So I've been emailing back and forth to a patient education liaison about my whole HHT(my hereditary disease), what my specialist says he has researched, and what is true. She works for the HHT international foundation. This is all she does is work with thousands of people with HHT, doctors that only research/treat HHT, and she herself knows pretty much all there is to the disease itself. And she is dumbfounded as to why I'm being treated this way. I have no higher risk than any other woman in the WORLD for uterine rupture trying for VBAC. And him telling me that I could have a spontaneous bleed from an unknown AVM in my uterus is unfounded because that is insanely rare! She emailed me all kinds of literature for me to give him. And I'm DEMANDING to see his "research" monday. I'm also calling some more midwives, seeing if one will pick me up, and telling everyone that keeps feeding me bs to sit and spin.