Oh Worm?

…but make it Nine Sols!

THIS CONTAINS SPOLERS SORTA??? IM GONNA SAY IT DOES JUST TO MAKE SURE!

Its hard to explain what my thought process was for this one so I’m not even gonna try ahaha…

Here’s a bonus fun fact about this, as I was starting to do lineart, I noticed that the little star-ish explosion at the start is exactly where little Heng is on the first shot AND I DIDNT DO IT ON PURPOSE ITS JUST AN UNFORTUNATE COINCIDENCE…unfortunate cause it makes me sad.

One bed..... @bakfoo did the voices for Yi and Kuafu

>Among the characters there are one or two White characters with minor and/or distinctly antagonistic roles.

>White tumblr users focus entirely on said White characters.

>Tag of Black led piece of media is filled with posts about White character(s)

19-year-old Khalil Al Habil's liver and kidneys are failing. Shrapnel damage from the bombardment that killed his baby brother Omar has gone mostly untreated due to a lack of funds and resources. The ill effects of this damage have progressed to the point that the organs are losing their ability to function. Khalil urgently needs 3 rounds of treatment to combat the effects of his deteriorating liver and kidneys.

We've paid off the first round of treatments but Khalil has two treatments that he still needs. The second costs about $1,250 usd, but we haven’t made much progress in more than a month and his condition is getting progressively worse. We need to meet this second goal ASAP!!!

Current: $10,052 out of $10,407 usd (12 May)

Need to raise: $355 usd

The lethargy and fatigue caused by his deteriorating organ function only make reaching out more difficult. He is in very, very bad shape, and I’m extremely worried about him.

He has gone so long between sessions that he requires additional medications to sustain him between treatments. With a price of $1500 for the treatment for his failing organs, and $500 for supplementary medications, this is where we are for round 3:

Current: $11,354 out of $12,407 usd (28 June)

That but with weight.

I have never seen another allergy that has been so viscerally hated and mocked by people working in education like nut allergies. I’ve seen fellow teachers cringe that their classroom was the “nut free” classroom that year. Support staff that are trained and willfully don’t follow cross contamination protocol in the lunchroom because it’s too “tedious” or “time-consuming”. Full preschools + childcare centers that refuse to accommodate nut allergies. Schools where the only free lunch is a PB&J. Before/after school programs and summer programs whose food curriculum has nuts and doesn’t provide an alternative activity.

Allergy discrimination is so so insidious and prevalent. It’s happening behind their back and it is everything from the exposure joke to possibly causing someone to go into anaphylaxis from willful ignorance.

I was not downplaying this. The stigma is real, and people are 100% willing to let people with allergies die.

When my mom tried to enroll me in preschool, the school principal refused any basic accommodations like asking everyone to wash their hands after lunch before re-entering the classroom, not bringing straight up peanuts to snack time, etc. There was no such thing as a nut free classroom at the time. The principal told my mom and me (I was 4 at the time and definitely in the room when this happened) “if she’s so sick, she belongs in a bubble, not at school.” THE FUCKING PRINCIPAL! My mom had to threaten legal action under the ADA to get them to comply.

Look, I was on a 504 accommodation plan under the ADA for the entirety of my formative education (elementary thru high school). That’s all 12 years!!! And yet I have had teachers hand me items I’m allergic to as a “reward”. I have had other kids intentionally try to send me into anaphylaxis. One girl in 3rd grade asked me why I “wasn’t dead yet” when she had put on a lotion with almonds in it and then held my hand. I’ve had other parents write letters to the school saying what a terrible inconvenience it was to them to not be able to send their kiddo to school with PB&J, demanding I be Removed to a special education only class if my “needs” were such a “burden” to others. During elementary school “parties” held in the classroom on holidays and for student birthdays, I was always sent to sit out in the hallway or go to the library, because even though parents were only supposed to bring safe foods into the room (they had a list of all my allergies) they never once got it right. Administrators fought me tooth and nail for the right to carry my epi pen and other meds on my person at all times. Why they thought I would start dealing benadryl on the playground, I do not know. At lunch, I was always sat at a specific segregated table labeled the “Nut Free Table” alone because who the fuck is going to sit there with the literally segregated outcast? But ONCE notably I was sat on one side of a line of blue masking tape down the table top with the rest of my class on the other. One side was the NUTS side!!! As if allergens would respect that tape barrier. (Spoiler alert: they do NOT!)

Literally from preschool to my senior year of high school, I was “the peanut kid”. Other parents gave my mom books about how to “cure your child’s food allergies from HOME” by micro dosing with things they are allergic to (please never ever ever even attempt anything like a food challenge with a known allergen outside of the care and supervision of a medical professional, holy shit that’s so dangerous). My mom joined the PTA in my last year of high school so that I could maybe participate in all the senior-focused events like pool parties and breakfast at school on the first Friday of the month. The number of times another parent either (a) decided it wasn’t worth it to care or (b) intentionally brought peanut products to an event to spite either me or my mom??? I literally could not count. It happened constantly.

College was better, but I still occasionally had people BALK when I asked them to please not eat a Nature Valley bar with whole nuts in it right the fuck next to me in lecture, thanks. Work parties and catered lunches were always impossible. A few conferences I went to as an undergrad were SUPPOSED to be nut-free, but always fucked up the catering. At one, they set up snack tables by every exit of the conference auditorium so that when people left after the talk, they all congregated around the exits and opened macadamia nut cookies and granola bars. When I had subsequently had a massive allergic reaction and needed help getting home (I’d walked) after taking like 200mg of benadryl, the staff offered me a stack of napkins and a lukewarm apology.

Food allergy is a disability which touches literally every aspect of a person’s life. Everytime I share with someone new about what it was like growing up with my allergies, they have never heard anything like it in their lives. They’re always like “holy shit, seriously??? People did that??? Kids tried to kill you??? Parents wanted you kicked out of the classroom????” Yeah, man. Yeah. My own brother (who doesn’t have any allergies at all) doesn’t understand why I don’t “eat more adventurously” and why I won’t travel internationally. So, saying it REALLY LOUDLY for people in the back: