#and now look at us
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etho gem n joel hanging out for so long ... they did this for ME specifically im their biggest fan omfg
#been needing them as a trio for an entire year now basically *looks at my superhero au*#like guys. i'm their og fan u don't understand#when i made that trio in my au i had a wish and a dream they had BARELY interacted with each other all together#and now look at us#insomnya stays winning!!!!!!!#nya talks#trafficblr#joel smallishbeans#smallishbeans#boat boys#smalletho#ethoslab#geminitay#wild life smp#wlsmp#wild life#life smp#traffic smp#wild life spoilers#wlsmp spoilers#wild life smp spoilers#the life series#life series spoilers
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in days like these .. i miss pixie hollow online ... underappreciated gem that was ..
#⊱✿⊰ ┊ ˢʰᵉ ʳᵉᵃˡˡʸ ⁱˢ ᵃ ᶠᵘⁿⁿʸ ᵍⁱʳˡ ( ooc )#[ always water talent ...#baby grill i remember when every disney mmo was out there#and now LOOK AT US#/LOOK AT US/#disney is afraid of our potential now .#i know they have kinda knock off versions of them now but like#remember the golden years ...#when we'd all log onto our beat up computers ..#and played games that we couldn't run ....#bc that was me girl .#that was me .
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#Cesc is the reason why I started watching the premier a million years ago when he signed for Arsenal#and now look at us#ben chilwell#chelsea#chelsea fc
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out of curiosity (and because I’ve seen some interesting tag games lately), out of all your oc ships, which is your most beloved? which one is THE otp? the one that if you had to pick only one to create for for the rest of your life that you would choose?
#for me it would be rafe and charlie#I sigh and kick my feet and twirl my hair whenever I think about them#and they were supposed to be just a one shot AU!#and now look at us#it’s been a year and a half of them#charlie and john are a close second though#their perverse love is all that sustains me some days#tbd later maybe
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if you told me two months ago that the hermits would do a two day long charity stream together irl and then roadtrip for a week afterwards where they stay together in one to two airbnbs depending on location and cook for each other and just enjoy the time off camera i would explode
#I'm looking at twitchcon related fic in my drafts#everything has this yearning to it#this knowledge that it's a temporary one time thing that might never happen again#the 'we have to make the most of this because we will never get the opportunity again'#and now look at us#look at us#who would have thought#not me#i have thoughts
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me when. i was a high school freshman when i started this blog and tomorrow i start college. thanks for being formative during my high school years guys <3 i’m still obsessed w this show
#it’s literally crazy#i was ending my freshman year of hs when ATLA came out on Netflix and I got to rewatch it for the first time since I was like. ten#and now look at us#who would have thought#not me#atla#avatar the last airbender#l’oreal sokka speaks
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the fact that no one can govern without a strong trifecta….our system sucks!
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#YEAH THAT SOUNDS ABOUT RIGHT#Christ what am I doing here#I joined in the middle of shocked Patrick and shortly before the mishapocalypse#And now look at us#whats even the memes now there hasn’t been a fresh one in a while
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look how far we’ve come
#number is subject to change honestly#remember in s1 and 2 when we were saying??? how? are there none?#and now look at us#being delusional works folks <3#ted lasso
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Neil Gaiman really Said "oh so it's a queerbait If they don't kiss huh? Alright then"
#and he was SO REAL FOR THAT#WAS IT WORTH IT?#I WAS SO HAPPY TO JUST HAVE SEASON 1 BUT AGAIN#AND NOW LOOK AT US#good omens season 2 spoilers#good omens season 2#good omens 2#good omens 2 spoilers#good omens spoilers#good omens#shippy says stuff
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hiiiii! 9 and 42!
Omg hi Mimi!
9:Got any piercings?
I have two holes in each ear lobe and one nostril pierced. I used to have one ear cartilage done but it closed up.
42:The last thing I ate
I had a sweet potato sushi roll and now I’m drinking a strawberry boba milk tea 🧋
#Mimi you are a celebrity to me#your polls always came across my dash even before I followed you#and now look at us#ask games#mail bag 💌#izvmimi
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and if i said this part of ms gaga’s paparazzi was my final push to make 42455 exist in my flying stars au. what then .
#he’s backstage at their shows …#this started bc of a joke i was gonna make abt making a miro harls paparazzi edit#and now look at us#flying stars band au#yap yap yapping
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Thinking that some ideas are destined to become shitposts and then finding out that they are actually good once i start working on them seems to be a trend with me lately
I mean who would have thought that fem!Shrek would turn out to be such an adorable little ray of sunshine, you know?
#but HAVE YOU SEEN HER?#also in the beginning i thought Princess Charming would be a hilarious shitpost too#and now look at us#we made it to the trending page#now that is truly hilarious if you ask me#ravangie rambles
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THANK YOU.
Tbh I did not expect you to actually respond and add to this post, but I am THOROUGHLY grateful you have. But I also would like to inform you(and anyone else that's uncertain about their ability to repost this)
Self diagnosis is valid.
Being officially diagnosed is a luxury.
Often one that is usually only given to those that show extreme or undeniable traits. And even then, you still could be denied.
I was 12 when I was diagnosed with autism. People have known something was "off" since I was 4.
I was able to feel the sideways curves in my spine and see that my shoulders were uneven before I got diagnosis for "mild" scoliosis at 19, after living a life complaining of back and rib pain.
I've felt my joints, all the way from my fingers to my toes, all fall out of place since I was 10, often times having to have my own mother massage my knees back into place so that I could walk, and even spraining my ankles simply going upstairs. All of which fell on deaf ears for the entire 20+ years of my life despite countless professionals, from muscular skeletal to rheumatoid specialists and even physical therapists confirming that I have hEds and possibly early signs of rheumatoid arthritis. And yet they still cannot diagnose it because they "can't treat it"
And the reason I say all of this is because I used to worry the same thing. If maybe by claiming this diagnosis as my own, that somehow I was doing something wrong. Or taking something away from someone else. However, I want to let you all in on a little secret.
If you're actively experiencing symptoms, you're not faking it.
You might label the symptoms wrong, yes, but that doesn't mean that they're not there. People get officially misdiagnosed all the time! Because a lot of medical things have a bunch of overarching symptoms that overlap! And you could have so many things going on all at once!
And sure. You're not a doctor. So you might miss something or assign too much importance to it, but that's fine! You're allowed to make mistakes!
Unless you are actively pushing a harmful narrative or making life harder for them, you are not taking anything away from those who are officially diagnosed.
Wear your headphones in public, ask your friend to lower the music, buy a shower chair and lie to the cashier telling them it's for your grandma, pick up a super fluffy stuffed animal just because the texture is calming, take a look at the cool little canes at the thrift shop, do whatever helps you.
There's enough headphones and shower chairs and weighted stuffed animals for the rest of us to enjoy. You're not wasting anything that you find useful. And also, sometimes your friends are just slightly deaf and used to feeling the bass shake their entire car. It's okay to tell them that you're not.
It's okay to ask for some help bringing your groceries out to the car.
It's okay to ask someone to repeat what they said a third time.
It's okay to ask if you can see something again to make sure that you understand.
It's okay to tell people you'd rather not be touched right now.
It's okay to tell people that you want to be touched after telling them previously not to!
It's okay! And this even goes for nondisabled people too! Please reblog this post, even if you have nothing to say or add. Because maybe then, it might find it's way to somebody else who needs it. Whether that be a friend or loved one, a beloved moot, a follower, or just some random homie who comes across it by chance.
Even if you just like the way things are said, or think that the words are nice, that's more than enough reason to throw this post on your blog.
So go for it.
Press the nice shiny button.
Be an ally.
I dare you.
Local PSA: invisible disability does NOT mean you can live your life like a "normal person" invisible disability meant that if a stranger looks at you in public they wouldn't know what's going on.
Like if a wheelchair user were to decide to run into a corner store to grab a candy bar because they know that their legs can last that long without, the cashier wouldn't know.
Or someone with "mild" scoliosis walking upright through their shoulder leans slightly to the left. Maybe they just have bad posture. The lady in the next isle thinks to herself.
The person with EDS or POTS or whatever sort of condition wearing compression gloves out and about. Perhaps it's a fashion statement?
Or what about the people with intestinal issues? They can look like "normal people" too.
You never know what someone is going through.
You never know what they might need to survive or if they're on the edge of a flare up or even if they are currently going through one just by one look.
I think both disabled and non disabled need to realize this. You're not "no longer disabled" because you can "live without" disability aids. They're there to help you. To make your life easier. If living without a cane is going to make it more likely you'll fall over and hurt yourself, use the cane.
If you need to sit down to do dishes or cut vegetables because you need to save your legs for taking out the trash, sit down.
If you need a shower chair because you don't know if you'll pass out, use the shower chair.
People are going to judge you regardless for multiple reasons out of your control.
I'd rather they judge you while you're being safe.
You don't need to struggle to be "normal."
You can just be you.
However that looks for you.
Use your disability aids.
#obviously I'm being a little silly#y'all don't have to do anything if you're TRULY unsure or don't want to#but like it's possible#you could do it#i actively encourage it actually#the amount of people who've been reached by this post alone is so much more than i could have ever dreamed#and since it's picking up traction yet again#i think it's nice that so many people are able to share all of their stories with me again#because like#i love you#you know?#i love listening to you all talk#i love hearing about how you've connected with others experiences and how you feel less alone#that is literally what this post was for#this post was born out of my own isolation as I began experiencing what it meant to truly have an invisible disability#one that impacted my day to day life in such large ways despite everyone else being nonethewiser and even doctors insisting that i was fine#a lot of the original disabilities that I included in the original post ARE based off of my personal experiences! like the compression!#or sitting down to do tasks. i STILL do that! even now that my legs are stronger.#and now look at us#all of us are slightly less alone now. look at us go.#I'm proud of us.#so yes#everyone's allowed to share this post#disabled or not#you'll never know who needs it#late diagnosed autistic#self diagnosis#self diagnosis is valid#diagnosis#invisible disability
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i used to be so good at writing strong, thoroughly-researched, thoroughly-edited essays.
as a kid in hs, my teacher literally came up to me, holding my 40 page essay on the intersection of the European witch hunts and capitalism/exploitation/gender roles (it was supposed to be 7 pages...whoops) and went like "this is literally a master's-degree level thesis. what are you doing?? you could literally use this as your final dissertation in a master's program, what the fuck."
NOW??? NOW?? you'd think I'd be oh so skilled. but alas. i can barely piece together two ideas. adhd skill-regression is so so real. im SOBBING
#this is just me ranting sorry#im very tired and hungry#and i want to sleep but brain go brrrrr#well i used to be nice and smart and now im neither of those or however the song goes#pretty sure he was exaggerating cause looking back. it was good. but some of the wording was a lil wonky#adhd#actually adhd#executive dysfunction#actually neurodiverse#adhd paralysis#adult adhd#attention deficit hyperactivity disorder#adhd hacks#academia#neurodivergent#adhd skill regression#confessions of a burnt out gifted kid#<< i guess#former gifted kid#burnt out gifted kid#gifted kid burnout#realizing i sound rly pretentious here sorry -- formal speech patterns i picked up as an autistic child and never put down again haha
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Dick who climbed on anything as a child. Even in public, especially in public. The moment Bruce looks away, he is climbing something to get as high as possible. The first times, it gave Bruce an heart attack. Now, it's just a headache.
People pass by and ask if they should call the firefighters, and Bruce tiredly tell them "He is fine, he can get down on his own.", like people with cats.
Imagine, you're walking out of some building, only to see a 10 years old standing on top of a lamppost, having a discussion with his dad guardian at the bottom.
"Dick, get down."
"Make me."
"Get down or you're grounded."
#bruce wayne#dick grayson#batman#robin#dc comics#my ramblings#sometimes Bruce doesn't even know how Dick got where he is#he looked away for a second and now Dick is in the ceiling#of course Dick doesn’t get down because he knows the threat is empty Bruce is using his “tired dad” voice not his “disappointed dad” voice#really different for a Batkid you can still get away with a lot with the “tired dad”
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