. nothing that can't be changed by the user's theme and can't be copy-pasted and turned into whatever format a person needs in order for the text to be accessible for their specific needs.
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My friend @winterpower98 is going to school to become an ASL interpreter, so we've been practicing together for a few months. I mostly just checked her signing and didn't sign myself because I was slower and didn't want to take up her valuable practice time clumsily trying to sign. Still, I intend to learn if for nothing else than having a way to communicate when I had a migraine.
Then I got sick.
I'm honestly not sure what's wrong with me, but in early January, I got a bad cough, asthma issues, and other various NASTY symptoms (leaving out to not get too tmi). The symptoms got worse quickly and I ended up at doctors and urgent cares and ERs. They found that I didn't have any of the major contagious things, but still my lungs were crap, my voice was nearly gone (just a whisper), and I was badly malnourished and dehydrated. One very scary phone call from a relative and two days of forcing my raw voice to work well enough to talk to police and relatives later, I lost my voice completely (save for little squeaks and rumbles). That was six weeks ago.
Winter and I didn't practice ASL the first two or three weeks I was sick (and I was honestly in no shape to do it anyway). Being mute was... okay at first. Annoying but manageable. But then as time went on, it got ROUGH. Being trapped in my own head and unable to convey things in real time took a toll on my mental health that I honestly wasn't expecting. Imaging being unable to even laugh or make frustrated noises or make sounds when you're crying hard and having a panic attack? It was hell! I couldn't got to therapy, see a doctor by myself (had to write a script for whomever came with me), contact services and doctors that didn't have messaging/email (they'd call back anyway despite me saying that I was completely unable to talk), tell people what I needed during a panic attack or sensory overload, or get my intrusive thoughts out (I say the out loud and work through them to see they aren't logical). When one doctor got really frustrated with me and proceeded to insult and lecture me for a solid 30 minutes (in front of my other friend who got very close to losing her temper), there was no way to report it because I had to CALL to place a complaint. I was limited to typing on my phone when I needed to communicate and even THAT was slow and not always possible (can't type during a coughing fit or if I had to leave my phone charging). Getting people's attention to notice me or read a message was also difficult, so I had to sit quietly AND patiently AND ignored so much of the time that I eventually broke down crying.
Eventually, I started doing a little ASL again. I wasn't expecting how hard it would be to sign things when I had only watched before. My movements were slow and clunky, sometimes I did the wrong sign, and I could only "talk" to one person, but the growing pains were worth the feeling of ACTUALLY communicating again. It's only been a few weeks, but I can already express my emotions/frustration and convey simple concepts during a conversation (instead of typing and having the conversation move on before I finish or just not feeling like my words were worth the effort on top of breaking the flow of a conversation). Yesterday, my bestie/roommate decided to start practicing the ASL alphabet and asked for a list of words I used the most so she could understand me too.
ASL has giving me back some of my autonomy. With a few signs and some finderspelling, I was able to tell Winter that I needed to eat, wanted leftovers, there was a bowl in the fridge, and to please add water (easier to swallow with my irritated throat). I can ask how people are, tell them how I'm doing, or just be a little goofy because I want to (like quoting NADDPOD and telling my friends "fuck you, I love you, eat a rat").
While being unable to talk for 6 weeks (and limited a bit before that) is nothing compared to the experiences of the deaf/Deaf, mute, and nonverbal communities, it made me realize how hard it is to navigate the world when your speech is impaired. It also made me develop a new appreciation for ASL. Originally, learning ASL was a novelty to me that might come in handy when I had a hemiplegic migraine (makes it hard to talk), but it was mostly to help Winter in her studies. Now it just feels... important. Like something more people should learn, be aware of, and accomodate for.
Tldr; Being unable to talk for over 6 weeks (and probably many more weeks after that) made me realize how important being able to communicate is to mental health, how society is not made to accomodate people with limited to no verbal communication ability, why learning ASL is so important, some of the struggles that people with limited to no verbal communication go through, and the fact that I am privileged in a way that I've never considered before.
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