Hi all! First off I just want to say that I’m so grateful this Reddit page exists; it’s taught me so much about what to ask for regarding endometriosis care (this is a serious lack of education within the medical industry!). After 5 years of chronic pain, I started taking the steps to get help. I was referred to get a transvaginal ultrasound via my PCP. Thanks to y’all, I know that it’s pretty common for Endo to not get spotted. I got the unfortunate results that they did not see any endo. What are recommendations for next steps? Should I push for a Laparoscopic Surgery? Are there things I should be aware of when it comes to asking for next steps? I’m trying my best not to be disheartened by the ultrasound results. For some context: my mom had endo and had to undergo laparoscopic surgery in her late 20s. Her sister had a hysterectomy due to endo and her other sister had fibroids. My grandma (her mom) also have endo. I feel like it’s basically a given that the chronic cramping, bloating, painful periods and inflammation I’ve experienced can be attributed to Endo.   submitted by   /u/Leather-Sun619 [link]   [comments]