429
me_irl (lemmy.blahaj.zone)
submitted 4 days ago by [email protected] to c/[email protected]
you are viewing a single comment's thread
view the rest of the comments
[-] [email protected] 43 points 4 days ago

Translation: “I’m out of my depth here. I don’t know how to help. I would refer you to the right person but I don’t even have a good, professional referral network.”

[-] [email protected] 37 points 4 days ago

If your lucky. Often it’s just “I’m too overworked and busy to take you seriously”.

Or “I don’t believe you / think you are exaggerating”.

[-] [email protected] 19 points 4 days ago* (last edited 4 days ago)

I still remember the time I was like 17, hiking, and got bit by a tick just over my belt buckle, and a rash started to develop and the doctor was like “it’s a byproduct of an allergy to your belt” and prescribed me steroids. I basically begged for a Lyme disease test. If I didn’t get that test and those meds at the time (after testing positive for lyme), life would be way more fucked up right now

[-] [email protected] 5 points 3 days ago

Lucky the tests worked for you as they are notoriously inaccurate!

load more comments (1 replies)
this post was submitted on 16 Jul 2025
429 points (98.2% liked)

Chronic Illness

510 readers
1 users here now

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 1 year ago
MODERATORS