How did they know you still had endomitosis still on you?

Yes, I have gastroparesis, IBS, Gerd, etc ... It's been a struggle for years. I almost had to a colostomy bag because the Endo was so bad on bowels and go track last year I believe. I've had five surgeries as well. I'm currently going to speak to the GI doctor today because I'm having issues just even drinking anything and I barely am able to eat anything. I understand the frustration. I hope you found a good GI doctor you need someone who works with Endo patients as well a specialist. I hope everything works out. Good luck. Unfortunately, Endo grows everywhere.

Sunshine, my last surgery the surgeons left livevendo in my rt ureter and pelvic cul de sac due to the depth of the endometriosis.

Thank you for sharing your story and I'm sorry you're going through this and have gone through it for so long! I have been dealing with various issues for 20 years. To be frank, I've always thought my issue was with my GI tract, which I think is one reason it took so long to get a proper diagnosis. I have been diagnosed with "IBS" but I always say that's what they diagnose you with when they don't know what is wrong with you. I feel like nothing has helped me. No diet changes, no medicating, nothing.