Something something about the alien hand call in 7x05 and Buck being the one being strangled.
Something something about Buck grappling with this new part of himself and coming out to people. Something something about the ‘fear’ of being judged or treated differently having him in a stranglehold because it’s still new to him and he doesn’t have it figured out himself yet.
Something something about being in 2 minds about telling people, about revealing himself - because the alien hand syndrome in this call occurs when the brains two lobes are separated - the connection severed - the brain is split in two
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i think "nonbinary" can be useful but a lot of times the way it is being used isn't helpful to actually discussing nonbinary people, especially since it is a HUGE umbrella term with very few boundaries. like there are nonbinary men & women, so positioning "nonbinary" as something intrinsically separate from man/woman isn't accurate. or there are times where it would be more useful to name the specific group (like multigender people, androgynes, abinary/aphorians) rather than a much vaguer term
in general the problem is that our language to describe nonbinary existence is basically some scraps held together with duct tape. there's sooo many ways in which nonbinary people are erased or binaried through language. not just through the lack of gender neutral options but the la of blatantly genderqueer ones.
i kinda feel like as of right now, nonbinary-ness is pretty slapdash & all over the place and it would be helpful to have a large-scale discussion on what terminology would be best for discussing things like exorsexism and it's various aspects, and how to talk about nonbinary people without homogenizing us, while ALSO acknowledging the need for umbrella terms that can cover a range of individual identities, even if people don't personally identify with the umbrella term itself. & on that note we should also probably discuss the issue of. like. perfectionism wrt nonbinary language & the way that potentially useful terms get lost bc of it. I don't think nonbinary people can really achieve meaningful equality and inclusion on the same level until we are able to have equally diverse and useful ways of describing ourselves, and a stronger understanding of how we relate to each other as a community.
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Like OK so I've been reading a fic with trans wolfwood in it that is so. HONEST. About how it affected him and still affects him. In a way that's very much not an average cis writer portrayal of a trans character.
Like. Either this writer is trans or did plenty of research, but it just feels REAL to me. And it has me thinking about my own way of writing trans Wolfwood.
I'm not there yet. But I've been thinking about it. The ways that what the EOM did fucked him up... but it also acted as HRT that affirmed his gender. So what do you do when you're in a body you don't recognize, but looks much more like a man than ever before? There's some gender euphoria in a way, but dysphoria at the same time bc you didn't grow into this. You didn't watch yourself transition. Suddenly you just Were this, and it's not you, but also it's nice to finally be seen as a man, but it also feels wrong to feel grateful for any part of what they did to you...
On and on and on
You see? This is what I want to think about with him. This is why trans Wolfwood is so compelling to me. It's just so Complicated, he'd have such Complicated feelings about his body and the way he lives with it. He learns this new body, it starts to feel more like his, but he also mourns the fact that he didn't get to watch it grow into this like he should've.
That kind of thing.
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hello! im a beginner artist and i recently found your blog! ive found inspiration in your art (if that's okay) and i really like your shading style but cant really replicate it in a way i like.. (hopefully this isnt inappropriate to admit) do you mind doing a brief tutorial? many thanks! your art is very lovely
HIII sorry it took so long to respond i was kinda busy... but THANKS! heres some process pics and also a long winded rant about art... hope its helpful
i used this piece cus its one of my recent artworks that i did a lot more rendering for... usually its a bit more condensed than this, but yeah. gradients are. poggers
ive only recently gotten comfortable w this "artstyle" so i'm not exactly the. authority here. but yeah! just some notes and thoughts... wish you all the best on your journey soldier. firm handshake.
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i have a neurologist appointment in about a month that i'm quite nervous about due to previously being dismissed/not having my concerns listened to, so gonna post this to ask for some advice on getting Taken Seriously or if anyone knows things about the type of condition i might have about what i should be asking them to do/test.
might be quite long so putting it under a read more, and tw for medical stuff and doctors being dismissive. also i am So So Tired and therefore not able to think very clearly so apologies if i've messed up any of the medical info about conditions i mention and apologise just generally for the rambliness of my writing.
summary of why i'm going:
bunch of disabling symptoms that have continually progressed over the past 5+ years, including: muscle weakness, fatigue, muscle twitches/small spasms, nerve pain, blurry vision, lack of coordination (have this from autism, however has gotten significantly worse recently so might also be related to neuro stuff). first symptoms were difficulty having my arms over my head (like having to take multiple breaks while putting my hair into a ponytail because i couldn't hold my arms over my head for the like.. three minutes to do a ponytail) and blurry vision (that optometrist has said seems like might be due to a systemic disease because of how variable it is) since i was 13, which was seven years ago. i started getting more impairing symptoms when i was 15, and began needing a wheelchair for anything that required standing or walking for more than 10 - 15 minutes. i'm currently 20 and need my wheelchair whenever i leave the house, i can't leave the house or do things around the house often, i can stand for a max of like four minutes and can't hold my hands above my head for more than like 30 seconds to one minute. pretty much all my symptoms get a lot worse with any exertion.
GP thinks i have myasthenia gravis, but the test for acetylcholine receptor antibodies was negative and he doesn't have the ability to do other tests.
the neurologist has already said he thinks i have functional neurological disorder and that i should do CBT and pysio to improve my functioning (i already know CBT is horrible for me, i'm in other therapy which is good, i've done some psyio before but she just taught me some stretches and that was it, more psyio could be good but it'd have to be with someone who isn't trying to do a graded exercise therapy type thing since i get PEM). he has mentioned doing a spine MRI but this hasn't been done yet. he said he doesn't want to do further testing for myasthenia gravis but i will probably try to get him to agree to doing a repetitive nerve stimulation EMG or something.
i also have scapular winging on the side of my body with worse muscular symptoms which has also caused a lot of nerve pain, and i might also have some sort of spine issues (straightening of cervical lordosis was seen on a CT scan, they said it was probably due to muscle spasms, and i get a lot of neck pain which might be due to that? as well as a ton of back pain along my spine. might have CCI but haven't been tested yet). since it seems like i'm getting some structural changes in areas where i also get a lot of the pain and weakness and spasms i'm hoping if i bring that up the neurologist might maybe look more at organic causes + the state of those structural changes but i dunno.
he did a basic neurological exam in my initial appointment with him and said that i have give way weakness/waxing and waning weakness because when he got me to do the pushing my limbs against resistance i could do okay for a couple seconds but couldn't maintain it. he also said in the letter that i had positive hoovers sign however i am.. very confused by this because from my understanding hoovers sign is mainly looked at when someone has one limb that's at least somewhat "normal" and one that either can't be moved or is very weak, and then the person can't move the weak leg but when asked to push the stronger leg against resistance they push the weak leg down. both my legs are strong enough that i can stand and whilst one leg is a bit weaker they're relatively similar. i lifted and pushed against resistance with both legs so.... i am not sure how hoovers is applicable here? does anyone know why it was applied and if that was correct or if i should be challenging that? he's saying that the give way weakness and positive hoovers are indicators that the problem is "non-organic" and therefore should be treated with CBT and pysio.
i'm not sure what i think is actually going on. i think myasthenia gravis might make sense, but also so could other neuromuscular diseases like a mitochondrial disease or something. also very possible it's myalgic encephalomyelitis (aka chronic fatigue syndrome) but obviously that one is a diagnosis of exclusion so i want to rule other things out if possible. i want to know what's going on so i can have the best chance of being as well as is possible for me. i know CBT is not right for me and whilst some type of pysio could help a bit/prevent some decline (based on past experience i know it won't Cure Me but obviously it can help a bit to build some muscle or maintain range of motion and things like that which are important) if there's other things i can do on top of that i want to.
i've tried to do research to work out the best tests to ask for and i think EMG might be good but also know a normal EMG doesn't typically pick up myasthenia gravis so it needs to also have repetitive nerve stimulation i think?
i can't see a different neurologist at least not anytime soon, so i need to get this neurologist to do as much to help as possible. a social worker from where i get therapy is coming to the appointment to help me so that should be good but i need to work out what the best way to advocate for myself is and what tests are going to be the most useful to ask for.
if anyone has any advice for getting doctors to take you seriously or for any tests i should be advocating for or conditions i should be looking into or anything i would really appreciate it <3 (emoticon description: heart)
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Things I have learned (or re-learned) from the first three weeks of my eight-week grad school class:
Why I'm not going into freelance editing (or any type of long-form editing) as a career.
Why I'm not going into journalism/newspaper editing as a career.
Why one should not write about difficult life experiences when one is already stressed and annoyed.
How much I hate group projects.
Related: how far I can push the limits of my patience.
Also related: How to send a very polite, professional email when I would rather like to bite the person I'm emailing.
Things I have learned from the first three weeks of my eight-week grad school class that I was actually supposed to learn:
The difference between a news story and a feature story and the types of openings you can use for a feature story.
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I feel like some people are saying that also because there is literal clips of shubble and lexie straight up saying his friends knew he was abusing her and wouldn't care to say anything until it was public
I understand, but what they said is hardly enough to straight up start pointing fingers at the exact ccs involved. Especially when they’re saying things now. Like, we don’t know who they’re referring to, and saying “wow why didn’t you say anything earlier” to someone going “you manipulated me” is just point blank kinda fucked. I understand and sympathize with people’s anger, but in this situation with a cc that has had many of his associates come out and describe his behavior as hurting them personally, like, you just can’t be sure if the person you’re pointing is truly complicit or literally another victim
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