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

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.

founded 4 months ago

MODERATORS

[email protected]

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"Don't do sick" until you're sick... (lemmy.blahaj.zone)

submitted 1 month ago by [email protected] to c/[email protected]

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[–] [email protected] 7 points 1 month ago (1 children)

I just want to offer my two cents as someone who is disabled. I understand you viewpoint, and I don’t think it makes you ableist, but the sentiment definitely leaves a bad taste in my mouth.

1.) You can have that opinion without being ableist, but it’s a pretty insensitive thing to express. I understand you’re probably not going around telling disabled people that, but it can come across as “a disabled life isn’t worth it”, whether you mean it or not.

2.) It’s a blanket sentiment that raises the bar of what you consider to be disabled. Would you really rather die than have autism or ADHD? Or maybe POTS? Or IBD? Disabled is a very broad term that encompasses far more than profound physical disabilities.

Between those two, as someone who is disabled, I’m left wondering whether someone is implying my life isn’t worth living, or that they don’t consider me disabled enough. Again, not trying to come at you or call you ableist, just trying to explain how it could possibly come across poorly.

[–] [email protected] 4 points 1 month ago

I see and agree with both points. I definitely keep such choices to a very tight circle (like I gave instructions to my partner and family in what to do should I end up in certain situations - also called biological testament in Italian).

I also mentioned that indeed I would consider certain disabilities a deal breaker for me not to keep living, definitely not all disabilities. I would actually say that there are things that I want to do in life, and if I can't - for whatever reason - that would be a reason not to live for me. Whether it's a disability, a material condition, etc. It's not really relevant - a disability can simply be a proxy not to be able to do something.

For example, I fought tooth and nail to ensure that my grandma would receive the proper care when she had dementia (which is a disabling condition I would say?). I also took care of her directly, and I would do that again a thousand times. However, should I get a similar condition, I let my family know that I would like to be euthanized, I don't want to live like that.

Finally, this perspective is really really personal, it is bound to my experiences and my idea to the point that it can't simply apply to anybody else. I would definitely never go to anybody and say "if I were in your shoes I would rather die", but even if I thought that, this is a meaningless statement for another person. It's of course extremely rude to say this, so once again, I am saying it for the sake of a theoretical discussion.

Overall for me this is a matter of free will and agency over your own body, it's in anthithesis with the religious view that considers your body not yours and suffering a noble thing in itself.