Why does it take so lengthy to diagnose endometriosis, in line with one knowledgeable?

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Woman having pain in the bedroom

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It is estimated that one in ten women around the world is affected by endometriosis. This corresponds to 176 million people. For the past decade, activists and charities have worked tirelessly to raise the profile of the condition that can cause sufferers to weaken chronic pain. However, research suggests that there are still misconceptions related to endometriosis in the medical community and society that prevent people from getting the help they need. Why does endometriosis take so long to diagnose? Studies have shown that sufferers had to wait an average of seven and a half years before getting answers from doctors about symptoms and a diagnosis of endometriosis.

Endometriosis has tissue elsewhere in your body that is similar to the lining of the womb. Research has looked at what causes endometriosis, but the cause is unknown. Endometriosis lesions can be found on the ovaries, fallopian tubes, pelvic side walls, bladder, intestines and intestines, among others.

The most common symptom associated with endometriosis is chronic pain. In a similar way to the way the lining of the uterus loosens on a monthly basis, endometriosis lesions can swell and bleed. However, the blood cannot leave the body. This can be completely debilitating, and research has shown that it can take an average of seven years for patients to get an endometriosis diagnosis.

“Normalizing painful symptoms is a big problem. And there is still very little detection of endometriosis by the general practitioner. That is where a young woman would go with her painful symptoms, “says Lone Hummelshoj, executive director of the World Endometriosis Society and the World Endometriosis Research Foundation.” If these symptoms are dismissed as primary dysmenorrhea, for some people it may not be a doctor conduct further examinations, which will help delay diagnosis and timely treatment of symptomatic endometriosis. “

Due to the fact that there is no simple test that can diagnose endometriosis and there are a number of misconceptions and myths associated with the condition, patients can manage their symptoms for years without the help of doctors. Currently, a clinician can only test endometriosis through laparoscopy. This is where a small camera is inserted into the pelvis so the doctor can look for signs of endometriosis. This can be invasive, and some patients even have difficulty seeing a doctor who is experienced in treating endometriosis to perform such a procedure.

“In a prospective study conducted by the World Endometriosis Research Foundation (WERF), we found that 50% of people referred to a gastroenterologist with bowel problems actually had endometriosis and no bowel problems. People with painful symptoms need to see a gynecologist, and it’s not about going to a gynecologist, “says Hummelshoj.” It has to be someone who specializes in treating endometriosis, or who can turn to someone who is. “

WERF’s studies have also shown that some symptoms of endometriosis are shared with other conditions. This could explain why some people have to wait years between their first appointment and being diagnosed with endometriosis.

While activists have campaigned to raise awareness about the disease, many myths and misconceptions related to endometriosis still exist. Many people with painful symptoms associated with endometriosis experience them as early as their teens. However, due to misunderstandings, they are not diagnosed until many years later. If you are of legal age to have a period, you could have endometriosis. Similarly, the pill has been introduced as a cure for endometriosis in the past. There is no cure for endometriosis, only ways to deal with symptoms. Some have also proposed a hysterectomy as a cure for endometriosis. By definition, endometriosis is “endometrial tissue” that grows outside the uterus. So removing the uterus will not eliminate the symptoms.

The normalization of menstrual pain and the myths associated with endometriosis make it difficult for people to be diagnosed quickly. The pain associated with the condition is chronic and can make working, socializing, and completing everyday tasks incredibly difficult. More research needs to be done on the disease that affects so many people around the world.

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