this post was submitted on 12 Jun 2025
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Chronic Illness

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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

  1. Be excellent to each other

  2. Absolutely no ableism. This includes harmful stereotypes: lazy/freeloaders etc

  3. 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.

  4. No denialism or minimisation This applies challenges faced by chronically ill people.

  5. 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.

founded 11 months ago
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Alt Text:

Disabled fantasy: Being able to sit in the room with all the doctors who ever asked if you were maybe just making your symptoms up...while they experience your symptoms. And ask them if they're making them up

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[–] [email protected] 22 points 1 week ago (8 children)
[–] [email protected] 5 points 1 week ago (7 children)

As someone with chronic fatigue due to long covid i can relate to this hard. I only had to wait 2 years to start with some experimental meds tho so not all is bad.

[–] [email protected] 2 points 1 week ago (3 children)

Chronic Fatigue ≠ ME/CFS [Hallmark symptom of ME/CFS is PEM]

So sorry to hear you got post-COVID tho. Hope your baseline improves.

[–] [email protected] 1 points 1 week ago

I might want to add, "hope that your baseline improves " is a very good way of expressing well wishes to someone where you know that "get well soon" is just not the right way for someone with a chronic disease that doesn't get much or any better soon!!! Love it, will steal this ^^

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