#chronic illness spoonie
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Anyone taking requests for Worst/DOFP!Logan?
I want someone to write a fic or headcanon about Logan (preferably the Worst or DOFP) in a relationship with a spoonie/Chronic (mental or physical) Illness reader/OC where they have limitations to what they can do and/or even pain days especially on bad weather days.
(More details below cut)
I want to see the reader having to explain shit to Logan about their mental and/or physical health. I
I want to see Logan realizing they have much to learn about himself too and this starts up questions that he has about his own mental and/or physical health with how it applies.
I want to see how Logan and the (non-healing-factor) reader have arguments and how they resolve them.
It doesn’t even have to be a sexual ending. Just want to read the real lifeness and dedication of the relationship and to each other. Do they do couple’s therapy to learn how to recognize and be able to address/understand each other’s emotional needs?
I want to see the reader help Logan through PTSD Nightmares. With his initial reaction being claws/attack/fight, how do they handle that so they don’t get injured, you know, especially the first time!?
I want to see Logan help the reader through a depression spiral and/or aftermath of self-harm and vice versa.
The reader could also be Wade/Deadpool too.
Tagging because I saw posts: @pleasantlycrazyworld
#trigger warning#fanfic request#logan howlett#wolverine#worst wolverine#dofp! logan#reader insert or headcanon#chronic illness spoonie#mental health#Logan has ptsd#dedication to each other#tw self harm or depression spiral#tw ptsd nightmare
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able bodied people will freak out when they see an ambulatory mobility aid user not using their aids but won't question it when a hiker only uses a walking stick or trekking poles when they're hiking. they're the same thing.
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Kinda fucked up that we all coo and sympathize with "former gifted kids" but never talk about the students who had to stay late after school or over the summer for remedial classes/clubs, who struggled to get above a C, who were given up on or punished. Who tried so hard to understand or just couldn't. Who were grouped with the "stupid kids" (a classmate called us that in remedial math btw)
Autistic kids and adhders who can't relate to their gifted peers and are constantly alienated by them. Kids who struggled in school due to dealing with a chronic or mental illness or physical/learning/developmental disability. Those of us who have had to drop out of highschool or college. Kids who worked so hard and wanted to be seen as smart, but never were. Who watched as their peers seem to fly by them in school, while they were left behind. Who were bullied and put down by those in the gifted and honors classes. Whose confidence was absolutely destroyed by education.
I love you all and I'm so sorry the school system failed you. I'm sorry you weren't properly accommodated and given the education you deserved. I'm sorry people put you down for something that they never had to fight for.
#wrenfea.exe#was going to keep this in drafts for a bit but wanted to post to give my solidarity with morg#gifted kids act like they are the most oppressed but in my experience they love feeling better than other people#disability#chronic disability#chronic pain#spoonie#chronic illness#physical disability#autism
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"everyone should care about accessibility because most people will become disabled at some point in their life" is a logical argument and I understand its popularity
however, everyone should care about accessibility because disabled people are fellow human beings living in the same society as you who deserve the same rights as you
thank you good night
#chronically ill#chronic pain#spoonie#cripplepunk#chronic illness#disability activism#disability#disabled
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#spooniestrong#spoonie#disability#chronic illness#chronic pain#ableism#disabled#autoimmine disease#autoimmune
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This makes so much sense
#chronic illness#chronically ill#chroniclesofchronicillness#chronic pain#invisible illness#invisible disability#spoonie#mental health#pots#svt#trigeminal neuralgia#potsandspoonies#100 percent
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#fibromyalgia#chronic illness#chronic pain#chronic fatigue#fibro#spoonie#chronically ill#invisible illness
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Chronic pain pisses me off cause I'm not even incapacitated for like a cool or badass reason instead my body is throwing the world's biggest temper tantrum because it's raining outside
#it feels like i got jumped by seven people but NO#if my body is going to make me feel like ive been stabbed five thousand times i should at least get a sword fight out of it im just saying#fibromyalgia#fibropain#fibro problems#fibro flare#fibro#chronic pain#chronic fatigue#chronic illness#hypermobility#hypermobile#hypermobility syndrome#spoonie#disabled#actually disabled#disability#c punk#cripple punk
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anyone else ever wish they could lie down harder? Like, I'm already horizontal, but I need more horizontal. I need to be absorbed by the floor. I think that would fix me
#My orthostatic tolerance is currently zero#POTS#postural orthostatic tachycardia syndrome#me/cfs#fibromyalgia#chronic illness#disability#migraine#gastroparesis#chronic pain#chronic fatigue#chronic fatigue syndrome#myalgic encephalomyelitis#spoonie#mast cell activation syndrome#MCAS#dysautonomia#chronic migraine#joint pain#hEDS#ehlers danlos syndrome#hypermobility#hypermobile ehlers danlos#interstitial cystitis
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i hate when i, a completely healthy person (very chronically ill), get sick (flare up) for no reason at all (i exerted myself way past my limit just cuz i didn’t wanna be “annoying”)
#chronic illness#actually chronically ill#chronically ill#potsie#pots#pots syndrome#spoonie#spoonies
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hi, you there who are or are thinking about spending all day in bed, it’s okay, I’m not telling you to get up. I’d just like to do a quick check in to make sure you’ve got everything you need to be comfortable and safe.
Have you gotten up to take any meds you need?
Do you need to open or close your windows or curtains/blinds to make your environment nicer? (Fresh air, keep the cold out, sunlight/darkness)
Do you have a water bottle or a glass of water easily accessible? (Can also be juice, cordial, a meal replacement drink or anything else)
Do you have any over the counter or prescription as required meds you might need, like painkillers or anti nausea meds?
Is your phone or laptop charged?
Are you wearing comfortable clothing?
Do you have enough blankets/pillows to be warm and comfortable?
Do you have any snacks like fruit or chips or muesli bars in case you can’t get up to make a meal?
Are you able to change positions in bed (or sit up if you’re able)?
Do you have any regulation tools like fidgets, ear plugs, or journaling/art books or low energy hobbies you might want?
Are you being gentle and patient with yourself and your body today?
Thanks for doing this check in with me. I like to have some of these things prepared on my nightstand, or all together in the same space in my room so I don’t have to do as much work on low energy days. It can also help to have someone else prepare or get these things for you if you’re unable. Hope you have an uncomplicated day.
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me carrying a stuffed animal around while being disabled is not "infantilizing disability"
I am an actually disabled person who carries a stuffed animal as comfort bc disability is hard
what's "infantilizing disability" is assuming that just bc I carry a stuffed animal I'm not capable of making decisions for myself. or that having a stuffed animal makes me a less serious, adult person than you are.
#disability#disabled#chronically ill#chronic pain#spoonie#cripple punk#cripplepunk#chronic illness#crutch user#actually autistic
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Having dreams crushed by disability is such a deeply traumatic experience, the realization that you’ll never be able to do the thing you want most in life because your body isn’t able to handle it. Waking up the day after you received the news and feeling that utter sense of heartbreak in your chest. Watching people go on and do those things while you sit on the sidelines, forced to watch bitterly. That feeling of being trapped, imprisoned by your inability to do what you love. The grief, the anger, the sadness. All because your body doesn’t allow you to.
#someone tell me to go to bed#poison is the posts#poison is the cripplepunk#disability#disabled#chronically ill#chronic pain#chronic illness#physically disabled#heds#hypermobile eds#hypermobile ehlers danlos#pots syndrome#pots#spoonie#cripplepunk
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Useful information
#chronic illness#chronic pain#disability#pots syndrome#postural orthostatic tachycardia syndrome#chronic fatigue#invisible disability#spoonie#fibromyalgia#potsie#tiktok
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Sorry I Spent all mY spoons this week already and it's fucking Tuesday. We're heading to the knives
#actually spoonie#chronic pain#fibromyalgia#actually mentally ill#chronic illness#aroace agender#spoonie#chronic fatigue#disability#actually disabled#chronic disability#spoon theory
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