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"Oh you're so lucky, I wish I could spend so much time in bed"
(lemmy.blahaj.zone)
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this post was submitted on 17 Sep 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
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Be excellent to each other
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Absolutely no ableism. This includes harmful stereotypes: lazy/freeloaders etc
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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.
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No denialism or minimisation This applies challenges faced by chronically ill people.
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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
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No this is real and happens all the time.
I have neuropathy and it just literally does not matter what I tell 99% of people, they'll almost all say I am lying and lazy and get angry when I tell them 'ok, I can try to go out and do this physical thing, but I'll be in screaming pain after an hour or two and need to rest for the next two days.'
Last two girlfriends I had literally did not give a shit, kept pushing me far beyond the limits I told them I had and then got angry at me about it.
One refused to stop going on rides at a county fair so that she could let me sit in her car before my phone died. I ended up writhing in pain outside her car for 2 hours before she noticed.
Another had me walking around for about 8 hours 3 days in a row for a convention, after we both agreed I could only do about 2 hours a day. Had to take a week off work to recover. So I paid for the whole outing, then lost a week of work pay, and the net result was she was angry I ruined the whole experience for her.
People do not fucking register non obvious illnesses. Even mental illnesses, at least among younger people, now have better social acceptance than chronic pain.
You can tell people who tell you they love you that what is easy for them is excruciating for you and they don't understand why causing you to be in excruciating pain and then belittling you about it causes you to be angry.
I finally got SSDI and just live alone now, cut off contact with everyone. Never been less stressed out, haven't had this good of at least mental health in over a decade.
Don't have people constantly shaming me and guilt tripping me. So, so much less stress.
:( that's awful, I'm glad you cut those people off. Hopefully you find better someday
I hope you find better people in your life, my partner is also dealing with undiagnosed chronic pain (we're going through appointments still), i can't say i understand what you feel but i know how it affects her, and that's probably pretty similar. You deserve better, hope you find relief and better friends.