Hi, Everyone. I need your help again, please. I'm going to be meeting with a Gastroenterologist. She will be doing an endoscopy on me without any kind of numbing or anesthesia. I only hope to do this once and hopefully not need to do it again for years, if ever. I am also hoping someday (this fall or next year) to maybe see KDM or one of the ME/CFS Doctors in the Bay Area. The only doctor of our medical condition I've been able to see so far is Dr. Chia. (He did blood work that shows I have enteroviruses.) Here's my questions: Is there anything in particular they (the ME/CFS doctors) would look for regarding me having ME/CFS that I could ask her to biopsy/test for? And should I/could I have anything sent to their labs? Thank you for any ideas, and knowledge, it helps a lot.