I don't know if anyone has posted about this yet (I haven't seen anything but it's entirely possible I missed it) but March is Endometriosis Awareness Month, and I was wondering if anyone here would be interested in reading a bit about this crappy disease and what some great resources are. I know a lot of information that doctors, hospitals, and even websites give out is really out of date and not necessarily accepted as fact anymore, which is really hard for women because there is already so little known about endo and the way it affects our lives.
If there isn't a lot of interest I will stick to papering my Facebook wall and Twitter account with endo facts and info, but if you guys are interested too I would love to write something about it here and provide some information and great resources. Most of the information I have is for Australia and the US, but I know a lot of European countries have some good resources as well. Endometriosis can be devastating but I've found that information is power, because there is no worse feeling in the world than someone telling you your pain and illness is entirely in your head.