incognito as a human

it feels so long since ive actually draw him grr i hope i did your vision justice eb! <33

you too! i hope your car breaks down and. and

It's totally just normal tea. I think 😅✨️

Never once did they wear one in canon, in fact, wearing suits instead. In junior high they were a jumpsuit, which avoids them wearing a gendered uniform.

only one instance exists and that is in a gag comic. With a car and a friendly titan.

Wether you interpret Hange as a woman, a man or nonbinary, Hange is specifically shown to present themselves with masculine or neutral fashion. At least respect that.

It's less of an issue regarding Hange's gender as a specific issue, and more of an issue regarding general societal impressions of women. In our society, women can absolutely wear pants, but anyone who wears a skirt is either a woman, or womanly. Hange, who is explicitly uncomfortable in skirts/dresses, is still made to wear a dress in fanon. Unless you have a setting where it's taboo for Hange to not wear a dress (in which case, they probably would still not wear one, lol), I don't see why you would put them in one, especially in cases where they're portrayed as uncomfortable, but still made to wear the dress.

My point is that no one can police how you portray Hange, and supposedly, their gender is up to reader interpretation. However, the dilemma lies in the alteration of their character (or appearance, in terms of dress or even anatomy, in some art, where there's enhancement on their breasts, hips, etc., even alterations to height) based on gender. If Hange is a woman to you, they are already a woman; there's no point in "making" them into one.

If my posts—whether on this blog or on my Attack on Titan side blog ( @scarletskiesinthepaths )—have ever meant something to you, and you’d like to support me, here’s my Ko-Fi:

Even a small donation helps more than I can say.

There is absolutely no pressure. I write my posts because I’m passionate about the subjects, not because I expect payment. But for those wondering why I’m fundraising:

I am poor and disabled. My current wheelchair (a TiLite Aero Z) was measured improperly and is actively harming me. I was born with two rare, genetic disabilities—classical-like Ehlers-Danlos syndrome type 1 (which resulted in congenital hip dysplasia) and a progressive, childhood-onset generalized dystonia-plus syndrome that fewer than 50 people worldwide have been diagnosed with. Both conditions make walking extremely difficult, and I rely on my wheelchair daily.

Unfortunately, the way my current chair is set up causes my hips to dislocate and compresses nerves in my spine. Every time I use it, I end up in severe pain, and I’ve been told by my doctors I’m at real risk of developing cauda equina syndrome if I don’t get a properly fitted wheelchair soon.

While I do have health insurance, I’m responsible for a 30% coinsurance after meeting my deductible. I’ve already met the deductible, but my share for the wheelchair still comes to $2,500—an amount I simply cannot afford on my own, especially with how many other expenses I currently have.

If you’re able to donate, it would mean the world to me. If you can’t, reblogs are also deeply appreciated. Thank you for taking the time to read this, and thank you to anyone who can help, financially or otherwise.

Ko-Fi link:

As of today (8/24/25), I have raised $420/$2,500.

If possible, please continue sharing this post or my Ko-Fi link. Even a simple reblog helps a lot!

If my posts—whether on this blog or on my Attack on Titan side blog ( @scarletskiesinthepaths )—have ever meant something to you, and you’d like to support me, here’s my Ko-Fi:

Even a small donation helps more than I can say.

There is absolutely no pressure. I write my posts because I’m passionate about the subjects, not because I expect payment. But for those wondering why I’m fundraising:

I am poor and disabled. My current wheelchair (a TiLite Aero Z) was measured improperly and is actively harming me. I was born with two rare, genetic disabilities—classical-like Ehlers-Danlos syndrome type 1 (which resulted in congenital hip dysplasia) and a progressive, childhood-onset generalized dystonia-plus syndrome that fewer than 50 people worldwide have been diagnosed with. Both conditions make walking extremely difficult, and I rely on my wheelchair daily.

Unfortunately, the way my current chair is set up causes my hips to dislocate and compresses nerves in my spine. Every time I use it, I end up in severe pain, and I’ve been told by my doctors I’m at real risk of developing cauda equina syndrome if I don’t get a properly fitted wheelchair soon.

While I do have health insurance, I’m responsible for a 30% coinsurance after meeting my deductible. I’ve already met the deductible, but my share for the wheelchair still comes to $2,500—an amount I simply cannot afford on my own, especially with how many other expenses I currently have.

If you’re able to donate, it would mean the world to me. If you can’t, reblogs are also deeply appreciated. Thank you for taking the time to read this, and thank you to anyone who can help, financially or otherwise.

Ko-Fi link:

(A Marco drawing by me coming soon)

I GOT THE NEW JEAN 😍😩 ooohh beautiful adorable handsome gorgeous 💕