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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 

 

Upcoming Webinar

 

As part of Endometriosis Awareness Month, this EFIC webinar brings together authors of two recent European Journal of Pain studies to explore emerging insights into the mechanisms of endometriosis-associated pain. Despite its high prevalence, pain in endometriosis remains complex, heterogeneous, and challenging to assess and manage. The session will highlight new evidence on sensory profiles, quantitative sensory testing, and bodily–emotional pain mapping in people with endometriosis, offering a deeper understanding of peripheral and central pain mechanisms beyond lesion-based explanations. Speakers will discuss how these findings contribute to improved pain phenotyping and what they may mean for clinical assessment, research design, and future pain management strategies.

When?
17 March 2026

12:30 PM CET

Register here:
https://us06web.zoom.us/webinar/register/WN_XKj8kKN8RaKqVZ-quF_XHA#/registration

 

Further Reading

 

The role of catastrophizing in enhancing pain interference and depressive symptoms in endometriosis: A longitudinal examination

Quantitative sensory testing in endometriosis patients with cyclic vs. non-cyclic pain—A case–control study

Pain, emotions, interoception, and bodily sensations in patients with endometriosis

For detailed information about endometriosis, please visit the Endometriosis Awareness Month website: https://endometriosisassn.org/ 

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