my fav calvin n hobbes joke and no one ever puts it anywhere
occasionally subtle
$LAYYYTER

izzy's playlists!
KIROKAZE
Cosmic Funnies

ellievsbear
sheepfilms
"I'm Dorothy Gale from Kansas"

blake kathryn
hello vonnie
Not today Justin

Origami Around

Jar Jar Binks Fan Club
todays bird
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TMBGareOK. The Official They Might Be Giants tumblr
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Kiana Khansmith
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let's talk about Bridgerton tea, my ask is open
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@krazycat6167
my fav calvin n hobbes joke and no one ever puts it anywhere
zinetober day 12....
I would scoop this up so fast if I saw this for sale at a booth.
So this is not a plea for money. This is something that surprised me, and chatting with people on discord, they were unaware of as well.
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.
its a battle every time i shower
hope you don't mind op
I'm very excited to see your project hail mary posting, but every time I see the #phm my brain tries to fill it in as phineas hnd merb
PHINEAS HND MERB
nuclear power is impressive until you get up to why. "we use the most precisely engineered machinery ever created to split atoms to release energy" oh yeah how come? "boil water to turn a fan" get the fuck out
The power of atom turns out to be, yet again, the power of steam
Quote of the day
My mom likes to tell me about how when I was a little kid riding public transport with her I'd always smile and giggle and chat with weird old ladies who smelled like cat pee and homeless folks and strangers dressed in bizarre outfits but any time a tidy and respectable businessman in a suit and tie waved at me I'd immediately clam up, and she takes a great deal of pride in my supposed inherentability to clock personalities but the truth is I do vaguely remember those bus rides, and it was never about the clothes or the hair or the smell, but more because everyone "strange" asked interesting questions and listened to what I had to say and seemed to think about what I said while the neat and tidy and rigid folks only ever acted like they were going through the motions, which was boring as hell and also pretty annoying
Well-to-do finance manager with tidy shoes: "Why hello, sweetheart. Can you say 'hi'? Aren't you cute. Are you on a trip with your mom?"
4 year old me: why must we do this
Fantastic old woman in the leopard print coat: "Why yes, my tooth IS real silver! Nobody ever asks me that. Do you like cats?"
4 year old me, suddenly paying attention: Finally, A Person Of Intellect
today I found out my mother doesn't know what dandelions are and now I'm wondering what other strange secrets she's been quietly harboring
Where do you live that you don't have dandelions?
we have dandelions EVERYWHERE, they are basically our State Weed, it is absolutely impossible that my mom has never interacted with a dandelion before, this requires further investigation
So after extensive interrogation I have an update:
my mom is in fact aware that dandelions exist. she temporarily forgot the name and there was some miscommunication.
the truth is actually weirder
she's aware dandelions look like this
she is familiar with this flower. she knows the name of this flower. she declines to believe, however, that these are also dandelions
she does not believe these are the same plant. I tried to explain, and she thought I was either misinformed or lying. so I asked her what exactly did she think the yellow ones were called?
she answered, with complete confidence: Daffodils.
gosh I enjoy this website
then wtf is a daffodil......................
More of you need to learn about these ☝️
it's wild that popular discourse around migraines is that there are too many people who claim to have migraines but "just have bad headaches". this is the exact opposite of my experience? i'm still trying to convince several of my friends that their "bad tension headaches" that are unilateral, throbbing, cause light sensitivity, nausea, etc, are migraines lmao. migraine is underdiagnosed and undertreated by every metric i can think of.
this narrative is not harmless! it prevents people from getting treatment that could really benefit them. so i would like it to die. thank you.
As a guy who went to see a neurologist only to "rule out migraines" because I thought I had "tension headaches at worst and also it's not that bad really" only to realize by tracking my headache days that I have very bad chronic migraines just with no aura (most people with migraines don't have them), I co-sign this 100%.
Just starting abortive medications already improved my quality of life so much and now that my doctor started me on preventatives, I might actually be able to have more than a handful of headache-free days each month.
Migraine is frequently misdiagnosed as chronic sinusitis or tension headaches according to research. Mostly because people have a very rigid (inaccurate) idea of what it actually is.
But even if it's not migraine, you still deserve treatment for your headaches. Just because someone else has them worse than you doesn't mean you don't deserve relief.
Learning about the different types of migraine and headache disorders can help you better understand your symptoms and discuss them with you
yeah i found out awhile back that the 'pressure headaches' that i get that 'aren't that bad' (but still leave me feeling sick and dysfunctional all day) were migraines. i now take a low dose of a preventative medication and the number of shitty rain days i have per month has dropped from like ten to two. it's great.
In my experience anyone who has chronic pain of any kind ALWAYS under diagnoses it in part cause people who DON'T have chronic pain always tell them how it's Not That Bad Just Get Over It and it takes a lot of fighting to get anyone (including doctors) to do anything about it. Fucked if I know why. Everyone seems to think we're making it up. I've never met anyone who is making it up.
at some point in being autistic it becomes really clear that everyone wants you to come up with solutions to problems you've never been helped with
i don't know how to fix our communicative problems, you're the source of it and it's exhausting to be treated as irrational for not responding correctly to small talk, do you think you could help a disabled bitch out and not put the onus of solving the problem on me, the one who is constantly excluded and treated as a freak
and then when you point this out they're like "but we literally put up with you, could you do something for us please?" and it's like. you put up with me?
Hey can you guys reblog Cheeseburger so he can take a sunbeam nap on lots of blogs. No other reason I just want you guys to see him.
So, Cheeseburger died on November 21st after an unfairly short battle with an unfairly rare cancer that is rarely seen in cats. I only got to spend a month with him after his diagnosis, and losing him has been the greatest heartbreak of my entire life so far. He was my best friend and my soul cat, and he was there for me when I was completely alone, for twelve long years.
I made this transparent PNG the night he died in preparation for one of the many ways I was going to memorialize him--a surface rug in his likeness that I planned on laying directly in the line of his favourite sunbeam. And I uploaded that PNG here, because this is the website where people post their cats.
I was not expecting the reception I got. Many people have pointed out that this post has more reblogs than likes, and how insane that is in 2025 when reblog culture is at an all time low. I didn't even talk about the fact that Burger passed away in the original post, it wasn't a tearjerker reblog bait or anything like that. People just loved Burger that much, in the same way I fell in love with him at first sight. He was such an ugly kitten.
Anyways, it's really special to me that so many people have reblogged my best friend. I made this PNG to memorialize him in a completely different way, and you all wound up doing just that in ways I never even imagined.
Thank you. Wherever he is, I know the sun is shining.
reblog to stare at your mutuals like this
Layered cliffs under clear sky by qing ying