This is an automated archive made by the Lemmit Bot.

The original was posted on /r/ehlersdanlos by /u/Fun-Savings2349 on 2023-10-05 13:10:44.

I think it’s so funny that a lot of the physically well people we’ve had problems with regarding eds whether it’s friends, family, or partners will be so quick to dismiss us or ignore our reactions to our symptoms, but expect sympathy when they get a viral illness or a cold… it’s just odd how they forget they only have to experience those mildly uncomfortable symptoms for at most a week, but it’s everyday for us. Just imagine how dramatic the people in your life would be if they had even HALF the eds symptom list.