At what point did you realize it wasn’t just PCOS, and was endo too?

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I 21F was diagnosed with PCOS this fall. I got a cyst removed, and was in and out of appointments after. I was seeing two doctors at the time in my University’s town. One who was trying to tell me PCOS isn’t real, and another who was saying my symptoms were sounding like endo after she diagnosed me with PCOS. I since left the town, after severe trauma medically, and personally. So right now i’m starting over medically. I am young and have a really high libido, but I have pain during intercourse/ or alone pleasure, I am having severe cramps (butthole lightning) in my anus area, horrid back aches, and my periods can be irregular but when I have them i’m going through Ultras in a hour. For awhile now my periods consist of clots around the size of my palm. GI wise I am either on the verge of shitting my pants, or i’m constipated to no end. The uterus pain is constantly, and will go up my back or down my leg. The only thing I feel like i’m good at anymore is sleeping ALL THE TIME. I can sleep for 16 hrs and be exhausted. Every single one of my blood tests they say “you’re fine” “this is kind of high, this is kind of low, but you’re fine change your diet, and take birth control” I am at the point I always feel like something is wrong, that i’m just so emotional. Should I start pushing more for them to check for endo?? Or is this just the joy of pcos?? Thank you to anyone who replies.   submitted by   /u/Standard-Ground758 [link]   [comments]