Got my biopsy results and he said it’s endo , which makes no sense as they have always been adamant I don’t have any. So I’ve had a hyesterctomy nearly two years ago for ovarian cysts and pain for years, and have been ok for a year and a half then agony and severe diaorhea. They thought I had kidney infection but it was a big cyst they thought was ovarian remnant syndrome. My point is where has the endo come from if I haven’t had it before and have no ovaries anyway... so disheartened I’ve emailed my consultant for more information... I want a follow up to tell me exactly what was found and why.
Feels like endometriosis is just shoved aside and ignored as we all sit here in agony
Stay safe stay well