Thank you all very much. It seems everybody wants a national action plan, and I know that the September funding was mainly about access, but how would you see some of that money going to actually map out what's there and not there? From what I'm hearing from Dr. Jolly, I think if young women knew about it.... As a humble family doctor, I had lots of patients come in and say, “Do you think it could be endometriosis?”
If you build that health literacy, sometimes it shortens how long it takes to get the imaging or all of that. My question is on what would be in an action plan.
Also, in the specialized imaging, it sounds like it's only going to be in certain places across the country. Is there a way that could happen virtually with technicians in various places, but the actual imaging happening in the specialized sites? In the referral system, again, how do we make sure it's equitable across the country, without people having to get on a plane? Is it just that it's not on the billing schedule, or is it that there are wait times and people then choose to go private or go to the States?
Anybody can have a go at any of it.