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For over 20 years, Jen Moore endured intense pain during her menstrual cycles, a struggle that began at the tender age of 11. A recent diagnosis has finally shed light on her condition, unraveling a long-standing medical mystery.
Now 35 and living in Cambridge, England, Moore initially faced debilitating pain during her periods. Medical professionals suggested birth control pills to alleviate her suffering, yet the pain persisted unchecked. Despite seeking help, doctors dismissed her distress as “normal,” labeling her merely as someone unlucky to experience heavy menstrual periods.
The COVID-19 lockdown marked a significant turning point in Moore’s journey. After halting contraceptive use for the first time in 22 years, she found herself grappling with debilitating pain and frequent fainting spells due to severe blood loss. An ultrasound examination offered little relief; physicians reported no signs of endometriosis, deepening her frustration.
Determined to find answers, Moore opted to pay for an MRI scan out of her own pocket. This decision ultimately led to the diagnosis of endometriosis and adenomyosis—conditions where uterine lining cells grow inappropriately, often causing severe pain.
Moore recounted her experiences, stating, “At the time, I thought it was normal because I didn’t know any different.” Reflecting on her childhood, she expressed sadness over the lack of understanding surrounding her painful periods, which persisted despite assurances from doctors that they would eventually cease.
Even today, Moore feels “rage” over her medical ordeal and sadness for her younger self, who was unaware of the struggles ahead. Nevertheless, she finds solace in the growing movement of individuals advocating for better recognition and treatment of endometriosis. “I feel hope that generations are standing up and that they don’t want to tolerate this anymore,” she stated compellingly.
Despite her diagnosis, Moore described feelings of exhaustion and frustration, indicating that no aspect of her life remains untouched by her condition. Chronic pain has shaped her existence, with periods so severe that a week every month left her nearly immobile. She has also discovered endometriosis affecting her bowels and bladder, complicating her situation.
Moore reflected on the significant damage her body has sustained over the years due to undiagnosed endometriosis, noting: “That’s a lot of damage to unpick, so surgeries are never magic and [don’t] always provide a pain-free life.” She acknowledged that a considerable amount of endometriosis remains, leaving her to confront her situation head-on.
Janet Lindsay, CEO of Wellbeing of Women, echoed the urgency of recognizing endometriosis. “For too long, women’s pain has been dismissed or misunderstood,” she emphasized. There is a pressing need for improved awareness, early diagnoses, and enhanced support for those living with this debilitating condition.
The conversation surrounding endometriosis has gained momentum, with individuals like Bindi Irwin sharing their struggles. Irwin revealed her own decade-long battle with misdiagnosis before undergoing surgery for endometriosis.
According to the Mayo Clinic, endometriosis occurs when tissue similar to the uterine lining grows outside the uterus, commonly affecting the pelvic region. This condition can lead to severe pain and fertility issues, impacting the lives of countless women.
As more patients like Moore share their stories, the hope remains that awareness and understanding will lead to better outcomes for future generations. For those suffering silently, recognizing their pain is the first step toward advocacy and improved care.