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I have a whole ARFID side blog i havent touched in 3 years but im gonna make a long rant post about my experience with ARFID here and it may not be linear but it will be out of my head
Its a lot.
As far as i am aware i was born with ARFID, my mom swears i used to eat veggies as a baby, but i have no recollection of this and i do remember a few things pretty far back.
I remember my moms chevy cutlass, but the only thing i remember about it was that it had a hood ornament, i remember trying to reach out and grab it. My mom said i had to be no older than 2 in order to remember that.
I remember one of my first babysitters having a very frustrating time trying to get me to eat. I remember crying and screaming that i didnt want to try the food. It was green beans and mashed potatos and one other thing, maybe carrots. I remember her yelling at me. I remember going hungry. I remember my mom telling me to next time just say no thank you. i remember the next time she brought me food i said no thank you, my babysitter didnt looked pleased but she didnt yell at me this time.
Thus begun the cycle of going hungry just to not have people make a fuss over my eating habits.
My family never really sat down around the dinner table to eat. My mom never did the "You're gonna sit here til that plate is empty" She didnt have the patience to do that. But she did try to force a spoon full of whatever she made. So many nights of "Just try one bite" "Please, just try one bite" "One Bite" "Try. It."
When i finally gave in and tried to even just chew on what she gave me- gagging, most of the time immediately as soon as it hits my tongue. Would spit whatever i tried back out into the trash. Then my mother would say i was faking it.
My mom just thought i was being difficult.
I got tired of being called a liar.
My mom does this thing, and she does this to show affection, she'll lightly pinch a bit of extra skin from the side of your torso or upper arm or outer thigh and squeeze it a couple times. Sometimes it tickles, especially the torso. She'd tickle me and when i'd tell her to stop she's always laughs and say "But i cant help it!!"
Well one of these pressure campaigns to get me to try something, gag, say im faking. I broke down crying, telling my mom im not faking it, that i couldnt help it. Why was it okay for my mom to have things she cant help but i not for me? I told my mom that the same way she cant help it, i couldnt help it.
I think after that my mom switched gears. She stopped trying to force me to eat new things. Instead resigned that i was just a picky eater and i'd eventually grow out of it. claiming my grandpa and granny were picky eaters too.
Dinner time came around every night with the same question "What do YOU want to eat?" I became the deciding factor on what fast food we'd be getting for dinner. It made me feel guilty. My sister would want chinese or mexican food, and unless my dad was okay with going two places instead of one. What i would eat trumped whatever anyone else wanted. It didnt feel fair to my sister, but my parents didnt want me to starve. If i had to make food at home it was deep-fried fries and frozen nuggets.
Years go by of the same song and dance. PB w/ no J, a chocolate pudding cup, and a carton of 2% milk for lunch at school everyday. Every. Day. From Pre-K to my highschool graduation. Thats what i ate for lunch. My mom bought me these crayola themed sandwich boxes because i wouldn't eat a smashed sandwich.
I always had a hard time doing the dishes, putting up the dishes i had no issues with. But cleaning the old food off made me sick to my stomach. My sister usually was the one to load the dishwasher while i was the one to put the dishes up. I wear gloves when doing dishes now. Mom didnt think to give me any as a child, what gloves would fit me?
I remember turning 10. I remember making a vow to try to eat more now that i was 10. I felt like i failed, and started to wonder if i was broken. As i got older i started to wonder when was the "Growing Out" part of being a picky eater. i remember my childhood friend inviting me to have dinner at his place with his grandparents, i wanna say we were 7 or 8 years old? His grandpa was the one to call and ask if i wanted to come over. He was alway kind, the flower bed he build in the front lawn of his old house is still there. Anyway, I remember telling him no thank you and that its because i was a picky eater, I think I remember him saying they were having steaks. I actually really like steak now. I hung up the phone and my mom told me not to mention that I was a picky eater. I didnt understand why I shouldn't give them the reason I was declining. I felt ashamed. I'm a picky eater, but other people shouldn't know.
Hard for your peers at school not to notice you're the only one to bring your own lunch everyday and its the same thing everyday. I never had to change school districts, so the classmates that I graduate with knew that i had always been like this. I have had my pudding cup stolen a couple of times, started taking my lunch pale with me to the line for my carton of milk.
Senior year rolls around, got through the first semester okay, winter break i cut my long hair short for the first time in forever, a month into second semester here my government history teacher talking about this new thing called covid. We go into Spring break, spring break goes by, lockdown, it felt like forever, but feels so far away now. Have to worry about socially navigating through prom? Nope. Have to worry about my grades? Nope. "You're grades are frozen so they cannot go down, but we are assigning online work, if you do that and turn it in, it can go up. Looking at the As, Bs and one C on my last report card.
"I aint doing shit the rest of the school year."
and i didnt. fuck yeah. instead i was smoking weed and shaving bark off of big sticks for walking sticks and wondering what it means to be a good person.
Over the entire lockdown the only people i had to worry about my eating with was my own family, it was great, i had already survived 17 years of that.
When i finally graduated, my mom in celebration threw out my crayola sandwish cases, exclaiming in relieve that she no longer has to worry about them.
She didnt ask me first. I was mad at her, saying that i wanted to keep them.
Eventually got a job, easy enough not to eat in front of coworkers, just sat and ate in my car instead. Self isolation? Never heard of it. Coworkers bringing up food and giving opinions on which foods they like more, inevitably asking the question, "Have you ever had ____?" and the following interaction feeling like a quick time event of "Did i select the right dialog option for you to not question my eating habits further or am i gonna get called a picky eater?"
When i eventually open up about my eating habits my boss at the time told me it was my parents fault. I have heard it all by that point. Its me being difficult, Im just a picky eater, its my parents fault for spoiling me.
Year into that job im like "I dont wanna do this for the rest of my life" No longer under covid lockdown #2, i enroll in Votech. Going their to learn how to work on computers. Its going awesome, having a blast, genuinely the most fun i have had at a place of learning, Had a 2 hour lunch window to go and eat where ever i wanted, there was a nice grilled cheese place near by, i go there every day, they dont question shit, they just know i want that american on white and nothing else.
Im making friends chatting with my class mates when it happens. The fucking canon event happens. One of my classmates mentions they have an eating disorder that makes them extremely picky. I almost dont believe them myself. I go "Wait what was it called?" "its called ARFID"
I go to the oracle Google. This was before AI took over the search engine so i could trust the little summary blurb at the top search results. I don't believe my eyes. I'm looking at the list of symptoms like a god damn check list. I'm disbelief. I'm a bit hysterical. I see when it became diagnosable. 2013. I became angry, embittered, frustrated. I could have gotten help when i was twelve. My mother could have gotten me help when i was twelve. I remember back in 2012-2013 a CNN segment about the new diagnosable disorder, it gave a phone number on the screen for people who think they have it to call. I told my mom if we should, she brushed me off as just a picky eater. I was angry. I could have gotten help sooner, but my mother refused to believe that her child was suffering. I was angry. But I finally felt like there could be help for me. I finally felt like I wasn't alone.
I spend hours absorbing as much knowledge I can about the disorder I'd been living with forever. What resources are out there for help. Where can i get help, what does help even look like. Most help, turns out, is for childern. It makes sense. ARFID appears during childhood. But i never got to grow out of being picky, i was an adult now. These resource are for parents.
I found one book. Just one. Called "The picky eaters recovery guide." Again with being called picky but i digress, it was for adults dealing with ARFID. First few chapters go into describing this disorder and giving 3 examples of how it appears. I related to Kojos story the most. I cried thinking "They put my childhood into words on paper" I sobbed.
Unfortunately I'm not the most avid reader. I read a bit further and quickly realized that i was not going to be able to pull myself up by my bootstraps and climb over this wall all by myself. I needed a professional. Learning that there was more psychological hurdles in my way i sought out a therapist that specialized in eating disorders.
First session i have with her im explaining my symptoms and i start trembling, not like im a little chilly, like my nervous system is firing on all cylinders, trembling. Im telling her that im extremely picky, it feels like a mental block, i dont think its anorexia or bulimia. I never care about my weight. I never cared about calorie count. I didnt binge eat then feel guilty and throw it back up. (I actually dont know a lot about bulimia, im sorry if thats not the correct mindset of bulimia) I just wish i could eat like eveyone else. My therapist says i might have ARFID, i told her i know thats why im seeing you. She asks me how my body is feeling. im confused and ask what? She goes "Well your entire body is shaking" and i go "Oh because someone finally believes me."
I start seeing her twice a month, she wants me to work on getting outpatient care and i agree because i have heard stories and i do not want to be inpatient. She says i need a dietitian. Im native, i go to the native clinic, i ask to see a dietitian, they assign me a dietitian, i start talking with that dietitian, she's not completely familiar with ARFID, says she still has to go through the training for it (ARFID wasnt a thing when she was in school for her job).
She asks if i am okay with seeing one of their pediatric dietitians, says she'd be more familiar with ARFID i say yes.
New dietitian is only maybe a year or two older than me. Not too long out of college. I ask her if she has other ARFID patients, she says only few but I'm her first adult case. We get along great, almost like a second therapist.
I was finally getting help. I finally felt like i could fight back against this and enjoy the process of eating instead of seeing it as a daily maintenance chore to keep my body running. It hasnt been easy, especially in the beginning. I cried the first couple session i had to try foods in office. I had to describe the food, what it looked like, what it smelled like, what it felt to the touch, what it tasted like, what the texture was like. But im not allowed to use negative words. I cant say its gross, i can say it smells bad, i cant say the texture is bad. I can only use Good or Neutral terms.
Trying someone new is eaiser than it ever has been for me, there's still the initial hesitation, i will still decline when offered to try most foods, but i dont gag nearly as often as i found before, and that in itself has been a major improvement.
Thanksgivings.
I hate thanksgiving dinner. My least favorite it holiday where it is almost required for you to eat. Someone always asks. I always feel ungrateful for not eating of the food. Usually just kept in my room or outside if it was at extended another person house. Most fast food places are closed Thanksgiving. Cant get something before heading over. What's a bit more self starvation to stave of social isolation?
Mostly wanted to disappear or be invisible on that day.
The first thanksgiving after starting outpatient care. I feel like i can finally be at the table and be prepare for the question of "whys arent you eating" Dinner is held at my older sisters house, eating and conversation has been happening. I go check up on my nephew playing video games in his room. I over hear my mom answer someone question for me. Incorrectly. I rush in to try to explain what it actually feels like. Im frustrated with my mother. Dinner is over, we head back home. I go into my room and scroll on my phone. My mom enters my room and lays down on my bed next to me.
She tells me she thinks i need to be trying more.
Trying more?
I snap.
I hysterically laugh, i start screaming at the top of my lungs
"I am trying! I am trying so fucking hard! This is literally the hardest thing i will probably ever have to do in my life! I didnt ever think there would be help for me! Im sorry Im not better on your schedule! Im sorry i wasnt better yesterday! But i got myself more help in the past three months for my eating disorder than you did my entire goddamn childhood!"
Screaming matches between me and my mother as this time were not uncommon. I usually was the one to start it. It usually ended up with my dad having to intervene.
But this time my mother was silent, she didn't yell back. My dad came running when he heard me yelling and as he got to the threshold of my room my mother turned around and said to my father "I started it."
My mother at somepoint tried to say that she had suffered from ARFID just as much as i had. I tried to correct her in saying that she has only has second hand experience with ARFID, and only i have first hand experience with it. We argued back n forth on this for a minute before i finally told her "Just like how you threw out my sandwich cases, when i move out, you will no longer have to put up with this. But I Will." I think that got through to her.
My mom isnt a villain, she's not an evil women. I love my mother very much. But she has been the aggressor in most of my ARFID related memories. And i definitely took some of my resentment of her miss care out on her when i was older with the screaming matches. We have come to an understanding.
Not too long ago i was talking with her about something with my childhood, and she's was the one to bring up that she recognizes now why i had such trouble with the dishes. Saying if she only knew what she knows now.
I'm at the stage in my care where i need to start adding outside foods into my routine eat, which is easier said than done. I'm not done with recovery, and i may never be completely done fighting this, but I'm doing better than i did before, and I'm not done fighting.
i feel so defensive and protective of people with ARFID like if i had a disorder that made my brain register 90% of food as poison for no reason and i had a bazillion people on the internet constantly calling me a manchild who needs to just grow up and stop being a picky eater i would start killing people
people with ARFID and people with very few autism safe foods and people with contamination OCD and people in ED recovery and everyone else with a complicated relationship with food that no one takes seriously GET BEHIND ME!!!!!!!
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I mean, in some very interesting Technically Correct ways, they didn't actually die? Now, they're very much no longer alive. But the forces involved are such that they didn't get any of the usual cellular processes of death, they simply went from biology to physics in less time than it takes a signal to travel down your optic nerve.
in 2026 let’s start actually noticing and taking seriously the true scale and impact of jkrs transmisogyny and how she’s been funneling decades of royalties and ip owner cash directly into anti trans lobbying thats been making the uk hell while gradually worsening conditions elsewhere through impacting the zeitgeist
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crazy how i find myself thinking i've got a handle on it all finally and then i see the ways that other people tangle their lives together so easily and live so easily together with their friends and i feel like that girl at the top of the stairs painting by norman rockwell
Ya'know that lady that has multiple archeological native american skulls despite the different tribes asking for their ancestors skulls back and her saying "Nuh-uh mine now"
Yeah anyway be a shame if someone broke into her house.
I feel like I need to share this because idk if Europeans are familiar with the presence of Aldi in the US, but at least especially in my area they’ve been growing a lot recently. Like Aldi bought out some local failing grocery chains where I live (Louisiana) and have opened Aldis in all these somewhat rural communities and small towns, which for the record I’m fine with
But as a result of this they are advertising a lot more in my area and also in many cases, the people in these areas have never been confronted with Aldi or any European grocery store. So the ads that Aldi is pushing out to its new US customer base feature a cowboy shopping at Aldi who is explaining to new Aldi customers how Aldi works. Like this cowboy is explaining you gotta put a quarter in the shopping cart and why there are very little name brands. A cowboy is how they want to reach their American customer base. They gave us a cowboy
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Gotta add previous tags on here, because this is gonna live rent free in my head from now on. The stars are real, constellations are not. Damn. Tags by @smoreofbabylon (if you don’t want me to put you on blast like this I’ll delete lol!)
H̸̪̎ô̴͉w̵̒̇ͅd̶̙̤̈́y̷̯͚̒. @hipoppokunurious - Tumblr Blog | Tumlook