March marks Endometriosis Awareness Month, an annual initiative led by The Endometriosis Association to raise awareness of this common but often under-reported chronic disease. Educational events and fundraising efforts occur throughout the month in order to shed light on the challenges faced by those living with endometriosis, and emphasise the urgent need for better quality research, diagnosis, and treatment options.
Endometriosis is a complex hormonal and immune disease affecting an estimated 190 million women and individuals worldwide. One of its most debilitating symptoms is chronic pain, which significantly impacts quality of life. It is widely recognised, yet awareness and education about endometriosis remain limited, leading to an average diagnostic delay of several years. According to Lavefjord, et al., (2025), published in The European Journal of Pain, Endometriosis is commonly understudied, despite the fact that individuals with Endometriosis suffer pain on over 26 days of the month on average.
Research also emphasises the link to a higher risk of developing additional health disorders, highlighting the necessity of increased support. Recognising The Endometriosis Association as a vital advocate since 1993, this month is a critical opportunity to raise awareness, provide patient support, and advocate for research funding. Chronic pain is the most prominent and distressing symptoms of endometriosis. This usually surfaces through:
- Painful periods
- Pain during or after sexual activity
- Painful urination or bowel movements during menstruation
- Chronic abdominal and pelvic pain
For detailed information about endometriosis, please visit the Endometriosis Awareness Month website: https://endometriosisassn.org/
Download the open-access article on The European Journal of Pain here: https://onlinelibrary.wiley.com/doi/epdf/10.1002/ejp.4781
For more information, feel free to watch these previous two webinars on Endometriosis on EFIC’s YouTube page.
