hi everyone, looking for some advice & to see if anyone has the same symptoms as me.
I have been on the waitlist for diagnostic laparoscopy surgery for suspected endometriosis for over a year now and have been trying to get a diagnosis for around 8 years.
My symptoms seem to be getting worse recently especially ibs type symptoms around ovulation - is this common for anyone else with endo/suspected endo & if so do you have any tips for helping it? It adds to the pelvic pain and discomfort & finding it really hard to manage the pain and symptoms at the mo. When the pain is really bad it makes me feel quite alone as hard to explain to those around me so just wondering if anyone gets similar symptoms too?
any advice greatly appreciated, thank you 🤍