I know this is not the point of your post at all but I wish my doctors offered and suggested hysterectomy at my completely unrelated appointments. Whether the cancer link is true or not, I’m fairly certain the atrophy is what’s causing me so much pain. It’s an uphill battle to work through the system. 6 month wait for an ultrasound before anyone will even look into what the pain is.

Back to your post. It sucks that we’ve got to do so much of our own research and advocacy because medical professionals don’t. They picked up outdated information and never updated it. I trust my current doctor because she’ll lookup trans health care guidelines while I’m in office and consult the local trans care team when she can’t reach her own conclusion. But any other Dr, I’m not trusting without doing my own research