#chronic-illness — Public Fediverse posts
Live and recent posts from across the Fediverse tagged #chronic-illness, aggregated by home.social.
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If I had a dollar for the amount of blood tests and urine samples I have had to do over the years with disability(and especially recently with additional health stuff), I'd be able to afford my groceries and bills without issue😂😅
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RE: https://social.saarland/@achim/117220772698874452
Fühle dich von ❤ gedrückt, liebe @afelia ! Ich wünsche dir, dass dein Zustand sich bald bessert 🌻
Und ich danke dir für deine wie immer wahren und wohl gewählten Worte. Die Frage nach dem Wert ist für mich in einem Crash immer noch fast unerträglich. Wortmeldungen wie deine sind da bisweilen sehr wertvoll und tröstend. Danke, dass du sichtbar bleibst! 🫂
#mecfs #chronischkrank #chronicillness -
This is shameful discriminatory and misogynistic reporting.
People aren’t choosing disability to be “cool”.
Young women don’t have to “prove” to you that they’re sick.
Disability rates are skyrocketing because we’ve left a disabling virus rip through the population for over 6 years.
The insinuation that disabled women who post about their experiences are “entrenching a culture of economic inactivity” is ableism.
They want to shame us into being silent about our suffering.
Make noise.
Let’s tell the Telegraph this disgusting article should be retracted
https://www.telegraph.co.uk/news/2026/09/05/disability-became-cool/
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Can anyone spot me a few e-gift cards for groceries? it would help me out a lot.
On my wishlist. https://throne.com/kswriteshere
#mutualaid #directaid #disabled #artist #queer #lgbtq #poverty @[email protected] @[email protected] @disabledvoices @[email protected] @[email protected] @creativearts @povertyandinequality #spoonie #chronicpain #chronicillness @spoonie @queer
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4/
“It can be helpful to explore abandoning (or at least curbing) an achievement-orientation to life (i.e., life is about a checklist of completed accomplishments) and instead adopting an experience-orientation to life (i.e., life is about having all kinds of varied pleasant and difficult experiences that we can use for various things like connection or growth).”#chronicillness #spoonie #mecfs #longcovid
@mecfs @longcovid -
One of my chronic conditions has been flaring badly lately and my doctor wouldn't renew my prescription for the one med that's been getting me out of bed for the past year, and also wouldn't order any diagnostics or refer me to the relevant specialist. My partner has been telling me for years: You need a new doctor. So, yes, he's right. But also that's easy to say.
#chronicillness -
You won't believe this. I did 2 minutes of yoga this morning and it completely cured my genetic joint problems and restored my mental health!
Ok. Not really. I'm actually just stuck on the floor and tooting this while I figure out how to get up.
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OH FOR....
Being allergic to my MEDICAL ALERT BRACELET is a NEW FUCKING LOW.
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The Looking Glass
Alice peers through a looking glass and discovers another version of herself—one untouched by pain, grief, fear, and survival. What follows is a quiet reckoning with freedom, resilience, imagination, and the strange ways we learn to recognize ourselves.https://kandiblaze.wordpress.com/2026/09/04/the-looking-glass/
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My pain medication was lowered a week ago due to it likely being the source of the swelling in my legs. I've barely been able to function because of the pain. I've also been having to go to a nursing care centre daily for wound care for 3 days now, and sitting on the exam table for 40+ minutes makes my pain way worse. Today I needed physical help getting back into the car, because I was so sore and weak. I also had to cancel an outing today due to pain. #ChronicIllness #Fibromyalgia
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RE: https://lgbtqia.space/@aceofcosmicspace/117209647785511701
Thank you! I only need $30 to go to reach my goal to get the food I need now. Please help if you can. Boosts help too♥️
#boost #mutualaid #disabled #disability #chronicillness #community #bisexual #lgbtqia #trans #assist
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RE: https://me.dm/@kshernandez/117205123370324265
If I had misspelled kitties as tiddies, I wonder if anyone would've matched this 35 by now... tiddies.
#mutualaid #directaid #disabled #artist #queer #lgbtq #poverty @[email protected] @[email protected] @disabledvoices @[email protected] @[email protected] @creativearts @povertyandinequality #spoonie #chronicpain #chronicillness @spoonie @queer
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From Canada 🇨🇦
‘Prov[ing] What You Already Know’: The Overreliance on Medical Evidence in Adjudicating Ontario Disability Support Program Applications
Free fulltext:
https://digitalcommons.osgoode.yorku.ca/jlsp/vol38/iss1/6/#MEcfs #chronicillness #Disability #PwME #CFS #hiddenillness
#invisibleillness
#ChronicIllnesses
#Spoonies
#Spoonie
@mecfs -
Who can match the 35 received today
A great #WhiskersWednesday shot from a favorite #Twitch stream. #CatsofMastodon
I'm hoping these lovely kitties will inspire folks to help me with my #urgent move goal.
Do they? Can you?
All is appreciated!Deets and ways to aid: https://linktr.ee/khernandez
#mutualaid #directaid #disabled #artist #queer #lgbtq #poverty @[email protected] @[email protected] @disabledvoices @[email protected] @[email protected] @creativearts @povertyandinequality #spoonie #chronicpain #chronicillness @spoonie @queer
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my allergy shots didn’t get delivered yesterday as this is a specific medication can only be given exactly 2 weeks apart not even a day early if I get them of my current schedule I’ll
Have to cancel & reschedule 12 appointments so the next two weeks I need extra support & if I go MIA you know why 😂 -
What irritates me here is that for those of us with POTS could likely have benefit from something like this by increasing oxygen to the brain even though bloodflow is reduced...
Then I wake up and realize this is America where we don't give a shit about giving people better lives, just finding optimal ways of killing more people for profit.
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RE: https://mastodon.social/@ellespeaks/117199420020373951
$25 due in 12hrs!
for my co pay or i have to cancel the appt 🆘️⚠️Im disabled, queer + estranged from family since losing my gram September 2024. Anything helps!
V: d_fay
Pp: peach77
Kofi: https://ko-fi.com/ellespeaks#mutualaid #MutualAidSavesLives #MutualAidRequest #helpfolkslive #disabled #spoonie #chronicillness #lgbtq #crowdfunding #gofundme #directaid #queer #hunger #poverty @[email protected] @[email protected] @disabledvoices @[email protected] @[email protected] @queer @disability #disabledmutualaid @povertyandinequality
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Classes officially start today.
It’s eclipsed by:
I see my Rheumatologist this afternoon because of this massive flare up I have been in for a month that’s nothing like what I’ve experienced before.
I’ve very likely failed this biologic (#5) and have to switch meds. The med I’m most likely to try next that’ll stop all of this pain?
… there is a shortage of.
FML I hate being chronically ill.
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Living with ME & fibromyalgia: ‘In 10 years, I had 10 pregnancies. It was a decade of loss, & a fight to get the family we wanted’ (Paywall)
Link for Dublin Fringe Festival's "Chronically Hopeful", Sept 6-9
https://www.fringefest.com/festival/whats-on/chronically-hopeful
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The Class Work Project have a call out for submissions on disability and chronic illness for their next issue of their journal Lumpen.
https://theclassworkproject.com/lumpen-19-call-for-submissions/