Hi everyone, so after 3 years of fighting i was finally diagnosed with endometriosis a couple of months ago by MRI.
Initially i was told that i have deep infiltrating endo on my uterus and my bladder. Because of it being on my bladder they were contemplating referring me to a specialist endo clinic to have it removed.
However today my gyne called me to say that it actually isnt on my bladder or my uterus and that its just in my ligaments (still deep infiltrating) so they can do the surgery there (my local hospital). So now im completely unsure what to believe baring in mind that when my MRI was first looked at i was told that there was no endo whatsoever!!! Kind of just ranting but if anyone has any advice on what i should do that would be very much appreciated!
**for context, I’m being treated in France
Thank you x