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A woman who endured excruciating menstrual pain for two decades finally received a diagnosis that shed light on a long-standing mystery, which began troubling her long before she entered her teenage years.
Jen Moore, a 35-year-old former wedding cake baker from Cambridge, England, faced debilitating menstrual cramps since she was just 11 years old. She described her inability to stand up straight when the painful periods began, a shocking experience for someone so young.
Desperate for relief, Moore turned to medical professionals who prescribed birth control pills in an effort to reduce her painful symptoms. However, years of using contraceptives yielded little respite. Doctors repeatedly assured her that her experience was “normal,” attributing her suffering to bad luck rather than a serious medical condition.
During the COVID lockdown, Moore stopped taking contraceptives after 22 years and revealed that the absence of medication transformed her reality. “I didn’t recognize the person I became,” she stated, explaining that she often fainted due to the severe pain and excessive blood loss.
When seeking further evaluation, Moore underwent an ultrasound, which failed to detect any signs of endometriosis. Unsatisfied with this result, she took the initiative to pay for an MRI, which ultimately led to a diagnosis of endometriosis and adenomyosis. Both conditions occur when the uterine lining grows outside its normal location.
Reflecting on her ordeal, Moore expressed feelings of heartbreak and anger toward the healthcare system. “At the time, I thought it was normal because I didn’t know any different,” she noted. Despite her mother’s efforts to seek help, medical professionals dismissed their concerns, claiming that her painful periods would eventually subside.
Moore lamented, “I feel rage at what happened to me… and heartbroken, thinking about myself as an 11-year-old who had no idea she was about to go through so many of these things.” Nevertheless, she also feels hopeful, noting that younger generations are becoming more vocal about their pain and demanding changes.
Despite her diagnosis, Moore continues to grapple with the consequences of endometriosis, which has caused damage to her organs for 22 years. She confessed, “There is still a lot of endometriosis for me,” emphasizing that surgeries are not a guaranteed cure.
Janet Lindsay, CEO of Wellbeing of Women, advocates for heightened awareness of endometriosis. She expressed that for too long, women’s pain has been overlooked and misunderstood. There is an urgent need for better diagnostic practices, increased awareness, and stronger support systems for those suffering from this painful condition.
This case adds to a growing narrative around women’s health issues that often remain underreported or dismissed. Last year, Bindi Irwin, daughter of the late Steve Irwin, also opened up about her diagnosis of endometriosis after years of being misdiagnosed for various diseases.
Irwin stated, “I was tested for everything… I had every blood test and scan imaginable.” Her experience parallels Moore’s and highlights the critical need for healthcare reform concerning women’s pain and reproductive health.
According to the Mayo Clinic, endometriosis is a condition where cells similar to the uterine lining grow outside of the uterus, which can result in significant pain and fertility issues. This chronic illness affects countless women, often leading to years of suffering before a proper diagnosis is made.
As awareness increases, it becomes evident that women’s health deserves greater attention and advocacy. Moore’s experience, while deeply personal, represents the struggle many face when seeking understanding and validation in their health journeys.
Lauryn Overhultz of Fox News Digital contributed reporting.