Hi everyone, I'm new here ☀️
and I wanted to ask about your experiences with diagnostic laparoscopy.
Some time ago I went to see a endometriosis specialist and during an ultrasound she discovered something that "could very well be endometriosis but could just as well not be", as she put it (so basically a 50/50 chance I guess). (Actually had an appointment with her twice and she said so both times).
She said I was welcome to book an appointment for laparoscopy, but afterwards I probably would have to take the pill anyways, so I might just as well take it now and not go through surgery. The decision is completely up to me, she didn't make any recommendations.
I struggle to make a decision.
I experience so many symptoms that other women diagnosed with endometriosis experience (especially chronic fatigue) - sometimes I see posts by other women and these are my symptoms exactly.
However, my period doesn't seem to be nearly as painful as for some women affected by endometriosis. I find it to be really painful, but by no means am I close to fainting, like I've heard other women say.
I know some women go without any symptoms at all, but my other symptoms being so strong and the pain not being that strong (compared to other women)...? Is that even possible?
(I know, I should have asked my doctor about this 😅).
I also know, ultimately I have to take the decision based on what feels right to me, but I was hoping for some input; what are your experiences with diagnostic laparoscopy (particularly compared to taking the pill)?
Looking forward to your input! Have a lovely day 🌸