As someone already considered disabled before my endo diagnosis, I am on medicare for insurance. They won’t allow me to see anyone for Excision, let alone an expert, it’s all hormone treatments, go to a gastric specialist for a colonoscopy, have an ultrasound, if anything. I consider myself “lucky” my endo physically blocked a surgeon from reaching a surgical site as it is probably the only reason I was finally diagnosed, (it was with histologic confirmation, samples from the unrelated surgery were sent and confirmed to be endo adhesions and I had endometriomas on the ovary.)