Jenna Ortega talking about how she choreographed the iconic dance scene by herself. WEDNESDAY (2022- )
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Jenna Ortega talking about how she choreographed the iconic dance scene by herself. WEDNESDAY (2022- )

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I'm a fucking terrible person and an even shittier dog owner
whenever I decide anything I need 15 people to say "that's a good idea" to me otherwise I feel like I'm making a catastrophic decision that will ruin my life. in a chill way I'm chill
I adjusted to be chronically ill. And then I adjusted to being chronically ill and immunocompromised during a pandemic where people openly don't care if I live or die. But I don't want to adjust to just randomly having debilitating pain. This is not what i signed up for.
It would be one thing if this new pain was once every few months and had a very probable explanation (thank you ER doctors) like the other non-IBD-flare-up pain I've had for the last few years. But this new pain has been almost every single day for over a month now.
On the few good days I'll only be in pain for like 3 hours, but on the bad days I'm in mod/severe pain an average of 7 hours. It's a distraction at work, it keeps me from walking my dog and from eating normally, and it keeps me lying in bed for the majority of the day when I don't have to work.
I saw my doctor a couple of weeks ago when my pain was finally lessening and she had a reasonable guess of the cause and out me in a temporary med, but the pain started coming back just a few days after I started the med and I am miserable.
I don't want this body. I don't want to be broken, to be a physical or emotional burden.
And like my mental health is also fucked up.. No one is going to love me in this body.

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Fuck the whole “who’s gonna die this year” who’s death are you MANIFESTING. I’ll go first. JK Rowling
Maybe if instead of the vague cutesy term "brain fog" we use the more directly accurate term "neurological damage", that will help ppl stop seeing that as a "minor" outcome of covid
Brain fog is a term that has been in use by disabled people for a specific type of symptom for at least 30 years. Instead of blaming disabled people for not being taken seriously when they try to discuss issues they face in the most understandable way possible, let's look at why doctors refuse to take patients seriously when they say "I can't think clearly, like a thick fog has covered my brain"
Brain fog was never a "cutesy term" before covid, and it isnt the fault of people who experience it that it's the best way we can think of to talk about this symptom when hey, we're experiencing it
Abled people are treating basically every part of long covid as "minor" and its affecting people who have experienced these symptoms their entire lives severely. It's not disabled people's fault abled people refuse to take our illnesses seriously and it's not the fault of the terms we made for ourselves and use
Ok like 100% guaranteed way to make me laugh is to send me a joke that takes out the superlative/adjective from a phrase that should have one like
easily one of the days i've had all week
world's...dad
drinks that taste
this is by far one of the posts youve made
this is one of the world's most sounds
one of the seattle colleges
it won't fail
one of the jokes ever

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gays! clean your room
okay i’m curious bc my parents were relatively young having me but idk what age difference is “normal” between parents and kids as i’ve met people with plenty of variations. so if you want, reblog this and tag (don’t comment) how old your parents were when they had you. my mom was 25 and my dad was 21.
alright ladies time for wretched woman winter. my poor nerves. i need to lie down
women only want one thing and its other women

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oh so when PETER PARKER gets sensory overload he has spidey senses but when I do I HAVE AUTISM
you both have autism hope this helps