#and now look at us
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insomnya777 · 29 days ago
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etho gem n joel hanging out for so long ... they did this for ME specifically im their biggest fan omfg
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peculiarbeauty · 10 days ago
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in days like these .. i miss pixie hollow online ... underappreciated gem that was ..
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canirove · 6 months ago
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detectivelokis · 2 years ago
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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?
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skizz-that-man · 7 months ago
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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
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sokka-with-his-hair-down · 1 year ago
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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
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bisexualalienss · 18 days ago
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the fact that no one can govern without a strong trifecta….our system sucks!
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cryptvokeeper · 9 months ago
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miastree · 2 years ago
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look how far we’ve come
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shippy-from-apocalypse · 1 year ago
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Neil Gaiman really Said "oh so it's a queerbait If they don't kiss huh? Alright then"
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whats-her-quirk · 1 year ago
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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 🧋
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starscelly · 1 year ago
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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 .
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ravangie · 2 years ago
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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?
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sunnywalnut · 9 days ago
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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.
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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
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littlefankingdom · 4 months ago
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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."
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