The diagnosis wait time for endometriosis has stretched to nearly a decade, especially in Wales, according to recent research by Endometriosis UK. Women endure prolonged pain and dismissive attitudes from healthcare providers, with many visiting their GP numerous times before diagnosis. Despite efforts to raise awareness, inadequate access to specialist care persists, leaving patients unsupported. The Welsh government acknowledges the need for improvement but more comprehensive reforms are essential to address the systemic barriers to timely diagnosis and treatment.
What steps do you believe are necessary to improve the timely diagnosis and treatment of endometriosis, and how can society better support individuals affected by this condition?
It’s so disheartening to hear about the significant delays in diagnosis, especially considering the immense physical and emotional toll it takes on women. It’s frustrating to see how often symptoms are dismissed or trivialized
I think there needs to be more awareness about this condition so that women can seek help sooner. What do you think needs to happen to speed up the diagnosis of endometriosis and make sure people get the specialist care they need? And how can we all pitch in to support those dealing with this condition?
I think there needs to be greater recognition of the impact of endometriosis on individuals’ lives. By raising awareness about it, hopefully, reduction of waiting time would follow naturally
