After years of pain, food allergy tests and supposed IBS, I had my first significant appointment for endometriosis today, getting an internal and external ultrasound. Although I was pleased to hear that my ovaries and uterus did not look inflamed, I wasn't really told any other information and will have to wait to talk things through with my doctor.
I was disappointed when the technician told me they can't really see anything on scans like this and don't know why they get asked to do them, but the chances of them offering to do a laparoscopy are slim because of how invasive they are.
I left feeling a little bit lost - what if I do have endo but they don't deem it significant enough to properly investigate with a laparo? Do I just live in this no mans land of undiagnosed? How can you treat something without truly knowing what it is?
How difficult did you all find it to get a laparo? Did your results from your ultrasound differ to what was found in a laparo if you were offered one?
All advice welcome x