…you look up dysautonomia because someone says that the symptoms you’re experiencing fit pretty well into dysautomanias description, and lo and behold, they do.
Can’t say I’m all that surprised, seeing as quite a few other EDS sufferers have it, so if I did officially get it, it wouldn’t be all that weird, just more painful and a lot more annoying.
Anyway, to continue on this tangent, do you want to know what having EDS feels like? A fellow Zebra wrote a blog post about the most horrible things about having EDS, illustrated with memes, and in a very cute font too! Please go check it out!
Love to all!