#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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#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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"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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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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just a kind reminder to please be kind to the people you know with gastrointestinal disorders/conditions! they're embarassing, often very painful - sometimes debilitating - and very hard to talk about without oversharing a lot more than most are comfortable with.
if someone you know:
- spends a lot/long time in the restroom
- has a colostomy bag
- requires diapers or similar implements
- experiences a lot of gas and/or bloating
- requires tube feeding or other alternative methods of nutrition
- has food restrictions (e.g. cannot handle a lot of spices, certain proteins, etc.)
- eats a lot, or only a little
or other similar factors of their life...
please be patient and understanding, it's hard having guts that really like disagreeing with you!
#chronically ill#chronic illness#spoonie#disability#i dont know too many specific conditions so apologies for vague tags
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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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#fibromyalgia#chronic illness#chronic pain#chronic fatigue#fibro#spoonie#chronically ill#invisible illness
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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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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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I found an extremely dope disability survival guide for those who are homebound, bedbound, in need of disability accommodations, or would otherwise like resources for how to manage your life as a disabled person. (Link is safe)
It has some great articles and resources and while written by people with ME/CFS, it keeps all disabilities in mind. A lot of it is specific to the USA but even if you're from somewhere else, there are many guides that can still help you. Some really good ones are:
How to live a great disabled life- A guide full of resources to make your life easier and probably the best place to start (including links to some of the below resources). Everything from applying for good quality affordable housing to getting free transportation, affordable medication, how to get enough food stamps, how to get a free phone that doesn't suck, how to find housemates and caregivers, how to be homebound, support groups and Facebook pages (including for specific illnesses), how to help with social change from home, and so many more.
Turning a "no" into a "yes"- A guide on what to say when denied for disability aid/accommodations of many types, particularly over the phone. "Never take no for an answer over the phone. If you have not been turned down in writing, you have not been turned down. Period."
How to be poor in America- A very expansive and helpful guide including things from a directory to find your nearest food bank to resources for getting free home modifications, how to get cheap or free eye and dental care, extremely cheap internet, and financial assistance with vet bills
How to be homebound- This is pretty helpful even if you're not homebound. It includes guides on how to save spoons, getting free and low cost transportation, disability resources in your area, home meals, how to have fun/keep busy while in bed, and a severe bedbound activity master list which includes a link to an audio version of the list on Soundcloud
Master List of Disability Accommodation Letters For Housing- Guides on how to request accommodations and housing as well as your rights, laws, and prewritten sample letters to help you get whatever you need. Includes information on how to request additional bedrooms, stop evictions, request meetings via phone, mail, and email if you can't in person, what you can do if a request is denied, and many other helpful guides
Special Laws to Help Domestic Violence Survivors (Vouchers & Low Income Housing)- Protections, laws, and housing rights for survivors of DV (any gender), and how to get support and protection under the VAWA laws to help you and/or loved ones receive housing and assistance
Dealing With Debt & Disability- Information to assist with debt including student loans, medical debt, how to deal with debt collectors as well as an article with a step by step guide that helped the author cut her overwhelming medical bills by 80%!
There are so many more articles, guides, and tools here that have helped a lot of people. And there are a lot of rights, resources, and protections that people don't know they have and guides that can help you manage your life as a disabled person regardless of income, energy levels, and other factors.
Please boost!
#signal boost#please reblog#I'm so so glad this has gotten the traction that it has!#chronic pain#chronic illness#disability#fibromyalgia#cfs#chronic fаtiguе ѕуndrоmе#actually disabled#spoonie#me/cfs#cfs/me#long covid#important#invisible disability#ehlers danlos syndrome#lyme disease#chronically ill#cpunk#cripplepunk#it's a bummer that it's so US centric but if you're outside of the US you can look into similar programs#I hope that other countries have options like these#the US seems so behind when it comes to medical care and disability resources. and i mean it is#but it's good to know all of your rights as a disabled person or if you ever become disabled
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