I’m forced to because I make the most ridiculous spelling mistakes that completely change the comment.
“With” autocorrects to “without”.
“is” autocorrects to “isn’t”
Finally worked out why though - my right eye is impaired and I type exclusively with my right thumb (on mobile) so I’m not actually pressing the keys I think I am and I’m often hitting the “predict word” button instead of the space bar.
Looking forward to getting tactile keys on phones again!
My job somehow shifted from teaching IT to seniors to teaching SOSE to migrants
It has simultaneously been the most challenging, and most rewarding change.
I’m forced to edit myself down from my preferred 5000 word lecture to about 150 words with clip art.
It’s slowly helping me become less of a rambler.
Except for the “post restraint collapse”, I get home and I can’t hold it in anymore, cue the explosive verbal diarrhoea.
At work, fewer words are better.
But in my own personal life I feel that the fewer words I employ to convey the way I feel the less nuance I’m embedding in my message and what is communication if not the conveyance of the core message, failing to express myself clearly would be counter-productive so surely explaining in more detail is beneficial, hello? Are you still listening? Why have your eyes glazed over.
Call her doctor
I should have been more specific. Find a time when she’s not doing anything urgent, tell her it’s time to call the doctor, pick up her phone and dial the doctor, put them on speaker and put the phone down next to you while you body double your partner as they gone through the motions of locking in the appointment.
While on the phone your partner can also give third party authorisation. It’s the first thing I do when I meet a new provider, I give third party authorisation to my partner and mother so they can make appointments on my behalf (they can’t get results for me, but they can schedule things for me)
Call her doctor, make an appointment, save it in her calendar, remind her in the lead up, drive her there, get the referral. Walk her to the post box to send it off, sit next to her to phone the intake office to confirm they got the referral, set appointments on her phone for every 6 months to sit with her and call to check the cancellation list until you get an appointment. Drive her to that appointment.
If she has ADHD, the steps involved in getting a diagnosis are bigger than Mt Everest, she will need a neurotypical Sherpa.
He’s also not a racist!
Yeah it’s pretty regulated here, you present your evidence for being a medical cannabis candidate to your GP/PCP (or they tell you they think you’re a candidate) who refers to you to a clinic that specialises in cannabis, the intake appointment was 2 hours long, they prescribe specific products based on your symptoms and needs, then script gets sent to a compounding chemist and you go and pick up the medication from the chemist, the same chemist that you’d go to for advil and beta blockers.
As if there wouldn’t be a black market for menthols if they were the only product to be banned.
And if my yeasty poison goes bad, I’ll just pour it over some poisonous leaves, I love salad.
Don’t forget to season it with minerals you chipped off a rock in a dried out lake bed.
I can’t imagine they’d prescribe oil that needs to be further processed by the patient. The printed dosage instructions from my doctor just say to take 0.5ml sublingual, and the pharmacist didn’t say anything otherwise. It was topaz t25 oil, my friends tried some because I was convinced it was the wrong product or something, and it worked for them.
I have issues with other drugs too, like I still puke when dosed up on ondansatron, and the reason Im prescribed cannabis is because I can’t take opiods for my chronic pain condition, even 8mg of codeine causes my respiratory rate to drop dangerously low. My chronic pain is the result of a genetic disorder, so I’ve just assumed I metabolised things badly, though Ive asked several doctor about it and because I’m in the public healthcare system I can’t access CYP2D6 testing to know for sure.
This is a common misconception with “charity shops” in the UK and “opportunity (op) shops” in Australia.
The assumption is that the charity/opportunity is for people doing it tough to be able to buy cheap clothes and home goods.
But the “charity” is because many shops like this are partner retailers of larger charity organisations, eg: the “profit” from Salvos stores helps indirectly fund Salvation Army Housing and food relief programs.
The opportunity comes from who they hire, if you’re disabled or elderly, these shops are more likely to hire you than other retail providers.
But of course, a large number of charity and op shops abuse their staff as much as Amazon and Walmart do. Wage theft and unethical labour practices galore
I quit caffeine a month ago (my neurologist is convinced my redbull “addiction” was causing the migraines I’ve been having since I was 6) and it’s no skin off my back to quit for 6 months to prove him wrong.
Only the insomnia!
I used to have a red bull right before bed to help me relax and sleep soundly, now I’ve got nothing (weed makes me want to clean my house then throw up)
I haven’t had any caffeine cravings, but I have started hallucinating from the sleep deprivation. I was told caffeine withdrawals usually only last 2 weeks so I’m wondering if this is just my natural sleep cycle shining through.
I’ve got a sublingual melatonin tincture that I need to remember to use because it helps somewhat, but despite multiple alarms and post it notes near my bed I completely forget I have it as an option.
My neurologist told me to give up caffeine, been 1 month so far. Genuinely haven’t noticed a difference in my life yet, turns out in the short term I was addicted to the taste of redbull, not the caffeine.
I’m thinking I’ll have to give up weed too since I’ve started getting hyperemesis every other time I smoke. (I’m prescribed a thc oil but I genuinely feel nothing when I take it, even if I take 10x the dose, so 🤷 )
And if I’m giving up weed I might as well give up cigarettes too…
Not nicotine though, you’ll pry nicotine from my cold, stroke induce dead hands. I’ll be chewing on this gum till the noise in my head stops.
I managed to go all of 22-28 never once being carded for anything.
When I hit 30 I started getting carded for things I’d never been carded for before, even the milk bar I’d bought smokes at for 10 years, same guy and his son running it, suddenly started carding me.
That’s how I learned the ID that I’d been carrying around for 10-11 years since getting my photo ID in highschool was functionally useless, because hardly anywhere would accept it as legal ID despite it being legal ID.
I had to keep the website for the government list of ID boolmarkef so I could show doubtful cashiers that my ID was indeed federally accepted, legal and valid ID.
I went to try and get a different type of ID last year which is how it found out that despite being born in my country to a citizen of my country, and having my birth recorded and receiving my birth certificate. Somehow I’m not actually a citizen of my own country and I can’t get a passport…so I’m trying to navigate that system but that’s extra fun and confusing because I have neurodevelopmental issues and no one to help me understand what I need to to do.
I just want to be able to buy alcohol as a person in their 30s, without having to jump through impossible hoops to prove that I’m not not 17.
I’ve got smile lines and the beginnings of crows feet, I am weathered! Why am it getting carded now
It helps that I’d had several previous surgeries, so I’d had practice at keeping my cool. Plus my surgeon was in discussion with me for months with multiple consultations to really understand the issue, I don’t think I could have possibly been in safer hands.
Well either it’s 1 in 10,0000 in my country, or the department of health, my surgeon and GP are all missing a zero… which isn’t more likely because there’s no way our risk would be that much higher than the UK, and the NHS public health resources is 100,000.
Depending on what you’re treating, 50% sounds pretty good.
I remember when I went for my last surgery and I was signing all the consent forms, my doctor was emphasising the 17% chance of this known lifelong complication, and the increased 4% chance of general anaesthesia fatality (compared to 1 in 10,000 for general public).
My mum was freaking out because when she had the same surgery she’d been seen much earlier in the disease process, she wasn’t expecting such a “high” risk of complications in my care.
But all I was hearing is that there’s an over 80% chance it will be a success. Considering how limited and painful my life was by the thing we were treating, it was all no brainier, I liked those odds. Plus my condition is diagnosed 1 in 100,000 people, so how much data could my surgeon really have on the rate of risk, the sample size would be laughable.
Still the best decision of my life, my surgeon rolled his skilled dice, I had zero complications (other than slow wound healing but we expected and prepared for that). I threw my crutches in the trash 2 years later, and ran for the first time in my life at 27 years old after being told at 6 years old that I’d be a full time wheelchair user by 30.
Unfortunately the models are have trained on biased data.
I’ve run some of my own photos through various “lens” style description generators as an experiment and knowing the full context of the image makes the generated description more hilarious.
Sometimes the model tries to extrapolate context, for example it will randomly decide to describe an older woman as a “mother” if there is also a child in the photo. Even if a human eye could tell you from context it’s more likely a teacher and a student, but there’s a lot a human can do that a bot can’t, including having common sense to use appropriate language when describing people.
Image descriptions will always be flawed because the focus of the image is always filtered through the description writer. It’s impossible to remove all bias. For example, because of who I am as a person, it would never occur to me to even look at someone’s eyes in a portrait, let alone write what colour they are in the image description. But for someone else, eyes may be super important to them, they always notice eyes, even subconsciously, so they make sure to note the eyes in their description.
I guess my question would be, why do you need the picture as a visual aid, is the accompanying body text confusing without that visual aid? and if so, by having no alt text, you accept that you will leave VI people confused and only sighted people will have the clarification needed.
If your including a picture of a table with nothing on it, there’s a reason, so yes, that alt text is perfectly reasonable.
Personally I wish there was a way to enable two types of alt text on images, for long and quick context.
Because I understand your concern about unnecessary detail, if I’m in a rush “a table with nothing on it” will do for quicker context, but there are times when it’s appropriate to go much deeper, “a picture of a hard wood rustic coffee table, taken from a high angle, natural sunlight, there are no objects on the table.”
I think so, but I don’t have the mental energy at the moment to sit down and figure out if the AI detection software is accessible either. I know some of my colleagues use programs to check student work for LLM plagerism, but I don’t assign work that can be done via an LLM so I haven’t looked into that, and that’s different from the AI images.
Yes and no, applying for accommodations is as fun and easy as pulling out your own teeth with a rubber chicken.
It took months to get the paperwork organised and the conversations started around accommodations I needed for my disability, I realised halfway through I had to simplify what I was asking for and just deal with some less than accessible issues because the process of applying for disability accommodations was not accessible and I was getting rejected for simple requests like “can I reserve a seat in the front row because I can’t get up the stairs, and I can’t get there early because I need to take the service elevator to get to the lecture hall, so I’m always waiting on the security guard”
My teachers knew I had a physical disability and had mobility accommodations, some of them knew that the condition I had also caused a degree of sensory disability, but I had nothing formal on the paperwork about my hearing and vision loss because I was able to self manage with my existing tools.
I didn’t need my teachers to do anything differently so I didn’t see the point in delaying my education and putting myself through the bureaucratic stress of applying for visual accommodations when I didn’t need them to be provided to me from the university itself.
Obviously if I’d gotten a result of “you cheated” I’d immediately get that paperwork in to prove I didn’t cheat, my voice over reader just gave me the ChatGPT instructions and I didn’t realise it wasn’t part of the assignment… But that could take 3-4 months to finalise the accommodation process once I become aware that there is a genuine need to have that paperwork in place.