#me/cfs
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they say you can't pour from an empty cup but i've been doing it my whole life and aside from all of these mysterious ailments it's working out great for me
#joke#burnout#burned out#people pleaser#chronic illness#disability#disabled#chronic fatigue#support needs#neurodivergent#neurodiversity#memes#cfs#cfs/me#me/cfs#fibromyalgia#pots syndrome#pots
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Disabled and chronically ill people are allowed to enjoy things and do things they like (if they’re able) while still being sick and disabled. Yes, even if they aren’t employed. Hope this helps.
#disabled#disability#epilepsy#pots#chronic illness#me/cfs#myalgic encephalomyelitis#autoimmune disease#hashimotos#postural orthostatic tachycardia syndrome#wheelchair user#dysautonomia#spoonie#pots syndrome#chronically ill#chronic fatigue
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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'm really worried for all of us. I want us to be as well as possible and for that to be the case we really gotta stay informed:










(resources compiled by sp0receress and agitpropnabsurdity on IG, I just copied em to share here)
best way to protect yourself is to wear a mask (n95 or kn95) wherever possible and do social events outside if you're not gonna mask. though the latter isn't foolproof, I read a case study of a jogger infecting a bunch of people in a park. it can happen.
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sometimes I forget standing up isn’t painful and difficult for most people so I’ll be watching something like game changer and see the people standing behind their podiums the whole episode and think ‘wow don’t they need to sit down. how can they still think coherent thoughts’ and then I’m like oh. yeah. I have a disease
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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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#covid#covid aint over#covid 19#coronavirus#wear a mask#masks are sexy#masking#mask up#masks#facemask#face mask#disabled liberation#long Covid#me/cfs#chronic illness#uk politics#us politics
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Reblog if you understand that disability is not a monolith and two people with the same disability do not have identical experiences ✨
#actually disabled#chronic disability#me/cfs#autoimmune disorder#chronic fatigue#chronic fatigue syndrome#chronic illness#chronic pain#disability#actually autistic#invisible disability#disabilities#sensory processing disorder#autoimmune disease#disabled#thyroid disease#fibro#fibromyalgia#hashimotos#high support needs#hyperlexia#autistic things#thyroid#cane user#wheelchair user#chronically ill#sensory issues#sensory overload#special interest
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Do any other chronically ill or disabled people feel like they're watching themselves rot away due to how little they can do as a result of their conditions
#chronic illness#chronically ill#disabled#disability#spoonie#chronic illness vent#cfs#me/cfs#migraines
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chronic illness really makes the weirdest ‘would you rather’ scenarios come to life.
like, would you rather: show up to christmas with no presents for anyone or show up having not showered for a week?
would you rather: feed yourself or do the dishes?
you can choose both but your penalty is to spend an unknown amount of time bedbound afterwards.
#me/cfs#chronically ill#cpunk#crip punk#cripple punk#myalgic encephalomyelitis#disabled#chronic illness#pots#potsie#spoonie#1k
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The ever-excellent Michiel Tack eviscerates the Miller et al BMJ editorial on ME/CFS in his e-letter, "The risk of blaming patients for their lack of recovery" which includes much more hard data than their weak, speculative editorial
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Fatigue feels like you have sandbags tied to your feet while trying to walk. It feels like you haven’t slept in weeks. It feels like gravity is pulling you down. It feels like cotton balls are in your head, clouding everything.
Fatigue is NOT the equivalent to being tired.
#disabled#chronic illness#epilepsy#me/cfs#myalgic encephalomyelitis#pots#pots syndrome#postural orthostatic tachycardia syndrome#dysautonomia#autoimmune disease#hashimotos#long covid#disability#chronic fatigue
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Anyone else with chronic pain ever get really absorbed in a project and dissociate from your body while you're working but then you finish and you come back to your body and you're just like AAAAAAAHHH! WHAT'S WRONG?? oh yeah. The horrors. Never mind
#my body is ouchie#chronic illness#disability#fibromyalgia#me/cfs#migraine#postural orthostatic tachycardia syndrome#chronic fatigue#chronic pain#gastroparesis#pots#hEDS#ehlers danlos syndrome#hypermobile ehlers danlos#hypermobility#the horrors persist but so do I#the horrors#interstitial cystitis#I no longer desire internal organs#or bones#oof ouch my bones#dysautonomia
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I still can't believe we've just stopped talking about covid. it's so surreal to watch it destroy people's lives and most people have no idea what's happening. I can't believe we're putting kids in the position of getting covid over and over again.
if you have new weird symptoms or conditions popping up seemingly out of nowhere, it could very well be as a result of having had covid. if you're collapsing into bed at the end of your workweek, bone tired, it could be because of having had covid.
it causes multi systemic issues, damages blood vessels and the brain, triggers the development of chronic conditions and autoimmune diseases and more. pots and mcas are really common. symptoms can look a lot of ways because the impact of covid is multi systemic.
I know this is alarming. but I gotta say, having had postviral illness for many years, getting started on treating these things has improved my quality of life significantly. there is no cure for a lot of it, but life can still be made better with the right medicine.
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Long Covid Justice on COVID and LONG COVID from the mask ban teach-in
COVID/SARS-CoV-2 basics
It is NOT seasonal, like the flu is.
Spreads through air, like smoke.
The 6 feet apart rule is no longer great prevention advice.
Handwashing is a great hygiene practice, but transmission via surfaces is unlikely.
Vaccines do NOT prevent transmission. They reduce symptoms and severity for some.
You can transmit [COVID] while completely asymptomatic. Around half of transmission is as asymptomatic or presymptomatic. Everyone's immune system is different.
Being indoors increases risk of transmission, but you can still get it in crowded outdoor spaces.
What is Long Covid?
Long Covid is a set of health issues after someone has COVID-19
New health issues, ongoing issues, or worsening of previous symptoms and conditions.
It is a biological disease that affects hundreds of millions of people globally. It is a mass disabling condition and crisis.
It can cause significant disability and can be fatal.
Anyone can develop it, and up to 10% of people with COVID will.
Severity of initial infection doesn't correlate to potential to develop Long COVID.
It can be very hard to get a diagnosis and proper treatment or care for Long COVID.
Every time you get COVID infection, you increase your chances of developing Long COVID.
How do we prevent Long COVID? Layers of protection
Masking.
Air filtration.
Ventilation.
Vaccines.
Testing (right now Aug 2024, rapid tests are only about 20% reliable. Try to test two times in 24-48 hours).
Nasal sprays before and after exposure. (little data on these being effective against COVID but some are choosing to use them until more research comes out)
Mouthwashes with CPC (Cetylpyridinium Chloride) before and after exposure. (Must be used for at least 60 seconds)
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