FundMECFSResearch@lemmy.blahaj.zoneM to

Chronic Illness@lemmy.worldEnglish · 6 days ago

Ahhh more ableist classics

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Ahhh more ableist classics

lemmy.blahaj.zone

FundMECFSResearch@lemmy.blahaj.zoneM to

Chronic Illness@lemmy.worldEnglish · 6 days ago

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6 days ago
Yeah, no question. Pain is still pain. There’s just an aspect of discovering how much more you can endure than you thought you could until what was once unbearable is just your normal.

Chronic Illness@lemmy.world

chronicillness@lemmy.world

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A community/support group for chronically ill people. While anyone is welcome, our number one priority is keeping this a safe space for chronically ill people.

This is a support group, not a place for people to spout their opinions on disability.

Rules

Be excellent to each other
Absolutely no ableism. This includes harmful stereotypes: lazy/freeloaders etc
No quackery. Does an up-to date major review in a big journal or a major government guideline come to the conclusion you’re claiming is fact? No? Then don’t claim it’s fact. This applies to potential treatments and disease mechanisms.
No denialism or minimisation This applies challenges faced by chronically ill people.
No psychosomatising psychosomatisation is a tool used by insurance companies and governments to blame physical illnesses on mental problems, and thereby saving money by not paying benefits. There is no concrete proof psychosomatic or functional disease exists with the vast majority of historical diagnoses turning out to be biomedical illnesses medicine has not discovered yet. Psychosomatics is rooted in misogyny, and consisted up until very recently of blaming women’s health complaints on “hysteria”.

Did your post/comment get removed? Before arguing with moderators consider that the goal of this community is to provide a safe space for people suffering from chronic illness. Moderation may be heavy handed at times. If you don’t like that, find or create another community that prioritises something else.

Visibility: Public

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