Endometriosis Awareness Month: More than just a ‘women’s problem’
Why does a disease which causes pain and infertility, and which affects around 1 in 10 people with uteruses*, take up to ten years to diagnose?
Endometriosis is common and debilitating. Deposits of tissue resembling the lining of the womb are left in places they would not normally occur. The ovaries, tubes and walls of the pelvis are common targets. The bladder and bowel can be affected and, on rare occasions, far-flung body parts such as the liver can be involved. With every period the deposits bleed, setting off a vicious cycle of inflammation and scarring.
People with endometriosis commonly experience very painful periods and painful sex. Some will also have pelvic pain which can last throughout the cycle. Bowel symptoms, such as bloating and diarrhoea, are common and are often put down to irritable bowel syndrome. Symptoms of bladder irritation are experienced by two-thirds of sufferers. Fertility is often reduced. In advanced cases, scarring in the pelvis makes it difficult for an egg and sperm to meet and fertilise. Even in mild cases, a cocktail of inflammatory substances in the pelvis can be toxic to eggs and embryos.
The daily effects of living with chronic illness, including managing pain and associated fatigue, extend to all areas of women’s lives. Depression and anxiety are very common. The impact on relationships and sex, plans for a family, and career and productivity, can be immense. To add further difficulty, many will have a long and difficult journey towards diagnosis and proper management, with multiple attendances at their General Practitioner and Emergency Care.
Some will have been told outright, or by implication, that they are simply not managing the normal business of being a woman. From a medical point of view, they can be considered challenging patients, because they attend frequently and never seem to get better.
Why is this difficult to talk about?
There are a number of reasons for the long delay in diagnosis. Firstly, endometriosis touches on a number of issues which are considering challenging, if not exactly taboo, in our culture. It is a disease of people with uteruses – and one which involves direct discussion of sex, periods and fertility. For many people, it also involves chronic pain, another difficult topic. Secondly, young people may be told, by parents and doctors, that period pain is a normal part of the experience of being someone who menstruates. Thirdly, classical teaching for doctors has been that endometriosis is a disease of older people. As a result, it was not something which was usually considered a problem in teenagers and young people.
How, then, can we improve things for this large and somewhat disenfranchised group of patients? In recent years, the growing evidence base around endometriosis has started to improve our understanding. We know that it can and does present in young women, and indeed that it may be aggressive at this stage. We now know that it is associated with other health problems such as asthma and eczema, and that it seems to also be linked with more serious autoimmune problems, such as inflammatory bowel disease. There seems to be a genetic link – and it is more likely where a family member are also affected.
With this improved knowledge comes the power to recognise and to treat earlier. The key message for women and doctors is that disabling period pain is not normal. Women who are routinely struggling with severe period pain or pain during sex should seek medical advice.
Doctors who are considering the diagnosis should then refer women to a gynaecologist with a special interest in endometriosis, or, ideally, to a specialist treatment centre. To diagnose endometriosis properly, a small operation known as a laparoscopy is needed. Patches of endometriosis can be treated surgically, or through hormonal medical treatments, such as the pill. Women can connect with other women through contact with an active network of support groups.
Through better recognition of the common symptoms, people can receive a timely diagnosis and can then start to consider their management options. Only then will we start to improve the long diagnostic delay and quality of life for women with endometriosis.
*Not all people who menstruate or have Endometriosis identify as a womxn
About the Author
Jenny Johnston is an academic General Practitioner and educationalist. Her research employs a range of methodologies, including grounded theory, phenomenology and discourse analysis. Her Ph.D. work explores the construction of professional identity in general practice training. Other current projects focus on using sociocultural theory to explore assessment processes. As a clinician, her academic work is grounded in the need to improve patient care through high quality medical education research.