{"version":"1.0","type":"rich","provider_name":"Acast","provider_url":"https://acast.com","height":250,"width":700,"html":"<iframe src=\"https://embed.acast.com/$/61722772c2948100146d29f4/619ecd402acda800133e6c34?\" frameBorder=\"0\" width=\"700\" height=\"250\"></iframe>","title":"Endometriosis sufferers got an apology. What next? ","thumbnail_width":200,"thumbnail_height":200,"thumbnail_url":"https://open-images.acast.com/shows/61722772c2948100146d29f4/1635304037293-b334bebfed39c3fcba21c48ae4f9043c.jpeg?height=200","description":"<p>Back in 2017, Health Minister Greg Hunt issued a rare apology to Australian women.</p><p>He directed it towards the one in ten who suffer from endometriosis, noting that the condition should have been acknowledged at an earlier time. In a much more powerful way.</p><p>His apology came on behalf of all those in parliament and from the medical system.</p><p>The apology, during an Endo Active event in Canberra, featuring a number of different advocacy groups and “Endo Warriors\" in the room, marked a major turning point for those who suffer from endometriosis in Australia.</p><p>Because previously, endometriosis had gone largely ignored or overlooked.</p><p>On this week’s Women’s Health Project, we’re exploring endometriosis in Australia: how far we’ve come, and the very long way we have to go.</p><p>It takes an average six and a half years for someone to be diagnosed with endometriosis. And even that is an improvement: that figure is down from an average seven to 12 years a decade ago.</p>","author_name":"Agenda Media"}