Endometriosis affects women, girls, transgender men, and gender-diverse and non-binary people of all races, ethnicities, and socio-economic groups. The symptoms of endometriosis can be highly individual and may depend on location and severity of the disease, even though there is not always a connection between the extent of the disease and the symptoms. Some people have very little endometriosis but a lot of pain, while others have severe endometriosis without experiencing any symptoms at all.
The most common symptom of endometriosis is pain, which can present in a variety of ways.
In addition to pain, you may experience:
It is difficult to live with chronic pain. People with endometriosis experience higher rates of other pain conditions such as irritable bowel syndrome, migraines, and fibromyalgia. There is also an increased risk of ovarian and other gynaecological cancers.
The severity and frequency of these symptoms, including pain, can increase as people age. For people who do experience one or multiple symptoms, endometriosis can have a large effect on their social life, school or professional aspirations, health, and finances. Ongoing symptoms like severe pain, fatigue, and infertility can prevent people from going to work or school. Painful sex or bleeding during sex can lead to avoiding intercourse and can put stress on a person or relationship. Together, these can impact people’s quality of life, result in social exclusion, diminish self-esteem, and heighten their anxiety or depression. Feelings of uncertainty, anxiety, and depression may be higher among people who feel that they have been dismissed by friends, family, or medical professionals, and among those who have experienced systemic oppressions, delays to diagnosis, and medical trauma. Said feelings may also appear in realms where culturally safe, trauma-informed, and/or gender-affirming care is not available.