South Australia faces endometriosis treatment delays, report says

Women in South Australia with endometriosis are facing long waits for diagnosis and treatment. A parliamentary inquiry has found that many suffer due to access issues and a lack of awareness about the condition. Deanna Flynn Wallis, who has struggled with endometriosis since she was 13, shared her story during the inquiry. After years of pain and multiple procedures, she says her symptoms continue to affect her life. She has faced infertility and has undergone various treatments, including a hysterectomy. The inquiry, led by Labor MP Catherine Hutchesson, took a year to gather evidence. Hutchesson, who suffers from endometriosis, emphasized the need for better public awareness. Many women reported being dismissed by doctors who told them to take painkillers instead of offering proper treatment. The report highlights that at least one in seven women in Australia has endometriosis. Major factors causing delays include social normalization of pain, limited access to healthcare providers, treatment costs, and inadequate education around the condition. The recommendations aim to enhance training for medical staff, launch a public health campaign, and improve education in schools. Hutchesson stressed the importance of informing young women about what constitutes abnormal pain and encouraging them to seek help. Health Minister Chris Picton expressed the government's commitment to reform. He stated that treating endometriosis must change, and acknowledged the need for society and medical professionals to listen to women's experiences. Flynn Wallis called the release of the report a historic moment. She plans to continue advocating for better treatment and support for others affected by endometriosis, humorously noting her intention to be more persistent in pushing for changes.