free palestine 🇵🇸

You may need to learn how to set up your paints and such… but this is what people did, live, while the show aired. That’s what the show was for. I had family members create lovely works of art they enjoyed, which I still have on my walls, because William Alexander and Bob Ross both said:

SCREW METICULOUS CLASSICAL ART PRACTICES — JUST GRAB A PALETTE KNIFE AND BIG OLD BRUSH AND PAINT!

They freed a whole generation of people who were taught to paint detail and realism and exact representation of reality — people who largely gave up this kind of thing because it got tedious.

I watched the joy of family members as they rediscovered art as a messy fun spontaneous half hour activity.

Discovered last year I couldn’t look at my 2015 MacBook Air without it triggering nausea and migraines, and figured the screen died. Have been getting by on my phone, but concluded I really need a laptop again.

Saved up, realised I could afford a brand new MacBook Neo, and got one.

-And I couldn’t spend more than five minutes looking at the screen without massive eye strain, nausea, vertigo, and if I pushed it, I-need-to-lie-down-in-a-dark-room-for-hours migraines.

Looking up MacBook and Eyestrain explained what is going on. The liquid retina displays that Apple currently has uses Pulse Width Modulation or PWM. In order to give the screens a deeper depth of colour and contrast, PWM flickers between several hundred to thousand times a second.

And there is currently no way to turn it off. There are settings and apps to reduce it, but there is no way to stop the screen from flickering. Checked Apple forums, called Apple Support, and the time I could look at the screen kept shrinking. Got the laptop Tuesday, returned it Friday, today is Sunday and I’m still dealing with a vertigo migraine.

For MacBooks, it seems to vary on the computer model and the software it uses. In retrospect, the issue with my MacBook Air started after a major software update.

And it’s not just an Apple thing. Current Windows and Android screens do the same thing. There’s even a Reddit for people who are sensitive to PWM flickers to help find computers and screens that won’t trigger eyestrain and headaches.

So, yeah. This week has been a learning experience. But for those who are prone to headaches and migraines, this may be something to be aware of, cause I was not.

And this forces you to decide whether your autonomy matters to you more than the approval of the group - while they'll still act like you're on thin ice either way, if you give in at this point they know you're theirs forever, because now they've established a foothold, you've shown a moral weakness, which they will brand you with so it can be used against you in the future ("hey RICE-addict here doesn't want help break into the city records office") to force you to double-down and isolate you further.

See that bit at the bottom? Don't do that. Insert ParamedicGuy.gif going "Don't."

Other malicious spam comments I've gotten seemed designed to make an author question their writing, or outright encourage them to delete their stories from AO3. This one is different, in that it tries to get you to destroy the work on your own computer.

If you ran that command, it basically locates your Documents folder, then deletes everything in it, including all subfolders. It also does it without any prompt, so you have no chance to second guess your actions.

This is just fucking trolling.

Coincidentally, we just did training on a cyberattack similar to this, called a ClickFix attack. You can read about how that works here.

As a general rule, if ANYONE or ANY WEBSITE tells you unsolicited* to do anything in Powershell, CMD RUN, command prompt, shell command, or something similar, DON'T.

*There are legit reasons for running commands in PowerShell or the command prompt, but in those cases you are likely seeking out a solution to a problem you are already experiencing. Don't just run random commands on your computer as recommended by some unlogged-in guest on a fan fiction site.

Always think and consider before taking action, and get a second opinion from a trusted source. When I got this comment I was pretty sure what the command would do, and it took me about three seconds of googling to confirm it.

Ive been on estrogen since I was 16, 2 years and three months... and my cramps are debilitating. I turn suicidal for a week every month and i sometimes throw up from the stinging/dull pain combo. there is bloating, severe depression, mood swings and extreme dysphoria.

My endocrinologist said that i should beware because my brain is decepting me and that can hinder meaningful conversation in my last meetup a month ago. i swear that im not making this up.

painkillers dont even work on my third/fourth day (i start counting the first day from when i get depressed, the other symptoms start the next day, and there is alot of sharp, radiating cramps, headache and other shittery the third day)

what should i do? am i really such a fraudster? i cant keep going on like this. its reducing my quality of life. is it really possible for me to have this much pain at a 26-27 day cycle??

So, I don't say this lightly: your endocrinologist should go to to hell! You're not a fraud and your brain isn't "deceiving" you. Those are literal textbook symptoms of something like PMDD and it's actually vile of him to straight-up diminish your symptoms and do nothing about it.

My first suggestion is get a different endocrinologist, if you can. That person is committing medical neglect against you and its loaded with medical trans/misogyny. If you can, you do not want to have to continue dealing with that.

Secondly, I want to suggest you try to find an OB/GYN. You have a few choices for dealing with it. If your AGAB is on file, it might be hard to find one that will take you, especially depending on where you live.

If you AGAB is not on file, it'll be easier to get in but medical misogyny, coupled with medical transmisogyny/transphobia is going to make getting help harder.

This does not mean you're faking it or that it's not worth trying [speaking as someone who cannot get diagnosed partially because of bigotry!], it just means people are bigoted assholes sometimes.

You might have to try numerous doctors. I cannot emphasis this enough: if you can, take someone with you! Doctors WILL treat you better.

Sometimes even going to the ER when you're experiencing these symptoms to have them run tests to narrow-down what disability you're dealing with can help. But do not let your endocrinologist force you into believing that the pain you're living with is normal or okay.

I'm not sure if this helps but I hope so, Anon! Let me know if you have any other questions or need anything else, fr. <3333