i’m newly diagnosed with endometriosis through exclusion and symptoms. i’ve been having frequent bouts of sharp ripping, tight and burning pain on my right side. i got an ultrasound back in february at my old obgyn and they did everything they could to find my right ovary but couldn’t. the doctor i saw said it was normal for that to happen and brushed it off. he also said that because i’m only 20, i’m too young to deal with endometriosis and too young for a lap. i felt weird about it so i sought out a second opinion. i had been reading other womens stories about their endometriosis adhesions and it made me wonder if that could possibly be why my ovary is “missing”. i finally met up with an incredible doctor and we did a scan yesterday and low and behold, my right ovary is still nowhere to be seen. instead of brushing it off, my new doctor said he thinks it could be stuck to another organ from adhesions and that he thinks we should look into finding out where it is. it was so relieving to hear that! sometimes a little validation goes a long way. i was wondering if anyone else had this same problem? thanks for any replies!