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#Autism Support Items
noisycowboyglitter · 2 months
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Puzzle Sloth: Advocating for Autism Awareness Until All Pieces Fit
Discover the enchanting world of the Until All Pieces Fit Puzzle Sloth. This captivating puzzle invites you on a whimsical journey through the lush rainforest, where a lovable sloth patiently works on piecing together the intricate details of its arboreal home.
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Buy now:19.95$
The design celebrates the slow and steady approach to life, a quality often associated with sloths. Just as the sloth meticulously assembles its puzzle, we encourage you to embrace a mindful and patient approach to your own challenges. Each piece you connect brings you closer to completing the picture, much like the steps we take in achieving our goals.
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The Until All Pieces Fit Puzzle Sloth is more than just a game; it's a reminder to appreciate the journey and find joy in the process. It's a gentle nudge to slow down, take a deep breath, and savor the moment. Whether you're a puzzle enthusiast or simply seeking a relaxing pastime, this puzzle offers a delightful escape into a world of tranquility.
Let the sloth's serene demeanor inspire you to approach life with patience, persistence, and a touch of playful curiosity. As you piece together the puzzle, allow yourself to unwind and connect with your inner peace.
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April is designated as National Autism Awareness Month to shed light on autism spectrum disorder (ASD). This neurodevelopmental condition affects communication, social interaction, and behavior. The month-long observance aims to increase understanding, acceptance, and support for individuals with autism and their families.
By raising awareness, we challenge misconceptions and stereotypes surrounding autism. It's an opportunity to celebrate the unique strengths and abilities of individuals on the spectrum. Through education, advocacy, and community involvement, we strive to create a more inclusive society where everyone feels valued and supported.
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Join us in spreading awareness about autism throughout the month of April. Let's work together to build a world where individuals with autism can reach their full potential and live fulfilling lives.
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crazycatsiren · 3 months
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Unfortunately, Lijjian the capybara Squishmallow is too big to fit on the bed when the husband and I are both on it.
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germplush · 1 month
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we got Proloquo2Go this month! we still working hard on our app we got this so far.. theres sm we need to update on it so we can use every day.. we work on it every day.. if anyone has any tips let us know!!
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littlethingsmart · 11 months
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(source)
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Would like advice on what to name this lil dude (frog bracelet my partner got me to accompany my lil autistic and anxious self when we go run errands and such)! Full disclosure he will not be named exclusively by highest votes, but it will help lead my decision. Additional name ideas in tags or replies are welcome as well!
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genderqueerdykes · 7 months
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Disabled homeless trans lesbian artist in need; new items added to our Ko-fi shop!
We are currently homeless and living out of a hotel- I am spending $38/night every night that I'm here. I'm working with an apartment complex that is waiting for approval from the government to get me my unit. I still haven't been approved and I have been working with them since October. I am severely disabled with having autism, hEDS, fibromyalgia, schizophrenia, PTSD & other conditions. Even reblogging this post helps. We've added a lot of new items, we're very excited for these! We hope you enjoy them as much as we do! Thank you if you decide to support us, it goes a long way!
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abyss-is-lame · 3 months
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ZZZ Headcanons because I headCANon
also i havent finished the game (im on like mid/end of ch2) so some of these may be canon
Anby has autism. Nothing can change my mind. She is autism.
Nekomata has a lot of cat items, like cat beds, scratching posts, toys, etc. and is a catnip addict. She regularly uses toy mice as forms of payment, and gets sad when its not accepted
Even though Billy is an AI, he sucks at anything math-related
Nicole is under the trans umbrella, cis fem to a ___girl xenogender (probably cybergender/cybergirl)
Corin can and will absolutely destroy you if you piss her off enough, she'll go from nice little goober to the worst pain you've ever felt
Soukaku is picky when it comes to food, if even 1 thing is messed up she'll refuse to eat it
Soldier 11 and Anby literally cannot be separated, and they would both full well die for eachother, and regularly get noodles together
Koleda is an absolute gremlin, and sometimes needs to be held back by the entire Belobog team like a feral animal
Grace will always say random embarrassing events that happened to Koleda when she's with the Belobog team, just for shits and giggles
Ben is treated like an emotional support teddy-bear by the Belobog team (mostly Koleda)
Anton is like the Kirishima of ZZZ. No idea how to explain it
Lycaon is strictly a carnivore, and sometimes just eats corpses in the Hollows because he can
Rina is like Corin's mom, basically helping Corin to function properly and not just cease existing from anxiety
Ellen has anger issue and can't listen to 'No', she will throw hands (and fins) to get her way
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foldingfittedsheets · 2 months
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my bed mattress is nearly 2 decades old now but it's still like the comfiest bed i've ever slept in (my autism may have a role in this), is it really necessary to replace it?
Hmgh. It… depends. As someone who Bonds with items especially in my comfort zone like bed and couch this is tough to answer.
A few signs that you do in fact need to replace it:
The bed has a divot where you sleep. These will always impact good sleep and support. Automatic replace.
You are tossing, turning, waking up unrested, or achey. Be very attentive to how you feel upon waking. If you need to keep a diary of how often you wake up unachey and check in after two weeks. If you're conssitently not sleeping great the mattress is letting you down.
If you're waking up congested. 90% of people do not have adequate well maintained mattress protectors. Beds can double their weight every ten years due to dead skin, dust mites and their assorted corpses as they live their life cycles, and general dust. All these thing can cause allergic congestion and is also just Not Great to breathe all night.
All this being said. I nor anyone else is gonna come take your bed from you. You can do whatever you like with your bed, ten years is when I recommend people tune in and asses their situation.
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babygorewhore · 10 months
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You’re everything.
Eddie Munson x fem reader
Eddie Munson comes home and sees the bedroom destroyed. Your mental health has taken a toll and you feel worthless. But he’s always there to remind you how much he loves you and how he’s always willing to help you pick up the pieces.
Warnings! Hurt comfort. Mental illness. I wrote this with the reader having BPD and autism. This is based on my experience. I haven’t seen much on those two issues. Feelings of worthlessness. Mild self harm. Anger episode. Anxiety. I hope this comforts you because you’re worthy of love and Eddie would love you no matter what. Also the photo used is just for aesthetic. Not proofread.
Thank you to my friends, Dolly, Mae and Em for helping me with this. I love you girls.
Eddie pushed open the apartment door, with his hip, a few grocery bags lined down his arm because he refused to make two trips. “Hey, sweetheart, I’m back!” He shut the door with his foot, did a quick unfocused glance around the living room.
“Fuck, the store was packed! I think you would have stayed in the car, baby.” He set down the bags and started putting away the cold items. Eddie yawned afterwards, closing the refrigerator and stretched. His black, stolen back sweatshirt rising above his stomach.
It dawned on him that you haven’t responded at all. “Baby?” He called again. No answer. He frowned and approached the bedroom door and he gasped when he saw the scene.
The bed was torn apart. Blankets thrown off and the pillows dented. Eddie went to take a step before he looked on the ground. Stim toys were all over the floor. Stuffed animals and even clothes. A few shirts were ripped. He didn’t see you. “Princess, what’s going-“
A hole was in the wall next to the closet. A small one but it went deep in the plaster. Eddie moved quickly. Surveying the damage, he saw a bloody imprint. Knuckles. Eddie sighed. You were having an episode. He should have known. You didn’t answer his texts. You hated phone calls. This wasn’t the first time this happened. Eddie on a number of times had to sit by your side during dark hours.
But he loved you. You were beautiful. His everything. It wasn’t one sided. If anything, you gave too much to him. You were always supporting him. Even when he was unbearable. You stood by him. He would do whatever you needed. He needed you. He wanted you. Eddie knew immediately where you were then.
He gently opened the closet door and he saw you. You were wearing a large t shirt, it went past your thighs and loose plaid pajama pants.
Over ear headphones on, your phone face down on the floor and you were stimming. Rocking back and forth. You were panting, your face flushed and he could see your eyes squeezed shut. Eddie saw your right hand. Your knuckles were bloody and bruised.
He didn’t want to startle you so Eddie opened the door further, enough for you to hear it over music.
Eddie’s heart ached when you turned to look at him. Your eyes were blood shot. Your lips bleeding from what he knew, you bit them or picking at them. Your nails had blood underneath them from biting the nail. You were a wreck. But you were his special girl.
“Hey…” He said, swallowing. “Baby, I-what happened?”
You tried to stand but ended up sprawled on the ground. He went to help you but you jerked away, pulling yourself up.
“I’m so fucking mad right now.” You were almost yelling. But you sounded out of breath. “I-I took my meds but I’m still like this. My heart hurts, I just feel like I want to crawl out of my skin. Everything is too loud!” You weren’t crying but you were growing hysterical. You started pacing.
“Why am I like this? Why can’t I just be normal? Why do I get so upset over the smallest things?” Eddie was standing close but he didn’t reach yet. You were tugging at your shirt. He knew you were getting hot.
“I can’t deal with this. I can’t feel this way! Im so sick of feeling like I’m useless because I can’t even talk on the phone to my boyfriend because I hate how it makes me feel! You shouldn’t have to deal with me.”
“Sweetheart, will you just come here for a second?” Eddie tried to prompt.
“No!” You stopped moving and placed your hands on your chest. “Eddie. I don’t want you to see me like this. Again. Maybe you should leave. I don’t want to keep freaking you out.”
Eddie moved then. And he gently grasped your elbows and looked down. Eye contact was difficult for you and he never wanted to force it. But he tilted your chin, happy if you just looked at his forehead. “Princess. I’m not leaving you. I would never.” He leaned forward, rubbing his nose against yours. “I’m just happy you didn’t break your hand.” He pulled away, glad you weren’t moving away. “You’re burning up. Let’s get to the couch, it’s too warm in here.”
Eddie wrapped his arm around your waist, helping you walk around the mess and he sat you down on the couch. “I’ll be right back, babe.” You grabbed his hand. “I promise.” He smiled at you. You slowly let go.
He tried not to show his panic as he looked for the first aid kit. Eddie came back to the living room, kneeling in front of you. “Let me see that hand.” He asked, pulling it towards him. It was shaking. He was careful, dabbing it with saline and you winced. “I’m sorry, baby.” Eddie went through the motions, remembering how to wrap an injured hand from his own share of punching walls.
After the bandage was around your hand, he pressed a kiss on top. He maneuvered his way up and sat beside you. Eddie held your leg that was bouncing. “Babe…I know for a while things have been really hard for you. And seeing all that today, I see you’re in a lot of pain. And I just want to help you. I love you so much. You know that right?” You covered your face with your hands.
“Eddie, you shouldn’t. I feel like I don’t have enough good days. I’m so tired of always telling you how bad my day was, or that I want to have a meltdown about fucking textures or sounds. I just wish I could be normal for you.” Eddie shook his head, taking your hands down.
“Hey. Hey. I would never trade you for anything. I would never want anyone other than you. The only thing I wish I could change, is how you feel about yourself. Baby, you are so much more than what you struggle with. You’re kind, funny, like so funny I almost snort and I can’t even breathe. You understand me, you are so caring and you let me be annoying when I smoke too much weed. I could go on for days.” You lifted your head. And looked at him. And held eye contact.
“You’re more than bad days, baby. I love you so much. And I know you were listening to our song, right? The one I told you to play when things get bad?” You nodded. Smiling a little. Eddie feigned shock.
“Is that-is that a smile? That’s my girl.” It widened and he grinned, cupping your cheeks.
“Come on. Sing one line with me. And then, I’m gonna go pick up the bedroom. I’m going to make you something to eat and then we’re going to watch your favorite movies.”
“Do I have to sing?” You complained.
“Sorry, baby. Those are the rules.” Eddie winked, still holding tight to your face.
“And I don’t want the world to see me, cuz I don’t think that they’d understand.” Eddie leaned in, pressing his lips softly to yours. Gently because of the picked apart flesh.
“I’m proud of you, sweetheart.” You wrapped your arms around his shoulders and squeezed tightly. Eddie followed suit and hugged you around the waist.
“I love you so much, Eddie.”
Eddie breathed you in. It wouldn’t fix what you felt. But you wouldn’t have to battle anything alone.
Tagging. @xxhellfirebunnyxx @reidsbtch @take-everything-you-can @emsgoodthinkin @monstxrteeth @battymunson @scene-and-dandylover @lithium80sblog @elaine-in-the-membrane
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autistpride · 4 months
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AUTISM ACCEPTANCE
Teacher AU from April's prompts by @wolfstarmicrofic
Wordcount: 998
Remus had been waiting for this day for years. Nearly a decade, but the waitlist was seven years long and he was low on the priority list because he wasn’t in a mental health crisis and had a somewhat stable home and job situation, but after nine years, he finally got the calls.
Remus first began to suspect he might be autistic when he began teaching. Remus taught at the primary level, year one, and all of the students in his class were autistic. He related to his students and seemed to understand them on a level most of the other teachers could not. He spent his own money changing his room up, buying sensory tools and various items. In the end his students thrived and Remus was so proud of them.
As the years passed, Remus gained a reputation for being quirky, odd, and a bit too into the fandom for the book series he was into. But despite being a bit of a “loner” and not developing much of a relationship with his coworkers, Remus was beloved by his students and as a result, their families.
Remus set up his assessments during the half term, or tried too, but his final meeting was during a school day and that was unfortunately unable to be rescheduled due to the psychologists busy schedule. 
Remus explained to his students the day before his appointment that he would not be at the classroom Friday morning. He would be at a doctor’s appointment and they would have a substitute teacher until lunch time. Naturally they had questions, as all curious children do.
“Mr. Lupin, are you sick?”
“No, Hermione, I’m not sick. Just a meeting.” 
“Do you promise you’ll be back at lunch time to get us from the playground?”
“Yes, Harry, I promise. I will be standing at the side ready to collect you from the playground at the end of your break.”
“Do you have a baby in you?”
This one caused Remus to snort. “No Ron, I don’t have a baby in my belly. I know you have a little sister coming soon though huh?” Remus asked the boy who beamed and nodded. 
“Are you going to die?”
“No I am absolutely not dying, Draco. You don’t have to worry. You are going to be stuck with me all year!” Remus said in a low tone crouched down and wiggling his fingers like a monster.
This caused a bout of giggles from the young children and Remus chuckled before helping them pack up for the day.
Friday morning he rose early, packed everything he needed for the day, and rode the bus the hour to the city. He sat and listened as the psychologist explained he did in fact meet the criteria for autism and after years of waiting, he was officially diagnosed. The psychologist explained that it wasn’t uncommon for trans males to go undiagnosed their whole lives because many doctors were biassed against females as well as people of colour. They kept asking if Remus was okay, if he was upset or needed any support because they knew that hearing this information was a lot. 
But Remus just felt relief and peace. He finally felt like it all made since, his whole life
The bus ride back to the village Remus teared up as he texted his best friend Lily that he got it and she replied instantly with many hugs and heart emojis and then a message saying that she knew he would and that she was proud of him.
Remus walked from the bus stop to the school and buzzed in through the staff entrance in the back with his badge. He placed all his stuff in his locker in the staff lounge, made sure his badge was the right way on his lanyard, and made his way to the enclosed play area where his students would be.
Slowly, one at a time, his students noticed his arrival and ran around finding the other classmates to tell them that he was there. Then without warning they screamed and ran over to him, tackling him with hugs, causing Remus to laugh as he hugged them back.
Soon the students were all lining up to go back into the classrooms, but Remus was confused, the substitute wasn’t there. He asked where Mr. Black was and Luna said that he stayed behind because he had something he had to do in the classroom since Mr. Lupin would be there to get them. Remus was confused and puzzled because he had prepared all the materials for the day’s lessons and there was nothing that needed to be prepared during the lunch period. 
They made their way back to the classroom in a line, Remus walking backwards like a professional at this point, directing his students in their songs for things like planets, continents and oceans, and skip counting as they walked. They entered the classroom one at a time ahead of him and when he turned to walk through the doorway he froze.
His entire classroom was decorated for a party, his students sitting on the reading rug holding onto little drawings. In the back, Sirius held up a small cake. “Congratulations!” written on the whiteboard in Sirius’ beautiful loopy cursive. 
Remus’ hands quickly covered his mouth in surprise as he looked around and took it all in. “Oh,” he whispered.
“Class what do we say to Mr. Lupin?” Sirius asked with a cheeky grin.
The entire class erupted into screams of “ONE OF US! ONE OF US!” 
Remus threw his head back and laughed despite the happy tears that welled in his eyes. 
Remus had never felt confident before in his life. Never felt like he actually fit someplace before until now. 
And if he bit his lip to try to hide his smirk and raised his eyebrows at Sirius when he had Sirius’ number in his phone after years of pining, well who could blame him. 
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noisycowboyglitter · 2 months
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Empowerment Through Art: "I Wear Purple for Someone" Butterfly Products
"The Purple Butterfly: A Symbol of Solidarity and Remembrance"
The sight of a purple butterfly holds profound meaning in the realm of awareness and remembrance. This hue, often associated with the fight against Alzheimer's disease, becomes a unifying emblem that transcends individual experiences, forging a sense of collective empowerment and support.
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Buy now:19.95$
When someone wears purple in honor of the butterfly, it is a powerful declaration of their commitment to standing by the side of those affected by this devastating illness. The purple butterfly represents the resilience, compassion, and unwavering spirit of the Alzheimer's community, serving as a touchstone for the shared journey of those living with the disease and their loved ones.
This symbolic gesture becomes a rallying cry, amplifying the voices of those whose lives have been touched by Alzheimer's. It is a testament to the enduring human capacity for empathy, a acknowledgment of the challenges faced, and a steadfast promise to continue the fight for a cure.
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As the purple butterfly takes flight, it carries with it the collective memories, hopes, and determination of all those who wear it. It is a poignant reminder that, even in the face of unimaginable adversity, the human spirit can soar, finding strength in the embrace of a community united by a common cause.
"Raising Awareness, Fostering Understanding: The Fight Against Alzheimer's"
Alzheimer's Awareness is a clarion call that echoes through communities worldwide, uniting individuals in a collective effort to confront this formidable challenge. As this devastating neurodegenerative disease continues to impact millions of lives, awareness serves as a powerful catalyst for change.
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Through educational initiatives, support networks, and advocacy campaigns, Alzheimer's Awareness shines a light on the realities faced by those living with the condition and their caregivers. It dispels misconceptions, fosters empathy, and mobilizes resources to advance research, improve care, and unlock the mysteries of this perplexing illness.
Most importantly, Alzheimer's Awareness empowers those affected, giving voice to their experiences and inspiring a sense of hope. It recognizes the resilience and adaptability required to navigate the journey, while also championing the tireless efforts of those dedicated to finding a cure and bettering the lives of all touched by Alzheimer's.
"Ethereal Elegance: Butterfly-Inspired Gifts that Captivate the Senses"
Butterfly-themed gifts hold a captivating allure, seamlessly blending the delicate charm of nature's winged wonders with timeless sophistication. These enchanting offerings cater to those who appreciate the beauty of the natural world, becoming cherished keepsakes that infuse spaces with a sense of wonder.
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From delicate jewelry pieces featuring intricate butterfly motifs to whimsical home accents that flutter with grace, these gifts transcend the boundaries of mere decoration. They serve as touchstones, evoking cherished memories and fostering a deeper connection to the fragile yet resilient cycle of life.
In the embrace of the butterfly, these gifts become a celebration of the ethereal elegance that permeates the human experience.
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crazycatsiren · 1 year
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Taking a plushie with me when I leave the house, 5 stars, highly recommend!
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germplush · 12 days
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8/29/24 | Olive Dot here. spend time with my owners Dreamdrop but later went out to a bar with their roommate. i was there for support. we went to a bar for the first time and ordered a drink. after we had subway. good day! proud of them - Olive Dot
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tealottie · 5 days
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What are your headcanons about Della?
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I have so many, but tbh my favorite headcanons have to do with her having PTSD - so i can't promise this will be a fun post
MASTERLIST OF DELLA HEADCANONS BELOW:
Appearance:
Scars from the Moon
One across her beak on left side
Scars on her arms and legs
Other markings
Stretch marks especially on her tummy and butt
A few stretch marks on her chest and thighs
Freckles on her beak (because she had triplets and ducks IRL sometimes get freckles after pregnancy)
Other
Chubby pear shape
DD cup size
Squishy belly
Big eyes
Fluffy unkempt feathers (she's bad at preening)
Thin hair (also bad at taking care of it)
Short beak
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Queer Headcanons:
Homoromantic
Bisexual
Prefers to just call herself a lesbian
Ciswoman (doesn't mind they/them pronouns and probably finds it entertaining if she's referred to as he/him)
Supports all of her queer babies
She also does not actively seek out romance, but she isn't offput by the idea entirely
Mental Health and Neurodiverse Headcanons:
PTSD
Hates being alone at any given moment and had to ask Donald if she could room with him in the houseboat for a few months
Genuinely cannot look at her reflection and will be needing exposure therapy
Does not like the feeling of movement underwater because it reminds her of the moon's gravity
Terrified that she'll never be fully capable of being a mom because of the 10 years she missed
Cringes at any moon or space themed items now - sometimes triggers her on a bad day or if she looks at them for too long
Her hair being too long is a trigger for her, so she always keeps it shoulder length or above
She ALWAYS feels cold even if her body temperature is normal and sometimes it drives her crazy
Lots of nightmares about what-ifs - what if it was my kids instead of me, what if it was my brother instead of me, what if i didnt have oxychew, what if i never met the Moonlanders, etc etc etc
The taste of black licorice will genuinely send her spiraling, and because it lingers - it wrecks her for days (she hates similar flavors such as rootbeer)
Finds a lot of joy in warm places so she now loves to be out in the sun
Had a period of time where she wasn't really talking with Penumbra because of the severity of her triggers/ptsd
Both finds peace in dead silence, but it also brings her back to the moon as well - she has a very complex relationship with isolation
Prefers silver over gold (even though she doesn't wear jewelry, she likes silver on others and silver on things such as zippers and buttons)
Spent quite a few years terrified of flying after the horror of her own trauma set in, but it threw her into a big depression since piloting is her passion
Hates taking care of her stump because she doesn't like taking her prosthetic leg off - she sees it as her own, so she hates taking it off even though she knows she needs to when sleeping or showering
She has a hard time looking at her stump and scars because on one hand; sick as hell battle wounds, but on the other; damn was that the worst time in my entire life
Depression and Anxiety
Even before crashlanding on the moon, she dealt with depression and social anxiety
She has a bit of a hard time keeping her room tidy and taking care of herself, but she's phenomenal at putting other people first
Feels as though she's not attractive enough
Wants to be a ray of sunshine in other peoples' lives
She's very scared that she won't be enough for people and therefore she must put 110% into everything she does for others
ADHD and Autism
Her sensory issues tend to directly conflict with her PTSD issues - like she hates silence because of the moon, but sometimes she gets overstimulated by noise and needs the silence or alone time
She does not sleep until her body physically passes out because the change in activity is hard for her to deal with
Goes insane if she feels understimulated because her brain begins to shut down and she dissociates
Many, many stims (sometimes doubles as grounding with PTSD): bouncing her leg, various hand motions, feeling the fabric of her clothes, physical affection with her loved ones, playing with the tightness of her prosthetic (loosening and then tightening it over and over), shaking her head to feel her hair around her shoulders (and solidifying that what she's feeling is earth gravity)
Really hard time understanding social cues that makes her come across as rather ditzy
Special interest in aircraft technology and was a top student at her flight school
Love/Hate relationship with reading because if she enjoys what she's reading she gets invested, but if she's understimulated, the words jumble together in her mind
Not good at math for a similar reason
Fish are a huge sensory nightmare for her; the scales, the smell, the taste, etc
Is generally pretty sensory-seeking, but has a few Hard Nos on textures (such as slimy scales)
Other:
I headcanon Della having compulsive sexual behavior disorder, and her libido especially spiked after being on the moon for 10 years, and it makes her feel really gross at times
Due to said hypersexuality, she gets intrusive thoughts that piss her off
Because of the moon not really having a clear indicator of night and day, Della lost her circadian rhythm and struggles with a Hell combination of non-24 and ADHD insomnia
The lack of general sleep makes it hard for her to lose weight and so she's insecure about that
Physical Disabilities:
Because she was on the moon for so long, the zero gravity and lack of proper breathable oxygen took a huge toll on her, physically
She developed really bad asthma and will likely be recovering from it for the rest of her life
Her lungs can only intake so much oxygen at a time, so she also struggles with shortness of breath
Upon returning to earth, her body was really broken down from the cold atmosphere - causing her to not be able to regulate her body temperature properly
Her bones were weakened upon arrival, so she has to spend years recovering physically from it
Her stump is irritated a lot because she doesn't like taking care of it properly
She owns crutches for when she needs to take breaks from her prosthetic just because of the discomfort when wearing it
She is not afraid to hit Donald with a crutch BTW
IF THERE ARE ANY OTHER SPECIFIC HEADCANONS THAT YOU ARE CURIOUS ABOUT, SHOOT ME AN ASK! <3
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AITA for not saying please/thank you?
So this is an ongoing argument with my roommate. I (22nb) am autistic, and T (55f) has ADHD.
Now to get this out of the way, i do say thank you. I was always taught to wait a moment after receiving something, take a bite or appreciate what you were given for a breath, before thanking someone so that you could add something more to it. My roommate and I both agree that i do say thank you the vast majority of the time, but the problem for her is that i do not say it fast enough.
T often gives me a "tHaNk yOu" while the item in question is still being passed. This seems ridiculous to me as i haven't even been fully given it yet.
In addition, i have the dishes as my household chore, and i do them daily, despite almost never making any dishes myself. I do this to both support T and her diet, as well as contribute to the household that i live in.
T thanks me near daily for doing the dishes. This always seems weird and unnecessary to me, as it is my responsibility. I have told her this. I dont expect to be thanked for doing my own laundry, after all. In return, T gets upset that i dont notice and thank her for taking out the garbage/recycling/compost, to which she is the main contributor to and is under her responsibilities.
As for please: i do say this much more rarely. I think it feels overly preformative and fake, and i typical choose more "would you mind closing my door for me" "if its not too much of a hassle, could you toss me my waterbottle" "id appreciate it if you could preheat the oven while you're in the kitchen"
I think that these work perfectly fine as a replacement. Please just has always felt wrong and fake. No one else in my entire life has ever commented on this before.
Thirdly; T has been upset that i don't respond to her apologies appropriately. After she is snappy at me (due to her emotional disregulation from ADHD) (last time it was because i asked if she was using the oven instead of asking if i could use the oven myself, for reference) there is a 50/50 shot that she will come and apologize.
I dont often accept apologies. Apologies are for the person saying them to get it off their chests, or to make you put it behind them. Usually, ill say something like "it was just one of those days, y'know?" Or "its alright, water under the bridge"
Because i was always taught that apologies came with a promise of change, and T can't (or won't) change how she re-directs her frustration at unrelated things to things ive done "wrong". When she told me the correct response was "i forgive you", i decided to not engage instead of telling her directly that i didnt forgive her (because i am certain she will do it again). (I usually dont engage with her when shes irritated: she never notices and just wants to say her piece so im not being rude here)
She said that i was being disrespectful, "like always", and when i suggested it may be more difficult for me due to my autism, she said that we made plenty of accommodations for me (which i think is false), and that i just needed to do this for her comfort. That please/thank yous were something she needed to feel appreciated and i should be making more accommodations for her.
To me, i feel like she is getting really caught up on semantics and is being a little controlling about it. But maybe its just a boundary? I dont know if i could commit to changing my language for her though, i feel like i will just start forgetting after awhile because it feels so fake. Shouldn't it be better for me to say things genuinely than just for her approval?
AITA for not saying please/thank you?
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3liza · 7 months
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corset has become one of those things where I wonder why I feel so bleughhh and then I realize I'm not wearing it or haven't laced it up, stupid,
and then I do and instantly have blood in my brain again and start zooming around my house faster and thinking clearer. it's interesting how so much of this illness is purely mechanical. squeeze one part of your body to move fluids to another part of your body. apply pressure to an area that is sore and hurting and it feels better. idiot. moron
one of the lectures about POTS/EDS at the Dysautonomia Conference I think in 2022 ended with the presenter recommending corseting (she phrased it as "abdominal compression" because corset scary) by using waist trainer wraps for patients to immediately get some relief and restore homeostatic fluid dispersal to the parts of the body that need it. compression garments are recommended in the scientific literature for tons of stuff that doctors don't communicate to patients, including autism. not necessarily a corset corset with steel boning that looks like a fetish club item, but just general physical mechanical support for all these patients whose problems are either rooted in or comorbid with tissue laxity and bad orthostasis. if it's loose, add reinforcement. very simple mechanical principle we all understand intrinsically but somehow don't think of applying to our daily EDC of shit to handle our problems.
I have a friend with Problems Syndrome who describes the sensation of something being pulled downward uncomfortably from their chest and throat when they aren't tensing their abdominal muscles constantly. I do that too, it all has to be held in, held still, tensed and gripped or you feel like your body is collapsing like one of those string toys
anyway this is not to say "get a corset", because it's not the right thing for everyone obviously. also it's a lot of trouble to buy them and try them and break them in and not everyone wants to look like an extra from Sweeney Todd every day. I have that option because I'm a goth that works from home. I'm just blogging, don't take this as medical advice or even casual advice. I was just inspired to jot down my thoughts after thinking "why do I feel so shitty" today, lacing up the corset I had loosened earlier, and immediately regaining about 15% of my function.
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