hey everyone! I am having my first ever rheumatology appointment in a few days, and I was wondering what I should expect? Or if there’s anything I should be prepared for? (Both in good and bad scenarios haha)(types of testing, things that might be shut off etc.) The rheumatologist is unfortunately not EDS aware, but he allowed me to send over a list of information about it. Slightly hopeful given that he hasn’t kicked me out of his appointment list. I’ve prepared a full list of symptoms, sorted into multiple categories already. Just a little nervous. Am honestly not expecting a good outcome because well, we all know🤣. But at the same tome i hope to be able to stand my ground without feeling too crazy

Posted by Deleted (ade58139) at 2022-10-21 11:38:35 UTC