We couldn't go one meeting without someone being on mute.
I just want to say quickly that I think when you speak with people who have endometriosis, a lot of the mental health concerns they experience come from being disbelieved by their health care providers, by their families, by their friends, by their communities. A lot of the burden comes from that.
I think in addressing some of the delayed diagnosis issues, we'll also have an opportunity to mitigate the effects on mental health—not completely but certainly, I think, in a significant proportion.