this post was submitted on 21 Dec 2024
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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.

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

😃 "And! Just so you know, dear...you've been APPROVED for MAiD! Only if you want to go there though." 😔

[–] [email protected] 4 points 2 days ago

Yes because she requested it?

I requested ADHD medication and was approved for that. If I don’t want to take it or if I want to stop taking it that’s my choice.

This is kind of how healthcare works so I don’t understand the sarcasm.

I think her approval for MAiD also boosts the visibility of her disease and how, again, all countries (not just Canada) care for people with this condition (spoiler: they don’t).

Telling this story in the media is a last ditch effort to get adequate care. Otherwise, she doesn’t want to live like this. Sounds reasonable.

Other countries like the US would probably just prefer she die homeless, poor, and quietly in the street somewhere, while still denying her care for her condition.