This is an automated archive made by the Lemmit Bot.
The original was posted on /r/cfs by /u/Dryrange12 on 2025-07-31 04:20:47+00:00.
I feel like most advice people offer are almost never adjusted to people with chronic illnesses and essentially CFS or Dysautonomia.
It’s tough. Everywhere I go I’m labeled either lazy or a faker lol
I don’t go for looking for empathy online but it’s the same even in person
Title is a bit harsh. Couldn’t find the correct term.
You must log in or register to comment.