Endometriosis Is Often Ignored in Teenage Girls

Key points
- Senie Byrne began menstruating at 15, and she quickly became an expert in pain management.
- "They told me that it was all part of being a woman, and that there was nothing they could do for me," said Ms.
- Finally, when she was 21, a doctor performed a laparoscopy to see what was going on.
- Byrne said she was somewhat relieved to finally have a name for what had been ailing her.
Senie Byrne began menstruating at 15, and she quickly became an expert in pain management. Every month, it felt as if 1,000 darts had plunged into her abdomen; she sometimes passed out from the cramps. She was often nauseated, constipated and exhausted. At times, she had diarrhea. She said she saw 22 doctors over the years, but none took her seriously.
"They told me that it was all part of being a woman, and that there was nothing they could do for me," said Ms. Byrne, 29, who works in financial services in Leesburg, Va. One doctor gave her a prescription for Prozac, telling her it was all in her head.
Finally, when she was 21, a doctor performed a laparoscopy to see what was going on. The diagnosis: severe endometriosis, a hormone and immune system disease in which uterine tissue is found outside the uterus, causing lesions in the ovaries, fallopian tubes, abdominal lining, bowel or bladder. While it is not known how or why uterine cells form in other parts of the body, the lesions can cause inflammation and debilitating pain.
Ms. Byrne said she was somewhat relieved to finally have a name for what had been ailing her. "I knew something was wrong when I was 15, but no one listened to me," she said.
An estimated 89 million women worldwide, including 6.5 million in the United States and Canada, have endometriosis, according to the Endometriosis Association, a research and advocacy group. Symptoms can include debilitating periods, painful bowel movements with menstruation, inflammation, internal bleeding, scar tissue and infertility.
But those numbers are rough, experts say, because many young girls with endo, as it is called, do not find out until years later. In fact, research from the Endometriosis Association estimates that it can take up to 10 years from the onset of pain for a doctor to give a diagnosis of endometriosis, largely because many physicians do not believe the disease affects teenagers. By that time, the damage has been done.
"The medical teaching on endometriosis was that it's a disease of women in their reproductive years, not adolescents," said Mary Lou Ballweg, the president and executive director of the Endometriosis Association. "Many times, we hear that girls are told they're too young to have the disease, they're trying to get out of school, or that they're exaggerating. Add the misconception that pain with menstruation is normal, and you get a bundle of confusion. And not the least, most gynecologists are uncomfortable treating adolescent gynecological problems, and pediatricians don't."
Jill Fuersich, 31, a preschool teacher in Manhattan, first had her period when she was 12. She often missed school days and social events because she was in agony. "The doctors said that it was normal to have a period that was painful," she said.
She bounced among gynecologists and gastroenterologists for a decade until she finally received a endometriosis diagnosis at 23. She was given birth control pills and a progesterone IUD, which were supposed to ease the symptoms. They did not.
Written and revised by
David Cohen, M.D.
Our doctors write and review articles for accuracy and keep them up to date.
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